BDBM60981 (2,3-diphenyl-1,2,4-thiadiazol-5-ylidene)-methyl-amine;hydrobromide::CHEMBL161867::MLS002153327::N-methyl-2,3-diphenyl-1,2,4-thiadiazol-5-imine;hydrobromide::SCH-202676 hydrobromide::SMR001230740::cid_11957689
SMILES C\N=c1/nc(-c2ccccc2)n(s1)-c1ccccc1
InChI Key InChIKey=FFUBTEITUNMMOK-FOCLMDBBSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 60981
TargetDNA dC->dU-editing enzyme APOBEC-3G(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.59E+4nMT: 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
Affinity DataIC50: 460nMAssay Description:Inhibition of full length His-NTMT1 (1 to 222 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3) assessed as SAH production by Mtase...More data for this Ligand-Target Pair
Affinity DataEC50: 2.80E+3nMAssay Description:Effective concentration for displacement of [3H]-CCPA from human adenosine A1 receptor after 60 minMore data for this Ligand-Target Pair
TargetDNA dC->dU-editing enzyme APOBEC-3A(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+5nMT: 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