Ki Summary

Reaction Details

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Target

Gonadotropin-releasing hormone receptor

Ligand

BDBM50470126

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_100131 (CHEMBL858015)

0.166±n/a nM

Citation

Haviv, F; Fitzpatrick, TD; Nichols, CJ; Bush, EN; Diaz, G; Bammert, G; Nguyen, AT; Johnson, ES; Knittle, J; Greer, J In vitro and in vivo activities of reduced-size antagonists of luteinizing hormone-releasing hormone. J Med Chem37:701-5 (1994) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Gonadotropin-releasing hormone receptor

Name:

Gonadotropin-releasing hormone receptor

Synonyms:

GNRHR_RAT | GnRH receptor | GnRH-R | Gnrhr

Type:

PROTEIN

Mol. Mass.:

37767.60

Organism:

Rattus norvegicus

Description:

ChEMBL_1335047

Residue:

327

Sequence:

MANNASLEQDQNHCSAINNSIPLTQGKLPTLTLSGKIRVTVTFFLFLLSTAFNASFLVKL
QRWTQKRKKGKKLSRMKVLLKHLTLANLLETLIVMPLDGMWNITVQWYAGEFLCKVLSYL
KLFSMYAPAFMMVVISLDRSLAVTQPLAVQSKSKLERSMTSLAWILSIVFAGPQLYIFRM
IYLADGSGPAVFSQCVTHCSFPQWWHEAFYNFFTFSCLFIIPLLIMLICNAKIIFALTRV
LHQDPRKLQLNQSKNNIPRARLRTLKMTVAFGTSFVICWTPYYVLGIWYWFDPEMLNRVS
EPVNHFFFLFAFLNPCFDPLIYGYFSL

BDBM50470126

n/a

Name

BDBM50470126

Synonyms:

CHEMBL266032

Type

Small organic molecule

Emp. Form.

C64H82N14O11

Mol. Mass.

1223.4231

SMILES

CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(C)=O |wU:57.63,12.20,77.91,wD:45.57,31.44,63.79,23.28,5.4,(17.4,.92,;17.4,-.62,;16.08,-1.39,;14.73,-.64,;13.42,-1.39,;14.7,.87,;15.92,1.76,;15.41,3.21,;13.87,3.21,;13.44,1.75,;12.1,.99,;12.09,-.55,;10.78,1.76,;10.79,3.33,;12.12,4.07,;12.14,5.61,;13.48,6.4,;13.48,7.92,;14.83,8.68,;12.16,8.71,;9.44,1.02,;8.09,1.79,;8.12,3.34,;6.75,1.03,;6.75,-.51,;8.08,-1.29,;9.41,-.52,;8.06,-2.83,;5.42,1.82,;4.08,1.05,;4.07,-.49,;2.76,1.83,;2.77,3.37,;2.29,4.83,;.83,5.31,;.83,6.86,;2.31,7.33,;2.93,8.75,;4.47,8.91,;5.37,7.66,;4.75,6.24,;3.21,6.08,;1.42,1.06,;.07,1.85,;.07,3.39,;-1.27,1.08,;-1.27,-.46,;.06,-1.23,;.04,-2.79,;1.38,-3.57,;2.73,-2.8,;4.05,-3.57,;2.74,-1.26,;1.39,-.48,;-2.59,1.88,;-3.93,1.11,;-3.95,-.45,;-5.26,1.89,;-5.25,3.42,;-3.91,4.19,;-6.61,1.12,;-7.94,1.91,;-7.92,3.45,;-9.29,1.14,;-9.29,-.4,;-7.98,-1.19,;-6.54,-.56,;-5.52,-1.71,;-6.31,-3.05,;-5.84,-4.52,;-6.89,-5.66,;-8.39,-5.34,;-8.85,-3.86,;-7.82,-2.73,;-10.61,1.91,;-11.95,1.15,;-11.99,-.38,;-13.28,1.95,;-13.27,3.49,;-11.92,4.26,;-11.95,5.8,;-10.57,6.54,;-9.26,5.77,;-9.26,4.23,;-10.61,3.46,;-14.62,1.18,;-15.82,2.14,;-17.24,1.56,;-15.6,3.65,)|

Structure