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Compile Data Set for Download or QSAR

Found 621 hits with Last Name = 'marelli' and Initial = 'uk'   
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
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530090
PNG
(CHEMBL4443665)
Show SMILES CC(C)C[C@@H]1NC(=O)CNC(=O)[C@H](CCCCNC(=O)CCCCCNC(=O)CCc2ccc3C=C4C(C)=CC(C)=[N+]4[B-](F)(F)n23)N(C)C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r,c:37,40,t:34|
Show InChI InChI=1S/C58H90BF2N15O12/c1-34(2)27-41-53(84)71-40(15-13-25-66-58(62)63)52(83)67-32-49(79)70-42(31-51(81)82)54(85)72-43(28-35(3)4)56(87)74-26-14-17-45(74)57(88)73(7)44(55(86)68-33-50(80)69-41)16-10-12-24-64-47(77)18-9-8-11-23-65-48(78)22-21-38-19-20-39-30-46-36(5)29-37(6)75(46)59(60,61)76(38)39/h19-20,29-30,34-35,40-45H,8-18,21-28,31-33H2,1-7H3,(H,64,77)(H,65,78)(H,67,83)(H,68,86)(H,69,80)(H,70,79)(H,71,84)(H,72,85)(H,81,82)(H4,62,63,66)/t40-,41-,42-,43-,44-,45+/m0/s1
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n/an/a 0.0600n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530090
PNG
(CHEMBL4443665)
Show SMILES CC(C)C[C@@H]1NC(=O)CNC(=O)[C@H](CCCCNC(=O)CCCCCNC(=O)CCc2ccc3C=C4C(C)=CC(C)=[N+]4[B-](F)(F)n23)N(C)C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r,c:37,40,t:34|
Show InChI InChI=1S/C58H90BF2N15O12/c1-34(2)27-41-53(84)71-40(15-13-25-66-58(62)63)52(83)67-32-49(79)70-42(31-51(81)82)54(85)72-43(28-35(3)4)56(87)74-26-14-17-45(74)57(88)73(7)44(55(86)68-33-50(80)69-41)16-10-12-24-64-47(77)18-9-8-11-23-65-48(78)22-21-38-19-20-39-30-46-36(5)29-37(6)75(46)59(60,61)76(38)39/h19-20,29-30,34-35,40-45H,8-18,21-28,31-33H2,1-7H3,(H,64,77)(H,65,78)(H,67,83)(H,68,86)(H,69,80)(H,70,79)(H,71,84)(H,72,85)(H,81,82)(H4,62,63,66)/t40-,41-,42-,43-,44-,45+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-6


(Homo sapiens (Human))
BDBM50530099
PNG
(CHEMBL4441624)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CCCCN)N(C)C(=O)[C@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC1=O |r|
Show InChI InChI=1S/C51H75N13O11/c1-30(2)25-35-45(70)57-31(3)43(68)62-38(27-33-17-9-6-10-18-33)49(74)64-24-14-21-40(64)50(75)63(4)39(20-11-12-22-52)48(73)61-36(26-32-15-7-5-8-16-32)46(71)59-34(19-13-23-55-51(53)54)44(69)56-29-41(65)58-37(28-42(66)67)47(72)60-35/h5-10,15-18,30-31,34-40H,11-14,19-29,52H2,1-4H3,(H,56,69)(H,57,70)(H,58,65)(H,59,71)(H,60,72)(H,61,73)(H,62,68)(H,66,67)(H4,53,54,55)/t31-,34-,35-,36-,37-,38-,39-,40+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta6 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-6


(Homo sapiens (Human))
BDBM50530099
PNG
(CHEMBL4441624)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CCCCN)N(C)C(=O)[C@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC1=O |r|
Show InChI InChI=1S/C51H75N13O11/c1-30(2)25-35-45(70)57-31(3)43(68)62-38(27-33-17-9-6-10-18-33)49(74)64-24-14-21-40(64)50(75)63(4)39(20-11-12-22-52)48(73)61-36(26-32-15-7-5-8-16-32)46(71)59-34(19-13-23-55-51(53)54)44(69)56-29-41(65)58-37(28-42(66)67)47(72)60-35/h5-10,15-18,30-31,34-40H,11-14,19-29,52H2,1-4H3,(H,56,69)(H,57,70)(H,58,65)(H,59,71)(H,60,72)(H,61,73)(H,62,68)(H,66,67)(H4,53,54,55)/t31-,34-,35-,36-,37-,38-,39-,40+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta6 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50112984
PNG
(CHEMBL3601428)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)N(C)C(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C58H79N15O9/c1-7-8-19-43(67-35(2)74)52(77)68-45-31-50(75)63-25-14-13-21-46(51(59)76)70(3)57(82)49(29-39-32-65-42-20-12-11-18-41(39)42)73(6)56(81)47(22-15-26-64-58(60)61)71(4)54(79)44(28-36-23-24-37-16-9-10-17-38(37)27-36)69-53(78)48(72(5)55(45)80)30-40-33-62-34-66-40/h9-12,16-18,20,23-24,27,32-34,43-49,65H,7-8,13-15,19,21-22,25-26,28-31H2,1-6H3,(H2,59,76)(H,62,66)(H,63,75)(H,67,74)(H,68,77)(H,69,78)(H4,60,61,64)/t43-,44-,45+,46+,47+,48+,49+/m1/s1
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n/an/a 0.5n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC4 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-3


