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BDBM50030562 CHEMBL3354130

SMILES: NS(=O)(=O)c1ccc(NC(=O)NS(=O)(=O)c2ccccc2Cl)cn1

InChI Key: InChIKey=FTPGKSNIJAXUPQ-UHFFFAOYSA-N

Data: 4 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50030562   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Carbonic anhydrase 12


(Homo sapiens (Human))
BDBM50030562
PNG
(CHEMBL3354130)
Show SMILES NS(=O)(=O)c1ccc(NC(=O)NS(=O)(=O)c2ccccc2Cl)cn1
Show InChI InChI=1S/C12H11ClN4O5S2/c13-9-3-1-2-4-10(9)24(21,22)17-12(18)16-8-5-6-11(15-7-8)23(14,19)20/h1-7H,(H2,14,19,20)(H2,16,17,18)
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Article
PubMed
4.60n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase 12 preincubated for 15 mins by stopped flow CO2 hydration method


J Med Chem 57: 9152-67 (2014)


Article DOI: 10.1021/jm501314c
BindingDB Entry DOI: 10.7270/Q2CV4K97
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50030562
PNG
(CHEMBL3354130)
Show SMILES NS(=O)(=O)c1ccc(NC(=O)NS(=O)(=O)c2ccccc2Cl)cn1
Show InChI InChI=1S/C12H11ClN4O5S2/c13-9-3-1-2-4-10(9)24(21,22)17-12(18)16-8-5-6-11(15-7-8)23(14,19)20/h1-7H,(H2,14,19,20)(H2,16,17,18)
PDB
MMDB

NCI pathway
Reactome pathway
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PC sid
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Article
PubMed
9.70n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase 9 preincubated for 15 mins by stopped flow CO2 hydration method


J Med Chem 57: 9152-67 (2014)


Article DOI: 10.1021/jm501314c
BindingDB Entry DOI: 10.7270/Q2CV4K97
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50030562
PNG
(CHEMBL3354130)
Show SMILES NS(=O)(=O)c1ccc(NC(=O)NS(=O)(=O)c2ccccc2Cl)cn1
Show InChI InChI=1S/C12H11ClN4O5S2/c13-9-3-1-2-4-10(9)24(21,22)17-12(18)16-8-5-6-11(15-7-8)23(14,19)20/h1-7H,(H2,14,19,20)(H2,16,17,18)
PDB
MMDB

Reactome pathway
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PC sid
UniChem

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Article
PubMed
38n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration method


J Med Chem 57: 9152-67 (2014)


Article DOI: 10.1021/jm501314c
BindingDB Entry DOI: 10.7270/Q2CV4K97
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50030562
PNG
(CHEMBL3354130)
Show SMILES NS(=O)(=O)c1ccc(NC(=O)NS(=O)(=O)c2ccccc2Cl)cn1
Show InChI InChI=1S/C12H11ClN4O5S2/c13-9-3-1-2-4-10(9)24(21,22)17-12(18)16-8-5-6-11(15-7-8)23(14,19)20/h1-7H,(H2,14,19,20)(H2,16,17,18)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
58n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration method


J Med Chem 57: 9152-67 (2014)


Article DOI: 10.1021/jm501314c
BindingDB Entry DOI: 10.7270/Q2CV4K97
More data for this
Ligand-Target Pair