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BDBM50211374 CHEMBL2371967::c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7-Pip8-Trp9-Lys10)-NH2

SMILES: [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O

InChI Key: InChIKey=DFDCZNQATCGDRV-LNVKHAPMSA-N

Data: 4 IC50  2 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50211374   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Melanocortin receptor 5 (MC5R)


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
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n/an/an/an/a 0.450n/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Agonist activity at human MC5R expressed in CHO cells assessed as cAMP accumulation


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
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n/an/a 3.90E+3n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]NDPalphaMSH from human cloned MC3R expressed in CHO cells


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
PDB

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n/an/a 710n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]NDPalphaMSH from human cloned melanocortin receptor 1b expressed in CHO cells


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair
Melanocortin receptor 5 (MC5R)


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
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n/an/a 2.70n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]NDPalphaMSH from human cloned MC5R expressed in CHO cells


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
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n/an/a 720n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]NDPalphaMSH from human cloned MC4R expressed in CHO cells


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50211374
PNG
(CHEMBL2371967 | c-Nle4-cyclo(Asp5-Tic6-D-4,4'-Bip7...)
Show SMILES [H][C@@]12CCCCN1C(=O)[C@H](Cc1ccc(cc1)-c1ccccc1)NC(=O)[C@]1([H])Cc3ccccc3CN1C(=O)[C@H](CC(=O)NCCCC[C@H](NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC2=O)C(N)=O)NC(=O)[C@H](CCCC)NC(C)=O
Show InChI InChI=1S/C60H72N10O9/c1-3-4-21-47(64-37(2)71)55(74)67-50-34-53(72)62-29-14-12-23-46(54(61)73)65-56(75)48(32-43-35-63-45-22-11-10-20-44(43)45)66-57(76)51-24-13-15-30-69(51)59(78)49(31-38-25-27-40(28-26-38)39-16-6-5-7-17-39)68-58(77)52-33-41-18-8-9-19-42(41)36-70(52)60(50)79/h5-11,16-20,22,25-28,35,46-52,63H,3-4,12-15,21,23-24,29-34,36H2,1-2H3,(H2,61,73)(H,62,72)(H,64,71)(H,65,75)(H,66,76)(H,67,74)(H,68,77)/t46?,47-,48-,49-,50-,51-,52-/m0/s1
PDB

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n/an/an/an/a 130n/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Agonist activity at human melanocortin receptor 1b expressed in CHO cells assessed as cAMP accumulation


J Med Chem 50: 2520-6 (2007)


Article DOI: 10.1021/jm0614275
BindingDB Entry DOI: 10.7270/Q2JQ10QM
More data for this
Ligand-Target Pair