Compile Data Set for Download or QSAR

Found 66 hits Enz. Inhib. hit(s) with all data for entry = 50035119   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087247 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES Cn1nc(s\c1=N/S(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)cc1)S(N)(=O)=O Show InChI InChI=1S/C19H16ClN5O6S3/c1-25-18(32-19(23-25)33(21,27)28)24-34(29,30)14-5-3-13(4-6-14)22-10-11-8-17(26)31-16-9-12(20)2-7-15(11)16/h2-9,22H,10H2,1H3,(H2,21,27,28)/b24-18-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	0.5	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087247 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES Cn1nc(s\c1=N/S(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)cc1)S(N)(=O)=O Show InChI InChI=1S/C19H16ClN5O6S3/c1-25-18(32-19(23-25)33(21,27)28)24-34(29,30)14-5-3-13(4-6-14)22-10-11-8-17(26)31-16-9-12(20)2-7-15(11)16/h2-9,22H,10H2,1H3,(H2,21,27,28)/b24-18-	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	0.600	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087247 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES Cn1nc(s\c1=N/S(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)cc1)S(N)(=O)=O Show InChI InChI=1S/C19H16ClN5O6S3/c1-25-18(32-19(23-25)33(21,27)28)24-34(29,30)14-5-3-13(4-6-14)22-10-11-8-17(26)31-16-9-12(20)2-7-15(11)16/h2-9,22H,10H2,1H3,(H2,21,27,28)/b24-18-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087246 (3-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-N...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCNCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C15H14ClN5O5S2/c16-9-1-2-10-8(5-13(23)26-11(10)6-9)7-18-4-3-12(22)19-14-20-21-15(27-14)28(17,24)25/h1-2,5-6,18H,3-4,7H2,(H2,17,24,25)(H,19,20,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087265 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES NS(=O)(=O)c1nnc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)s1 Show InChI InChI=1S/C18H14ClN5O6S3/c19-11-1-6-14-10(7-16(25)30-15(14)8-11)9-21-12-2-4-13(5-3-12)33(28,29)24-17-22-23-18(31-17)32(20,26)27/h1-8,21H,9H2,(H,22,24)(H2,20,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087258 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-ethyl-am...) Show SMILES NS(=O)(=O)c1ccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)cc1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-1-10-20-14(11-22(27)32-21(20)12-15)13-25-16-2-8-19(9-3-16)34(30,31)26-17-4-6-18(7-5-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087265 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES NS(=O)(=O)c1nnc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)s1 Show InChI InChI=1S/C18H14ClN5O6S3/c19-11-1-6-14-10(7-16(25)30-15(14)8-11)9-21-12-2-4-13(5-3-12)33(28,29)24-17-22-23-18(31-17)32(20,26)27/h1-8,21H,9H2,(H,22,24)(H2,20,26,27)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	4	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087265 (5-{4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES NS(=O)(=O)c1nnc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)s1 Show InChI InChI=1S/C18H14ClN5O6S3/c19-11-1-6-14-10(7-16(25)30-15(14)8-11)9-21-12-2-4-13(5-3-12)33(28,29)24-17-22-23-18(31-17)32(20,26)27/h1-8,21H,9H2,(H,22,24)(H2,20,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	5	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087256 (3-[4-(7-chloro-2-oxo-2H-4-chromenylmethylamino)phe...) Show SMILES NS(=O)(=O)c1cccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)c1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-4-9-20-14(10-22(27)32-21(20)11-15)13-25-16-5-7-18(8-6-16)34(30,31)26-17-2-1-3-19(12-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087264 (5-[(Z)-7-Chloro-2-oxo-2H-chromen-4-ylmethylimino]-...) Show SMILES Cn1nc(s\c1=N/Cc1cc(=O)oc2cc(Cl)ccc12)S(N)(=O)=O Show InChI