Reaction Details |
| Report a problem with these data |
Target | Nuclear receptor subfamily 0 group B member 1 |
---|
Ligand | BDBM97208 |
---|
Substrate/Competitor | n/a |
---|
IC50 | >277.93±n/a nM |
---|
Citation | PubChem, PC Luminescence-based cell-based high throughput dose response assay for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): repression of SF-1 (NR5A1) activated StAR promoter by full-length DAX-1 PubChem Bioassay(2013)[AID] |
---|
More Info.: | Get all data from this article |
---|
|
Nuclear receptor subfamily 0 group B member 1 |
---|
Name: | Nuclear receptor subfamily 0 group B member 1 |
Synonyms: | AHC | DAX1 | NR0B1 | NR0B1_HUMAN |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 51729.22 |
Organism: | Homo sapiens (Human) |
Description: | gi_5016090 |
Residue: | 470 |
Sequence: | MAGENHQWQGSILYNMLMSAKQTRAAPEAPETRLVDQCWGCSCGDEPGVGREGLLGGRNV
ALLYRCCFCGKDHPRQGSILYSMLTSAKQTYAAPKAPEATLGPCWGCSCGSDPGVGRAGL
PGGRPVALLYRCCFCGEDHPRQGSILYSLLTSSKQTHVAPAAPEARPGGAWWDRSYFAQR
PGGKEALPGGRATALLYRCCFCGEDHPQQGSTLYCVPTSTNQAQAAPEERPRAPWWDTSS
GALRPVALKSPQVVCEAASAGLLKTLRFVKYLPCFQVLPLDQQLVLVRNCWASLLMLELA
QDRLQFETVEVSEPSMLQKILTTRRRETGGNEPLPVPTLQHHLAPPAEARKVPSASQVQA
IKCFLSKCWSLNISTKEYAYLKGTVLFNPDVPGLQCVKYIQGLQWGTQQILSEHTRMTHQ
GPHDRFIELNSTLFLLRFINANVIAELFFRPIIGTVSMDDMMLEMLCTKI
|
|
|
BDBM97208 |
---|
n/a |
---|
Name | BDBM97208 |
Synonyms: | 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-1-[2,5-dimethyl-1-(thiophen-2-ylmethyl)pyrrol-3-yl]ethanone | 2-[(5-amino-1,3,4-thiadiazol-2-yl)thio]-1-[2,5-dimethyl-1-(2-thenyl)pyrrol-3-yl]ethanone | 2-[(5-amino-1,3,4-thiadiazol-2-yl)thio]-1-[2,5-dimethyl-1-(thiophen-2-ylmethyl)-3-pyrrolyl]ethanone | 2-[(5-azanyl-1,3,4-thiadiazol-2-yl)sulfanyl]-1-[2,5-dimethyl-1-(thiophen-2-ylmethyl)pyrrol-3-yl]ethanone | MLS000336319 | SMR000253873 | cid_4880179 |
Type | Small organic molecule |
Emp. Form. | C15H16N4OS3 |
Mol. Mass. | 364.509 |
SMILES | Cc1cc(C(=O)CSc2nnc(N)s2)c(C)n1Cc1cccs1 |
Structure |
|