Reaction Details |
| Report a problem with these data |
Target | Cytochrome P450 26B1 |
---|
Ligand | BDBM50253810 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1567868 (CHEMBL3789263) |
---|
IC50 | 0.460000±n/a nM |
---|
Citation | Diaz, P; Huang, W; Keyari, CM; Buttrick, B; Price, L; Guilloteau, N; Tripathy, S; Sperandio, VG; Fronczek, FR; Astruc-Diaz, F; Isoherranen, N Development and Characterization of Novel and Selective Inhibitors of Cytochrome P450 CYP26A1, the Human Liver Retinoic Acid Hydroxylase. J Med Chem59:2579-95 (2016) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Cytochrome P450 26B1 |
---|
Name: | Cytochrome P450 26B1 |
Synonyms: | CP26B_HUMAN | CYP26A2 | CYP26A2 | CYP26B1 | Cytochrome P450 26A2 | Cytochrome P450 26B1 | Cytochrome P450 retinoic acid-inactivating 2 | Cytochrome P450RAI-2 | P450RAI2 | Retinoic acid-metabolizing cytochrome |
Type: | PROTEIN |
Mol. Mass.: | 57525.03 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_115648 |
Residue: | 512 |
Sequence: | MLFEGLDLVSALATLAACLVSVTLLLAVSQQLWQLRWAATRDKSCKLPIPKGSMGFPLIG
ETGHWLLQGSGFQSSRREKYGNVFKTHLLGRPLIRVTGAENVRKILMGEHHLVSTEWPRS
TRMLLGPNTVSNSIGDIHRNKRKVFSKIFSHEALESYLPKIQLVIQDTLRAWSSHPEAIN
VYQEAQKLTFRMAIRVLLGFSIPEEDLGHLFEVYQQFVDNVFSLPVDLPFSGYRRGIQAR
QILQKGLEKAIREKLQCTQGKDYLDALDLLIESSKEHGKEMTMQELKDGTLELIFAAYAT
TASASTSLIMQLLKHPTVLEKLRDELRAHGILHSGGCPCEGTLRLDTLSGLRYLDCVIKE
VMRLFTPISGGYRTVLQTFELDGFQIPKGWSVMYSIRDTHDTAPVFKDVNVFDPDRFSQA
RSEDKDGRFHYLPFGGGVRTCLGKHLAKLFLKVLAVELASTSRFELATRTFPRITLVPVL
HPVDGLSVKFFGLDSNQNEILPETEAMLSATV
|
|
|
BDBM50253810 |
---|
n/a |
---|
Name | BDBM50253810 |
Synonyms: | CHEMBL459505 | N-(4-(2-ethyl-1-(1H-1,2,4-triazol-1-yl)butyl)phenyl)benzo[d]thiazol-2-amine | R-115866 | R115866 | US9963439, Talarozole |
Type | Small organic molecule |
Emp. Form. | C21H23N5S |
Mol. Mass. | 377.506 |
SMILES | CCC(CC)C(c1ccc(Nc2nc3ccccc3s2)cc1)n1cncn1 |
Structure |
|