InChI=1S/C13H11ClN4O4S2/c1-18-12(23-13(17-18)24(15,20)21)16-6-7-4-11(19)22-10-5-8(14)2-3-9(7)10/h2-5H,6H2,1H3,(H2,15,20,21)/b16-12-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	6	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087255 (5-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-[...) Show SMILES NS(=O)(=O)c1nnc(NCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C12H9ClN4O4S2/c13-7-1-2-8-6(3-10(18)21-9(8)4-7)5-15-11-16-17-12(22-11)23(14,19)20/h1-4H,5H2,(H,15,16)(H2,14,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087259 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-ethyl-am...) Show SMILES CCN(Cc1cc(=O)oc2cc(Cl)ccc12)C1CC(C)S(=O)(=O)c2sc(cc12)S(N)(=O)=O Show InChI InChI=1S/C20H21ClN2O6S3/c1-3-23(10-12-7-18(24)29-17-8-13(21)4-5-14(12)17)16-6-11(2)31(25,26)20-15(16)9-19(30-20)32(22,27)28/h4-5,7-9,11,16H,3,6,10H2,1-2H3,(H2,22,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	8	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087262 (5-(5,7-Dioxo-5,7-dihydro-pyrrolo[3,4-b]pyridin-6-y...) Show SMILES NS(=O)(=O)c1nnc(NN2C(=O)c3cccnc3C2=O)s1 Show InChI InChI=1S/C9H6N6O4S2/c10-21(18,19)9-13-12-8(20-9)14-15-6(16)4-2-1-3-11-5(4)7(15)17/h1-3H,(H,12,14)(H2,10,18,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	8	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM10884 ((2S,4S)-4-(ethylamino)-2-methyl-1,1-dioxo-2H,3H,4H...) Show SMILES CCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(cc12)S(N)(=O)=O |r| Show InChI InChI=1S/C10H16N2O4S3/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16)/t6-,8-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB PubMed	9	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087246 (3-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-N...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCNCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C15H14ClN5O5S2/c16-9-1-2-10-8(5-13(23)26-11(10)6-9)7-18-4-3-12(22)19-14-20-21-15(27-14)28(17,24)25/h1-2,5-6,18H,3-4,7H2,(H2,17,24,25)(H,19,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	12	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087251 (4-Chloro-6-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)...) Show SMILES NS(=O)(=O)c1cc(c(NCc2cc(=O)oc3cc(Cl)ccc23)cc1Cl)S(N)(=O)=O Show InChI InChI=1S/C16H13Cl2N3O6S2/c17-9-1-2-10-8(3-16(22)27-13(10)4-9)7-21-12-5-11(18)14(28(19,23)24)6-15(12)29(20,25)26/h1-6,21H,7H2,(H2,19,23,24)(H2,20,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	12	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087258 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-ethyl-am...) Show SMILES NS(=O)(=O)c1ccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)cc1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-1-10-20-14(11-22(27)32-21(20)12-15)13-25-16-2-8-19(9-3-16)34(30,31)26-17-4-6-18(7-5-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	14	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087255 (5-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-[...) Show SMILES NS(=O)(=O)c1nnc(NCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C12H9ClN4O4S2/c13-7-1-2-8-6(3-10(18)21-9(8)4-7)5-15-11-16-17-12(22-11)23(14,19)20/h1-4H,5H2,(H,15,16)(H2,14,19,20)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	15	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087264 (5-[(Z)-7-Chloro-2-oxo-2H-chromen-4-ylmethylimino]-...) Show SMILES Cn1nc(s\c1=N/Cc1cc(=O)oc2cc(Cl)ccc12)S(N)(=O)=O Show InChI InChI=1S/C13H11ClN4O4S2/c1-18-12(23-13(17-18)24(15,20)21)16-6-7-4-11(19)22-10-5-8(14)2-3-9(7)10/h2-5H,6H2,1H3,(H2,15,20,21)/b16-12-	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	16	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087246 (3-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-N...