BDBM50262065 4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide::CHEMBL513185

SMILES: COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=LSCBKQOZIVXZJF-UHFFFAOYSA-N

Data: 4 KI  2 IC50

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 6 hits for monomerid = 50262065   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of human cloned CA2 by CO2 hydration assay				Bioorg Med Chem Lett 18: 4624-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.010 BindingDB Entry DOI: 10.7270/Q2959JF0
					More data for this Ligand-Target Pair
Carbonic Anhydrase VA (Homo sapiens (Human))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	10.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of human recombinant CA5A by CO2 hydration assay				Bioorg Med Chem Lett 18: 4624-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.010 BindingDB Entry DOI: 10.7270/Q2959JF0
					More data for this Ligand-Target Pair
Carbonic Anhydrase VB (Homo sapiens (Human))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	51.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of human recombinant CA5B by CO2 hydration assay				Bioorg Med Chem Lett 18: 4624-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.010 BindingDB Entry DOI: 10.7270/Q2959JF0
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	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	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of human cloned CA1 by CO2 hydration assay				Bioorg Med Chem Lett 18: 4624-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.010 BindingDB Entry DOI: 10.7270/Q2959JF0
					More data for this Ligand-Target Pair
Prostaglandin E synthase/G/H synthase 2 (Homo sapiens (Human))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of human recombinant COX2 by fluorescence assay				Bioorg Med Chem 21: 4288-95 (2013) Article DOI: 10.1016/j.bmc.2013.04.074 BindingDB Entry DOI: 10.7270/Q2DV1NTZ
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase (cyclooxygenase) (Ovis aries (Sheep))	BDBM50262065 (4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)benze...) Show SMILES COc1ccc(cc1)-c1cn(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C15H14N4O3S/c1-22-13-6-2-11(3-7-13)15-10-19(18-17-15)12-4-8-14(9-5-12)23(16,20)21/h2-10H,1H3,(H2,16,20,21)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of ovine COX1 by fluorescence assay				Bioorg Med Chem 21: 4288-95 (2013) Article DOI: 10.1016/j.bmc.2013.04.074 BindingDB Entry DOI: 10.7270/Q2DV1NTZ
					More data for this Ligand-Target Pair