Reaction Details  Report a problem with these data
Target
Nuclear receptor subfamily 0 group B member 1
Ligand
BDBM76503
Substrate
n/a
IC50
>67536±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]
Target
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:
MAGENHQWQGSILYNMLMSAKQTRAAPEAPETRLVDQCWGCSCGDEPGVGREGLLGGRNVALLYRCCFCGKDHPRQGSILYSMLTSAKQTYAAPKAPEATLGPCWGCSCGSDPGVGRAGLPGGRPVALLYRCCFCGEDHPRQGSILYSLLTSSKQTHVAPAAPEARPGGAWWDRSYFAQRPGGKEALPGGRATALLYRCCFCGEDHPQQGSTLYCVPTSTNQAQAAPEERPRAPWWDTSSGALRPVALKSPQVVCEAASAGLLKTLRFVKYLPCFQVLPLDQQLVLVRNCWASLLMLELAQDRLQFETVEVSEPSMLQKILTTRRRETGGNEPLPVPTLQHHLAPPAEARKVPSASQVQAIKCFLSKCWSLNISTKEYAYLKGTVLFNPDVPGLQCVKYIQGLQWGTQQILSEHTRMTHQGPHDRFIELNSTLFLLRFINANVIAELFFRPIIGTVSMDDMMLEMLCTKI
  
Inhibitor
Name:
BDBM76503
Synonyms:
3-chloranyl-N-(5-methyl-1,3-thiazol-2-yl)-1-benzothiophene-2-carboxamide | 3-chloro-N-(5-methyl-1,3-thiazol-2-yl)-1-benzothiophene-2-carboxamide | 3-chloro-N-(5-methyl-2-thiazolyl)-1-benzothiophene-2-carboxamide | 3-chloro-N-(5-methylthiazol-2-yl)benzothiophene-2-carboxamide | MLS000334487 | SMR000249245 | cid_2523343
Type:
Small organic molecule
Emp. Form.:
C13H9ClN2OS2
Mol. Mass.:
308.806
SMILES:
Cc1cnc(NC(=O)c2sc3ccccc3c2Cl)s1
Structure:
Search PDB for entries with ligand similarity: