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PubMed code 22712585

Compile data set for download or QSAR
Found 106 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kJ/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50049479
PNG
((S)-6-Amino-2-{(R)-2-[(S)-2-{(S)-2-[(R)-2-[(S)-2-a...)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O
Show InChI InChI=1S/C46H56N12O6/c1-27(54-44(62)39(20-29-23-51-35-15-7-5-13-32(29)35)57-43(61)34(48)22-31-25-50-26-53-31)42(60)56-40(21-30-24-52-36-16-8-6-14-33(30)36)46(64)58-38(19-28-11-3-2-4-12-28)45(63)55-37(41(49)59)17-9-10-18-47/h2-8,11-16,23-27,34,37-40,51-52H,9-10,17-22,47-48H2,1H3,(H2,49,59)(H,50,53)(H,54,62)(H,55,63)(H,56,60)(H,57,61)(H,58,64)/t27-,34-,37-,38+,39+,40-/m0/s1
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n/an/a 6.08n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50370294
PNG
(Examorelin | HEXARELIN | US9708370, Hexareline)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c(C)[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O
Show InChI InChI=1S/C47H58N12O6/c1-27-34(33-15-7-9-17-37(33)54-27)23-41(58-44(62)35(49)22-31-25-51-26-53-31)45(63)55-28(2)43(61)57-40(21-30-24-52-36-16-8-6-14-32(30)36)47(65)59-39(20-29-12-4-3-5-13-29)46(64)56-38(42(50)60)18-10-11-19-48/h3-9,12-17,24-26,28,35,38-41,52,54H,10-11,18-23,48-49H2,1-2H3,(H2,50,60)(H,51,53)(H,55,63)(H,56,64)(H,57,61)(H,58,62)(H,59,65)/t28-,35-,38-,39+,40-,41+/m0/s1
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n/an/a 15.9n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394979
PNG
(CHEMBL18872)
Show SMILES Cc1[nH]c2ccccc2c1C[C@@H](NC(=O)[C@@H](Cc1c(C)[nH]c2ccccc12)NC(=O)C(C)(C)N)C(N)=O
Show InChI InChI=1S/C28H34N6O3/c1-15-19(17-9-5-7-11-21(17)31-15)13-23(25(29)35)33-26(36)24(34-27(37)28(3,4)30)14-20-16(2)32-22-12-8-6-10-18(20)22/h5-12,23-24,31-32H,13-14,30H2,1-4H3,(H2,29,35)(H,33,36)(H,34,37)/t23-,24-/m1/s1
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n/an/a 62.9n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395006
PNG
(CHEMBL2163473)
Show SMILES C[C@H](NC(=O)N(Cc1cccc2ccccc12)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H56N12O6/c1-29(54-47(65)59(58-44(62)37(49)24-34-26-51-28-53-34)27-32-16-11-15-31-14-5-6-17-35(31)32)43(61)56-41(23-33-25-52-38-19-8-7-18-36(33)38)46(64)57-40(22-30-12-3-2-4-13-30)45(63)55-39(42(50)60)20-9-10-21-48/h2-8,11-19,25-26,28-29,37,39-41,52H,9-10,20-24,27,48-49H2,1H3,(H2,50,60)(H,51,53)(H,54,65)(H,55,63)(H,56,61)(H,57,64)(H,58,62)/t29-,37?,39-,40+,41-/m0/s1
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n/an/a 465n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395024
PNG
(CHEMBL2163444 | US9708370, CP-2A(v))
Show SMILES C[C@H](N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)NNC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C41H51N11O6/c1-24(43)37(54)48-35(21-27-23-46-31-16-8-6-14-29(27)31)40(57)51-52-41(58)50-34(20-26-22-45-30-15-7-5-13-28(26)30)39(56)49-33(19-25-11-3-2-4-12-25)38(55)47-32(36(44)53)17-9-10-18-42/h2-8,11-16,22-24,32-35,45-46H,9-10,17-21,42-43H2,1H3,(H2,44,53)(H,47,55)(H,48,54)(H,49,56)(H,51,57)(H2,50,52,58)/t24-,32-,33+,34-,35+/m0/s1
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n/an/a 568n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394997
PNG
(CHEMBL2163482 | US9708370, DBG-253-6)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1cccc2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H56N12O6/c1-29(54-45(63)41(23-33-25-52-38-19-8-7-18-36(33)38)56-44(62)37(49)24-34-26-51-28-53-34)43(61)58-59(27-32-16-11-15-31-14-5-6-17-35(31)32)47(65)57-40(22-30-12-3-2-4-13-30)46(64)55-39(42(50)60)20-9-10-21-48/h2-8,11-19,25-26,28-29,37,39-41,52H,9-10,20-24,27,48-49H2,1H3,(H2,50,60)(H,51,53)(H,54,63)(H,55,64)(H,56,62)(H,57,65)(H,58,61)/t29-,37-,39-,40+,41+/m0/s1
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n/an/a 723n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395005
PNG
(CHEMBL2163474)
Show SMILES C[C@H](NC(=O)N(CCc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H56N12O6/c1-28(51-44(62)56(21-19-29-12-4-2-5-13-29)55-41(59)34(46)24-32-26-48-27-50-32)40(58)53-38(23-31-25-49-35-17-9-8-16-33(31)35)43(61)54-37(22-30-14-6-3-7-15-30)42(60)52-36(39(47)57)18-10-11-20-45/h2-9,12-17,25-28,34,36-38,49H,10-11,18-24,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,62)(H,52,60)(H,53,58)(H,54,61)(H,55,59)/t28-,34?,36-,37+,38-/m0/s1
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n/an/a 729n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395009
PNG
(CHEMBL2163470)
Show SMILES Cc1[nH]c2ccccc2c1C[C@@H](NC(=O)[C@@H]1Cc2cccc3CC[C@H](N)C(=O)N1c23)C(=O)N[C@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C57H70N12O7/c1-33-40(39-19-6-8-21-43(39)63-33)31-48(68-56(75)49-30-36-17-13-16-35-24-25-41(60)57(76)69(49)50(35)36)55(74)65-45(23-10-12-27-59)52(71)67-47(29-37-32-62-42-20-7-5-18-38(37)42)54(73)66-46(28-34-14-3-2-4-15-34)53(72)64-44(51(61)70)22-9-11-26-58/h2-8,13-21,32,41,44-49,62-63H,9-12,22-31,58-60H2,1H3,(H2,61,70)(H,64,72)(H,65,74)(H,66,73)(H,67,71)(H,68,75)/t41-,44-,45+,46+,47-,48+,49-/m0/s1
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n/an/a 750n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394996
PNG
(CHEMBL2163348 | US9708370, DBG-253-7)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H55N11O7/c1-26(51-42(60)38(21-29-23-49-34-12-6-5-11-32(29)34)54-41(59)33(46)22-30-24-48-25-50-30)40(58)53-36(20-28-14-16-31(56)17-15-28)44(62)55-37(19-27-9-3-2-4-10-27)43(61)52-35(39(47)57)13-7-8-18-45/h2-6,9-12,14-17,23-26,33,35-38,49,56H,7-8,13,18-22,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,58)(H,54,59)(H,55,62)/t26-,33-,35-,36-,37+,38+/m0/s1
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n/an/a 771n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395003
PNG
(CHEMBL2163476 | US9708370, DBG-188p)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C44H53N13O6/c45-17-9-8-16-35(39(47)58)52-41(60)36(18-26-10-2-1-3-11-26)54-42(61)37(19-27-22-49-33-14-6-4-12-30(27)33)55-44(63)57-56-43(62)38(20-28-23-50-34-15-7-5-13-31(28)34)53-40(59)32(46)21-29-24-48-25-51-29/h1-7,10-15,22-25,32,35-38,49-50H,8-9,16-21,45-46H2,(H2,47,58)(H,48,51)(H,52,60)(H,53,59)(H,54,61)(H,56,62)(H2,55,57,63)/t32-,35-,36+,37-,38+/m0/s1
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n/an/a 808n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395009
PNG
(CHEMBL2163470)
Show SMILES Cc1[nH]c2ccccc2c1C[C@@H](NC(=O)[C@@H]1Cc2cccc3CC[C@H](N)C(=O)N1c23)C(=O)N[C@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C57H70N12O7/c1-33-40(39-19-6-8-21-43(39)63-33)31-48(68-56(75)49-30-36-17-13-16-35-24-25-41(60)57(76)69(49)50(35)36)55(74)65-45(23-10-12-27-59)52(71)67-47(29-37-32-62-42-20-7-5-18-38(37)42)54(73)66-46(28-34-14-3-2-4-15-34)53(72)64-44(51(61)70)22-9-11-26-58/h2-8,13-21,32,41,44-49,62-63H,9-12,22-31,58-60H2,1H3,(H2,61,70)(H,64,72)(H,65,74)(H,66,73)(H,67,71)(H,68,75)/t41-,44-,45+,46+,47-,48+,49-/m0/s1
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n/an/a 1.11E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394983
PNG
(CHEMBL2163466)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H61N11O6/c1-29(2)28-58(57-46(63)41(55-43(60)38-20-12-22-50-38)25-32-27-52-36-18-9-7-16-34(32)36)47(64)56-40(24-31-26-51-35-17-8-6-15-33(31)35)45(62)54-39(23-30-13-4-3-5-14-30)44(61)53-37(42(49)59)19-10-11-21-48/h3-9,13-18,26-27,29,37-41,50-52H,10-12,19-25,28,48H2,1-2H3,(H2,49,59)(H,53,61)(H,54,62)(H,55,60)(H,56,64)(H,57,63)/t37-,38-,39+,40-,41+/m0/s1
