Ki Summary

Reaction Details

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Target

Melanocortin receptor 5

Ligand

BDBM50158406

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_430381 (CHEMBL915324)

EC50

0.18±n/a nM

Citation

Joseph, CG; Wang, XS; Scott, JW; Bauzo, RM; Xiang, Z; Richards, NG; Haskell-Luevano, C Stereochemical studies of the monocyclic agouti-related protein (103-122) Arg-Phe-Phe residues: conversion of a melanocortin-4 receptor antagonist into an agonist and results in the discovery of a potent and selective melanocortin-1 agonist. J Med Chem47:6702-10 (2004) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Melanocortin receptor 5

Name:

Melanocortin receptor 5

Synonyms:

MC5R_MOUSE | Mc5r | Melanocortin receptor 5 | Melanocortin receptor 5 (MC5R)

Type:

Enzyme

Mol. Mass.:

36966.58

Organism:

Mus musculus (Mouse)

Description:

P41149

Residue:

325

Sequence:

MNSSSTLTVLNLTLNASEDGILGSNVKNKSLACEEMGIAVEVFLTLGLVSLLENILVIGA
IVKNKNLHSPMYFFVGSLAVADMLVSMSNAWETVTIYLLNNKHLVIADTFVRHIDNVFDS
MICISVVASMCSLLAIAVDRYITIFYALRYHHIMTARRSGVIIACIWTFCISCGIVFIIY
YESKYVIICLISMFFTMLFFMVSLYIHMFLLARNHVKRIAASPRYNSVRQRTSMKGAITL
TMLLGIFIVCWSPFFLHLILMISCPQNVYCSCFMSYFNMYLILIMCNSVIDPLIYALRSQ
EMRRTFKEIVCCHGFRRPCRLLGGY

BDBM50158406

n/a

Name

BDBM50158406

Synonyms:

Ac-Nle-c[Asp-His-DPhe-Arg-Trp-Lys]-NH2 | CHEMBL224277

Type

Small organic molecule

Emp. Form.

C53H73N15O11

Mol. Mass.

1096.2406

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](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)C1CC(O)=O)C(N)=O |r,wU:39.41,50.52,21.80,12.11,wD:25.25,61.64,4.4,(29.19,-27.12,;27.85,-27.89,;26.52,-27.12,;25.19,-27.89,;23.86,-27.12,;22.52,-27.89,;22.52,-29.43,;21.19,-30.2,;23.86,-30.2,;23.86,-25.58,;25.18,-24.81,;22.48,-24.88,;22.48,-23.34,;21.24,-22.58,;19.81,-23.34,;19.81,-24.88,;18.47,-22.58,;18.62,-21.05,;17.36,-20.38,;17.37,-18.88,;18.67,-18.13,;18.73,-16.56,;20.05,-15.76,;21.28,-16.68,;21.28,-18.22,;22.59,-15.93,;22.59,-14.39,;21.26,-13.62,;19.85,-14.24,;18.82,-13.1,;19.59,-11.76,;19.11,-10.3,;20.14,-9.15,;21.65,-9.47,;22.13,-10.93,;21.1,-12.08,;23.88,-16.78,;25.15,-15.91,;25.15,-14.37,;26.41,-16.64,;26.41,-15.1,;27.75,-14.33,;27.75,-12.79,;29.08,-12.02,;29.08,-10.48,;27.75,-9.71,;30.41,-9.71,;27.75,-15.87,;29.06,-16.67,;30.39,-15.9,;29,-18.19,;30.33,-18.96,;31.65,-18.19,;33.01,-18.98,;34.33,-18.22,;34.33,-16.7,;33,-15.93,;31.67,-16.7,;28.58,-18.63,;27.75,-21.04,;29.24,-21.45,;26.85,-22.56,;27.89,-23.7,;29.39,-23.37,;30.01,-21.96,;31.55,-22.11,;31.9,-23.61,;30.56,-24.37,;25.33,-22.28,;24.81,-20.84,;25.8,-19.66,;23.29,-20.57,;21.89,-20.56,;20.54,-20.19,;20.18,-18.84,;19.54,-21.18,;17.44,-15.73,;16.11,-16.61,;17.44,-14.19,)|

Structure