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CCNCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C15H14ClN5O5S2/c16-9-1-2-10-8(5-13(23)26-11(10)6-9)7-18-4-3-12(22)19-14-20-21-15(27-14)28(17,24)25/h1-2,5-6,18H,3-4,7H2,(H2,17,24,25)(H,19,20,22)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	16	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087262 (5-(5,7-Dioxo-5,7-dihydro-pyrrolo[3,4-b]pyridin-6-y...) Show SMILES NS(=O)(=O)c1nnc(NN2C(=O)c3cccnc3C2=O)s1 Show InChI InChI=1S/C9H6N6O4S2/c10-21(18,19)9-13-12-8(20-9)14-15-6(16)4-2-1-3-11-5(4)7(15)17/h1-3H,(H,12,14)(H2,10,18,19)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	18	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087252 (4,5-Dichloro-6-[(7-chloro-2-oxo-2H-chromen-4-ylmet...) Show SMILES NS(=O)(=O)c1cc(c(NCc2cc(=O)oc3cc(Cl)ccc23)c(Cl)c1Cl)S(N)(=O)=O Show InChI InChI=1S/C16H12Cl3N3O6S2/c17-8-1-2-9-7(3-13(23)28-10(9)4-8)6-22-16-12(30(21,26)27)5-11(29(20,24)25)14(18)15(16)19/h1-5,22H,6H2,(H2,20,24,25)(H2,21,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	18	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087259 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-ethyl-am...) Show SMILES CCN(Cc1cc(=O)oc2cc(Cl)ccc12)C1CC(C)S(=O)(=O)c2sc(cc12)S(N)(=O)=O Show InChI InChI=1S/C20H21ClN2O6S3/c1-3-23(10-12-7-18(24)29-17-8-13(21)4-5-14(12)17)16-6-11(2)31(25,26)20-15(16)9-19(30-20)32(22,27)28/h4-5,7-9,11,16H,3,6,10H2,1-2H3,(H2,22,27,28)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	25	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087264 (5-[(Z)-7-Chloro-2-oxo-2H-chromen-4-ylmethylimino]-...) Show SMILES Cn1nc(s\c1=N/Cc1cc(=O)oc2cc(Cl)ccc12)S(N)(=O)=O Show InChI InChI=1S/C13H11ClN4O4S2/c1-18-12(23-13(17-18)24(15,20)21)16-6-7-4-11(19)22-10-5-8(14)2-3-9(7)10/h2-5H,6H2,1H3,(H2,15,20,21)/b16-12-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	29	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087256 (3-[4-(7-chloro-2-oxo-2H-4-chromenylmethylamino)phe...) Show SMILES NS(=O)(=O)c1cccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)c1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-4-9-20-14(10-22(27)32-21(20)11-15)13-25-16-5-7-18(8-6-16)34(30,31)26-17-2-1-3-19(12-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	30	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087266 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-3...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(F)c1 Show InChI InChI=1S/C16H12ClFN2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	30	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087250 (3-Bromo-4-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)-...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(Br)c1 Show InChI InChI=1S/C16H12BrClN2O4S/c17-13-7-11(25(19,22)23)2-4-14(13)20-8-9-5-16(21)24-15-6-10(18)1-3-12(9)15/h1-7,20H,8H2,(H2,19,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	33	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087258 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-ethyl-am...) Show SMILES NS(=O)(=O)c1ccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)cc1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-1-10-20-14(11-22(27)32-21(20)12-15)13-25-16-2-8-19(9-3-16)34(30,31)26-17-4-6-18(7-5-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	33	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087256 (3-[4-(7-chloro-2-oxo-2H-4-chromenylmethylamino)phe...) Show SMILES NS(=O)(=O)c1cccc(NS(=O)(=O)c2ccc(NCc3cc(=O)oc4cc(Cl)ccc34)cc2)c1 Show InChI InChI=1S/C22H18ClN3O6S2/c23-15-4-9-20-14(10-22(27)32-21(20)11-15)13-25-16-5-7-18(8-6-16)34(30,31)26-17-2-1-3-19(12-17)33(24,28)29/h1-12,25-26H,13H2,(H2,24,28,29)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	36	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087255 (5-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-[...) Show SMILES NS(=O)(=O)c1nnc(NCc2cc(=O)oc3cc(Cl)ccc23)s1 Show InChI InChI=1S/C12H9ClN4O4S2/c13-7-1-2-8-6(3-10(18)21-9(8)4-7)5-15-11-16-17-12(22-11)23(14,19)20/h1-4H,5H2,(H,15,16)(H2,14,19,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	36	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087254 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-3...