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n/an/a 1.17E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395002
PNG
(CHEMBL2163477 | US9708370, DBG-201-A)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C48H61N13O6/c1-29(2)27-61(60-47(66)42(22-32-25-54-38-17-9-7-15-35(32)38)57-44(63)36(50)23-33-26-52-28-55-33)48(67)59-41(21-31-24-53-37-16-8-6-14-34(31)37)46(65)58-40(20-30-12-4-3-5-13-30)45(64)56-39(43(51)62)18-10-11-19-49/h3-9,12-17,24-26,28-29,36,39-42,53-54H,10-11,18-23,27,49-50H2,1-2H3,(H2,51,62)(H,52,55)(H,56,64)(H,57,63)(H,58,65)(H,59,67)(H,60,66)/t36-,39-,40+,41-,42+/m0/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395001
PNG
(CHEMBL2163478 | US9708370, DBG-253-1)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O6/c1-27(50-41(59)37(21-30-23-48-34-17-9-8-16-32(30)34)52-40(58)33(45)22-31-24-47-26-49-31)39(57)54-55(25-29-14-6-3-7-15-29)43(61)53-36(20-28-12-4-2-5-13-28)42(60)51-35(38(46)56)18-10-11-19-44/h2-9,12-17,23-24,26-27,33,35-37,48H,10-11,18-22,25,44-45H2,1H3,(H2,46,56)(H,47,49)(H,50,59)(H,51,60)(H,52,58)(H,53,61)(H,54,57)/t27-,33-,35-,36+,37+/m0/s1
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n/an/a 1.34E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394999
PNG
(CHEMBL2163480 | US9708370, DBG-253-3)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C49H58N12O6/c1-31(56-47(65)43(25-36-27-54-40-17-9-8-16-38(36)40)58-46(64)39(51)26-37-28-53-30-55-37)45(63)60-61(29-33-19-21-35(22-20-33)34-14-6-3-7-15-34)49(67)59-42(24-32-12-4-2-5-13-32)48(66)57-41(44(52)62)18-10-11-23-50/h2-9,12-17,19-22,27-28,30-31,39,41-43,54H,10-11,18,23-26,29,50-51H2,1H3,(H2,52,62)(H,53,55)(H,56,65)(H,57,66)(H,58,64)(H,59,67)(H,60,63)/t31-,39-,41-,42+,43+/m0/s1
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n/an/a 1.34E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395004
PNG
(CHEMBL2163475)
Show SMILES C[C@H](NC(=O)N(Cc1ccc(cc1)-c1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C49H58N12O6/c1-31(56-49(67)61(60-46(64)39(51)26-37-28-53-30-55-37)29-33-19-21-35(22-20-33)34-14-6-3-7-15-34)45(63)58-43(25-36-27-54-40-17-9-8-16-38(36)40)48(66)59-42(24-32-12-4-2-5-13-32)47(65)57-41(44(52)62)18-10-11-23-50/h2-9,12-17,19-22,27-28,30-31,39,41-43,54H,10-11,18,23-26,29,50-51H2,1H3,(H2,52,62)(H,53,55)(H,56,67)(H,57,65)(H,58,63)(H,59,66)(H,60,64)/t31-,39?,41-,42+,43-/m0/s1
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n/an/a 1.64E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395007
PNG
(CHEMBL2163472)
Show SMILES C[C@H](NC(=O)N(Cc1ccc(O)cc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O7/c1-26(50-43(62)55(24-28-14-16-31(56)17-15-28)54-40(59)33(45)21-30-23-47-25-49-30)39(58)52-37(20-29-22-48-34-12-6-5-11-32(29)34)42(61)53-36(19-27-9-3-2-4-10-27)41(60)51-35(38(46)57)13-7-8-18-44/h2-6,9-12,14-17,22-23,25-26,33,35-37,48,56H,7-8,13,18-21,24,44-45H2,1H3,(H2,46,57)(H,47,49)(H,50,62)(H,51,60)(H,52,58)(H,53,61)(H,54,59)/t26-,33?,35-,36+,37-/m0/s1
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n/an/a 1.80E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50049479
PNG
((S)-6-Amino-2-{(R)-2-[(S)-2-{(S)-2-[(R)-2-[(S)-2-a...)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O
Show InChI InChI=1S/C46H56N12O6/c1-27(54-44(62)39(20-29-23-51-35-15-7-5-13-32(29)35)57-43(61)34(48)22-31-25-50-26-53-31)42(60)56-40(21-30-24-52-36-16-8-6-14-33(30)36)46(64)58-38(19-28-11-3-2-4-12-28)45(63)55-37(41(49)59)17-9-10-18-47/h2-8,11-16,23-27,34,37-40,51-52H,9-10,17-22,47-48H2,1H3,(H2,49,59)(H,50,53)(H,54,62)(H,55,63)(H,56,60)(H,57,61)(H,58,64)/t27-,34-,37-,38+,39+,40-/m0/s1
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n/an/a 1.82E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50370294
PNG
(Examorelin | HEXARELIN | US9708370, Hexareline)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c(C)[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O
Show InChI InChI=1S/C47H58N12O6/c1-27-34(33-15-7-9-17-37(33)54-27)23-41(58-44(62)35(49)22-31-25-51-26-53-31)45(63)55-28(2)43(61)57-40(21-30-24-52-36-16-8-6-14-32(30)36)47(65)59-39(20-29-12-4-3-5-13-29)46(64)56-38(42(50)60)18-10-11-19-48/h3-9,12-17,24-26,28,35,38-41,52,54H,10-11,18-23,48-49H2,1-2H3,(H2,50,60)(H,51,53)(H,55,63)(H,56,64)(H,57,61)(H,58,62)(H,59,65)/t28-,35-,38-,39+,40-,41+/m0/s1
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n/an/a 2.08E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395001
PNG
(CHEMBL2163478 | US9708370, DBG-253-1)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O6/c1-27(50-41(59)37(21-30-23-48-34-17-9-8-16-32(30)34)52-40(58)33(45)22-31-24-47-26-49-31)39(57)54-55(25-29-14-6-3-7-15-29)43(61)53-36(20-28-12-4-2-5-13-28)42(60)51-35(38(46)56)18-10-11-19-44/h2-9,12-17,23-24,26-27,33,35-37,48H,10-11,18-22,25,44-45H2,1H3,(H2,46,56)(H,47,49)(H,50,59)(H,51,60)(H,52,58)(H,53,61)(H,54,57)/t27-,33-,35-,36+,37+/m0/s1
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n/an/a 2.77E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395002
PNG
(CHEMBL2163477 | US9708370, DBG-201-A)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C48H61N13O6/c1-29(2)27-61(60-47(66)42(22-32-25-54-38-17-9-7-15-35(32)38)57-44(63)36(50)23-33-26-52-28-55-33)48(67)59-41(21-31-24-53-37-16-8-6-14-34(31)37)46(65)58-40(20-30-12-4-3-5-13-30)45(64)56-39(43(51)62)18-10-11-19-49/h3-9,12-17,24-26,28-29,36,39-42,53-54H,10-11,18-23,27,49-50H2,1-2H3,(H2,51,62)(H,52,55)(H,56,64)(H,57,63)(H,58,65)(H,59,67)(H,60,66)/t36-,39-,40+,41-,42+/m0/s1
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n/an/a 2.89E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394995
PNG
(CHEMBL2163483 | US9708370, DBG-253-8)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H55N11O7/c1-26(51-42(60)38(21-29-23-49-34-12-6-5-11-32(29)34)54-41(59)33(46)22-30-24-48-25-50-30)40(58)53-36(20-28-14-16-31(56)17-15-28)44(62)55-37(19-27-9-3-2-4-10-27)43(61)52-35(39(47)57)13-7-8-18-45/h2-6,9-12,14-17,23-26,33,35-38,49,56H,7-8,13,18-22,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,58)(H,54,59)(H,55,62)/t26-,33-,35-,36+,37+,38+/m0/s1
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n/an/a 3.25E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394985
PNG
(CHEMBL2163464)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](C)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H59N11O6/c1-27(2)26-56(55-44(61)39(52-41(58)28(3)47)23-31-25-50-35-18-10-8-16-33(31)35)45(62)54-38(22-30-24-49-34-17-9-7-15-32(30)34)43(60)53-37(21-29-13-5-4-6-14-29)42(59)51-36(40(48)57)19-11-12-20-46/h4-10,13-18,24-25,27-28,36-39,49-50H,11-12,19-23,26,46-47H2,1-3H3,(H2,48,57)(H,51,59)(H,52,58)(H,53,60)(H,54,62)(H,55,61)/t28-,36+,37-,38+,39-/m1/s1
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n/an/a 3.61E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394998
PNG
(CHEMBL2163481 | US9708370, DBG-253-5)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(CCc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H56N12O6/c1-28(51-42(60)38(23-31-25-49-35-17-9-8-16-33(31)35)53-41(59)34(46)24-32-26-48-27-50-32)40(58)55-56(21-19-29-12-4-2-5-13-29)44(62)54-37(22-30-14-6-3-7-15-30)43(61)52-36(39(47)57)18-10-11-20-45/h2-9,12-17,25-28,34,36-38,49H,10-11,18-24,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,59)(H,54,62)(H,55,58)/t28-,34-,36-,37+,38+/m0/s1
