BDBM50157955 2-(4-Methyl-piperidin-1-yl)-N-(5-sulfamoyl-[1,3,4]thiadiazol-2-yl)-acetamide::2-(4-methylpiperidin-1-yl)-N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide::CHEMBL183442

SMILES CC1CCN(CC(=O)Nc2nnc(s2)S(N)(=O)=O)CC1

InChI Key InChIKey=YPZSGGRHSBFMRE-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50157955   

TargetCarbonic anhydrase 2(Human)
Harran University

Curated by ChEMBL
LigandPNGBDBM50157955(2-(4-Methyl-piperidin-1-yl)-N-(5-sulfamoyl-[1,3,4]...)
Affinity DataKi:  3.80nMAssay Description:Inhibitory potency against human cloned Carbonic anhydrase II expressed in Escherichia coli strain BL21More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed
TargetCarbonic anhydrase 1(Human)
Harran University

Curated by ChEMBL
LigandPNGBDBM50157955(2-(4-Methyl-piperidin-1-yl)-N-(5-sulfamoyl-[1,3,4]...)
Affinity DataKi:  8.20nMAssay Description:Inhibitory potency against human cloned Carbonic anhydrase I expressed in Escherichia coli strain BL21More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed
TargetCarbonic anhydrase 9(Human)
Harran University

Curated by ChEMBL
LigandPNGBDBM50157955(2-(4-Methyl-piperidin-1-yl)-N-(5-sulfamoyl-[1,3,4]...)
Affinity DataKi:  35nMAssay Description:Inhibitory potency against catalytic domain of human Carbonic anhydrase IX expressed in Escherichia coli strain BL21More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2012
Entry Details Article
PubMed