Reaction Details | |||
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Target | Corticotropin-releasing factor receptor 1 | ||
Ligand | BDBM50074512 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_51114 (CHEMBL664960) | ||
Ki | 5.2±n/a nM | ||
Citation | Chorvat, RJ; Bakthavatchalam, R; Beck, JP; Gilligan, PJ; Wilde, RG; Cocuzza, AJ; Hobbs, FW; Cheeseman, RS; Curry, M; Rescinito, JP; Krenitsky, P; Chidester, D; Yarem, JA; Klaczkiewicz, JD; Hodge, CN; Aldrich, PE; Wasserman, ZR; Fernandez, CH; Zaczek, R; Fitzgerald, LW; Huang, SM; Shen, HL; Wong, YN; Chien, BM; Arvanitis, A Synthesis, corticotropin-releasing factor receptor binding affinity, and pharmacokinetic properties of triazolo-, imidazo-, and pyrrolopyrimidines and -pyridines. J Med Chem42:833-48 (1999) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Corticotropin-releasing factor receptor 1 | |||
Name: | Corticotropin-releasing factor receptor 1 | ||
Synonyms: | CRF-R | CRF-R2 Alpha | CRF1 | CRFR | CRFR1 | CRFR1_HUMAN | CRH-R 1 | CRHR | CRHR1 | Corticotropin releasing factor receptor 1 | Corticotropin-releasing factor receptor 1 (CRF-1) | Corticotropin-releasing factor receptor 1 (CRF1) | Corticotropin-releasing hormone receptor 1 | ||
Type: | Enzyme | ||
Mol. Mass.: | 50744.31 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P34998 | ||
Residue: | 444 | ||
Sequence: |
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BDBM50074512 | |||
n/a | |||
Name | BDBM50074512 | ||
Synonyms: | Butyl-[9-(2-chloro-4,6-dimethoxy-phenyl)-2-methyl-9H-purin-6-yl]-ethyl-amine | CHEMBL355721 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H26ClN5O2 | ||
Mol. Mass. | 403.906 | ||
SMILES | CCCCN(CC)c1nc(C)nc2n(cnc12)-c1c(Cl)cc(OC)cc1OC |(15.41,-2.57,;14.07,-1.8,;12.72,-2.57,;11.39,-1.8,;10.06,-2.57,;8.73,-1.8,;8.73,-.24,;10.06,-4.11,;8.73,-4.88,;8.73,-6.42,;7.38,-7.19,;10.06,-7.19,;11.39,-6.42,;12.86,-6.89,;13.75,-5.63,;12.86,-4.39,;11.39,-4.88,;13.18,-8.38,;14.64,-8.87,;15.78,-7.82,;14.96,-10.37,;13.84,-11.39,;14.17,-12.91,;13.04,-13.96,;12.37,-10.93,;12.04,-9.43,;10.57,-8.96,;9.43,-9.99,)| | ||
Structure |