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TargetGonadotropin-releasing hormone receptor
LigandBDBM50121487
Substrate/Competitorn/a
Meas. Tech.ChEBML_71600
Ki 300±n/a nM
Citation Luthin, DRHong, YTompkins, EAnderes, KLPaderes, GKraynov, EACastro, MANared-Hood, KDCastillo, RGregory, MVazir, HMay, JMAnderson, MB Characterization of mono- and diaminopyrimidine derivatives as novel, nonpeptide gonadotropin releasing hormone (GnRH) receptor antagonists. Bioorg Med Chem Lett12:3635-9 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Gonadotropin-releasing hormone receptor
Name:Gonadotropin-releasing hormone receptor
Synonyms:GNRHR | GNRHR_HUMAN | GRHR | GnRH receptor | GnRH-R | Gonadotropin releasing hormone 1 (GnRHR1) | Gonadotropin-releasing hormone receptor | Gonadotropin-releasing hormone receptor (GnRH)
Type:Enzyme
Mol. Mass.:37749.45
Organism:Homo sapiens (Human)
Description:P30968
Residue:328
Sequence:
MANSASPEQNQNHCSAINNSIPLMQGNLPTLTLSGKIRVTVTFFLFLLSATFNASFLLKL
QKWTQKKEKGKKLSRMKLLLKHLTLANLLETLIVMPLDGMWNITVQWYAGELLCKVLSYL
KLFSMYAPAFMMVVISLDRSLAITRPLALKSNSKVGQSMVGLAWILSSVFAGPQLYIFRM
IHLADSSGQTKVFSQCVTHCSFSQWWHQAFYNFFTFSCLFIIPLFIMLICNAKIIFTLTR
VLHQDPHELQLNQSKNNIPRARLKTLKMTVAFATSFTVCWTPYYVLGIWYWFDPEMLNRL
SDPVNHFFFLFAFLNPCFDPLIYGYFSL
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  Blast E-value cutoff:
BDBM50121487
n/a
NameBDBM50121487
Synonyms:5-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-naphthalen-2-ylmethyl)-furan-2-carboxylic acid {4-[(4,6-dimethoxy-pyrimidin-2-ylamino)-methyl]-cyclohexylmethyl}-amide | CHEMBL333349
TypeSmall organic molecule
Emp. Form.C35H48N4O4
Mol. Mass.588.78
SMILESCOc1cc(OC)nc(NCC2CCC(CNC(=O)c3ccc(Cc4cc5c(cc4C)C(C)(C)CCC5(C)C)o3)CC2)n1 |(19.23,-16.95,;19.26,-18.68,;17.79,-19.57,;17.82,-21.3,;16.33,-22.18,;16.35,-23.9,;17.87,-24.75,;14.83,-21.35,;14.81,-19.62,;13.31,-18.78,;11.83,-19.65,;10.31,-18.81,;8.84,-19.69,;7.33,-18.86,;7.3,-17.14,;5.79,-16.3,;4.3,-17.19,;2.94,-16.47,;2.95,-15.04,;1.58,-17.19,;1.58,-18.63,;-1.14,-18.62,;-1.12,-17.18,;-2.5,-16.46,;-3.86,-17.19,;-5.22,-16.48,;-6.56,-17.19,;-6.56,-18.63,;-5.2,-19.33,;-3.86,-18.63,;-2.5,-19.33,;-7.91,-19.33,;-9.28,-20.04,;-6.56,-20.06,;-9.27,-18.63,;-9.27,-17.19,;-7.91,-16.47,;-9.28,-15.75,;-6.56,-15.75,;.22,-16.46,;8.79,-16.25,;10.29,-17.09,;16.27,-18.73,)|
Structure
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