Reaction Details |
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Target | Steroid 21-hydroxylase |
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Ligand | BDBM50249048 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1679701 (CHEMBL4029978) |
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IC50 | >10000±n/a nM |
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Citation | Hoyt, SB; Taylor, J; London, C; Ali, A; Ujjainwalla, F; Tata, J; Struthers, M; Cully, D; Wisniewski, T; Ren, N; Bopp, C; Sok, A; Verras, A; McMasters, D; Chen, Q; Tung, E; Tang, W; Salituro, G; Clemas, J; Zhou, G; MacNeil, D; Duffy, R; Xiong, Y Discovery of indazole aldosterone synthase (CYP11B2) inhibitors as potential treatments for hypertension. Bioorg Med Chem Lett27:2384-2388 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Steroid 21-hydroxylase |
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Name: | Steroid 21-hydroxylase |
Synonyms: | CP21A_HUMAN | CYP21 | CYP21A2 | CYP21B | Cytochrome P450 21 | Cytochrome P450 21A2 |
Type: | PROTEIN |
Mol. Mass.: | 55896.25 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1498865 |
Residue: | 494 |
Sequence: | MLLLGLLLLPLLAGARLLWNWWKLRSLHLPPLAPGFLHLLQPDLPIYLLGLTQKFGPIYR
LHLGLQDVVVLNSKRTIEEAMVKKWADFAGRPEPLTYKLVSKNYPDLSLGDYSLLWKAHK
KLTRSALLLGIRDSMEPVVEQLTQEFCERMRAQPGTPVAIEEEFSLLTCSIICYLTFGDK
IKDDNLMPAYYKCIQEVLKTWSHWSIQIVDVIPFLRFFPNPGLRRLKQAIEKRDHIVEMQ
LRQHKESLVAGQWRDMMDYMLQGVAQPSMEEGSGQLLEGHVHMAAVDLLIGGTETTANTL
SWAVVFLLHHPEIQQRLQEELDHELGPGASSSRVPYKDRARLPLLNATIAEVLRLRPVVP
LALPHRTTRPSSISGYDIPEGTVIIPNLQGAHLDETVWERPHEFWPDRFLEPGKNSRALA
FGCGARVCLGEPLARLELFVVLTRLLQAFTLLPSGDALPSLQPLPHCSVILKMQPFQVRL
QPRGMGAHSPGQNQ
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BDBM50249048 |
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n/a |
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Name | BDBM50249048 |
Synonyms: | CHEMBL4080256 |
Type | Small organic molecule |
Emp. Form. | C16H14F3N3O |
Mol. Mass. | 321.2971 |
SMILES | Cc1nn(-c2cncc(c2)[C@@](C)(O)C(F)(F)F)c2ccccc12 |r| |
Structure |
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