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SMILES: Cc1nc(no1)-c1csc(c1)S(N)(=O)=O

InChI Key: InChIKey=WSYKOUVIKYOXFB-UHFFFAOYSA-N

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 = 50531517   
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 2


(Homo sapiens (Human))
BDBM50531517
PNG
(CHEMBL4452965)
Show SMILES Cc1nc(no1)-c1csc(c1)S(N)(=O)=O
Show InChI InChI=1S/C7H7N3O3S2/c1-4-9-7(10-13-4)5-2-6(14-3-5)15(8,11)12/h2-3H,1H3,(H2,8,11,12)
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0.910n/an/an/an/an/an/an/an/a



Saint Petersburg State University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 assessed as reduction in CO2 hydration after 15 mins by phenol red staining-based stopped flow assay


Eur J Med Chem 164: 92-105 (2019)


Article DOI: 10.1016/j.ejmech.2018.12.049
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50531517
PNG
(CHEMBL4452965)
Show SMILES Cc1nc(no1)-c1csc(c1)S(N)(=O)=O
Show InChI InChI=1S/C7H7N3O3S2/c1-4-9-7(10-13-4)5-2-6(14-3-5)15(8,11)12/h2-3H,1H3,(H2,8,11,12)
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1.60n/an/an/an/an/an/an/an/a



Saint Petersburg State University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 9 assessed as reduction in CO2 hydration after 15 mins by phenol red staining-based stopped flow assay


Eur J Med Chem 164: 92-105 (2019)


Article DOI: 10.1016/j.ejmech.2018.12.049
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50531517
PNG
(CHEMBL4452965)
Show SMILES Cc1nc(no1)-c1csc(c1)S(N)(=O)=O
Show InChI InChI=1S/C7H7N3O3S2/c1-4-9-7(10-13-4)5-2-6(14-3-5)15(8,11)12/h2-3H,1H3,(H2,8,11,12)
PDB
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UniChem
Article
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8.10n/an/an/an/an/an/an/an/a



Saint Petersburg State University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 assessed as reduction in CO2 hydration after 15 mins by phenol red staining-based stopped flow assay


Eur J Med Chem 164: 92-105 (2019)


Article DOI: 10.1016/j.ejmech.2018.12.049
More data for this
Ligand-Target Pair
Carbonic anhydrase 12


(Homo sapiens (Human))
BDBM50531517
PNG
(CHEMBL4452965)
Show SMILES Cc1nc(no1)-c1csc(c1)S(N)(=O)=O
Show InChI InChI=1S/C7H7N3O3S2/c1-4-9-7(10-13-4)5-2-6(14-3-5)15(8,11)12/h2-3H,1H3,(H2,8,11,12)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
10n/an/an/an/an/an/an/an/a



Saint Petersburg State University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 12 assessed as reduction in CO2 hydration after 15 mins by phenol red staining-based stopped flow assay


Eur J Med Chem 164: 92-105 (2019)


Article DOI: 10.1016/j.ejmech.2018.12.049
More data for this
Ligand-Target Pair