| Reaction Details |
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 | Report a problem with these data |
| Target | Estrogen receptor |
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| Ligand | BDBM50185870 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_371967 (CHEMBL852960) |
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| IC50 | 1210±n/a nM |
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| Citation |  Wilkening, RR; Ratcliffe, RW; Tynebor, EC; Wildonger, KJ; Fried, AK; Hammond, ML; Mosley, RT; Fitzgerald, PM; Sharma, N; McKeever, BM; Nilsson, S; Carlquist, M; Thorsell, A; Locco, L; Katz, R; Frisch, K; Birzin, ET; Wilkinson, HA; Mitra, S; Cai, S; Hayes, EC; Schaeffer, JM; Rohrer, SP The discovery of tetrahydrofluorenones as a new class of estrogen receptor beta-subtype selective ligands. Bioorg Med Chem Lett16:3489-94 (2006) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Estrogen receptor |
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| Name: | Estrogen receptor |
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| Synonyms: | ER | ER-alpha | ESR | ESR1 | ESR1_HUMAN | Estradiol receptor | Estrogen receptor | Estrogen receptor (ER alpha) | Estrogen receptor (ER-alpha) | Estrogen receptor alpha (ER alpha) | Estrogen receptor alpha (ER) | NR3A1 | Nuclear receptor subfamily 3 group A member 1 |
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| Type: | Protein |
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| Mol. Mass.: | 66230.44 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P03372 |
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| Residue: | 595 |
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| Sequence: | MTMTLHTKASGMALLHQIQGNELEPLNRPQLKIPLERPLGEVYLDSSKPAVYNYPEGAAY
EFNAAAAANAQVYGQTGLPYGPGSEAAAFGSNGLGGFPPLNSVSPSPLMLLHPPPQLSPF
LQPHGQQVPYYLENEPSGYTVREAGPPAFYRPNSDNRRQGGRERLASTNDKGSMAMESAK
ETRYCAVCNDYASGYHYGVWSCEGCKAFFKRSIQGHNDYMCPATNQCTIDKNRRKSCQAC
RLRKCYEVGMMKGGIRKDRRGGRMLKHKRQRDDGEGRGEVGSAGDMRAANLWPSPLMIKR
SKKNSLALSLTADQMVSALLDAEPPILYSEYDPTRPFSEASMMGLLTNLADRELVHMINW
AKRVPGFVDLTLHDQVHLLECAWLEILMIGLVWRSMEHPGKLLFAPNLLLDRNQGKCVEG
MVEIFDMLLATSSRFRMMNLQGEEFVCLKSIILLNSGVYTFLSSTLKSLEEKDHIHRVLD
KITDTLIHLMAKAGLTLQQQHQRLAQLLLILSHIRHMSNKGMEHLYSMKCKNVVPLYDLL
LEMLDAHRLHAPTSRGGASVEETDQSHLATAGSTSSHSLQKYYITGEAEGFPATV
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| BDBM50185870 |
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| n/a |
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| Name | BDBM50185870 |
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| Synonyms: | 9a-ethyl-7-hydroxy-4-methyl-1,2,9,9a-tetrahydrofluoren-3-one | CHEMBL212675 |
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| Type | Small organic molecule |
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| Emp. Form. | C16H18O2 |
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| Mol. Mass. | 242.3129 |
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| SMILES | CCC12Cc3cc(O)ccc3C1=C(C)C(=O)CC2 |t:13| |
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| Structure | 
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