(Homo sapiens (Human))
BDBM50235980
PNG
(2-((2S,5R,8S,11S)-5-benzyl-11-(3-guanidinopropyl)-...)
Show SMILES [#6]-[#6](-[#6])-[#6@@H]-1-[#7](-[#6])-[#6](=O)-[#6@@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6]-1=O |r|
Show InChI InChI=1S/C27H40N8O7/c1-15(2)22-25(41)33-17(10-7-11-30-27(28)29)23(39)31-14-20(36)32-18(13-21(37)38)24(40)34-19(26(42)35(22)3)12-16-8-5-4-6-9-16/h4-6,8-9,15,17-19,22H,7,10-14H2,1-3H3,(H,31,39)(H,32,36)(H,33,41)(H,34,40)(H,37,38)(H4,28,29,30)/t17-,18-,19+,22-/m0/s1
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n/an/a 0.540n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of vitronectin binding to Integrin alphaVbeta3 receptor (unknown origin) by competitive ELISA


J Med Chem 56: 1509-19 (2013)


Article DOI: 10.1021/jm301221x
BindingDB Entry DOI: 10.7270/Q2FJ2J4B
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-3


(Homo sapiens (Human))
BDBM50235980
PNG
(2-((2S,5R,8S,11S)-5-benzyl-11-(3-guanidinopropyl)-...)
Show SMILES [#6]-[#6](-[#6])-[#6@@H]-1-[#7](-[#6])-[#6](=O)-[#6@@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6]-1=O |r|
Show InChI InChI=1S/C27H40N8O7/c1-15(2)22-25(41)33-17(10-7-11-30-27(28)29)23(39)31-14-20(36)32-18(13-21(37)38)24(40)34-19(26(42)35(22)3)12-16-8-5-4-6-9-16/h4-6,8-9,15,17-19,22H,7,10-14H2,1-3H3,(H,31,39)(H,32,36)(H,33,41)(H,34,40)(H,37,38)(H4,28,29,30)/t17-,18-,19+,22-/m0/s1
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Division of Organic Chemistry CSIR-National Chemical Laboratory (NCL)

Curated by ChEMBL


Assay Description
Inhibition of vitronectin binding to recombinant human integrin alphaV (Phe31 to Val992 residues) beta3 (Gly27 to Asp718 residues) expressed in CHO c...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127039
BindingDB Entry DOI: 10.7270/Q2RJ4P16
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-6


(Homo sapiens (Human))
BDBM50530110
PNG
(CHEMBL4575627)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC1=O |r|
Show InChI InChI=1S/C43H64N12O11/c1-23(2)19-28-38(62)48-24(3)36(60)53-30(20-26-11-6-5-7-12-26)41(65)55-18-10-15-32(55)42(66)54-17-9-14-31(54)40(64)49-25(4)35(59)51-27(13-8-16-46-43(44)45)37(61)47-22-33(56)50-29(21-34(57)58)39(63)52-28/h5-7,11-12,23-25,27-32H,8-10,13-22H2,1-4H3,(H,47,61)(H,48,62)(H,49,64)(H,50,56)(H,51,59)(H,52,63)(H,53,60)(H,57,58)(H4,44,45,46)/t24-,25-,27-,28-,29-,30-,31-,32+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta6 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-6


(Homo sapiens (Human))
BDBM50530110
PNG
(CHEMBL4575627)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC1=O |r|
Show InChI InChI=1S/C43H64N12O11/c1-23(2)19-28-38(62)48-24(3)36(60)53-30(20-26-11-6-5-7-12-26)41(65)55-18-10-15-32(55)42(66)54-17-9-14-31(54)40(64)49-25(4)35(59)51-27(13-8-16-46-43(44)45)37(61)47-22-33(56)50-29(21-34(57)58)39(63)52-28/h5-7,11-12,23-25,27-32H,8-10,13-22H2,1-4H3,(H,47,61)(H,48,62)(H,49,64)(H,50,56)(H,51,59)(H,52,63)(H,53,60)(H,57,58)(H4,44,45,46)/t24-,25-,27-,28-,29-,30-,31-,32+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta6 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-IIb/beta-3


(Homo sapiens (Human))
BDBM50004058
PNG
((2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-yl...)
Show SMILES CCCCS(=O)(=O)N[C@@H](Cc1ccc(OCCCCC2CCNCC2)cc1)C(O)=O
Show InChI InChI=1S/C22H36N2O5S/c1-2-3-16-30(27,28)24-21(22(25)26)17-19-7-9-20(10-8-19)29-15-5-4-6-18-11-13-23-14-12-18/h7-10,18,21,23-24H,2-6,11-17H2,1H3,(H,25,26)/t21-/m0/s1
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n/an/a 0.950n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of fibrinogen binding to Integrin alpha2bbeta3 receptor (unknown origin) by competitive ELISA


J Med Chem 56: 1509-19 (2013)


Article DOI: 10.1021/jm301221x
BindingDB Entry DOI: 10.7270/Q2FJ2J4B
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Integrin alpha-IIb/beta-3


(Homo sapiens (Human))
BDBM50004058
PNG
((2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-yl...)
Show SMILES CCCCS(=O)(=O)N[C@@H](Cc1ccc(OCCCCC2CCNCC2)cc1)C(O)=O
Show InChI InChI=1S/C22H36N2O5S/c1-2-3-16-30(27,28)24-21(22(25)26)17-19-7-9-20(10-8-19)29-15-5-4-6-18-11-13-23-14-12-18/h7-10,18,21,23-24H,2-6,11-17H2,1H3,(H,25,26)/t21-/m0/s1
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n/an/a 1.20n/an/an/an/an/an/a



