Reaction Details |
| Report a problem with these data |
Target | Aryl hydrocarbon receptor |
---|
Ligand | BDBM50240990 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_510004 (CHEMBL1005597) |
---|
Ki | 6.8±n/a nM |
---|
Citation | Aiello, S; Wells, G; Stone, EL; Kadri, H; Bazzi, R; Bell, DR; Stevens, MF; Matthews, CS; Bradshaw, TD; Westwell, AD Synthesis and biological properties of benzothiazole, benzoxazole, and chromen-4-one analogues of the potent antitumor agent 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (PMX 610, NSC 721648). J Med Chem51:5135-9 (2008) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Aryl hydrocarbon receptor |
---|
Name: | Aryl hydrocarbon receptor |
Synonyms: | AHR_RAT | Ahr |
Type: | PROTEIN |
Mol. Mass.: | 96224.95 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_510004 |
Residue: | 853 |
Sequence: | MSSGANITYASRKRRKPVQKTVKPVPAEGIKSNPSKRHRDRLNTELDRLASLLPFPQDVI
NKLDKLSVLRLSVSYLRAKSFFDVALKSTPADRSRGQDQCRAQVRDWQDLQEGEFLLQAL
NGFVLVVTADALVFYASSTIQDYLGFQQSDVIHQSVYELIHTEDRAEFQRQLHWALNPSQ
CTDSAQGVDETHGLPQPAVYYTPDQLPPENTAFMERCFRCRLRCLLDNSSGFLAMNFQGR
LKYLHGQNKKGKDGALLPPQLALFAIATPLQPPSILEIRTKNFIFRTKHKLDFTPIGCDA
KGQLILGYTEVELCNKGSGYQFIHAADMLHCAESHIRMIKTGESGMTVFRLLAKHSRWRW
VQSNARLIYRNGRPDYIIATQRPLTDEEGREHLQKRSMTLPFMFATGEAVLYEISSPFSP
IMDPLPIRTKSNTSRKDWAPQSTPSKDSFHPNSLMSALIQQDESIYLCPPSSPAPLDSHF
LMDSMSECGSWQGSFAVASNEALLKHEEIRHTQDVNLTLSGGPSELFPDNKNNDLYSIMR
NLGIDFEDIRSMQNEEFFRTDSSGEVDFKDIDITDEILTYVQDSLNNSTLLNSACQQQPV
SQHLSCMLQERLQLEQQQQLQQQHPTQTLEPQRQLCQVEVPQHELGQKTKHMQVNGMFAS
WNPAPPVSFSCPQQERKHYSLFSGLQGTAQEFPYKSEVDSMPYTQNFAPCNQSLLPEHSK
GTQLDFPGRDFERSLHPNASNLEDFVSCLQVPENQRHGINSQSAMVSPQAYYAGAMSMYQ
CQAGPQHTPVDQMQYSPEIPGSQAFLSKFQSPSILNEAYSADLSSIGHLQTAAHLPRLAE
AQPLPDITPSGFL
|
|
|
BDBM50240990 |
---|
n/a |
---|
Name | BDBM50240990 |
Synonyms: | 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole | 5-fluoro-2-(3,4-dimethoxyphenyl)benzothiazole | CHEMBL373251 | NSC-721648 |
Type | Small organic molecule |
Emp. Form. | C15H12FNO2S |
Mol. Mass. | 289.325 |
SMILES | COc1ccc(cc1OC)-c1nc2cc(F)ccc2s1 |
Structure |
|