Reaction Details |
![](/images/Email.png) | Report a problem with these data |
Target | Cytochrome P450 11B2, mitochondrial |
---|
Ligand | BDBM50500186 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1545187 (CHEMBL3750668) |
---|
IC50 | 13±n/a nM |
---|
Citation | Papillon, JP; Lou, C; Singh, AK; Adams, CM; Ksander, GM; Beil, ME; Chen, W; Leung-Chu, J; Fu, F; Gan, L; Hu, CW; Jeng, AY; LaSala, D; Liang, G; Rigel, DF; Russell, KS; Vest, JA; Watson, C Discovery of N-[5-(6-Chloro-3-cyano-1-methyl-1H-indol-2-yl)-pyridin-3-ylmethyl]-ethanesulfonamide, a Cortisol-Sparing CYP11B2 Inhibitor that Lowers Aldosterone in Human Subjects. J Med Chem58:9382-94 (2015) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Cytochrome P450 11B2, mitochondrial |
---|
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
|
|
|
BDBM50500186 |
---|
n/a |
---|
Name | BDBM50500186 |
Synonyms: | CHEMBL3747069 |
Type | Small organic molecule |
Emp. Form. | C17H15ClN4O2S |
Mol. Mass. | 374.845 |
SMILES | CCS(=O)(=O)Nc1cncc(c1)-c1c(C#N)c2ccc(Cl)cc2n1C |
Structure |
|