Reaction Details | |||
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Target | Corticotropin-releasing factor receptor 1 | ||
Ligand | BDBM50087560 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEBML_51284 | ||
Ki | 3.5±n/a nM | ||
Citation | Hsin, LW; Webster, EL; Chrousos, GP; Gold, PW; Eckelman, WC; Contoreggi, C; Rice, KC Synthesis and biological activity of fluoro-substituted pyrrolo[2,3-d]pyrimidines: the development of potential positron emission tomography imaging agents for the corticotropin-releasing hormone type 1 receptor. Bioorg Med Chem Lett10:707-10 (2000) [PubMed] | ||
More Info.: | Get all data from this article, Assay Method | ||
Corticotropin-releasing factor receptor 1 | |||
Name: | Corticotropin-releasing factor receptor 1 | ||
Synonyms: | CRF-R | CRF1 | CRFR1_RAT | CRH-R 1 | Corticotropin releasing factor receptor | Corticotropin releasing factor receptor 1 | Corticotropin-releasing Factor Receptor 1 | Corticotropin-releasing hormone receptor 1 | Crhr | Crhr1 | ||
Type: | G Protein-Coupled Receptor (GPCR) | ||
Mol. Mass.: | 47870.75 | ||
Organism: | Rattus norvegicus (rat) | ||
Description: | Receptor binding assays were performed using rat cortex homogenate. | ||
Residue: | 415 | ||
Sequence: |
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BDBM50087560 | |||
n/a | |||
Name | BDBM50087560 | ||
Synonyms: | CHEMBL348967 | Ethyl-(4-fluoro-butyl)-[2,5,6-trimethyl-7-(2,4,6-trimethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine | ||
Type | Small organic molecule | ||
Emp. Form. | C24H33FN4 | ||
Mol. Mass. | 396.544 | ||
SMILES | CCN(CCCCF)c1nc(C)nc2n(c(C)c(C)c12)-c1c(C)cc(C)cc1C |(6.4,-1.55,;7.43,-2.71,;6.95,-4.16,;5.44,-4.49,;4.42,-3.34,;2.9,-3.66,;1.87,-2.52,;.37,-2.83,;7.98,-5.3,;7.5,-6.77,;8.54,-7.91,;8.07,-9.38,;10.04,-7.59,;10.5,-6.13,;11.92,-5.51,;11.76,-3.97,;12.9,-2.95,;10.25,-3.66,;9.62,-2.25,;9.48,-4.99,;13.25,-6.27,;13.25,-7.82,;11.9,-8.59,;14.58,-8.59,;15.92,-7.82,;17.24,-8.59,;15.92,-6.27,;14.58,-5.5,;14.56,-3.97,)| | ||
Structure |