Reaction Details |
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Target | Estrogen receptor beta |
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Ligand | BDBM50113776 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_65279 (CHEMBL676603) |
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Ki | >10000±n/a nM |
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Citation | Morgan, BP; Swick, AG; Hargrove, DM; LaFlamme, JA; Moynihan, MS; Carroll, RS; Martin, KA; Lee, E; Decosta, D; Bordner, J Discovery of potent, nonsteroidal, and highly selective glucocorticoid receptor antagonists. J Med Chem45:2417-24 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Estrogen receptor beta |
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Name: | Estrogen receptor beta |
Synonyms: | ER-beta | ESR2 | ESR2_HUMAN | ESTRB | Estradiol receptor beta (ERβ) | Estrogen receptor | Estrogen receptor (ER beta) | Estrogen receptor beta | Estrogen receptor beta (ER beta) | Estrogen receptor beta (ER) | NR3A2 | Nuclear receptor subfamily 3 group A member 2 | estrogen beta |
Type: | Protein |
Mol. Mass.: | 59238.43 |
Organism: | Homo sapiens (Human) |
Description: | Q92731 |
Residue: | 530 |
Sequence: | MDIKNSPSSLNSPSSYNCSQSILPLEHGSIYIPSSYVDSHHEYPAMTFYSPAVMNYSIPS
NVTNLEGGPGRQTTSPNVLWPTPGHLSPLVVHRQLSHLYAEPQKSPWCEARSLEHTLPVN
RETLKRKVSGNRCASPVTGPGSKRDAHFCAVCSDYASGYHYGVWSCEGCKAFFKRSIQGH
NDYICPATNQCTIDKNRRKSCQACRLRKCYEVGMVKCGSRRERCGYRLVRRQRSADEQLH
CAGKAKRSGGHAPRVRELLLDALSPEQLVLTLLEAEPPHVLISRPSAPFTEASMMMSLTK
LADKELVHMISWAKKIPGFVELSLFDQVRLLESCWMEVLMMGLMWRSIDHPGKLIFAPDL
VLDRDEGKCVEGILEIFDMLLATTSRFRELKLQHKEYLCVKAMILLNSSMYPLVTATQDA
DSSRKLAHLLNAVTDALVWVIAKSGISSQQQSMRLANLLMLLSHVRHASNKGMEHLLNMK
CKNVVPVYDLLLEMLNAHVLRGCKSSITGSECSPAEDSKSKEGSQNPQSQ
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BDBM50113776 |
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n/a |
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Name | BDBM50113776 |
Synonyms: | (R)-4a-Benzyl-7-methoxy-4,4a,9,10-tetrahydro-3H-phenanthren-2-one | CHEMBL78807 |
Type | Small organic molecule |
Emp. Form. | C22H22O2 |
Mol. Mass. | 318.4089 |
SMILES | COc1ccc2c(CCC3=CC(=O)CC[C@@]23Cc2ccccc2)c1 |t:9| |
Structure |
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