BDBM50097308 CHEMBL287145::{{2-[carboxymethyl-(2-{carboxymethyl-[(3-sulfamoyl-phenylcarbamoyl)-methyl]-amino}-ethyl)-amino]-ethyl}-[(3-sulfamoyl-phenylcarbamoyl)-methyl]-amino}-acetic acid

SMILES: NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1

InChI Key: InChIKey=WUXVVCVUHCWYDL-UHFFFAOYSA-N

Data: 10 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 10 hits for monomerid = 50097308   

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 12 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human recombinant CA12 by CO2 hydration stopped flow assay				Bioorg Med Chem Lett 18: 836-41 (2008) Article DOI: 10.1016/j.bmcl.2007.11.025 BindingDB Entry DOI: 10.7270/Q2JH3N16
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	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	9.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human recombinant CA9 by CO2 hydration stopped flow assay				Bioorg Med Chem Lett 18: 836-41 (2008) Article DOI: 10.1016/j.bmcl.2007.11.025 BindingDB Entry DOI: 10.7270/Q2JH3N16
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	69	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human recombinant CA2 by CO2 hydration stopped flow assay				Bioorg Med Chem Lett 18: 836-41 (2008) Article DOI: 10.1016/j.bmcl.2007.11.025 BindingDB Entry DOI: 10.7270/Q2JH3N16
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	155	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against Human carbonic anhydrase II				J Med Chem 45: 1466-76 (2002) BindingDB Entry DOI: 10.7270/Q2N29XN9
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	155	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi Curated by ChEMBL					Assay Description Inhibition of cloned isozyme, human carbonic anhydrase II				Bioorg Med Chem Lett 11: 575-82 (2001) BindingDB Entry DOI: 10.7270/Q2KW5GJQ
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	425	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi Curated by ChEMBL					Assay Description Inhibition of cloned isozyme, human carbonic anhydrase IV				Bioorg Med Chem Lett 11: 575-82 (2001) BindingDB Entry DOI: 10.7270/Q2KW5GJQ
					More data for this Ligand-Target Pair
Carbonic Anhydrase IV (Bos taurus (bovine))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	425	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against bovine carbonic anhydrase IV				J Med Chem 45: 1466-76 (2002) BindingDB Entry DOI: 10.7270/Q2N29XN9
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	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	578	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human recombinant CA1 by CO2 hydration stopped flow assay				Bioorg Med Chem Lett 18: 836-41 (2008) Article DOI: 10.1016/j.bmcl.2007.11.025 BindingDB Entry DOI: 10.7270/Q2JH3N16
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against Human carbonic anhydrase I				J Med Chem 45: 1466-76 (2002) BindingDB Entry DOI: 10.7270/Q2N29XN9
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50097308 (CHEMBL287145 | {{2-[carboxymethyl-(2-{carboxymethy...) Show SMILES NS(=O)(=O)c1cccc(NC(=O)CN(CCN(CCN(CC(O)=O)CC(=O)Nc2cccc(c2)S(N)(=O)=O)CC(O)=O)CC(O)=O)c1 Show InChI InChI=1S/C26H35N7O12S2/c27-46(42,43)20-5-1-3-18(11-20)29-22(34)13-32(16-25(38)39)9-7-31(15-24(36)37)8-10-33(17-26(40)41)14-23(35)30-19-4-2-6-21(12-19)47(28,44)45/h1-6,11-12H,7-10,13-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi Curated by ChEMBL					Assay Description Inhibition of cloned isozyme, human carbonic anhydrase I				Bioorg Med Chem Lett 11: 575-82 (2001) BindingDB Entry DOI: 10.7270/Q2KW5GJQ
					More data for this Ligand-Target Pair