Reaction Details |
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Target | 3-oxo-5-alpha-steroid 4-dehydrogenase 2 |
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Ligand | BDBM50368782 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_205047 (CHEMBL812406) |
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Ki | 1000±n/a nM |
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Citation | Abell, AD; Erhard, KF; Yen, H; Yamashita, DS; Brandt, M; Mohammed, H; Levy, MA; Holt, DA Preparative chiral HPLC separation of all possible stereoisomers of LY191704 and LY266111 and their in vitro inhibition of human types 1 and 2 steroid 5-reductases Bioorg Med Chem Lett4:1365-1368 (1994) Article |
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More Info.: | Get all data from this article, Assay Method |
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3-oxo-5-alpha-steroid 4-dehydrogenase 2 |
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Name: | 3-oxo-5-alpha-steroid 4-dehydrogenase 2 |
Synonyms: | 3-oxo-5-alpha-steroid 4-dehydrogenase 2 | 5 alpha-SR2 | 5α-Reductase 2 (5α-R2) | S5A2_HUMAN | SR type 2 | SRD5A2 | Steroid 5-alpha-reductase | Steroid 5-alpha-reductase 2 | Type II 5-alpha reductase |
Type: | Enzyme |
Mol. Mass.: | 28406.59 |
Organism: | Homo sapiens (Human) |
Description: | P31213 |
Residue: | 254 |
Sequence: | MQVQCQQSPVLAGSATLVALGALALYVAKPSGYGKHTESLKPAATRLPARAAWFLQELPS
FAVPAGILARQPLSLFGPPGTVLLGLFCLHYFHRTFVYSLLNRGRPYPAILILRGTAFCT
GNGVLQGYYLIYCAEYPDGWYTDIRFSLGVFLFILGMGINIHSDYILRQLRKPGEISYRI
PQGGLFTYVSGANFLGEIIEWIGYALATWSLPALAFAFFSLCFLGLRAFHHHRFYLKMFE
DYPKSRKALIPFIF
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BDBM50368782 |
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n/a |
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Name | BDBM50368782 |
Synonyms: | Bexlosteride | CHEMBL24955 | LY-191704 |
Type | Small organic molecule |
Emp. Form. | C14H16ClNO |
Mol. Mass. | 249.736 |
SMILES | CN1[C@@H]2CCc3cc(Cl)ccc3[C@H]2CCC1=O |
Structure |
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