Reaction Details |
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Target | Cytochrome P450 11B2, mitochondrial |
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Ligand | BDBM8905 |
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Substrate/Competitor | BDBM8582 |
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Meas. Tech. | CYP11B Assay |
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IC50 | 6±n/a nM |
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Citation | Voets, M; Antes, I; Scherer, C; Muller-Vieira, U; Biemel, K; Barassin, C; Marchais-Oberwinkler, S; Hartmann, RW Heteroaryl-substituted naphthalenes and structurally modified derivatives: selective inhibitors of CYP11B2 for the treatment of congestive heart failure and myocardial fibrosis. J Med Chem48:6632-42 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Cytochrome P450 11B2, mitochondrial |
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Name: | Cytochrome P450 11B2, mitochondrial |
Synonyms: | Aldosterone Synthase (CYP11B2) | Aldosterone synthase | Aldosterone-synthesizing enzyme | C11B2_HUMAN | CYP11B2 | CYPXIB2 | Cytochrome P450 11B2 | Cytochrome P450 11B2 (CYP11B2) | Cytochrome P450 11B2, mitochondrial | P-450Aldo | P-450C18 | Steroid 18-hydroxylase |
Type: | Protein |
Mol. Mass.: | 57582.15 |
Organism: | Homo sapiens (Human) |
Description: | P19099 |
Residue: | 503 |
Sequence: | MALRAKAEVCVAAPWLSLQRARALGTRAARAPRTVLPFEAMPQHPGNRWLRLLQIWREQG
YEHLHLEMHQTFQELGPIFRYNLGGPRMVCVMLPEDVEKLQQVDSLHPCRMILEPWVAYR
QHRGHKCGVFLLNGPEWRFNRLRLNPDVLSPKAVQRFLPMVDAVARDFSQALKKKVLQNA
RGSLTLDVQPSIFHYTIEASNLALFGERLGLVGHSPSSASLNFLHALEVMFKSTVQLMFM
PRSLSRWISPKVWKEHFEAWDCIFQYGDNCIQKIYQELAFNRPQHYTGIVAELLLKAELS
LEAIKANSMELTAGSVDTTAFPLLMTLFELARNPDVQQILRQESLAAAASISEHPQKATT
ELPLLRAALKETLRLYPVGLFLERVVSSDLVLQNYHIPAGTLVQVFLYSLGRNAALFPRP
ERYNPQRWLDIRGSGRNFHHVPFGFGMRQCLGRRLAEAEMLLLLHHVLKHFLVETLTQED
IKMVYSFILRPGTSPLLTFRAIN
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BDBM8905 |
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BDBM8582 |
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Name | BDBM8905 |
Synonyms: | 3-(6-Methoxy-2-naphthyl)pyridine | 3-(6-methoxynaphthalen-2-yl)pyridine | CHEMBL362968 | Pyridine-substituted naphthalene 2 | US9271963, 2 |
Type | Small organic molecule |
Emp. Form. | C16H13NO |
Mol. Mass. | 235.2805 |
SMILES | COc1ccc2cc(ccc2c1)-c1cccnc1 |
Structure |
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