Ki Summary

Reaction Details

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Target

Melanocortin receptor 5

Ligand

BDBM50217749

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_448695 (CHEMBL897841)

27000±n/a nM

Citation

Mutulis, F; Kreicberga, J; Yahorava, S; Mutule, I; Borisova-Jan, L; Yahorau, A; Muceniece, R; Azena, S; Veiksina, S; Petrovska, R; Wikberg, JE Design and synthesis of a library of tertiary amides: evaluation as mimetics of the melanocortins' active core. Bioorg Med Chem15:5787-810 (2007) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Melanocortin receptor 5

Name:

Melanocortin receptor 5

Synonyms:

Type:

Enzyme

Mol. Mass.:

36612.92

Organism:

Homo sapiens (Human)

Description:

P33032

Residue:

325

Sequence:

MNSSFHLHFLDLNLNATEGNLSGPNVKNKSSPCEDMGIAVEVFLTLGVISLLENILVIGA
IVKNKNLHSPMYFFVCSLAVADMLVSMSSAWETITIYLLNNKHLVIADAFVRHIDNVFDS
MICISVVASMCSLLAIAVDRYVTIFYALRYHHIMTARRSGAIIAGIWAFCTGCGIVFILY
SESTYVILCLISMFFAMLFLLVSLYIHMFLLARTHVKRIAALPGASSARQRTSMQGAVTV
TMLLGVFTVCWAPFFLHLTLMLSCPQNLYCSRFMSHFNMYLILIMCNSVMDPLIYAFRSQ
EMRKTFKEIICCRGFRIACSFPRRD

BDBM50217749

n/a

Name

BDBM50217749

Synonyms:

CHEMBL236020 | N-((Z)-2-chloro-3-phenyl-allyl)-N-[4-(4-guanidino-cyclohexylmethyl)-cyclohexyl]-4-(1H-indol-3-yl)-butyramide

Type

Small organic molecule

Emp. Form.

C35H46ClN5O

Mol. Mass.

588.226

SMILES

NC(N)=NC1CCC(CC2CCC(CC2)N(C\C(Cl)=C\c2ccccc2)C(=O)CCCc2c[nH]c3ccccc23)CC1 |(37.75,-39.73,;39.09,-40.5,;40.42,-39.74,;39.08,-42.05,;37.77,-42.88,;37.84,-44.42,;36.55,-45.24,;35.19,-44.53,;33.89,-45.37,;33.97,-46.9,;35.34,-47.61,;35.41,-49.14,;34.12,-49.98,;32.75,-49.28,;32.68,-47.74,;34.21,-51.51,;32.88,-52.45,;31.47,-51.64,;31.48,-50.01,;30.06,-52.44,;28.66,-51.62,;28.67,-50,;27.27,-49.18,;25.86,-49.99,;25.85,-51.62,;27.26,-52.43,;35.53,-52.26,;35.56,-53.78,;36.85,-51.47,;38.21,-52.22,;39.52,-51.42,;40.86,-52.17,;40.76,-53.71,;42.19,-54.29,;43.17,-53.1,;44.7,-53.04,;45.42,-51.69,;44.59,-50.39,;43.07,-50.45,;42.36,-51.8,;35.11,-43,;36.41,-42.17,)|

Structure