Reaction Details |
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Target | Cytochrome P450 11B2, mitochondrial |
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Ligand | BDBM280316 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibitory Effect on hCYP11B2 |
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pH | 7.4±n/a |
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Temperature | 298.15±n/a K |
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IC50 | 0.700±n/a nM |
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Comments | extracted |
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Citation | Ushirogochi, H; Sasaki, W; Onda, Y; Sakakibara, R; Akahoshi, F Disubstituted 1, 2, 4-triazine compound US Patent US10029993 Publication Date 7/24/2018 |
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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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BDBM280316 |
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n/a |
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Name | BDBM280316 |
Synonyms: | US10029993, Example 183 |
Type | Small organic molecule |
Emp. Form. | C18H24N4O |
Mol. Mass. | 312.4094 |
SMILES | Cc1ccccc1-c1cnnc(n1)N1CCC(CCCO)CC1 |
Structure |
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