BDBM75362 MLS-0435627.0001::[4-amino-3-(4-methylphenyl)-2-sulfanylidene-1,3-thiazol-5-yl]-[4-(2-fluorophenyl)piperazin-1-yl]methanone::[4-amino-3-(4-methylphenyl)-2-sulfanylidene-5-thiazolyl]-[4-(2-fluorophenyl)-1-piperazinyl]methanone::[4-amino-3-(p-tolyl)-2-thioxo-4-thiazolin-5-yl]-[4-(2-fluorophenyl)piperazino]methanone::[4-azanyl-3-(4-methylphenyl)-2-sulfanylidene-1,3-thiazol-5-yl]-[4-(2-fluorophenyl)piperazin-1-yl]methanone::cid_2385014
SMILES Cc1ccc(cc1)-n1c(N)c(sc1=S)C(=O)N1CCN(CC1)c1ccccc1F
InChI Key InChIKey=PMLLEJTXHYQOED-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 75362
TargetTyrosine-protein phosphatase non-receptor type 7(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.00E+5nMAssay 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
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: >1.00E+5nMAssay Description:Data Source: Burnham Center for Chemical Genomics (BCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) Networ...More data for this Ligand-Target Pair