Division of Organic Chemistry CSIR-National Chemical Laboratory (NCL)

Curated by ChEMBL


Assay Description
Inhibition of fibrinogen binding to human platelet integrin alpha2b beta3 by ELISA based solid phase binding assay


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127039
BindingDB Entry DOI: 10.7270/Q2RJ4P16
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530119
PNG
(CHEMBL4449438)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C37H61N11O10/c1-19(2)15-23-32(54)44-22(9-6-12-40-37(38)39)31(53)41-18-28(49)43-24(17-29(50)51)33(55)46-25(16-20(3)4)35(57)48-14-8-11-27(48)36(58)47-13-7-10-26(47)34(56)42-21(5)30(52)45-23/h19-27H,6-18H2,1-5H3,(H,41,53)(H,42,56)(H,43,49)(H,44,54)(H,45,52)(H,46,55)(H,50,51)(H4,38,39,40)/t21-,22-,23-,24-,25-,26-,27+/m0/s1
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n/an/a 1.30n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530119
PNG
(CHEMBL4449438)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C37H61N11O10/c1-19(2)15-23-32(54)44-22(9-6-12-40-37(38)39)31(53)41-18-28(49)43-24(17-29(50)51)33(55)46-25(16-20(3)4)35(57)48-14-8-11-27(48)36(58)47-13-7-10-26(47)34(56)42-21(5)30(52)45-23/h19-27H,6-18H2,1-5H3,(H,41,53)(H,42,56)(H,43,49)(H,44,54)(H,45,52)(H,46,55)(H,50,51)(H4,38,39,40)/t21-,22-,23-,24-,25-,26-,27+/m0/s1
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n/an/a 1.30n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50112890
PNG
(CHEMBL3600833)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-41(64-32(2)71)49(74)67-44-28-47(72)60-22-11-10-18-40(48(56)73)65-50(75)42(26-36-29-62-39-17-9-8-15-38(36)39)68-53(78)46(19-12-23-61-55(57)58)70(3)54(79)45(25-33-20-21-34-13-6-7-14-35(34)24-33)69-51(76)43(66-52(44)77)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,75)(H,66,77)(H,67,74)(H,68,78)(H,69,76)(H4,57,58,61)/t40-,41+,42-,43-,44-,45+,46-/m0/s1
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n/an/a 1.40n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC1 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530088
PNG
(CHEMBL4520646)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C37H61N11O10/c1-6-20(4)29-34(56)44-22(10-7-13-40-37(38)39)31(53)41-18-27(49)43-23(17-28(50)51)32(54)45-24(16-19(2)3)35(57)48-15-9-12-26(48)36(58)47-14-8-11-25(47)33(55)42-21(5)30(52)46-29/h19-26,29H,6-18H2,1-5H3,(H,41,53)(H,42,55)(H,43,49)(H,44,56)(H,45,54)(H,46,52)(H,50,51)(H4,38,39,40)/t20-,21-,22-,23-,24-,25-,26+,29-/m0/s1
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n/an/a 1.5n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530088
PNG
(CHEMBL4520646)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C37H61N11O10/c1-6-20(4)29-34(56)44-22(10-7-13-40-37(38)39)31(53)41-18-27(49)43-23(17-28(50)51)32(54)45-24(16-19(2)3)35(57)48-15-9-12-26(48)36(58)47-14-8-11-25(47)33(55)42-21(5)30(52)46-29/h19-26,29H,6-18H2,1-5H3,(H,41,53)(H,42,55)(H,43,49)(H,44,56)(H,45,54)(H,46,52)(H,50,51)(H4,38,39,40)/t20-,21-,22-,23-,24-,25-,26+,29-/m0/s1
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n/an/a 1.5n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50112894
PNG
(CHEMBL3600837)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-41(65-33(2)72)50(75)67-43-29-48(73)61-23-12-11-19-46(49(57)74)70(3)55(80)45(27-37-30-63-40-18-10-9-16-39(37)40)69-53(78)47(20-13-24-62-56(58)59)71(4)54(79)44(26-34-21-22-35-14-7-8-15-36(35)25-34)68-51(76)42(66-52(43)77)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,77)(H,67,75)(H,68,76)(H,69,78)(H4,58,59,62)/t41-,42+,43+,44-,45+,46+,47+/m1/s1
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n/an/a 1.60n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC3 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530098
PNG
(CHEMBL4584228)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C40H59N11O10/c1-22(2)18-28-38(60)51-17-9-14-30(51)39(61)50-16-8-13-29(50)37(59)45-23(3)33(55)48-26(19-24-10-5-4-6-11-24)35(57)47-25(12-7-15-43-40(41)42)34(56)44-21-31(52)46-27(20-32(53)54)36(58)49-28/h4-6,10-11,22-23,25-30H,7-9,12-21H2,1-3H3,(H,44,56)(H,45,59)(H,46,52)(H,47,57)(H,48,55)(H,49,58)(H,53,54)(H4,41,42,43)/t23-,25-,26-,27-,28-,29-,30+/m0/s1
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n/an/a 1.80n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530098
PNG
(CHEMBL4584228)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C40H59N11O10/c1-22(2)18-28-38(60)51-17-9-14-30(51)39(61)50-16-8-13-29(50)37(59)45-23(3)33(55)48-26(19-24-10-5-4-6-11-24)35(57)47-25(12-7-15-43-40(41)42)34(56)44-21-31(52)46-27(20-32(53)54)36(58)49-28/h4-6,10-11,22-23,25-30H,7-9,12-21H2,1-3H3,(H,44,56)(H,45,59)(H,46,52)(H,47,57)(H,48,55)(H,49,58)(H,53,54)(H4,41,42,43)/t23-,25-,26-,27-,28-,29-,30+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50112887
PNG
(CHEMBL3600736)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C54H71N15O9/c1-3-4-15-40(63-31(2)70)48(73)69-45-27-46(71)59-21-10-9-17-39(47(55)72)64-51(76)43(25-35-28-61-38-16-8-7-14-37(35)38)67-49(74)41(18-11-22-60-54(56)57)65-50(75)42(24-32-19-20-33-12-5-6-13-34(33)23-32)66-52(77)44(68-53(45)78)26-36-29-58-30-62-36/h5-8,12-14,16,19-20,23,28-30,39-45,61H,3-4,9-11,15,17-18,21-22,24-27H2,1-2H3,(H2,55,72)(H,58,62)(H,59,71)(H,63,70)(H,64,76)(H,65,75)(H,66,77)(H,67,74)(H,68,78)(H,69,73)(H4,56,57,60)/t39-,40+,41-,42+,43-,44-,45-/m0/s1
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n/an/a 2.40n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC4 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50112907
PNG
(CHEMBL3600918)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)67-45-30-49(74)62-24-13-12-20-46(50(58)75)70(3)55(80)44(28-38-31-64-41-19-11-10-17-40(38)41)69-52(77)47(21-14-25-63-57(59)60)71(4)54(79)43(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)48(72(5)56(45)81)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,76)(H,68,78)(H,69,77)(H4,59,60,63)/t42-,43-,44+,45+,46+,47+,48+/m1/s1
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n/an/a 2.5n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC3 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-3


(Homo sapiens (Human))
BDBM50429459
PNG
(CHEMBL2332367)
Show SMILES [#7]-[#6]-[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#7]-[#6]-1=O |r|
Show InChI InChI=1S/C27H41N9O7/c28-11-5-4-9-18-24(41)34-17(10-6-12-31-27(29)30)23(40)32-15-21(37)33-20(14-22(38)39)26(43)36-19(25(42)35-18)13-16-7-2-1-3-8-16/h1-3,7-8,17-20H,4-6,9-15,28H2,(H,32,40)(H,33,37)(H,34,41)(H,35,42)(H,36,43)(H,38,39)(H4,29,30,31)/t17-,18-,19+,20-/m0/s1
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n/an/a 2.60n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of vitronectin binding to Integrin alphaVbeta3 receptor (unknown origin) by competitive ELISA


J Med Chem 56: 1509-19 (2013)


Article DOI: 10.1021/jm301221x
BindingDB Entry DOI: 10.7270/Q2FJ2J4B
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112907
PNG
(CHEMBL3600918)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)67-45-30-49(74)62-24-13-12-20-46(50(58)75)70(3)55(80)44(28-38-31-64-41-19-11-10-17-40(38)41)69-52(77)47(21-14-25-63-57(59)60)71(4)54(79)43(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)48(72(5)56(45)81)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,76)(H,68,78)(H,69,77)(H4,59,60,63)/t42-,43-,44+,45+,46+,47+,48+/m1/s1
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n/an/a 2.80n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50112892
PNG
(CHEMBL3600835)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-41(64-32(2)71)49(74)69-45-28-47(72)60-22-11-10-18-40(48(56)73)65-52(77)44(26-36-29-62-39-17-9-8-15-38(36)39)67-50(75)42(19-12-23-61-55(57)58)66-51(76)43(25-33-20-21-34-13-6-7-14-35(34)24-33)68-53(78)46(70(3)54(45)79)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,77)(H,66,76)(H,67,75)(H,68,78)(H,69,74)(H4,57,58,61)/t40-,41+,42-,43+,44-,45-,46-/m0/s1
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n/an/a 3.20n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC3 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-3


(Homo sapiens (Human))
BDBM50545184
PNG
(CHEMBL4642869)
Show SMILES OC(=O)C(F)(F)F.NC(=N)NCCC[C@@H]1NC(=O)C2(CCCCC2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(O)=O)NC(=O)CNC1=O |r|
Show InChI InChI=1S/C28H40N8O7.C2HF3O2/c29-27(30)31-13-7-10-18-23(40)32-16-21(37)33-20(15-22(38)39)24(41)34-19(14-17-8-3-1-4-9-17)25(42)36-28(26(43)35-18)11-5-2-6-12-28;3-2(4,5)1(6)7/h1,3-4,8-9,18-20H,2,5-7,10-16H2,(H,32,40)(H,33,37)(H,34,41)(H,35,43)(H,36,42)(H,38,39)(H4,29,30,31);(H,6,7)/t18-,19+,20-;/m0./s1
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n/an/a 3.30n/an/an/an/an/an/a



Division of Organic Chemistry CSIR-National Chemical Laboratory (NCL)

Curated by ChEMBL


Assay Description
Inhibition of vitronectin binding to recombinant human integrin alphaV (Phe31 to Val992 residues) beta3 (Gly27 to Asp718 residues) expressed in CHO c...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127039
BindingDB Entry DOI: 10.7270/Q2RJ4P16
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112890
PNG
(CHEMBL3600833)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-41(64-32(2)71)49(74)67-44-28-47(72)60-22-11-10-18-40(48(56)73)65-50(75)42(26-36-29-62-39-17-9-8-15-38(36)39)68-53(78)46(19-12-23-61-55(57)58)70(3)54(79)45(25-33-20-21-34-13-6-7-14-35(34)24-33)69-51(76)43(66-52(44)77)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,75)(H,66,77)(H,67,74)(H,68,78)(H,69,76)(H4,57,58,61)/t40-,41+,42-,43-,44-,45+,46-/m0/s1
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n/an/a 3.40n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530140
PNG
(CHEMBL4445931)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C42H60N12O10/c1-22(2)17-30-40(63)54-16-8-13-32(54)41(64)53-15-7-12-31(53)39(62)48-23(3)35(58)51-28(18-24-20-46-26-10-5-4-9-25(24)26)37(60)50-27(11-6-14-45-42(43)44)36(59)47-21-33(55)49-29(19-34(56)57)38(61)52-30/h4-5,9-10,20,22-23,27-32,46H,6-8,11-19,21H2,1-3H3,(H,47,59)(H,48,62)(H,49,55)(H,50,60)(H,51,58)(H,52,61)(H,56,57)(H4,43,44,45)/t23-,27-,28-,29-,30-,31-,32+/m0/s1
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n/an/a 3.70n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530140
PNG
(CHEMBL4445931)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C42H60N12O10/c1-22(2)17-30-40(63)54-16-8-13-32(54)41(64)53-15-7-12-31(53)39(62)48-23(3)35(58)51-28(18-24-20-46-26-10-5-4-9-25(24)26)37(60)50-27(11-6-14-45-42(43)44)36(59)47-21-33(55)49-29(19-34(56)57)38(61)52-30/h4-5,9-10,20,22-23,27-32,46H,6-8,11-19,21H2,1-3H3,(H,47,59)(H,48,62)(H,49,55)(H,50,60)(H,51,58)(H,52,61)(H,56,57)(H4,43,44,45)/t23-,27-,28-,29-,30-,31-,32+/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50112887
PNG
(CHEMBL3600736)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C54H71N15O9/c1-3-4-15-40(63-31(2)70)48(73)69-45-27-46(71)59-21-10-9-17-39(47(55)72)64-51(76)43(25-35-28-61-38-16-8-7-14-37(35)38)67-49(74)41(18-11-22-60-54(56)57)65-50(75)42(24-32-19-20-33-12-5-6-13-34(33)23-32)66-52(77)44(68-53(45)78)26-36-29-58-30-62-36/h5-8,12-14,16,19-20,23,28-30,39-45,61H,3-4,9-11,15,17-18,21-22,24-27H2,1-2H3,(H2,55,72)(H,58,62)(H,59,71)(H,63,70)(H,64,76)(H,65,75)(H,66,77)(H,67,74)(H,68,78)(H,69,73)(H4,56,57,60)/t39-,40+,41-,42+,43-,44-,45-/m0/s1
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n/an/a 3.70n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC3 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50112894
PNG
(CHEMBL3600837)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-41(65-33(2)72)50(75)67-43-29-48(73)61-23-12-11-19-46(49(57)74)70(3)55(80)45(27-37-30-63-40-18-10-9-16-39(37)40)69-53(78)47(20-13-24-62-56(58)59)71(4)54(79)44(26-34-21-22-35-14-7-8-15-36(35)25-34)68-51(76)42(66-52(43)77)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,77)(H,67,75)(H,68,76)(H,69,78)(H4,58,59,62)/t41-,42+,43+,44-,45+,46+,47+/m1/s1
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n/an/a 3.90n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC1 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-6


(Homo sapiens (Human))
BDBM50110227
PNG
(3-{2-[4-(4-Methyl-pyridin-2-ylamino)-butyrylamino]...)
Show SMILES Cc1ccnc(NCCCC(=O)NCC(=O)NC(CC(O)=O)c2ccc(cc2)-c2cccc3ccccc23)c1
Show InChI InChI=1S/C31H32N4O4/c1-21-15-17-33-28(18-21)32-16-5-10-29(36)34-20-30(37)35-27(19-31(38)39)24-13-11-23(12-14-24)26-9-4-7-22-6-2-3-8-25(22)26/h2-4,6-9,11-15,17-18,27H,5,10,16,19-20H2,1H3,(H,32,33)(H,34,36)(H,35,37)(H,38,39)
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n/an/a 4n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of latency-associated peptide binding to Integrin alphaVbeta6 receptor (unknown origin) by competitive ELISA


J Med Chem 56: 1509-19 (2013)


