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TargetAryl hydrocarbon receptor
LigandBDBM50240990
Substrate/Competitorn/a
Meas. Tech.ChEMBL_510004 (CHEMBL1005597)
Ki 6.8±n/a nM
Citation Aiello, SWells, GStone, ELKadri, HBazzi, RBell, DRStevens, MFMatthews, CSBradshaw, TDWestwell, 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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50240990
n/a
NameBDBM50240990
Synonyms:2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole | 5-fluoro-2-(3,4-dimethoxyphenyl)benzothiazole | CHEMBL373251 | NSC-721648
TypeSmall organic molecule
Emp. Form.C15H12FNO2S
Mol. Mass.289.325
SMILESCOc1ccc(cc1OC)-c1nc2cc(F)ccc2s1
Structure
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