Reaction Details |
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Target | Cytochrome P450 11B2, mitochondrial |
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Ligand | BDBM362864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | HTRF-Based Assay |
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IC50 | 61.0±n/a nM |
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Citation | Bennett, DJ; Cai, J; Carswell, E; Cooke, A; Hoyt, SB; London, C; MacLean, J; Park, MK; Ratcliffe, P; Xiong, Y; Samanta, SK; Kulkarni, BA Pyrazolopyridyl compounds as aldosterone synthase inhibitors US Patent US9844553 Publication Date 12/19/2017 |
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More Info.: | Get all data from this article, 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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BDBM362864 |
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n/a |
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Name | BDBM362864 |
Synonyms: | 2-(5-methylpyridin-3-yl)-5-oxo-4,5,6,7- tetrahydropyrazolo[1,5-a]pyrimidine-3- carbonitrile | US9844553, 25 |
Type | Small organic molecule |
Emp. Form. | C13H11N5O |
Mol. Mass. | 253.2593 |
SMILES | Cc1cncc(c1)-c1nn2CCC(=O)Nc2c1C#N |
Structure |
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