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BDBM50184352 CHEMBL427205::c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2

SMILES: CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O

InChI Key: InChIKey=STHTUYXXUBUJIE-NMIKHESWSA-N

Data: 4 IC50  4 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 8 hits for monomerid = 50184352   
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 3


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/an/an/a 27n/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Activity against hMC3R transfected in HEK293 cells by intracellular cAMP accumulation


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocortin receptor 5 (MC5R)


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/a 110n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Inhibitory activity against hMC5R transfected in HEK293 cells


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Inhibitory activity against hMC1R transfected in HEK293 cells


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/an/an/a 3.00E+3n/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Activity against hMC4R transfected in HEK293 cells by intracellular cAMP accumulation


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/a 2.50E+3n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Inhibitory activity against hMC4R transfected in HEK293 cells


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Activity against hMC1R transfected in HEK293 cells by intracellular cAMP accumulation


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocortin receptor 5 (MC5R)


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
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n/an/an/an/a 180n/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Activity against hMC5R transfected in HEK293 cells by intracellular cAMP accumulation


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50184352
PNG
(CHEMBL427205 | c[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2)
Show SMILES CCCC[C@@H]1NC(=O)CC[C@H](NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC1=O)C(C)C)C(N)=O |wU:10.60,39.41,wD:50.57,28.30,14.14,4.3,(-1.88,-14.31,;-1.88,-15.85,;-.79,-16.58,;-.79,-18.09,;.43,-18.79,;2.13,-18.17,;2.13,-16.63,;.79,-15.87,;3.34,-15.85,;3.87,-14.57,;5.39,-14.36,;6.16,-15.69,;6.91,-17.02,;8.4,-16.61,;7.31,-18.51,;8.85,-18.51,;9.62,-19.85,;9.62,-21.39,;11.08,-21.87,;11.99,-20.64,;13.52,-20.48,;14.16,-19.09,;13.25,-17.83,;11.72,-17.98,;11.09,-19.38,;6.38,-19.73,;6.96,-21.15,;8.5,-21.14,;6.56,-22.63,;7.65,-23.73,;9.14,-23.32,;10.22,-24.41,;11.71,-24.02,;12.8,-25.1,;14.29,-24.71,;12.41,-26.59,;5.22,-23.39,;3.89,-22.62,;3.9,-21.08,;2.55,-23.38,;2.55,-24.92,;3.88,-25.69,;3.88,-27.23,;5.2,-28.01,;6.54,-27.24,;6.54,-25.69,;5.21,-24.92,;1.21,-22.61,;-.93,-22.79,;-.93,-24.3,;-2.04,-21.51,;-1.31,-20.3,;.09,-20.32,;1.32,-21.07,;-3.44,-21.49,;-4.12,-20.27,;-4.15,-22.69,;6.17,-13.03,;5.39,-11.69,;7.71,-13.03,)|
Show InChI InChI=1S/C42H59N11O7/c1-4-5-15-30-38(57)53-35(24(2)3)41(60)52-32(21-25-12-7-6-8-13-25)39(58)50-31(17-11-20-46-42(44)45)37(56)51-33(22-26-23-47-28-16-10-9-14-27(26)28)40(59)49-29(36(43)55)18-19-34(54)48-30/h6-10,12-14,16,23-24,29-33,35,47H,4-5,11,15,17-22H2,1-3H3,(H2,43,55)(H,48,54)(H,49,59)(H,50,58)(H,51,56)(H,52,60)(H,53,57)(H4,44,45,46)/t29-,30-,31-,32+,33-,35-/m0/s1
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 600n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Inhibitory activity against hMC3R transfected in HEK293 cells


J Med Chem 49: 1946-52 (2006)


Article DOI: 10.1021/jm0510326
BindingDB Entry DOI: 10.7270/Q2C24W1F
More data for this
Ligand-Target Pair