BDBM50221272 4-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-1-[alpha-(4-bromophenyl)-alpha-methyl methylene]semicarbazide::CHEMBL235501

SMILES CC(=NNC(=O)Nc1nnc(S)s1)c1ccc(Br)cc1

InChI Key InChIKey=VPIGZYKZWYUIHM-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50221272   

TargetCarbonic anhydrase 9(Homo sapiens (Human))
Assiut University

Curated by ChEMBL
LigandPNGBDBM50221272(4-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-1-[...)
Affinity DataKi:  6.85E+3nMAssay Description:Inhibition of catalytic domain of human cloned carbonic anhydrase9 by CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Assiut University

Curated by ChEMBL
LigandPNGBDBM50221272(4-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-1-[...)
Affinity DataKi:  1.13E+4nMAssay Description:Inhibition of human cloned carbonic anhydrase2 by CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Assiut University

Curated by ChEMBL
LigandPNGBDBM50221272(4-(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)-1-[...)
Affinity DataKi:  4.23E+4nMAssay Description:Inhibition of human cloned carbonic anhydrase1 by CO2 hydration methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed