Compile Data Set for Download or QSAR

Found 66 hits with Last Name = 'alim' and Initial = 'z'   

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))	BDBM50424254 (CHEMBL2314162) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(O)=O)-c2ccccc2)-c2cccc(c2)N=Nc2c(O)ccc3ccccc23)cc1 |w:31.33| Show InChI InChI=1S/C33H24N6O6S/c34-46(44,45)25-16-14-22(15-17-25)35-32(41)30-28(33(42)43)31(21-8-2-1-3-9-21)39(38-30)24-11-6-10-23(19-24)36-37-29-26-12-5-4-7-20(26)13-18-27(29)40/h1-19,40H,(H,35,41)(H,42,43)(H2,34,44,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Un-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM238298 (1-(3-aminophenyl)-4-benzoyl-5-phenyl-N-(4-sulfamoy...) Show SMILES Nc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(=O)c2ccccc2)c1-c1ccccc1 Show InChI InChI=1S/C29H23N5O4S/c30-21-12-7-13-23(18-21)34-27(19-8-3-1-4-9-19)25(28(35)20-10-5-2-6-11-20)26(33-34)29(36)32-22-14-16-24(17-15-22)39(31,37)38/h1-18H,30H2,(H,32,36)(H2,31,37,38)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	55	-41.4	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424250 (CHEMBL2314153) Show SMILES CC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)c1ccccc1 |w:4.4| Show InChI InChI=1S/C33H26N6O7S/c1-20(40)28(31(41)22-11-6-3-7-12-22)37-36-24-13-8-14-25(19-24)39-30(21-9-4-2-5-10-21)27(33(43)44)29(38-39)32(42)35-23-15-17-26(18-16-23)47(34,45)46/h2-19,36H,1H3,(H,35,42)(H,43,44)(H2,34,45,46)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	62	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Un-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM238299 (1-(3-azidophenyl)-4-benzoyl-5-phenyl-N-(4-sulfamoy...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(=O)c2ccccc2)-c2ccccc2)-c2cccc(c2)N=[N+]=[N-])cc1 Show InChI InChI=1S/C29H21N7O4S/c30-35-33-22-12-7-13-23(18-22)36-27(19-8-3-1-4-9-19)25(28(37)20-10-5-2-6-11-20)26(34-36)29(38)32-21-14-16-24(17-15-21)41(31,39)40/h1-18H,(H,32,38)(H2,31,39,40)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	64	-41.1	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193743 (Ethyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl...) Show SMILES CCCC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)OCC Show InChI InChI=1S/C29H28N12O9S4/c1-3-9-18(42)20(25(45)50-4-2)35-34-16-12-8-13-17(14-16)41-22(15-10-6-5-7-11-15)19(23(43)32-26-36-38-28(51-26)53(30,46)47)21(40-41)24(44)33-27-37-39-29(52-27)54(31,48)49/h5-8,10-14,34H,3-4,9H2,1-2H3,(H2,30,46,47)(H2,31,48,49)(H,32,36,43)(H,33,37,44)/b35-20-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	84	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193747 (Methyl 2-((3-(5-phenyl-3,4-bis((5-sulfamoyl-1,3,4-...) Show SMILES COC(=O)C(\N=N\c1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C30H24N12O10S5/c1-52-26(45)25(55(46,47)19-13-6-3-7-14-19)36-35-17-11-8-12-18(15-17)42-22(16-9-4-2-5-10-16)20(23(43)33-27-37-39-29(53-27)56(31,48)49)21(41-42)24(44)34-28-38-40-30(54-28)57(32,50)51/h2-15,25H,1H3,(H2,31,48,49)(H2,32,50,51)(H,33,37,43)(H,34,38,44)/b36-35+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	92	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424245 (CHEMBL2314158) Show SMILES CC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)OC(C)(C)C |w:4.4| Show InChI InChI=1S/C31H30N6O8S/c1-18(38)25(30(42)45-31(2,3)4)35-34-21-11-8-12-22(17-21)37-27(19-9-6-5-7-10-19)24(29(40)41)26(36-37)28(39)33-20-13-15-23(16-14-20)46(32,43)44/h5-17,34H,1-4H3,(H,33,39)(H,40,41)(H2,32,43,44)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	95	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424253 (CHEMBL2314161) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(c1)[N+]([O-])=O)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C25H21N5O7S/c1-2-37-25(32)21-22(24(31)27-17-11-13-20(14-12-17)38(26,35)36)28-29(23(21)16-7-4-3-5-8-16)18-9-6-10-19(15-18)30(33)34/h3-15H,2H2,1H3,(H,27,31)(H2,26,35,36)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	102	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM238298 (1-(3-aminophenyl)-4-benzoyl-5-phenyl-N-(4-sulfamoy...) Show SMILES Nc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(=O)c2ccccc2)c1-c1ccccc1 Show InChI InChI=1S/C29H23N5O4S/c30-21-12-7-13-23(18-21)34-27(19-8-3-1-4-9-19)25(28(35)20-10-5-2-6-11-20)26(33-34)29(36)32-22-14-16-24(17-15-22)39(31,37)38/h1-18H,30H2,(H,32,36)(H2,31,37,38)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	108	-39.8	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424247 (CHEMBL2314156) Show SMILES CCCC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)OCC |w:6.6| Show InChI InChI=1S/C31H30N6O8S/c1-3-9-24(38)26(31(42)45-4-2)35-34-21-12-8-13-22(18-21)37-28(19-10-6-5-7-11-19)25(30(40)41)27(36-37)29(39)33-20-14-16-23(17-15-20)46(32,43)44/h5-8,10-18,34H,3-4,9H2,1-2H3,(H,33,39)(H,40,41)(H2,32,43,44)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	111	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424249 (CHEMBL2314154) Show SMILES CCOC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)c1ccccc1 |w:6.6| Show InChI InChI=1S/C34H28N6O8S/c1-2-48-34(45)29(31(41)22-12-7-4-8-13-22)38-37-24-14-9-15-25(20-24)40-30(21-10-5-3-6-11-21)27(33(43)44)28(39-40)32(42)36-23-16-18-26(19-17-23)49(35,46)47/h3-20,37H,2H2,1H3,(H,36,42)(H,43,44)(H2,35,46,47)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	115	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193738 (1-(3-(2-(1,3-Dioxo-1-phenylbutan-2-ylidene)hydrazi...) Show SMILES CC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C31H24N12O8S4/c1-16(44)22(25(45)18-11-6-3-7-12-18)37-36-19-13-8-14-20(15-19)43-24(17-9-4-2-5-10-17)21(26(46)34-28-38-40-30(52-28)54(32,48)49)23(42-43)27(47)35-29-39-41-31(53-29)55(33,50)51/h2-15,36H,1H3,(H2,32,48,49)(H2,33,50,51)(H,34,38,46)(H,35,39,47)/b37-22-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	119	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193738 (1-(3-(2-(1,3-Dioxo-1-phenylbutan-2-ylidene)hydrazi...) Show SMILES CC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C31H24N12O8S4/c1-16(44)22(25(45)18-11-6-3-7-12-18)37-36-19-13-8-14-20(15-19)43-24(17-9-4-2-5-10-17)21(26(46)34-28-38-40-30(52-28)54(32,48)49)23(42-43)27(47)35-29-39-41-31(53-29)55(33,50)51/h2-15,36H,1H3,(H2,32,48,49)(H2,33,50,51)(H,34,38,46)(H,35,39,47)/b37-22-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	119	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424249 (CHEMBL2314154) Show SMILES CCOC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)c1ccccc1 |w:6.6| Show InChI InChI=1S/C34H28N6O8S/c1-2-48-34(45)29(31(41)22-12-7-4-8-13-22)38-37-24-14-9-15-25(20-24)40-30(21-10-5-3-6-11-21)27(33(43)44)28(39-40)32(42)36-23-16-18-26(19-17-23)49(35,46)47/h3-20,37H,2H2,1H3,(H,36,42)(H,43,44)(H2,35,46,47)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	126	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424251 (CHEMBL2314152) Show SMILES [#7]S(=O)(=O)c1ccc(-[#7]-[#6](=O)-c2nn(c(c2-[#6](-[#8])=O)-c2ccccc2)-c2cccc(-[#7]\[#7]=[#6](\[#6](=O)-c3ccccc3)-[#6](=O)-c3ccccc3)c2)cc1 Show InChI InChI=1S/C38H28N6O7S/c39-52(50,51)30-21-19-27(20-22-30)40-37(47)32-31(38(48)49)34(24-11-4-1-5-12-24)44(43-32)29-18-10-17-28(23-29)41-42-33(35(45)25-13-6-2-7-14-25)36(46)26-15-8-3-9-16-26/h1-23,41H,(H,40,47)(H,48,49)(H2,39,50,51)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	128	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM238299 (1-(3-azidophenyl)-4-benzoyl-5-phenyl-N-(4-sulfamoy...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(=O)c2ccccc2)-c2ccccc2)-c2cccc(c2)N=[N+]=[N-])cc1 Show InChI InChI=1S/C29H21N7O4S/c30-35-33-22-12-7-13-23(18-22)36-27(19-8-3-1-4-9-19)25(28(37)20-10-5-2-6-11-20)26(34-36)29(38)32-21-14-16-24(17-15-21)41(31,39)40/h1-18H,(H,32,38)(H2,31,39,40)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	129	-39.3	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424246 (CHEMBL2314157) Show SMILES COC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)C(C)C |w:5.5| Show InChI InChI=1S/C30H28N6O8S/c1-17(2)27(37)25(30(41)44-3)34-33-20-10-7-11-21(16-20)36-26(18-8-5-4-6-9-18)23(29(39)40)24(35-36)28(38)32-19-12-14-22(15-13-19)45(31,42)43/h4-17,33H,1-3H3,(H,32,38)(H,39,40)(H2,31,42,43)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	136	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424253 (CHEMBL2314161) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc(c1)[N+]([O-])=O)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C25H21N5O7S/c1-2-37-25(32)21-22(24(31)27-17-11-13-20(14-12-17)38(26,35)36)28-29(23(21)16-7-4-3-5-8-16)18-9-6-10-19(15-18)30(33)34/h3-15H,2H2,1H3,(H,27,31)(H2,26,35,36)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	144	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193744 (tert-Butyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulf...) Show SMILES CC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)OC(C)(C)C Show InChI InChI=1S/C29H28N12O9S4/c1-14(42)19(24(45)50-29(2,3)4)35-34-16-11-8-12-17(13-16)41-21(15-9-6-5-7-10-15)18(22(43)32-25-36-38-27(51-25)53(30,46)47)20(40-41)23(44)33-26-37-39-28(52-26)54(31,48)49/h5-13,34H,1-4H3,(H2,30,46,47)(H2,31,48,49)(H,32,36,43)(H,33,37,44)/b35-19-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	149	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193745 (1-(3-((2-Hydroxy-6-oxocyclohex-1-en-1-yl)diazenyl)...) Show SMILES [#7]S(=O)(=O)c1nnc(-[#7]-[#6](=O)-c2nn(c(c2-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)-c2ccccc2)-c2cccc(-[#7]\[#7]=[#6]-3/[#6](=O)-[#6]-[#6]-[#6]-[#6]-3=O)c2)s1 Show InChI InChI=1S/C27H22N12O8S4/c28-50(44,45)26-36-34-24(48-26)30-22(42)18-20(23(43)31-25-35-37-27(49-25)51(29,46)47)38-39(21(18)13-6-2-1-3-7-13)15-9-4-8-14(12-15)32-33-19-16(40)10-5-11-17(19)41/h1-4,6-9,12,32H,5,10-11H2,(H2,28,44,45)(H2,29,46,47)(H,30,34,42)(H,31,35,43)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	157	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424250 (CHEMBL2314153) Show SMILES CC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)c1ccccc1 |w:4.4| Show InChI InChI=1S/C33H26N6O7S/c1-20(40)28(31(41)22-11-6-3-7-12-22)37-36-24-13-8-14-25(19-24)39-30(21-9-4-2-5-10-21)27(33(43)44)29(38-39)32(42)35-23-15-17-26(18-16-23)47(34,45)46/h2-19,36H,1H3,(H,35,42)(H,43,44)(H2,34,45,46)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	159	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM238300 (4-benzoyl-1-(3-((2-hydroxy-4-oxopent-2-en-3-yl) di...) Show SMILES [#6]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2ccc(cc2)S([#7])(=O)=O)c(-[#6](=O)-c2ccccc2)c1-c1ccccc1)\[#6](-[#6])=O Show InChI InChI=1S/C34H28N6O6S/c1-21(41)30(22(2)42)38-37-26-14-9-15-27(20-26)40-32(23-10-5-3-6-11-23)29(33(43)24-12-7-4-8-13-24)31(39-40)34(44)36-25-16-18-28(19-17-25)47(35,45)46/h3-20,37H,1-2H3,(H,36,44)(H2,35,45,46)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	160	-38.8	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM238302 (4-benzoyl-1-(3-((3-hydroxy-1-oxo-1-phenylbut-2-en-...) Show SMILES CC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(=O)c2ccccc2)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C39H30N6O6S/c1-25(46)34(38(48)28-16-9-4-10-17-28)43-42-30-18-11-19-31(24-30)45-36(26-12-5-2-6-13-26)33(37(47)27-14-7-3-8-15-27)35(44-45)39(49)41-29-20-22-32(23-21-29)52(40,50)51/h2-24,42H,1H3,(H,41,49)(H2,40,50,51)/b43-34+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	166	-38.7	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424248 (CHEMBL2314155) Show SMILES CCOC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(C)=O |w:6.6| Show InChI InChI=1S/C29H26N6O8S/c1-3-43-29(40)24(17(2)36)33-32-20-10-7-11-21(16-20)35-26(18-8-5-4-6-9-18)23(28(38)39)25(34-35)27(37)31-19-12-14-22(15-13-19)44(30,41)42/h4-16,32H,3H2,1-2H3,(H,31,37)(H,38,39)(H2,30,41,42)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	197	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193742 (Diethyl 2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl-1,3...) Show SMILES [#6]-[#6]-[#8]-[#6](=O)-[#6](=[#7]/[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c1-c1ccccc1)\[#6](=O)-[#8]-[#6]-[#6] Show InChI InChI=1S/C28H26N12O10S4/c1-3-49-23(43)19(24(44)50-4-2)34-33-15-11-8-12-16(13-15)40-20(14-9-6-5-7-10-14)17(21(41)31-25-35-37-27(51-25)53(29,45)46)18(39-40)22(42)32-26-36-38-28(52-26)54(30,47)48/h5-13,33H,3-4H2,1-2H3,(H2,29,45,46)(H2,30,47,48)(H,31,35,41)(H,32,36,42)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	203	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193739 (Ethyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl...) Show SMILES CCOC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(C)=O Show InChI InChI=1S/C27H24N12O9S4/c1-3-48-23(43)18(13(2)40)33-32-15-10-7-11-16(12-15)39-20(14-8-5-4-6-9-14)17(21(41)30-24-34-36-26(49-24)51(28,44)45)19(38-39)22(42)31-25-35-37-27(50-25)52(29,46)47/h4-12,32H,3H2,1-2H3,(H2,28,44,45)(H2,29,46,47)(H,30,34,41)(H,31,35,42)/b33-18-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	208	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM238301 (4-benzoyl-1-(3-nitrophenyl)-5-phenyl-N-(4-sulfamoy...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(=O)c2ccccc2)-c2ccccc2)-c2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C29H21N5O6S/c30-41(39,40)24-16-14-21(15-17-24)31-29(36)26-25(28(35)20-10-5-2-6-11-20)27(19-8-3-1-4-9-19)33(32-26)22-12-7-13-23(18-22)34(37)38/h1-18H,(H,31,36)(H2,30,39,40)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	215	-38.1	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424251 (CHEMBL2314152) Show SMILES [#7]S(=O)(=O)c1ccc(-[#7]-[#6](=O)-c2nn(c(c2-[#6](-[#8])=O)-c2ccccc2)-c2cccc(-[#7]\[#7]=[#6](\[#6](=O)-c3ccccc3)-[#6](=O)-c3ccccc3)c2)cc1 Show InChI InChI=1S/C38H28N6O7S/c39-52(50,51)30-21-19-27(20-22-30)40-37(47)32-31(38(48)49)34(24-11-4-1-5-12-24)44(43-32)29-18-10-17-28(23-29)41-42-33(35(45)25-13-6-2-7-14-25)36(46)26-15-8-3-9-16-26/h1-23,41H,(H,40,47)(H,48,49)(H2,39,50,51)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	219	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193743 (Ethyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl...) Show SMILES CCCC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)OCC Show InChI InChI=1S/C29H28N12O9S4/c1-3-9-18(42)20(25(45)50-4-2)35-34-16-12-8-13-17(14-16)41-22(15-10-6-5-7-11-15)19(23(43)32-26-36-38-28(51-26)53(30,46)47)21(40-41)24(44)33-27-37-39-29(52-27)54(31,48)49/h5-8,10-14,34H,3-4,9H2,1-2H3,(H2,30,46,47)(H2,31,48,49)(H,32,36,43)(H,33,37,44)/b35-20-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	246	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424252 (CHEMBL2314151) Show SMILES [#6]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2ccc(cc2)S([#7])(=O)=O)c(-[#6](-[#8])=O)c1-c1ccccc1)\[#6](-[#6])=O Show InChI InChI=1S/C28H24N6O7S/c1-16(35)24(17(2)36)32-31-20-9-6-10-21(15-20)34-26(18-7-4-3-5-8-18)23(28(38)39)25(33-34)27(37)30-19-11-13-22(14-12-19)42(29,40)41/h3-15,31H,1-2H3,(H,30,37)(H,38,39)(H2,29,40,41)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	259	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193746 (1-(3-((2-Hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1...) Show SMILES [#6]C1([#6])[#6]-[#6](=O)\[#6](=[#7]/[#7]-c2cccc(c2)-n2nc(-[#6](=O)-[#7]-c3nnc(s3)S([#7])(=O)=O)c(-[#6](=O)-[#7]-c3nnc(s3)S([#7])(=O)=O)c2-c2ccccc2)-[#6](=O)-[#6]1 Show InChI InChI=1S/C29H26N12O8S4/c1-29(2)12-17(42)20(18(43)13-29)35-34-15-9-6-10-16(11-15)41-22(14-7-4-3-5-8-14)19(23(44)32-25-36-38-27(50-25)52(30,46)47)21(40-41)24(45)33-26-37-39-28(51-26)53(31,48)49/h3-11,34H,12-13H2,1-2H3,(H2,30,46,47)(H2,31,48,49)(H,32,36,44)(H,33,37,45)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	288	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193747 (Methyl 2-((3-(5-phenyl-3,4-bis((5-sulfamoyl-1,3,4-...) Show SMILES COC(=O)C(\N=N\c1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C30H24N12O10S5/c1-52-26(45)25(55(46,47)19-13-6-3-7-14-19)36-35-17-11-8-12-18(15-17)42-22(16-9-4-2-5-10-16)20(23(43)33-27-37-39-29(53-27)56(31,48)49)21(41-42)24(44)34-28-38-40-30(54-28)57(32,50)51/h2-15,25H,1H3,(H2,31,48,49)(H2,32,50,51)(H,33,37,43)(H,34,38,44)/b36-35+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	318	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424254 (CHEMBL2314162) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(O)=O)-c2ccccc2)-c2cccc(c2)N=Nc2c(O)ccc3ccccc23)cc1 |w:31.33| Show InChI InChI=1S/C33H24N6O6S/c34-46(44,45)25-16-14-22(15-17-25)35-32(41)30-28(33(42)43)31(21-8-2-1-3-9-21)39(38-30)24-11-6-10-23(19-24)36-37-29-26-12-5-4-7-20(26)13-18-27(29)40/h1-19,40H,(H,35,41)(H,42,43)(H2,34,44,45)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	318	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM238301 (4-benzoyl-1-(3-nitrophenyl)-5-phenyl-N-(4-sulfamoy...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(=O)c2ccccc2)-c2ccccc2)-c2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C29H21N5O6S/c30-41(39,40)24-16-14-21(15-17-24)31-29(36)26-25(28(35)20-10-5-2-6-11-20)27(19-8-3-1-4-9-19)33(32-26)22-12-7-13-23(18-22)34(37)38/h1-18H,(H,31,36)(H2,30,39,40)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	337	-36.9	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424244 (CHEMBL2314159) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(O)=O)-c2ccccc2)-c2cccc(c2)N=Nc2ccc(O)cc2)cc1 |w:31.33| Show InChI InChI=1S/C29H22N6O6S/c30-42(40,41)24-15-11-19(12-16-24)31-28(37)26-25(29(38)39)27(18-5-2-1-3-6-18)35(34-26)22-8-4-7-21(17-22)33-32-20-9-13-23(36)14-10-20/h1-17,36H,(H,31,37)(H,38,39)(H2,30,40,41)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	349	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50424243 (CHEMBL2314160) Show SMILES NS(=O)(=O)c1ccc(NC(=O)c2nn(c(c2C(O)=O)-c2ccccc2)-c2cccc(c2)C#N)cc1 Show InChI InChI=1S/C24H17N5O5S/c25-14-15-5-4-8-18(13-15)29-22(16-6-2-1-3-7-16)20(24(31)32)21(28-29)23(30)27-17-9-11-19(12-10-17)35(26,33)34/h1-13H,(H,27,30)(H,31,32)(H2,26,33,34)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	379	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424245 (CHEMBL2314158) Show SMILES CC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)OC(C)(C)C |w:4.4| Show InChI InChI=1S/C31H30N6O8S/c1-18(38)25(30(42)45-31(2,3)4)35-34-21-11-8-12-22(17-21)37-27(19-9-6-5-7-10-19)24(29(40)41)26(36-37)28(39)33-20-13-15-23(16-14-20)46(32,43)44/h5-17,34H,1-4H3,(H,33,39)(H,40,41)(H2,32,43,44)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	384	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193736 (1-(3-((2-Hydroxynaphthalen-1-yl)diazenyl)phenyl)-5...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)c2nn(c(c2C(=O)Nc2nnc(s2)S(N)(=O)=O)-c2ccccc2)-c2cccc(c2)\N=N\c2c(O)ccc3ccccc23)s1 Show InChI InChI=1S/C31H22N12O7S4/c32-53(47,48)30-40-38-28(51-30)34-26(45)22-24(27(46)35-29-39-41-31(52-29)54(33,49)50)42-43(25(22)17-8-2-1-3-9-17)19-11-6-10-18(15-19)36-37-23-20-12-5-4-7-16(20)13-14-21(23)44/h1-15,44H,(H2,32,47,48)(H2,33,49,50)(H,34,38,45)(H,35,39,46)/b37-36+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	411	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193741 (Ethyl 3-oxo-3-phenyl-2-(2-(3-(5-phenyl-3,4-bis((5-...) Show SMILES CCOC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C32H26N12O9S4/c1-2-53-28(48)23(25(45)18-12-7-4-8-13-18)38-37-19-14-9-15-20(16-19)44-24(17-10-5-3-6-11-17)21(26(46)35-29-39-41-31(54-29)56(33,49)50)22(43-44)27(47)36-30-40-42-32(55-30)57(34,51)52/h3-16,37H,2H2,1H3,(H2,33,49,50)(H2,34,51,52)(H,35,39,46)(H,36,40,47)/b38-23-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	435	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424252 (CHEMBL2314151) Show SMILES [#6]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2ccc(cc2)S([#7])(=O)=O)c(-[#6](-[#8])=O)c1-c1ccccc1)\[#6](-[#6])=O Show InChI InChI=1S/C28H24N6O7S/c1-16(35)24(17(2)36)32-31-20-9-6-10-21(15-20)34-26(18-7-4-3-5-8-18)23(28(38)39)25(33-34)27(37)30-19-11-13-22(14-12-19)42(29,40)41/h3-15,31H,1-2H3,(H,30,37)(H,38,39)(H2,29,40,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	448	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193742 (Diethyl 2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl-1,3...) Show SMILES [#6]-[#6]-[#8]-[#6](=O)-[#6](=[#7]/[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c1-c1ccccc1)\[#6](=O)-[#8]-[#6]-[#6] Show InChI