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n/an/a 3.74E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394986
PNG
(CHEMBL2163463)
Show SMILES CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)NN(CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H58N10O6/c1-4-40(56)50-39(24-31-26-49-35-19-11-9-17-33(31)35)44(60)54-55(27-28(2)3)45(61)53-38(23-30-25-48-34-18-10-8-16-32(30)34)43(59)52-37(22-29-14-6-5-7-15-29)42(58)51-36(41(47)57)20-12-13-21-46/h5-11,14-19,25-26,28,36-39,48-49H,4,12-13,20-24,27,46H2,1-3H3,(H2,47,57)(H,50,56)(H,51,58)(H,52,59)(H,53,61)(H,54,60)/t36-,37+,38-,39+/m0/s1
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n/an/a 3.86E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394982
PNG
(CHEMBL2163467)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(N)=O |r|
Show InChI InChI=1S/C42H49N11O5/c1-25(2)23-53(52-41(57)37(18-28-21-47-34-15-9-7-13-31(28)34)50-39(55)32(43)19-29-22-45-24-48-29)42(58)51-36(17-27-20-46-33-14-8-6-12-30(27)33)40(56)49-35(38(44)54)16-26-10-4-3-5-11-26/h3-15,20-22,24-25,32,35-37,46-47H,16-19,23,43H2,1-2H3,(H2,44,54)(H,45,48)(H,49,56)(H,50,55)(H,51,58)(H,52,57)/t32-,35+,36-,37+/m0/s1
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n/an/a 4.55E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394984
PNG
(CHEMBL2163465)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H57N11O6/c1-27(2)26-55(54-43(60)38(50-39(56)23-46)22-30-25-49-34-17-9-7-15-32(30)34)44(61)53-37(21-29-24-48-33-16-8-6-14-31(29)33)42(59)52-36(20-28-12-4-3-5-13-28)41(58)51-35(40(47)57)18-10-11-19-45/h3-9,12-17,24-25,27,35-38,48-49H,10-11,18-23,26,45-46H2,1-2H3,(H2,47,57)(H,50,56)(H,51,58)(H,52,59)(H,53,61)(H,54,60)/t35-,36+,37-,38+/m0/s1
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n/an/a 5.41E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395024
PNG
(CHEMBL2163444 | US9708370, CP-2A(v))
Show SMILES C[C@H](N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)NNC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C41H51N11O6/c1-24(43)37(54)48-35(21-27-23-46-31-16-8-6-14-29(27)31)40(57)51-52-41(58)50-34(20-26-22-45-30-15-7-5-13-28(26)30)39(56)49-33(19-25-11-3-2-4-12-25)38(55)47-32(36(44)53)17-9-10-18-42/h2-8,11-16,22-24,32-35,45-46H,9-10,17-21,42-43H2,1H3,(H2,44,53)(H,47,55)(H,48,54)(H,49,56)(H,51,57)(H2,50,52,58)/t24-,32-,33+,34-,35+/m0/s1
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n/an/a 6.06E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395019
PNG
(CHEMBL2163449 | US9708370, CP-2B(v))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H59N11O6/c1-27(2)26-56(55-44(61)39(52-41(58)28(3)47)23-31-25-50-35-18-10-8-16-33(31)35)45(62)54-38(22-30-24-49-34-17-9-7-15-32(30)34)43(60)53-37(21-29-13-5-4-6-14-29)42(59)51-36(40(48)57)19-11-12-20-46/h4-10,13-18,24-25,27-28,36-39,49-50H,11-12,19-23,26,46-47H2,1-3H3,(H2,48,57)(H,51,59)(H,52,58)(H,53,60)(H,54,62)(H,55,61)/t28-,36-,37+,38-,39+/m0/s1
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n/an/a 6.66E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395014
PNG
(CHEMBL2163454 | US9708370, 60 CP-3(iv))
Show SMILES C[C@H](N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O6/c1-25(42)36(52)47-34(22-29-23-44-31-18-10-9-17-30(29)31)38(54)45-26(2)37(53)49-50(24-28-15-7-4-8-16-28)40(56)48-33(21-27-13-5-3-6-14-27)39(55)46-32(35(43)51)19-11-12-20-41/h3-10,13-18,23,25-26,32-34,44H,11-12,19-22,24,41-42H2,1-2H3,(H2,43,51)(H,45,54)(H,46,55)(H,47,52)(H,48,56)(H,49,53)/t25-,26-,32-,33+,34+/m0/s1
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n/an/a 7.58E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395015
PNG
(CHEMBL2163453 | US9708370, CP-2B(i))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](C)C(N)=O |r|
Show InChI InChI=1S/C45H54N12O6/c1-26(2)24-57(56-44(62)39(19-30-22-50-36-16-10-8-14-33(30)36)53-41(59)34(46)20-31-23-48-25-51-31)45(63)55-38(18-29-21-49-35-15-9-7-13-32(29)35)43(61)54-37(17-28-11-5-4-6-12-28)42(60)52-27(3)40(47)58/h4-16,21-23,25-27,34,37-39,49-50H,17-20,24,46H2,1-3H3,(H2,47,58)(H,48,51)(H,52,60)(H,53,59)(H,54,61)(H,55,63)(H,56,62)/t27-,34-,37+,38-,39+/m0/s1
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n/an/a 7.59E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394983
PNG
(CHEMBL2163466)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H61N11O6/c1-29(2)28-58(57-46(63)41(55-43(60)38-20-12-22-50-38)25-32-27-52-36-18-9-7-16-34(32)36)47(64)56-40(24-31-26-51-35-17-8-6-15-33(31)35)45(62)54-39(23-30-13-4-3-5-14-30)44(61)53-37(42(49)59)19-10-11-21-48/h3-9,13-18,26-27,29,37-41,50-52H,10-12,19-25,28,48H2,1-2H3,(H2,49,59)(H,53,61)(H,54,62)(H,55,60)(H,56,64)(H,57,63)/t37-,38-,39+,40-,41+/m0/s1
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n/an/a 7.97E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395015
PNG
(CHEMBL2163453 | US9708370, CP-2B(i))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](C)C(N)=O |r|
Show InChI InChI=1S/C45H54N12O6/c1-26(2)24-57(56-44(62)39(19-30-22-50-36-16-10-8-14-33(30)36)53-41(59)34(46)20-31-23-48-25-51-31)45(63)55-38(18-29-21-49-35-15-9-7-13-32(29)35)43(61)54-37(17-28-11-5-4-6-12-28)42(60)52-27(3)40(47)58/h4-16,21-23,25-27,34,37-39,49-50H,17-20,24,46H2,1-3H3,(H2,47,58)(H,48,51)(H,52,60)(H,53,59)(H,54,61)(H,55,63)(H,56,62)/t27-,34-,37+,38-,39+/m0/s1
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n/an/a 8.17E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395007
PNG
(CHEMBL2163472)
Show SMILES C[C@H](NC(=O)N(Cc1ccc(O)cc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O7/c1-26(50-43(62)55(24-28-14-16-31(56)17-15-28)54-40(59)33(45)21-30-23-47-25-49-30)39(58)52-37(20-29-22-48-34-12-6-5-11-32(29)34)42(61)53-36(19-27-9-3-2-4-10-27)41(60)51-35(38(46)57)13-7-8-18-44/h2-6,9-12,14-17,22-23,25-26,33,35-37,48,56H,7-8,13,18-21,24,44-45H2,1H3,(H2,46,57)(H,47,49)(H,50,62)(H,51,60)(H,52,58)(H,53,61)(H,54,59)/t26-,33?,35-,36+,37-/m0/s1
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n/an/a 8.53E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394982
PNG
(CHEMBL2163467)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(N)=O |r|
Show InChI InChI=1S/C42H49N11O5/c1-25(2)23-53(52-41(57)37(18-28-21-47-34-15-9-7-13-31(28)34)50-39(55)32(43)19-29-22-45-24-48-29)42(58)51-36(17-27-20-46-33-14-8-6-12-30(27)33)40(56)49-35(38(44)54)16-26-10-4-3-5-11-26/h3-15,20-22,24-25,32,35-37,46-47H,16-19,23,43H2,1-2H3,(H2,44,54)(H,45,48)(H,49,56)(H,50,55)(H,51,58)(H,52,57)/t32-,35+,36-,37+/m0/s1
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n/an/a 9.01E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395016
PNG
(CHEMBL2163452 | US9708370, CP-2B(ii))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](C)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C42H57N13O6/c1-24(2)22-55(54-41(60)36(17-27-20-48-33-13-7-5-11-30(27)33)52-39(58)31(44)18-28-21-46-23-49-28)42(61)53-35(16-26-19-47-32-12-6-4-10-29(26)32)40(59)50-25(3)38(57)51-34(37(45)56)14-8-9-15-43/h4-7,10-13,19-21,23-25,31,34-36,47-48H,8-9,14-18,22,43-44H2,1-3H3,(H2,45,56)(H,46,49)(H,50,59)(H,51,57)(H,52,58)(H,53,61)(H,54,60)/t25-,31+,34+,35+,36-/m1/s1
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n/an/a 9.48E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395003
PNG