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(I)c1 Show InChI InChI=1S/C16H12ClIN2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	36	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50087262 (5-(5,7-Dioxo-5,7-dihydro-pyrrolo[3,4-b]pyridin-6-y...) Show SMILES NS(=O)(=O)c1nnc(NN2C(=O)c3cccnc3C2=O)s1 Show InChI InChI=1S/C9H6N6O4S2/c10-21(18,19)9-13-12-8(20-9)14-15-6(16)4-2-1-3-11-5(4)7(15)17/h1-3H,(H,12,14)(H2,10,18,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	39	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 human cloned Carbonic anhydrase I				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087248 (3-Chloro-4-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(Cl)c1 Show InChI InChI=1S/C16H12Cl2N2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	45	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM10884 ((2S,4S)-4-(ethylamino)-2-methyl-1,1-dioxo-2H,3H,4H...) Show SMILES CCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(cc12)S(N)(=O)=O |r| Show InChI InChI=1S/C10H16N2O4S3/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16)/t6-,8-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	45	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087252 (4,5-Dichloro-6-[(7-chloro-2-oxo-2H-chromen-4-ylmet...) Show SMILES NS(=O)(=O)c1cc(c(NCc2cc(=O)oc3cc(Cl)ccc23)c(Cl)c1Cl)S(N)(=O)=O Show InChI InChI=1S/C16H12Cl3N3O6S2/c17-8-1-2-9-7(3-13(23)28-10(9)4-8)6-22-16-12(30(21,26)27)5-11(29(20,24)25)14(18)15(16)19/h1-5,22H,6H2,(H2,20,24,25)(H2,21,26,27)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	49	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087251 (4-Chloro-6-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)...) Show SMILES NS(=O)(=O)c1cc(c(NCc2cc(=O)oc3cc(Cl)ccc23)cc1Cl)S(N)(=O)=O Show InChI InChI=1S/C16H13Cl2N3O6S2/c17-9-1-2-10-8(3-16(22)27-13(10)4-9)7-21-12-5-11(18)14(28(19,23)24)6-15(12)29(20,25)26/h1-6,21H,7H2,(H2,19,23,24)(H2,20,25,26)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	50	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087254 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-3...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(I)c1 Show InChI InChI=1S/C16H12ClIN2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	70	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087250 (3-Bromo-4-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)-...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(Br)c1 Show InChI InChI=1S/C16H12BrClN2O4S/c17-13-7-11(25(19,22)23)2-4-14(13)20-8-9-5-16(21)24-15-6-10(18)1-3-12(9)15/h1-7,20H,8H2,(H2,19,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	78	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087248 (3-Chloro-4-[(7-chloro-2-oxo-2H-chromen-4-ylmethyl)...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(Cl)c1 Show InChI InChI=1S/C16H12Cl2N2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	96	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087266 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-3...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)c(F)c1 Show InChI InChI=1S/C16H12ClFN2O4S/c17-10-1-3-12-9(5-16(21)24-15(12)6-10)8-20-14-4-2-11(7-13(14)18)25(19,22)23/h1-7,20H,8H2,(H2,19,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	110	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087257 (4-{2-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES NS(=O)(=O)c1ccc(CCNCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C18H17ClN2O4S/c19-14-3-6-16-13(9-18(22)25-17(16)10-14)11-21-8-7-12-1-4-15(5-2-12)26(20,23)24/h1-6,9-10,21H,7-8,11H2,(H2,20,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	120	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087263 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-b...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C16H13ClN2O4S/c17-11-1-6-14-10(7-16(20)23-15(14)8-11)9-19-12-2-4-13(5-3-12)24(18,21)22/h1-8,19H,9H2,(H2,18,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	125	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair				3D Structure (docked)