Article DOI: 10.1021/jm301221x
BindingDB Entry DOI: 10.7270/Q2FJ2J4B
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50112901
PNG
(CHEMBL3600912)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-42(65-33(2)72)50(75)68-45-29-48(73)61-23-12-11-19-41(49(57)74)66-51(76)43(27-37-30-63-40-18-10-9-16-39(37)40)67-52(77)46(20-13-24-62-56(58)59)70(3)54(79)44(26-34-21-22-35-14-7-8-15-36(35)25-34)69-53(78)47(71(4)55(45)80)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,76)(H,67,77)(H,68,75)(H,69,78)(H4,58,59,62)/t41-,42+,43-,44+,45-,46-,47-/m0/s1
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n/an/a 4n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC1 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50112907
PNG
(CHEMBL3600918)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C57H77N15O9/c1-6-7-18-42(66-34(2)73)51(76)67-45-30-49(74)62-24-13-12-20-46(50(58)75)70(3)55(80)44(28-38-31-64-41-19-11-10-17-40(38)41)69-52(77)47(21-14-25-63-57(59)60)71(4)54(79)43(27-35-22-23-36-15-8-9-16-37(36)26-35)68-53(78)48(72(5)56(45)81)29-39-32-61-33-65-39/h8-11,15-17,19,22-23,26,31-33,42-48,64H,6-7,12-14,18,20-21,24-25,27-30H2,1-5H3,(H2,58,75)(H,61,65)(H,62,74)(H,66,73)(H,67,76)(H,68,78)(H,69,77)(H4,59,60,63)/t42-,43-,44+,45+,46+,47+,48+/m1/s1
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n/an/a 4n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC4 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530125
PNG
(CHEMBL4541418)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O)[C@@H](C)O |r|
Show InChI InChI=1S/C42H63N11O11/c1-22(2)19-29-40(63)53-18-10-15-31(53)41(64)52-17-9-14-30(52)38(61)46-23(3)34(57)48-27(20-25-11-6-5-7-12-25)36(59)47-26(13-8-16-45-42(43)44)35(58)51-33(24(4)54)39(62)49-28(21-32(55)56)37(60)50-29/h5-7,11-12,22-24,26-31,33,54H,8-10,13-21H2,1-4H3,(H,46,61)(H,47,59)(H,48,57)(H,49,62)(H,50,60)(H,51,58)(H,55,56)(H4,43,44,45)/t23-,24+,26-,27-,28-,29-,30-,31+,33-/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530125
PNG
(CHEMBL4541418)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O)[C@@H](C)O |r|
Show InChI InChI=1S/C42H63N11O11/c1-22(2)19-29-40(63)53-18-10-15-31(53)41(64)52-17-9-14-30(52)38(61)46-23(3)34(57)48-27(20-25-11-6-5-7-12-25)36(59)47-26(13-8-16-45-42(43)44)35(58)51-33(24(4)54)39(62)49-28(21-32(55)56)37(60)50-29/h5-7,11-12,22-24,26-31,33,54H,8-10,13-21H2,1-4H3,(H,46,61)(H,47,59)(H,48,57)(H,49,62)(H,50,60)(H,51,58)(H,55,56)(H4,43,44,45)/t23-,24+,26-,27-,28-,29-,30-,31+,33-/m0/s1
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Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530103
PNG
(CHEMBL4546687)
Show SMILES CC(C)C[C@@H]1NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C36H59N11O10/c1-19(2)14-22-31(53)44-21(8-5-11-39-36(37)38)30(52)40-17-27(48)43-23(16-29(50)51)32(54)45-24(15-20(3)4)34(56)47-13-7-10-26(47)35(57)46-12-6-9-25(46)33(55)41-18-28(49)42-22/h19-26H,5-18H2,1-4H3,(H,40,52)(H,41,55)(H,42,49)(H,43,48)(H,44,53)(H,45,54)(H,50,51)(H4,37,38,39)/t21-,22-,23-,24-,25-,26+/m0/s1
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n/an/a 4.5n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530103
PNG
(CHEMBL4546687)
Show SMILES CC(C)C[C@@H]1NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C36H59N11O10/c1-19(2)14-22-31(53)44-21(8-5-11-39-36(37)38)30(52)40-17-27(48)43-23(16-29(50)51)32(54)45-24(15-20(3)4)34(56)47-13-7-10-26(47)35(57)46-12-6-9-25(46)33(55)41-18-28(49)42-22/h19-26H,5-18H2,1-4H3,(H,40,52)(H,41,55)(H,42,49)(H,43,48)(H,44,53)(H,45,54)(H,50,51)(H4,37,38,39)/t21-,22-,23-,24-,25-,26+/m0/s1
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n/an/a 4.5n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50112900
PNG
(CHEMBL3600843)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)N(C)C(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-42(65-33(2)72)50(75)67-44-29-48(73)61-23-12-11-19-41(49(57)74)66-51(76)43(27-37-30-63-40-18-10-9-16-39(37)40)68-53(78)46(20-13-24-62-56(58)59)70(3)55(80)47(26-34-21-22-35-14-7-8-15-36(35)25-34)71(4)54(79)45(69-52(44)77)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,76)(H,67,75)(H,68,78)(H,69,77)(H4,58,59,62)/t41-,42+,43-,44-,45-,46-,47+/m0/s1
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n/an/a 4.90n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC1 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112892
PNG
(CHEMBL3600835)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-41(64-32(2)71)49(74)69-45-28-47(72)60-22-11-10-18-40(48(56)73)65-52(77)44(26-36-29-62-39-17-9-8-15-38(36)39)67-50(75)42(19-12-23-61-55(57)58)66-51(76)43(25-33-20-21-34-13-6-7-14-35(34)24-33)68-53(78)46(70(3)54(45)79)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,77)(H,66,76)(H,67,75)(H,68,78)(H,69,74)(H4,57,58,61)/t40-,41+,42-,43+,44-,45-,46-/m0/s1
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n/an/a 5n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-5/beta-1


(Homo sapiens (Human))
BDBM50429464
PNG
(CHEMBL2332827)
Show SMILES NC(N)=NCCC[C@@H]1NC(=O)CNC(=O)C[C@H](NC(=O)[C@H](NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC1=O)c1ccccc1)C(O)=O |r,wU:16.47,7.6,wD:20.40,24.24,(29.78,-44.54,;28.45,-45.31,;27.11,-44.54,;28.45,-46.85,;27.11,-47.62,;27.11,-49.16,;25.77,-49.94,;25.77,-51.48,;24.44,-52.25,;23.1,-51.48,;23.1,-49.94,;21.77,-52.25,;21.79,-53.77,;23.13,-54.53,;24.46,-53.74,;23.15,-56.07,;24.49,-56.81,;24.51,-58.37,;25.85,-59.12,;27.18,-58.34,;25.87,-60.66,;27.21,-61.42,;29.78,-53.78,;31.12,-54.55,;29.77,-52.24,;31.08,-51.47,;32.4,-52.23,;32.56,-53.73,;34.05,-54.04,;34.8,-52.73,;36.28,-52.41,;36.75,-50.97,;35.72,-49.84,;34.24,-50.16,;33.78,-51.6,;28.45,-51.48,;27.11,-52.25,;27.11,-53.79,;24.54,-61.45,;23.2,-60.68,;21.87,-61.47,;21.89,-63.02,;23.25,-63.77,;24.56,-62.98,;25.82,-56.03,;27.16,-56.79,;25.8,-54.49,)|
Show InChI InChI=1S/C31H37N9O7/c32-31(33)34-12-6-11-21-27(43)38-22(13-18-15-35-20-10-5-4-9-19(18)20)28(44)40-26(17-7-2-1-3-8-17)29(45)39-23(30(46)47)14-24(41)36-16-25(42)37-21/h1-5,7-10,15,21-23,26,35H,6,11-14,16H2,(H,36,41)(H,37,42)(H,38,43)(H,39,45)(H,40,44)(H,46,47)(H4,32,33,34)/t21-,22+,23-,26+/m0/s1
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n/an/a 5.5n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of fibronectin binding to human Integrin alpha5beta1 receptor by competitive ELISA


J Med Chem 56: 1509-19 (2013)


Article DOI: 10.1021/jm301221x
BindingDB Entry DOI: 10.7270/Q2FJ2J4B
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-3


(Homo sapiens (Human))
BDBM50545181
PNG
(CHEMBL4633117)
Show SMILES OC(=O)C(F)(F)F.CC1(C)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC1=O |r|
Show InChI InChI=1S/C25H36N8O7.C2HF3O2/c1-25(2)23(40)32-15(9-6-10-28-24(26)27)20(37)29-13-18(34)30-17(12-19(35)36)21(38)31-16(22(39)33-25)11-14-7-4-3-5-8-14;3-2(4,5)1(6)7/h3-5,7-8,15-17H,6,9-13H2,1-2H3,(H,29,37)(H,30,34)(H,31,38)(H,32,40)(H,33,39)(H,35,36)(H4,26,27,28);(H,6,7)/t15-,16+,17-;/m0./s1
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n/an/a 5.5n/an/an/an/an/an/a



Division of Organic Chemistry CSIR-National Chemical Laboratory (NCL)