(CHEMBL2163476 | US9708370, DBG-188p)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C44H53N13O6/c45-17-9-8-16-35(39(47)58)52-41(60)36(18-26-10-2-1-3-11-26)54-42(61)37(19-27-22-49-33-14-6-4-12-30(27)33)55-44(63)57-56-43(62)38(20-28-23-50-34-15-7-5-13-31(28)34)53-40(59)32(46)21-29-24-48-25-51-29/h1-7,10-15,22-25,32,35-38,49-50H,8-9,16-21,45-46H2,(H2,47,58)(H,48,51)(H,52,60)(H,53,59)(H,54,61)(H,56,62)(H2,55,57,63)/t32-,35-,36+,37-,38+/m0/s1
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n/an/a 9.61E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394989
PNG
(CHEMBL2163460 | US9708370, 62 CP-AP-4)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)N1CCCN1C(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C47H57N13O6/c48-18-9-8-17-38(42(50)61)55-44(63)39(21-29-11-2-1-3-12-29)56-45(64)40(22-30-25-52-36-15-6-4-13-33(30)36)58-47(66)60-20-10-19-59(60)46(65)41(23-31-26-53-37-16-7-5-14-34(31)37)57-43(62)35(49)24-32-27-51-28-54-32/h1-7,11-16,25-28,35,38-41,52-53H,8-10,17-24,48-49H2,(H2,50,61)(H,51,54)(H,55,63)(H,56,64)(H,57,62)(H,58,66)/t35-,38-,39+,40-,41+/m0/s1
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n/an/a 9.81E+3n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394992
PNG
(CHEMBL2163437)
Show SMILES C[C@H](NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O6/c1-22(32(49)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36)41-31(48)23(2)42-35(52)46(20-25-13-7-4-8-14-25)45-33(50)27(37)18-26-19-39-21-40-26/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,52)(H,43,51)(H,44,49)(H,45,50)/t22-,23-,27?,28-,29+/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394987
PNG
(CHEMBL2163462 | US9708370, CP-AP-2)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCCN1C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C41H53N13O6/c1-24(49-39(58)34(17-25-20-46-31-11-4-2-9-28(25)31)50-38(57)30(43)19-27-22-45-23-48-27)37(56)51-35(18-26-21-47-32-12-5-3-10-29(26)32)40(59)53-15-8-16-54(53)41(60)52-33(36(44)55)13-6-7-14-42/h2-5,9-12,20-24,30,33-35,46-47H,6-8,13-19,42-43H2,1H3,(H2,44,55)(H,45,48)(H,49,58)(H,50,57)(H,51,56)(H,52,60)/t24-,30-,33-,34+,35-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395018
PNG
(CHEMBL2163450 | US9708370, 55 CP-2B(iv))
Show SMILES CC(C)CN(NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(51-36(54)25(3)47-37(55)30(42)19-28-21-44-23-46-28)40(58)50-34(18-27-20-45-31-14-8-7-13-29(27)31)39(57)49-33(17-26-11-5-4-6-12-26)38(56)48-32(35(43)53)15-9-10-16-41/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,55)(H,48,56)(H,49,57)(H,50,58)(H,51,54)/t25-,30+,32+,33-,34+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395020
PNG
(CHEMBL2163448 | US9708370, 47 CP-2A(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C41H46N12O6/c1-23(36(43)54)48-38(56)33(15-24-9-3-2-4-10-24)50-39(57)34(16-25-19-45-31-13-7-5-11-28(25)31)51-41(59)53-52-40(58)35(17-26-20-46-32-14-8-6-12-29(26)32)49-37(55)30(42)18-27-21-44-22-47-27/h2-14,19-23,30,33-35,45-46H,15-18,42H2,1H3,(H2,43,54)(H,44,47)(H,48,56)(H,49,55)(H,50,57)(H,52,58)(H2,51,53,59)/t23-,30-,33+,34-,35+/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394980
PNG
(CHEMBL2163469)
Show SMILES CC(C)CN(NC(=O)[C@H](N)Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |r|
Show InChI InChI=1S/C27H33N7O3/c1-16(2)15-34(33-26(36)21(28)11-17-13-30-22-9-5-3-7-19(17)22)27(37)32-24(25(29)35)12-18-14-31-23-10-6-4-8-20(18)23/h3-10,13-14,16,21,24,30-31H,11-12,15,28H2,1-2H3,(H2,29,35)(H,32,37)(H,33,36)/t21-,24+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395010
PNG
(CHEMBL2163458)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C38H50N12O6/c39-15-7-6-13-29(33(41)51)45-35(53)30(17-23-9-2-1-3-10-23)47-37(55)32-14-8-16-50(32)38(56)49-48-36(54)31(18-24-20-43-28-12-5-4-11-26(24)28)46-34(52)27(40)19-25-21-42-22-44-25/h1-5,9-12,20-22,27,29-32,43H,6-8,13-19,39-40H2,(H2,41,51)(H,42,44)(H,45,53)(H,46,52)(H,47,55)(H,48,54)(H,49,56)/t27-,29-,30+,31+,32-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395016
PNG
(CHEMBL2163452 | US9708370, CP-2B(ii))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](C)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C42H57N13O6/c1-24(2)22-55(54-41(60)36(17-27-20-48-33-13-7-5-11-30(27)33)52-39(58)31(44)18-28-21-46-23-49-28)42(61)53-35(16-26-19-47-32-12-6-4-10-29(26)32)40(59)50-25(3)38(57)51-34(37(45)56)14-8-9-15-43/h4-7,10-13,19-21,23-25,31,34-36,47-48H,8-9,14-18,22,43-44H2,1-3H3,(H2,45,56)(H,46,49)(H,50,59)(H,51,57)(H,52,58)(H,53,61)(H,54,60)/t25-,31+,34+,35+,36-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395022
PNG
(CHEMBL2163446 | US9708370, 49 CP-2A(iii))
Show SMILES C[C@H](NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C36H48N12O6/c1-21(32(50)45-29(15-22-9-3-2-4-10-22)34(52)44-28(31(39)49)13-7-8-14-37)43-36(54)48-47-35(53)30(16-23-18-41-27-12-6-5-11-25(23)27)46-33(51)26(38)17-24-19-40-20-42-24/h2-6,9-12,18-21,26,28-30,41H,7-8,13-17,37-38H2,1H3,(H2,39,49)(H,40,42)(H,44,52)(H,45,50)(H,46,51)(H,47,53)(H2,43,48,54)/t21-,26-,28-,29+,30+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395027
PNG
(CHEMBL2163441)
Show SMILES C[C@H](NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O7/c1-21(32(50)44-29(16-23-8-4-3-5-9-23)34(52)43-28(30(38)48)10-6-7-15-36)41-31(49)22(2)42-35(53)46(19-24-11-13-26(47)14-12-24)45-33(51)27(37)17-25-18-39-20-40-25/h3-5,8-9,11-14,18,20-22,27-29,47H,6-7,10,15-17,19,36-37H2,1-2H3,(H2,38,48)(H,39,40)(H,41,49)(H,42,53)(H,43,52)(H,44,50)(H,45,51)/t21-,22-,27?,28-,29+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395012
PNG
(CHEMBL2163456 | US9708370, 58 CP-3(ii))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](C)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O6/c1-22(33(51)46-30(32(40)50)14-8-9-15-38)45-37(55)49(20-24-10-4-3-5-11-24)48-34(52)23(2)44-36(54)31(16-25-18-42-29-13-7-6-12-27(25)29)47-35(53)28(39)17-26-19-41-21-43-26/h3-7,10-13,18-19,21-23,28,30-31,42H,8-9,14-17,20,38-39H2,1-2H3,(H2,40,50)(H,41,43)(H,44,54)(H,45,55)(H,46,51)(H,47,53)(H,48,52)/t22-,23+,28+,30+,31-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395013
PNG
(CHEMBL2163455 | US9708370, 59 CP-3(iii))
Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O6/c1-22(42-33(50)27(37)18-26-19-39-21-40-26)31(48)41-23(2)32(49)45-46(20-25-13-7-4-8-14-25)35(52)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,50)(H,43,51)(H,44,52)(H,45,49)/t22-,23+,27+,28+,29-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394988
PNG
(CHEMBL2163461 | US9708370, CP-AP-3)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N1CCCN1C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C39H52N12O6/c1-24(46-36(54)33(19-26-21-44-30-13-6-5-12-28(26)30)48-35(53)29(41)20-27-22-43-23-45-27)38(56)50-16-9-17-51(50)39(57)49-32(18-25-10-3-2-4-11-25)37(55)47-31(34(42)52)14-7-8-15-40/h2-6,10-13,21-24,29,31-33,44H,7-9,14-20,40-41H2,1H3,(H2,42,52)(H,43,45)(H,46,54)(H,47,55)(H,48,53)(H,49,57)/t24-,29-,31-,32+,33+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395013
PNG
(CHEMBL2163455 | US9708370, 59 CP-3(iii))
Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O6/c1-22(42-33(50)27(37)18-26-19-39-21-40-26)31(48)41-23(2)32(49)45-46(20-25-13-7-4-8-14-25)35(52)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,50)(H,43,51)(H,44,52)(H,45,49)/t22-,23+,27+,28+,29-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395025
PNG
