BDBM80566 (2E,5E)-2-[(4-fluorophenyl)imino]-5-[(5-methylthien-2-yl)methylene]-1,3-thiazolidin-4-one::(5E)-2-(4-fluoroanilino)-5-[(5-methyl-2-thienyl)methylene]-2-thiazolin-4-one::(5E)-2-(4-fluoroanilino)-5-[(5-methyl-2-thiophenyl)methylidene]-4-thiazolone::(5E)-2-(4-fluoroanilino)-5-[(5-methylthiophen-2-yl)methylidene]-1,3-thiazol-4-one::(5E)-2-[(4-fluorophenyl)amino]-5-[(5-methylthiophen-2-yl)methylidene]-1,3-thiazol-4-one::MLS001197019::SMR000555723::cid_1824334
SMILES Cc1ccc(C=C2SC(Nc3ccc(F)cc3)=NC2=O)s1
InChI Key InChIKey=OIDWNZWGFGJCON-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 80566
TargetDNA dC->dU-editing enzyme APOBEC-3A(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 3.22E+3nMT: 2°CAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetDNA dC->dU-editing enzyme APOBEC-3G(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 7.58E+3nMT: 2°CAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