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087260 (4-{[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-...) Show SMILES NS(=O)(=O)c1ccc(CNCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C17H15ClN2O4S/c18-13-3-6-15-12(7-17(21)24-16(15)8-13)10-20-9-11-1-4-14(5-2-11)25(19,22)23/h1-8,20H,9-10H2,(H2,19,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	145	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087263 (4-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-b...) Show SMILES NS(=O)(=O)c1ccc(NCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C16H13ClN2O4S/c17-11-1-6-14-10(7-16(20)23-15(14)8-11)9-19-12-2-4-13(5-3-12)24(18,21)22/h1-8,19H,9H2,(H2,18,21,22)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	170	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087257 (4-{2-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino...) Show SMILES NS(=O)(=O)c1ccc(CCNCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C18H17ClN2O4S/c19-14-3-6-16-13(9-18(22)25-17(16)10-14)11-21-8-7-12-1-4-15(5-2-12)26(20,23)24/h1-6,9-10,21H,7-8,11H2,(H2,20,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	225	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087260 (4-{[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-...) Show SMILES NS(=O)(=O)c1ccc(CNCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C17H15ClN2O4S/c18-13-3-6-15-12(7-17(21)24-16(15)8-13)10-20-9-11-1-4-14(5-2-11)25(19,22)23/h1-8,20H,9-10H2,(H2,19,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	240	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087261 (3-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-b...) Show SMILES NS(=O)(=O)c1cccc(NCc2cc(=O)oc3cc(Cl)ccc23)c1 Show InChI InChI=1S/C16H13ClN2O4S/c17-11-4-5-14-10(6-16(20)23-15(14)7-11)9-19-12-2-1-3-13(8-12)24(18,21)22/h1-8,19H,9H2,(H2,18,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	250	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087253 (2-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-b...) Show SMILES NS(=O)(=O)c1ccccc1NCc1cc(=O)oc2cc(Cl)ccc12 Show InChI InChI=1S/C16H13ClN2O4S/c17-11-5-6-12-10(7-16(20)23-14(12)8-11)9-19-13-3-1-2-4-15(13)24(18,21)22/h1-8,19H,9H2,(H2,18,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	270	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50087249 (4-[N'-(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-hydra...) Show SMILES NS(=O)(=O)c1ccc(NNCc2cc(=O)oc3cc(Cl)ccc23)cc1 Show InChI InChI=1S/C16H14ClN3O4S/c17-11-1-6-14-10(7-16(21)24-15(14)8-11)9-19-20-12-2-4-13(5-3-12)25(18,22)23/h1-8,19-20H,9H2,(H2,18,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	275	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 human cloned Carbonic anhydrase II				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM50087261 (3-[(7-Chloro-2-oxo-2H-chromen-4-ylmethyl)-amino]-b...) Show SMILES NS(=O)(=O)c1cccc(NCc2cc(=O)oc3cc(Cl)ccc23)c1 Show InChI InChI=1S/C16H13ClN2O4S/c17-11-4-5-14-10(6-16(20)23-15(14)7-11)9-19-12-2-1-3-13(8-12)24(18,21)22/h1-8,19H,9H2,(H2,18,21,22)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	280	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 bovine Carbonic anhydrase IV determined by esterase method				Bioorg Med Chem Lett 10: 673-6 (2000) BindingDB Entry DOI: 10.7270/Q2RV0P61
					More data for this Ligand-Target Pair

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