(CHEMBL2163443 | US9708370, CP-1B(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395026
PNG
(CHEMBL2163442 | US9708370, CP-1B(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O7/c1-21(33(52)46-30(32(40)51)9-5-6-14-38)44-36(55)31(15-24-17-42-29-8-4-3-7-27(24)29)47-34(53)22(2)45-37(56)49(19-23-10-12-26(50)13-11-23)48-35(54)28(39)16-25-18-41-20-43-25/h3-4,7-8,10-13,17-18,20-22,28,30-31,42,50H,5-6,9,14-16,19,38-39H2,1-2H3,(H2,40,51)(H,41,43)(H,44,55)(H,45,56)(H,46,52)(H,47,53)(H,48,54)/t21-,22+,28+,30+,31+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395012
PNG
(CHEMBL2163456 | US9708370, 58 CP-3(ii))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](C)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O6/c1-22(33(51)46-30(32(40)50)14-8-9-15-38)45-37(55)49(20-24-10-4-3-5-11-24)48-34(52)23(2)44-36(54)31(16-25-18-42-29-13-7-6-12-27(25)29)47-35(53)28(39)17-26-19-41-21-43-26/h3-7,10-13,18-19,21-23,28,30-31,42H,8-9,14-17,20,38-39H2,1-2H3,(H2,40,50)(H,41,43)(H,44,54)(H,45,55)(H,46,51)(H,47,53)(H,48,52)/t22-,23+,28+,30+,31-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395017
PNG
(CHEMBL2163451 | US9708370, CP-2B(iii))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(51-39(57)34(18-27-20-45-31-14-8-7-13-29(27)31)50-37(55)30(42)19-28-21-44-23-46-28)40(58)47-25(3)36(54)49-33(17-26-11-5-4-6-12-26)38(56)48-32(35(43)53)15-9-10-16-41/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,58)(H,48,56)(H,49,54)(H,50,55)(H,51,57)/t25-,30-,32-,33+,34+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394981
PNG
(CHEMBL2163468)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |r|
Show InChI InChI=1S/C33H40N10O4/c1-19(2)17-43(33(47)41-28(30(35)44)11-20-14-37-26-9-5-3-7-23(20)26)42-32(46)29(12-21-15-38-27-10-6-4-8-24(21)27)40-31(45)25(34)13-22-16-36-18-39-22/h3-10,14-16,18-19,25,28-29,37-38H,11-13,17,34H2,1-2H3,(H2,35,44)(H,36,39)(H,40,45)(H,41,47)(H,42,46)/t25-,28-,29+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395021
PNG
(CHEMBL2163447 | US9708370, 48 CP-2A(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C38H49N13O6/c1-21(34(53)47-30(33(41)52)12-6-7-13-39)46-36(55)31(14-22-17-43-28-10-4-2-8-25(22)28)49-38(57)51-50-37(56)32(15-23-18-44-29-11-5-3-9-26(23)29)48-35(54)27(40)16-24-19-42-20-45-24/h2-5,8-11,17-21,27,30-32,43-44H,6-7,12-16,39-40H2,1H3,(H2,41,52)(H,42,45)(H,46,55)(H,47,53)(H,48,54)(H,50,56)(H2,49,51,57)/t21-,27+,30+,31+,32-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395022
PNG
(CHEMBL2163446 | US9708370, 49 CP-2A(iii))
Show SMILES C[C@H](NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C36H48N12O6/c1-21(32(50)45-29(15-22-9-3-2-4-10-22)34(52)44-28(31(39)49)13-7-8-14-37)43-36(54)48-47-35(53)30(16-23-18-41-27-12-6-5-11-25(23)27)46-33(51)26(38)17-24-19-40-20-42-24/h2-6,9-12,18-21,26,28-30,41H,7-8,13-17,37-38H2,1H3,(H2,39,49)(H,40,42)(H,44,52)(H,45,50)(H,46,51)(H,47,53)(H2,43,48,54)/t21-,26-,28-,29+,30+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394987
PNG
(CHEMBL2163462 | US9708370, CP-AP-2)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCCN1C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C41H53N13O6/c1-24(49-39(58)34(17-25-20-46-31-11-4-2-9-28(25)31)50-38(57)30(43)19-27-22-45-23-48-27)37(56)51-35(18-26-21-47-32-12-5-3-10-29(26)32)40(59)53-15-8-16-54(53)41(60)52-33(36(44)55)13-6-7-14-42/h2-5,9-12,20-24,30,33-35,46-47H,6-8,13-19,42-43H2,1H3,(H2,44,55)(H,45,48)(H,49,58)(H,50,57)(H,51,56)(H,52,60)/t24-,30-,33-,34+,35-/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395011
PNG
(CHEMBL2163457 | US9708370, 57 CP-3(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)N(Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O6/c1-24(35(42)52)46-38(55)33(17-26-11-5-3-6-12-26)49-40(57)51(22-27-13-7-4-8-14-27)50-36(53)25(2)47-39(56)34(18-28-20-44-32-16-10-9-15-30(28)32)48-37(54)31(41)19-29-21-43-23-45-29/h3-16,20-21,23-25,31,33-34,44H,17-19,22,41H2,1-2H3,(H2,42,52)(H,43,45)(H,46,55)(H,47,56)(H,48,54)(H,49,57)(H,50,53)/t24-,25-,31-,33+,34+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395014
PNG
(CHEMBL2163454 | US9708370, 60 CP-3(iv))
Show SMILES C[C@H](N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)NN(Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O6/c1-25(42)36(52)47-34(22-29-23-44-31-18-10-9-17-30(29)31)38(54)45-26(2)37(53)49-50(24-28-15-7-4-8-16-28)40(56)48-33(21-27-13-5-3-6-14-27)39(55)46-32(35(43)51)19-11-12-20-41/h3-10,13-18,23,25-26,32-34,44H,11-12,19-22,24,41-42H2,1-2H3,(H2,43,51)(H,45,54)(H,46,55)(H,47,52)(H,48,56)(H,49,53)/t25-,26-,32-,33+,34+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395018
PNG
(CHEMBL2163450 | US9708370, 55 CP-2B(iv))
Show SMILES CC(C)CN(NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(51-36(54)25(3)47-37(55)30(42)19-28-21-44-23-46-28)40(58)50-34(18-27-20-45-31-14-8-7-13-29(27)31)39(57)49-33(17-26-11-5-4-6-12-26)38(56)48-32(35(43)53)15-9-10-16-41/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,55)(H,48,56)(H,49,57)(H,50,58)(H,51,54)/t25-,30+,32+,33-,34+/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395028
PNG
(CHEMBL2163440 | US9708370, CP-1B(iv))
Show SMILES C[C@H](N)C(=O)NN(Cc1ccc(O)cc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O7/c1-24(42)36(53)49-50(23-27-15-17-29(51)18-16-27)40(57)45-25(2)37(54)47-34(21-28-22-44-31-13-7-6-12-30(28)31)39(56)48-33(20-26-10-4-3-5-11-26)38(55)46-32(35(43)52)14-8-9-19-41/h3-7,10-13,15-18,22,24-25,32-34,44,51H,8-9,14,19-21,23,41-42H2,1-2H3,(H2,43,52)(H,45,57)(H,46,55)(H,47,54)(H,48,56)(H,49,53)/t24-,25-,32-,33+,34-/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394993
PNG
(CHEMBL2163485 | US9708370, CP-1A(iv))
Show SMILES C[C@H](N)C(=O)NN(Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O6/c1-25(42)36(52)49-50(24-28-15-7-4-8-16-28)40(56)45-26(2)37(53)47-34(22-29-23-44-31-18-10-9-17-30(29)31)39(55)48-33(21-27-13-5-3-6-14-27)38(54)46-32(35(43)51)19-11-12-20-41/h3-10,13-18,23,25-26,32-34,44H,11-12,19-22,24,41-42H2,1-2H3,(H2,43,51)(H,45,56)(H,46,54)(H,47,53)(H,48,55)(H,49,52)/t25-,26-,32-,33+,34-/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394988
PNG
(CHEMBL2163461 | US9708370, CP-AP-3)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N1CCCN1C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C39H52N12O6/c1-24(46-36(54)33(19-26-21-44-30-13-6-5-12-28(26)30)48-35(53)29(41)20-27-22-43-23-45-27)38(56)50-16-9-17-51(50)39(57)49-32(18-25-10-3-2-4-11-25)37(55)47-31(34(42)52)14-7-8-15-40/h2-6,10-13,21-24,29,31-33,44H,7-9,14-20,40-41H2,1H3,(H2,42,52)(H,43,45)(H,46,54)(H,47,55)(H,48,53)(H,49,57)/t24-,29-,31-,32+,33+/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394990
PNG
(CHEMBL2163459)
Show SMILES C[C@H](NC(=O)N1CCCN1C(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C39H52N12O6/c1-24(46-39(57)51-17-9-16-50(51)38(56)29(41)20-27-22-43-23-45-27)35(53)48-33(19-26-21-44-30-13-6-5-12-28(26)30)37(55)49-32(18-25-10-3-2-4-11-25)36(54)47-31(34(42)52)14-7-8-15-40/h2-6,10-13,21-24,29,31-33,44H,7-9,14-20,40-41H2,1H3,(H2,42,52)(H,43,45)(H,46,57)(H,47,54)(H,48,53)(H,49,55)/t24-,29-,31-,32+,33-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395023
PNG
(CHEMBL2163445 | US9708370, 50 CP-2A(iv))
Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NNC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C36H48N12O6/c1-21(43-33(51)26(38)17-24-19-40-20-42-24)32(50)47-48-36(54)46-30(16-23-18-41-27-12-6-5-11-25(23)27)35(53)45-29(15-22-9-3-2-4-10-22)34(52)44-28(31(39)49)13-7-8-14-37/h2-6,9-12,18-21,26,28-30,41H,7-8,13-17,37-38H2,1H3,(H2,39,49)(H,40,42)(H,43,51)(H,44,52)(H,45,53)(H,47,50)(H2,46,48,54)/t21-,26+,28+,29-,30+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395026
PNG
(CHEMBL2163442 | US9708370, CP-1B(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O7/c1-21(33(52)46-30(32(40)51)9-5-6-14-38)44-36(55)31(15-24-17-42-29-8-4-3-7-27(24)29)47-34(53)22(2)45-37(56)49(19-23-10-12-26(50)13-11-23)48-35(54)28(39)16-25-18-41-20-43-25/h3-4,7-8,10-13,17-18,20-22,28,30-31,42,50H,5-6,9,14-16,19,38-39H2,1-2H3,(H2,40,51)(H,41,43)(H,44,55)(H,45,56)(H,46,52)(H,47,53)(H,48,54)/t21-,22+,28+,30+,31+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394991
PNG
(CHEMBL2163438 | US9708370, 40 CP-1A(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O6/c1-22(33(51)46-30(32(40)50)14-8-9-15-38)44-36(54)31(16-25-18-42-29-13-7-6-12-27(25)29)47-34(52)23(2)45-37(55)49(20-24-10-4-3-5-11-24)48-35(53)28(39)17-26-19-41-21-43-26/h3-7,10-13,18-19,21-23,28,30-31,42H,8-9,14-17,20,38-39H2,1-2H3,(H2,40,50)(H,41,43)(H,44,54)(H,45,55)(H,46,51)(H,47,52)(H,48,53)/t22-,23+,28+,30+,31+/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394992
PNG
(CHEMBL2163437)
Show SMILES C[C@H](NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O6/c1-22(32(49)44-29(17-24-11-5-3-6-12-24)34(51)43-28(30(38)47)15-9-10-16-36)41-31(48)23(2)42-35(52)46(20-25-13-7-4-8-14-25)45-33(50)27(37)18-26-19-39-21-40-26/h3-8,11-14,19,21-23,27-29H,9-10,15-18,20,36-37H2,1-2H3,(H2,38,47)(H,39,40)(H,41,48)(H,42,52)(H,43,51)(H,44,49)(H,45,50)/t22-,23-,27?,28-,29+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395021
PNG
(CHEMBL2163447 | US9708370, 48 CP-2A(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C38H49N13O6/c1-21(34(53)47-30(33(41)52)12-6-7-13-39)46-36(55)31(14-22-17-43-28-10-4-2-8-25(22)28)49-38(57)51-50-37(56)32(15-23-18-44-29-11-5-3-9-26(23)29)48-35(54)27(40)16-24-19-42-20-45-24/h2-5,8-11,17-21,27,30-32,43-44H,6-7,12-16,39-40H2,1H3,(H2,41,52)(H,42,45)(H,46,55)(H,47,53)(H,48,54)(H,50,56)(H2,49,51,57)/t21-,27+,30+,31+,32-/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395023
PNG
(CHEMBL2163445 | US9708370, 50 CP-2A(iv))
Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NNC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C36H48N12O6/c1-21(43-33(51)26(38)17-24-19-40-20-42-24)32(50)47-48-36(54)46-30(16-23-18-41-27-12-6-5-11-25(23)27)35(53)45-29(15-22-9-3-2-4-10-22)34(52)44-28(31(39)49)13-7-8-14-37/h2-6,9-12,18-21,26,28-30,41H,7-8,13-17,37-38H2,1H3,(H2,39,49)(H,40,42)(H,43,51)(H,44,52)(H,45,53)(H,47,50)(H2,46,48,54)/t21-,26+,28+,29-,30+/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394980
PNG
(CHEMBL2163469)
Show SMILES CC(C)CN(NC(=O)[C@H](N)Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |r|
Show InChI InChI=1S/C27H33N7O3/c1-16(2)15-34(33-26(36)21(28)11-17-13-30-22-9-5-3-7-19(17)22)27(37)32-24(25(29)35)12-18-14-31-23-10-6-4-8-20(18)23/h3-10,13-14,16,21,24,30-31H,11-12,15,28H2,1-2H3,(H2,29,35)(H,32,37)(H,33,36)/t21-,24+/m1/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394986
PNG
(CHEMBL2163463)
Show SMILES CCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)NN(CC(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H58N10O6/c1-4-40(56)50-39(24-31-26-49-35-19-11-9-17-33(31)35)44(60)54-55(27-28(2)3)45(61)53-38(23-30-25-48-34-18-10-8-16-32(30)34)43(59)52-37(22-29-14-6-5-7-15-29)42(58)51-36(41(47)57)20-12-13-21-46/h5-11,14-19,25-26,28,36-39,48-49H,4,12-13,20-24,27,46H2,1-3H3,(H2,47,57)(H,50,56)(H,51,58)(H,52,59)(H,53,61)(H,54,60)/t36-,37+,38-,39+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395011
PNG
(CHEMBL2163457 | US9708370, 57 CP-3(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)N(Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O6/c1-24(35(42)52)46-38(55)33(17-26-11-5-3-6-12-26)49-40(57)51(22-27-13-7-4-8-14-27)50-36(53)25(2)47-39(56)34(18-28-20-44-32-16-10-9-15-30(28)32)48-37(54)31(41)19-29-21-43-23-45-29/h3-16,20-21,23-25,31,33-34,44H,17-19,22,41H2,1-2H3,(H2,42,52)(H,43,45)(H,46,55)(H,47,56)(H,48,54)(H,49,57)(H,50,53)/t24-,25-,31-,33+,34+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394989
PNG
(CHEMBL2163460 | US9708370, 62 CP-AP-4)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)N1CCCN1C(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C47H57N13O6/c48-18-9-8-17-38(42(50)61)55-44(63)39(21-29-11-2-1-3-12-29)56-45(64)40(22-30-25-52-36-15-6-4-13-33(30)36)58-47(66)60-20-10-19-59(60)46(65)41(23-31-26-53-37-16-7-5-14-34(31)37)57-43(62)35(49)24-32-27-51-28-54-32/h1-7,11-16,25-28,35,38-41,52-53H,8-10,17-24,48-49H2,(H2,50,61)(H,51,54)(H,55,63)(H,56,64)(H,57,62)(H,58,66)/t35-,38-,39+,40-,41+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395000
PNG
(CHEMBL2163479 | US9708370, DBG-253-2)
Show SMILES CC(C)CN(NC(=O)[C@H](C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(40(58)50-33(17-26-11-5-4-6-12-26)39(57)48-32(35(43)53)15-9-10-16-41)51-36(54)25(3)47-38(56)34(18-27-20-45-31-14-8-7-13-29(27)31)49-37(55)30(42)19-28-21-44-23-46-28/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,56)(H,48,57)(H,49,55)(H,50,58)(H,51,54)/t25-,30-,32-,33+,34+/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394979
PNG
(CHEMBL18872)
Show SMILES Cc1[nH]c2ccccc2c1C[C@@H](NC(=O)[C@@H](Cc1c(C)[nH]c2ccccc12)NC(=O)C(C)(C)N)C(N)=O
Show InChI InChI=1S/C28H34N6O3/c1-15-19(17-9-5-7-11-21(17)31-15)13-23(25(29)35)33-26(36)24(34-27(37)28(3,4)30)14-20-16(2)32-22-12-8-6-10-18(20)22/h5-12,23-24,31-32H,13-14,30H2,1-4H3,(H2,29,35)(H,33,36)(H,34,37)/t23-,24-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395010
PNG
(CHEMBL2163458)
Show SMILES NCCCC[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C38H50N12O6/c39-15-7-6-13-29(33(41)51)45-35(53)30(17-23-9-2-1-3-10-23)47-37(55)32-14-8-16-50(32)38(56)49-48-36(54)31(18-24-20-43-28-12-5-4-11-26(24)28)46-34(52)27(40)19-25-21-42-22-44-25/h1-5,9-12,20-22,27,29-32,43H,6-8,13-19,39-40H2,(H2,41,51)(H,42,44)(H,45,53)(H,46,52)(H,47,55)(H,48,54)(H,49,56)/t27-,29-,30+,31+,32-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395029
PNG
(CHEMBL2163439 | US9708370, CP-1A(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O6/c1-24(35(42)52)46-38(55)33(17-26-11-5-3-6-12-26)49-39(56)34(18-28-20-44-32-16-10-9-15-30(28)32)48-36(53)25(2)47-40(57)51(22-27-13-7-4-8-14-27)50-37(54)31(41)19-29-21-43-23-45-29/h3-16,20-21,23-25,31,33-34,44H,17-19,22,41H2,1-2H3,(H2,42,52)(H,43,45)(H,46,55)(H,47,57)(H,48,53)(H,49,56)(H,50,54)/t24-,25-,31-,33+,34-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395006
PNG
(CHEMBL2163473)
Show SMILES C[C@H](NC(=O)N(Cc1cccc2ccccc12)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H56N12O6/c1-29(54-47(65)59(58-44(62)37(49)24-34-26-51-28-53-34)27-32-16-11-15-31-14-5-6-17-35(31)32)43(61)56-41(23-33-25-52-38-19-8-7-18-36(33)38)46(64)57-40(22-30-12-3-2-4-13-30)45(63)55-39(42(50)60)20-9-10-21-48/h2-8,11-19,25-26,28-29,37,39-41,52H,9-10,20-24,27,48-49H2,1H3,(H2,50,60)(H,51,53)(H,54,65)(H,55,63)(H,56,61)(H,57,64)(H,58,62)/t29-,37?,39-,40+,41-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394991
PNG
(CHEMBL2163438 | US9708370, 40 CP-1A(ii))
Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C37H50N12O6/c1-22(33(51)46-30(32(40)50)14-8-9-15-38)44-36(54)31(16-25-18-42-29-13-7-6-12-27(25)29)47-34(52)23(2)45-37(55)49(20-24-10-4-3-5-11-24)48-35(53)28(39)17-26-19-41-21-43-26/h3-7,10-13,18-19,21-23,28,30-31,42H,8-9,14-17,20,38-39H2,1-2H3,(H2,40,50)(H,41,43)(H,44,54)(H,45,55)(H,46,51)(H,47,52)(H,48,53)/t22-,23+,28+,30+,31+/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395025
PNG
(CHEMBL2163443 | US9708370, CP-1B(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O7/c1-23(35(42)53)46-38(56)33(16-25-8-4-3-5-9-25)49-39(57)34(17-27-19-44-32-11-7-6-10-30(27)32)48-36(54)24(2)47-40(58)51(21-26-12-14-29(52)15-13-26)50-37(55)31(41)18-28-20-43-22-45-28/h3-15,19-20,22-24,31,33-34,44,52H,16-18,21,41H2,1-2H3,(H2,42,53)(H,43,45)(H,46,56)(H,47,58)(H,48,54)(H,49,57)(H,50,55)/t23-,24-,31-,33+,34-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395027
PNG
(CHEMBL2163441)
Show SMILES C[C@H](NC(=O)[C@H](C)NC(=O)N(Cc1ccc(O)cc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C35H49N11O7/c1-21(32(50)44-29(16-23-8-4-3-5-9-23)34(52)43-28(30(38)48)10-6-7-15-36)41-31(49)22(2)42-35(53)46(19-24-11-13-26(47)14-12-24)45-33(51)27(37)17-25-18-39-20-40-25/h3-5,8-9,11-14,18,20-22,27-29,47H,6-7,10,15-17,19,36-37H2,1-2H3,(H2,38,48)(H,39,40)(H,41,49)(H,42,53)(H,43,52)(H,44,50)(H,45,51)/t21-,22-,27?,28-,29+/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394990
PNG
(CHEMBL2163459)
Show SMILES C[C@H](NC(=O)N1CCCN1C(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C39H52N12O6/c1-24(46-39(57)51-17-9-16-50(51)38(56)29(41)20-27-22-43-23-45-27)35(53)48-33(19-26-21-44-30-13-6-5-12-28(26)30)37(55)49-32(18-25-10-3-2-4-11-25)36(54)47-31(34(42)52)14-7-8-15-40/h2-6,10-13,21-24,29,31-33,44H,7-9,14-20,40-41H2,1H3,(H2,42,52)(H,43,45)(H,46,57)(H,47,54)(H,48,53)(H,49,55)/t24-,29-,31-,32+,33-/m0/s1
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Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394998
PNG
(CHEMBL2163481 | US9708370, DBG-253-5)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(CCc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H56N12O6/c1-28(51-42(60)38(23-31-25-49-35-17-9-8-16-33(31)35)53-41(59)34(46)24-32-26-48-27-50-32)40(58)55-56(21-19-29-12-4-2-5-13-29)44(62)54-37(22-30-14-6-3-7-15-30)43(61)52-36(39(47)57)18-10-11-20-45/h2-9,12-17,25-28,34,36-38,49H,10-11,18-24,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,59)(H,54,62)(H,55,58)/t28-,34-,36-,37+,38+/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394984
PNG
(CHEMBL2163465)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H57N11O6/c1-27(2)26-55(54-43(60)38(50-39(56)23-46)22-30-25-49-34-17-9-7-15-32(30)34)44(61)53-37(21-29-24-48-33-16-8-6-14-31(29)33)42(59)52-36(20-28-12-4-3-5-13-28)41(58)51-35(40(47)57)18-10-11-19-45/h3-9,12-17,24-25,27,35-38,48-49H,10-11,18-23,26,45-46H2,1-2H3,(H2,47,57)(H,50,56)(H,51,58)(H,52,59)(H,53,61)(H,54,60)/t35-,36+,37-,38+/m0/s1
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n/an/a 1.05E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395019
PNG
(CHEMBL2163449 | US9708370, CP-2B(v))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H59N11O6/c1-27(2)26-56(55-44(61)39(52-41(58)28(3)47)23-31-25-50-35-18-10-8-16-33(31)35)45(62)54-38(22-30-24-49-34-17-9-7-15-32(30)34)43(60)53-37(21-29-13-5-4-6-14-29)42(59)51-36(40(48)57)19-11-12-20-46/h4-10,13-18,24-25,27-28,36-39,49-50H,11-12,19-23,26,46-47H2,1-3H3,(H2,48,57)(H,51,59)(H,52,58)(H,53,60)(H,54,62)(H,55,61)/t28-,36-,37+,38-,39+/m0/s1
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n/an/a 1.12E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394995
PNG
(CHEMBL2163483 | US9708370, DBG-253-8)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H55N11O7/c1-26(51-42(60)38(21-29-23-49-34-12-6-5-11-32(29)34)54-41(59)33(46)22-30-24-48-25-50-30)40(58)53-36(20-28-14-16-31(56)17-15-28)44(62)55-37(19-27-9-3-2-4-10-27)43(61)52-35(39(47)57)13-7-8-18-45/h2-6,9-12,14-17,23-26,33,35-38,49,56H,7-8,13,18-22,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,58)(H,54,59)(H,55,62)/t26-,33-,35-,36+,37+,38+/m0/s1
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n/an/a 1.20E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394996
PNG
(CHEMBL2163348 | US9708370, DBG-253-7)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H55N11O7/c1-26(51-42(60)38(21-29-23-49-34-12-6-5-11-32(29)34)54-41(59)33(46)22-30-24-48-25-50-30)40(58)53-36(20-28-14-16-31(56)17-15-28)44(62)55-37(19-27-9-3-2-4-10-27)43(61)52-35(39(47)57)13-7-8-18-45/h2-6,9-12,14-17,23-26,33,35-38,49,56H,7-8,13,18-22,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,60)(H,52,61)(H,53,58)(H,54,59)(H,55,62)/t26-,33-,35-,36-,37+,38+/m0/s1
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n/an/a 1.32E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394985
PNG
(CHEMBL2163464)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](C)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C45H59N11O6/c1-27(2)26-56(55-44(61)39(52-41(58)28(3)47)23-31-25-50-35-18-10-8-16-33(31)35)45(62)54-38(22-30-24-49-34-17-9-7-15-32(30)34)43(60)53-37(21-29-13-5-4-6-14-29)42(59)51-36(40(48)57)19-11-12-20-46/h4-10,13-18,24-25,27-28,36-39,49-50H,11-12,19-23,26,46-47H2,1-3H3,(H2,48,57)(H,51,59)(H,52,58)(H,53,60)(H,54,62)(H,55,61)/t28-,36+,37-,38+,39-/m1/s1
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n/an/a 1.33E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394999
PNG
(CHEMBL2163480 | US9708370, DBG-253-3)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C49H58N12O6/c1-31(56-47(65)43(25-36-27-54-40-17-9-8-16-38(36)40)58-46(64)39(51)26-37-28-53-30-55-37)45(63)60-61(29-33-19-21-35(22-20-33)34-14-6-3-7-15-34)49(67)59-42(24-32-12-4-2-5-13-32)48(66)57-41(44(52)62)18-10-11-23-50/h2-9,12-17,19-22,27-28,30-31,39,41-43,54H,10-11,18,23-26,29,50-51H2,1H3,(H2,52,62)(H,53,55)(H,56,65)(H,57,66)(H,58,64)(H,59,67)(H,60,63)/t31-,39-,41-,42+,43+/m0/s1
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n/an/a 1.35E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394994
PNG
(CHEMBL2163484 | US9708370, DBG-178p)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O7/c1-26(50-41(60)37(20-29-22-48-34-12-6-5-11-32(29)34)52-40(59)33(45)21-30-23-47-25-49-30)39(58)54-55(24-28-14-16-31(56)17-15-28)43(62)53-36(19-27-9-3-2-4-10-27)42(61)51-35(38(46)57)13-7-8-18-44/h2-6,9-12,14-17,22-23,25-26,33,35-37,48,56H,7-8,13,18-21,24,44-45H2,1H3,(H2,46,57)(H,47,49)(H,50,60)(H,51,61)(H,52,59)(H,53,62)(H,54,58)/t26-,33-,35-,36+,37+/m0/s1
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n/an/a 1.57E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395008
PNG
(CHEMBL2163471)
Show SMILES C[C@H](NC(=O)N(Cc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O6/c1-27(50-43(61)55(25-29-14-6-3-7-15-29)54-40(58)33(45)22-31-24-47-26-49-31)39(57)52-37(21-30-23-48-34-17-9-8-16-32(30)34)42(60)53-36(20-28-12-4-2-5-13-28)41(59)51-35(38(46)56)18-10-11-19-44/h2-9,12-17,23-24,26-27,33,35-37,48H,10-11,18-22,25,44-45H2,1H3,(H2,46,56)(H,47,49)(H,50,61)(H,51,59)(H,52,57)(H,53,60)(H,54,58)/t27-,33?,35-,36+,37-/m0/s1
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n/an/a 1.61E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395000
PNG
(CHEMBL2163479 | US9708370, DBG-253-2)