Curated by ChEMBL


Assay Description
Inhibition of vitronectin binding to recombinant human integrin alphaV (Phe31 to Val992 residues) beta3 (Gly27 to Asp718 residues) expressed in CHO c...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127039
BindingDB Entry DOI: 10.7270/Q2RJ4P16
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530124
PNG
(CHEMBL4537950)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C41H61N11O11/c1-22(2)18-28-39(62)52-17-9-14-31(52)40(63)51-16-8-13-30(51)38(61)45-23(3)33(56)47-26(19-24-10-5-4-6-11-24)35(58)46-25(12-7-15-44-41(42)43)34(57)50-29(21-53)37(60)48-27(20-32(54)55)36(59)49-28/h4-6,10-11,22-23,25-31,53H,7-9,12-21H2,1-3H3,(H,45,61)(H,46,58)(H,47,56)(H,48,60)(H,49,59)(H,50,57)(H,54,55)(H4,42,43,44)/t23-,25-,26-,27-,28-,29-,30-,31+/m0/s1
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n/an/a 5.80n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530124
PNG
(CHEMBL4537950)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C41H61N11O11/c1-22(2)18-28-39(62)52-17-9-14-31(52)40(63)51-16-8-13-30(51)38(61)45-23(3)33(56)47-26(19-24-10-5-4-6-11-24)35(58)46-25(12-7-15-44-41(42)43)34(57)50-29(21-53)37(60)48-27(20-32(54)55)36(59)49-28/h4-6,10-11,22-23,25-31,53H,7-9,12-21H2,1-3H3,(H,45,61)(H,46,58)(H,47,56)(H,48,60)(H,49,59)(H,50,57)(H,54,55)(H4,42,43,44)/t23-,25-,26-,27-,28-,29-,30-,31+/m0/s1
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n/an/a 5.80n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112894
PNG
(CHEMBL3600837)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-41(65-33(2)72)50(75)67-43-29-48(73)61-23-12-11-19-46(49(57)74)70(3)55(80)45(27-37-30-63-40-18-10-9-16-39(37)40)69-53(78)47(20-13-24-62-56(58)59)71(4)54(79)44(26-34-21-22-35-14-7-8-15-36(35)25-34)68-51(76)42(66-52(43)77)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,77)(H,67,75)(H,68,76)(H,69,78)(H4,58,59,62)/t41-,42+,43+,44-,45+,46+,47+/m1/s1
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n/an/a 6n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112888
PNG
(CHEMBL3600737)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](N(C)C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-40(64-32(2)71)49(74)68-44-28-47(72)60-22-11-10-19-46(48(56)73)70(3)54(79)45(26-36-29-62-39-17-9-8-15-38(36)39)69-50(75)41(18-12-23-61-55(57)58)65-51(76)42(25-33-20-21-34-13-6-7-14-35(34)24-33)66-52(77)43(67-53(44)78)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,76)(H,66,77)(H,67,78)(H,68,74)(H,69,75)(H4,57,58,61)/t40-,41+,42-,43+,44+,45+,46+/m1/s1
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n/an/a 6.10n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530122
PNG
(CHEMBL4577219)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C35H55N11O12/c1-17(2)13-22-33(57)46-12-6-9-24(46)34(58)45-11-5-8-23(45)32(56)40-18(3)28(52)43-21(15-27(50)51)31(55)42-19(7-4-10-38-35(36)37)29(53)39-16-25(47)41-20(14-26(48)49)30(54)44-22/h17-24H,4-16H2,1-3H3,(H,39,53)(H,40,56)(H,41,47)(H,42,55)(H,43,52)(H,44,54)(H,48,49)(H,50,51)(H4,36,37,38)/t18-,19-,20-,21-,22-,23-,24+/m0/s1
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n/an/a 6.30n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530122
PNG
(CHEMBL4577219)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O |r|
Show InChI InChI=1S/C35H55N11O12/c1-17(2)13-22-33(57)46-12-6-9-24(46)34(58)45-11-5-8-23(45)32(56)40-18(3)28(52)43-21(15-27(50)51)31(55)42-19(7-4-10-38-35(36)37)29(53)39-16-25(47)41-20(14-26(48)49)30(54)44-22/h17-24H,4-16H2,1-3H3,(H,39,53)(H,40,56)(H,41,47)(H,42,55)(H,43,52)(H,44,54)(H,48,49)(H,50,51)(H4,36,37,38)/t18-,19-,20-,21-,22-,23-,24+/m0/s1
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n/an/a 6.30n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Homo sapiens (Human))
BDBM50112901
PNG
(CHEMBL3600912)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O)C(N)=O |r|
Show InChI InChI=1S/C56H75N15O9/c1-5-6-17-42(65-33(2)72)50(75)68-45-29-48(73)61-23-12-11-19-41(49(57)74)66-51(76)43(27-37-30-63-40-18-10-9-16-39(37)40)67-52(77)46(20-13-24-62-56(58)59)70(3)54(79)44(26-34-21-22-35-14-7-8-15-36(35)25-34)69-53(78)47(71(4)55(45)80)28-38-31-60-32-64-38/h7-10,14-16,18,21-22,25,30-32,41-47,63H,5-6,11-13,17,19-20,23-24,26-29H2,1-4H3,(H2,57,74)(H,60,64)(H,61,73)(H,65,72)(H,66,76)(H,67,77)(H,68,75)(H,69,78)(H4,58,59,62)/t41-,42+,43-,44+,45-,46-,47-/m0/s1
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n/an/a 6.30n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC5 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50112890
PNG
(CHEMBL3600833)
Show SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(N)=N)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)NC1=O)C(N)=O |r|
Show InChI InChI=1S/C55H73N15O9/c1-4-5-16-41(64-32(2)71)49(74)67-44-28-47(72)60-22-11-10-18-40(48(56)73)65-50(75)42(26-36-29-62-39-17-9-8-15-38(36)39)68-53(78)46(19-12-23-61-55(57)58)70(3)54(79)45(25-33-20-21-34-13-6-7-14-35(34)24-33)69-51(76)43(66-52(44)77)27-37-30-59-31-63-37/h6-9,13-15,17,20-21,24,29-31,40-46,62H,4-5,10-12,16,18-19,22-23,25-28H2,1-3H3,(H2,56,73)(H,59,63)(H,60,72)(H,64,71)(H,65,75)(H,66,77)(H,67,74)(H,68,78)(H,69,76)(H4,57,58,61)/t40-,41+,42-,43-,44-,45+,46-/m0/s1
PDB

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UniProtKB/SwissProt

antibodypedia
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n/an/a 6.40n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [125I]-[Nle4,D-Phe7]-alpha-MSH from human MC4 receptor expressed in HEK293 cells after 40 mins by luminescence counting


J Med Chem 58: 6359-67 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00102
BindingDB Entry DOI: 10.7270/Q251410F
More data for this
Ligand-Target Pair
Integrin alpha-V/beta-8


(Homo sapiens (Human))
BDBM50530120
PNG
(CHEMBL4455010)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C1=O)c1ccccc1 |r|
Show InChI InChI=1S/C39H57N11O10/c1-21(2)18-26-37(59)50-17-9-14-28(50)38(60)49-16-8-13-27(49)35(57)44-22(3)32(54)48-31(23-10-5-4-6-11-23)36(58)46-24(12-7-15-42-39(40)41)33(55)43-20-29(51)45-25(19-30(52)53)34(56)47-26/h4-6,10-11,21-22,24-28,31H,7-9,12-20H2,1-3H3,(H,43,55)(H,44,57)(H,45,51)(H,46,58)(H,47,56)(H,48,54)(H,52,53)(H4,40,41,42)/t22-,24-,25-,26-,27-,28+,31-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.40n/an/an/an/an/an/a



Technische Universit£t M£nchen

Curated by ChEMBL


Assay Description
Inhibition of LAP binding to human integrin alphavbeta8 receptor after 1 hr by solid-phase binding assay


J Med Chem 62: 2024-2037 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01588
BindingDB Entry DOI: 10.7270/Q26T0R53
More data for this
Ligand-Target Pair
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