Show SMILES CC(C)CN(NC(=O)[C@H](C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(40(58)50-33(17-26-11-5-4-6-12-26)39(57)48-32(35(43)53)15-9-10-16-41)51-36(54)25(3)47-38(56)34(18-27-20-45-31-14-8-7-13-29(27)31)49-37(55)30(42)19-28-21-44-23-46-28/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,56)(H,48,57)(H,49,55)(H,50,58)(H,51,54)/t25-,30-,32-,33+,34+/m0/s1
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n/an/a 1.95E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395004
PNG
(CHEMBL2163475)
Show SMILES C[C@H](NC(=O)N(Cc1ccc(cc1)-c1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C49H58N12O6/c1-31(56-49(67)61(60-46(64)39(51)26-37-28-53-30-55-37)29-33-19-21-35(22-20-33)34-14-6-3-7-15-34)45(63)58-43(25-36-27-54-40-17-9-8-16-38(36)40)48(66)59-42(24-32-12-4-2-5-13-32)47(65)57-41(44(52)62)18-10-11-23-50/h2-9,12-17,19-22,27-28,30-31,39,41-43,54H,10-11,18,23-26,29,50-51H2,1H3,(H2,52,62)(H,53,55)(H,56,67)(H,57,65)(H,58,63)(H,59,66)(H,60,64)/t31-,39?,41-,42+,43-/m0/s1
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n/an/a 2.32E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395017
PNG
(CHEMBL2163451 | US9708370, CP-2B(iii))
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H56N12O6/c1-24(2)22-52(51-39(57)34(18-27-20-45-31-14-8-7-13-29(27)31)50-37(55)30(42)19-28-21-44-23-46-28)40(58)47-25(3)36(54)49-33(17-26-11-5-4-6-12-26)38(56)48-32(35(43)53)15-9-10-16-41/h4-8,11-14,20-21,23-25,30,32-34,45H,9-10,15-19,22,41-42H2,1-3H3,(H2,43,53)(H,44,46)(H,47,58)(H,48,56)(H,49,54)(H,50,55)(H,51,57)/t25-,30-,32-,33+,34+/m0/s1
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n/an/a 2.59E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394994
PNG
(CHEMBL2163484 | US9708370, DBG-178p)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1ccc(O)cc1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O7/c1-26(50-41(60)37(20-29-22-48-34-12-6-5-11-32(29)34)52-40(59)33(45)21-30-23-47-25-49-30)39(58)54-55(24-28-14-16-31(56)17-15-28)43(62)53-36(19-27-9-3-2-4-10-27)42(61)51-35(38(46)57)13-7-8-18-44/h2-6,9-12,14-17,22-23,25-26,33,35-37,48,56H,7-8,13,18-21,24,44-45H2,1H3,(H2,46,57)(H,47,49)(H,50,60)(H,51,61)(H,52,59)(H,53,62)(H,54,58)/t26-,33-,35-,36+,37+/m0/s1
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n/an/a 2.80E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394997
PNG
(CHEMBL2163482 | US9708370, DBG-253-6)
Show SMILES C[C@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)NN(Cc1cccc2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C47H56N12O6/c1-29(54-45(63)41(23-33-25-52-38-19-8-7-18-36(33)38)56-44(62)37(49)24-34-26-51-28-53-34)43(61)58-59(27-32-16-11-15-31-14-5-6-17-35(31)32)47(65)57-40(22-30-12-3-2-4-13-30)46(64)55-39(42(50)60)20-9-10-21-48/h2-8,11-19,25-26,28-29,37,39-41,52H,9-10,20-24,27,48-49H2,1H3,(H2,50,60)(H,51,53)(H,54,63)(H,55,64)(H,56,62)(H,57,65)(H,58,61)/t29-,37-,39-,40+,41+/m0/s1
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n/an/a 3.62E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395005
PNG
(CHEMBL2163474)
Show SMILES C[C@H](NC(=O)N(CCc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C44H56N12O6/c1-28(51-44(62)56(21-19-29-12-4-2-5-13-29)55-41(59)34(46)24-32-26-48-27-50-32)40(58)53-38(23-31-25-49-35-17-9-8-16-33(31)35)43(61)54-37(22-30-14-6-3-7-15-30)42(60)52-36(39(47)57)18-10-11-20-45/h2-9,12-17,25-28,34,36-38,49H,10-11,18-24,45-46H2,1H3,(H2,47,57)(H,48,50)(H,51,62)(H,52,60)(H,53,58)(H,54,61)(H,55,59)/t28-,34?,36-,37+,38-/m0/s1
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n/an/a 3.68E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395028
PNG
(CHEMBL2163440 | US9708370, CP-1B(iv))
Show SMILES C[C@H](N)C(=O)NN(Cc1ccc(O)cc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O7/c1-24(42)36(53)49-50(23-27-15-17-29(51)18-16-27)40(57)45-25(2)37(54)47-34(21-28-22-44-31-13-7-6-12-30(28)31)39(56)48-33(20-26-10-4-3-5-11-26)38(55)46-32(35(43)52)14-8-9-19-41/h3-7,10-13,15-18,22,24-25,32-34,44,51H,8-9,14,19-21,23,41-42H2,1-2H3,(H2,43,52)(H,45,57)(H,46,55)(H,47,54)(H,48,56)(H,49,53)/t24-,25-,32-,33+,34-/m0/s1
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n/an/a 3.69E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50394993
PNG
(CHEMBL2163485 | US9708370, CP-1A(iv))
Show SMILES C[C@H](N)C(=O)NN(Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C40H52N10O6/c1-25(42)36(52)49-50(24-28-15-7-4-8-16-28)40(56)45-26(2)37(53)47-34(22-29-23-44-31-18-10-9-17-30(29)31)39(55)48-33(21-27-13-5-3-6-14-27)38(54)46-32(35(43)51)19-11-12-20-41/h3-10,13-18,23,25-26,32-34,44H,11-12,19-22,24,41-42H2,1-2H3,(H2,43,51)(H,45,56)(H,46,54)(H,47,53)(H,48,55)(H,49,52)/t25-,26-,32-,33+,34-/m0/s1
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n/an/a 4.27E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395020
PNG
(CHEMBL2163448 | US9708370, 47 CP-2A(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)NNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C41H46N12O6/c1-23(36(43)54)48-38(56)33(15-24-9-3-2-4-10-24)50-39(57)34(16-25-19-45-31-13-7-5-11-28(25)31)51-41(59)53-52-40(58)35(17-26-20-46-32-14-8-6-12-29(26)32)49-37(55)30(42)18-27-21-44-22-47-27/h2-14,19-23,30,33-35,45-46H,15-18,42H2,1H3,(H2,43,54)(H,44,47)(H,48,56)(H,49,55)(H,50,57)(H,52,58)(H2,51,53,59)/t23-,30-,33+,34-,35+/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50395029
PNG
(CHEMBL2163439 | US9708370, CP-1A(i))
Show SMILES C[C@H](NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)N(Cc1ccccc1)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(N)=O |r|
Show InChI InChI=1S/C40H47N11O6/c1-24(35(42)52)46-38(55)33(17-26-11-5-3-6-12-26)49-39(56)34(18-28-20-44-32-16-10-9-15-30(28)32)48-36(53)25(2)47-40(57)51(22-27-13-7-4-8-14-27)50-37(54)31(41)19-29-21-43-23-45-29/h3-16,20-21,23-25,31,33-34,44H,17-19,22,41H2,1-2H3,(H2,42,52)(H,43,45)(H,46,55)(H,47,57)(H,48,53)(H,49,56)(H,50,54)/t24-,25-,31-,33+,34-/m0/s1
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n/an/a 5.10E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Platelet glycoprotein 4


(Rattus norvegicus)		BDBM50395008
PNG
(CHEMBL2163471)
Show SMILES C[C@H](NC(=O)N(Cc1ccccc1)NC(=O)C(N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C43H54N12O6/c1-27(50-43(61)55(25-29-14-6-3-7-15-29)54-40(58)33(45)22-31-24-47-26-49-31)39(57)52-37(21-30-23-48-34-17-9-8-16-32(30)34)42(60)53-36(20-28-12-4-2-5-13-28)41(59)51-35(38(46)56)18-10-11-19-44/h2-9,12-17,23-24,26-27,33,35-37,48H,10-11,18-22,25,44-45H2,1H3,(H2,46,56)(H,47,49)(H,50,61)(H,51,59)(H,52,57)(H,53,60)(H,54,58)/t27-,33?,35-,36+,37-/m0/s1
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n/an/a 7.24E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometry

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))		BDBM50394981
PNG
(CHEMBL2163468)
Show SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O |r|
Show InChI InChI=1S/C33H40N10O4/c1-19(2)17-43(33(47)41-28(30(35)44)11-20-14-37-26-9-5-3-7-23(20)26)42-32(46)29(12-21-15-38-27-10-6-4-8-24(21)27)40-31(45)25(34)13-22-16-36-18-39-22/h3-10,14-16,18-19,25,28-29,37-38H,11-13,17,34H2,1-2H3,(H2,35,44)(H,36,39)(H,40,45)(H,41,47)(H,42,46)/t25-,28-,29+/m0/s1
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n/an/a 8.56E+4n/an/an/an/an/an/a



Universit£ de Montr£al

Curated by ChEMBL


Assay Description
Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting method

J Med Chem 55: 6502-11 (2012)


Article DOI: 10.1021/jm300557t
BindingDB Entry DOI: 10.7270/Q22J6D00
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%