InChI=1S/C28H26N12O10S4/c1-3-49-23(43)19(24(44)50-4-2)34-33-15-11-8-12-16(13-15)40-20(14-9-6-5-7-10-14)17(21(41)31-25-35-37-27(51-25)53(29,45)46)18(39-40)22(42)32-26-36-38-28(52-26)54(30,47)48/h5-13,33H,3-4H2,1-2H3,(H2,29,45,46)(H2,30,47,48)(H,31,35,41)(H,32,36,42)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	461	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424247 (CHEMBL2314156) Show SMILES CCCC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)OCC |w:6.6| Show InChI InChI=1S/C31H30N6O8S/c1-3-9-24(38)26(31(42)45-4-2)35-34-21-12-8-13-22(18-21)37-28(19-10-6-5-7-11-19)25(30(40)41)27(36-37)29(39)33-20-14-16-23(17-15-20)46(32,43)44/h5-8,10-18,34H,3-4,9H2,1-2H3,(H,33,39)(H,40,41)(H2,32,43,44)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	485	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193741 (Ethyl 3-oxo-3-phenyl-2-(2-(3-(5-phenyl-3,4-bis((5-...) Show SMILES CCOC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C32H26N12O9S4/c1-2-53-28(48)23(25(45)18-12-7-4-8-13-18)38-37-19-14-9-15-20(16-19)44-24(17-10-5-3-6-11-17)21(26(46)35-29-39-41-31(54-29)56(33,49)50)22(43-44)27(47)36-30-40-42-32(55-30)57(34,51)52/h3-16,37H,2H2,1H3,(H2,33,49,50)(H2,34,51,52)(H,35,39,46)(H,36,40,47)/b38-23-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	487	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50424246 (CHEMBL2314157) Show SMILES COC(=O)C(=NNc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(O)=O)c1-c1ccccc1)C(=O)C(C)C |w:5.5| Show InChI InChI=1S/C30H28N6O8S/c1-17(2)27(37)25(30(41)44-3)34-33-20-10-7-11-21(16-20)36-26(18-8-5-4-6-9-18)23(29(39)40)24(35-36)28(38)32-19-12-14-22(15-13-19)45(31,42)43/h4-17,33H,1-3H3,(H,32,38)(H,39,40)(H2,31,42,43)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	490	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Non-competitive inhibition of human erythrocytes carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 21-7 (2012) Article DOI: 10.1016/j.bmc.2012.11.012 BindingDB Entry DOI: 10.7270/Q2NV9KJR
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM193737 (1-(3-(2-(2,4-Dioxopentan-3-ylidene)hydrazinyl)phen...) Show SMILES [#6]-[#6](=O)-[#6](=[#7]/[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c(-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)c1-c1ccccc1)\[#6](-[#6])=O Show InChI InChI=1S/C26H22N12O8S4/c1-12(39)18(13(2)40)32-31-15-9-6-10-16(11-15)38-20(14-7-4-3-5-8-14)17(21(41)29-23-33-35-25(47-23)49(27,43)44)19(37-38)22(42)30-24-34-36-26(48-24)50(28,45)46/h3-11,31H,1-2H3,(H2,27,43,44)(H2,28,45,46)(H,29,33,41)(H,30,34,42)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	494	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193745 (1-(3-((2-Hydroxy-6-oxocyclohex-1-en-1-yl)diazenyl)...) Show SMILES [#7]S(=O)(=O)c1nnc(-[#7]-[#6](=O)-c2nn(c(c2-[#6](=O)-[#7]-c2nnc(s2)S([#7])(=O)=O)-c2ccccc2)-c2cccc(-[#7]\[#7]=[#6]-3/[#6](=O)-[#6]-[#6]-[#6]-[#6]-3=O)c2)s1 Show InChI InChI=1S/C27H22N12O8S4/c28-50(44,45)26-36-34-24(48-26)30-22(42)18-20(23(43)31-25-35-37-27(49-25)51(29,46)47)38-39(21(18)13-6-2-1-3-7-13)15-9-4-8-14(12-15)32-33-19-16(40)10-5-11-17(19)41/h1-4,6-9,12,32H,5,10-11H2,(H2,28,44,45)(H2,29,46,47)(H,30,34,42)(H,31,35,43)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	508	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM238302 (4-benzoyl-1-(3-((3-hydroxy-1-oxo-1-phenylbut-2-en-...) Show SMILES CC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2ccc(cc2)S(N)(=O)=O)c(C(=O)c2ccccc2)c1-c1ccccc1)\C(=O)c1ccccc1 Show InChI InChI=1S/C39H30N6O6S/c1-25(46)34(38(48)28-16-9-4-10-17-28)43-42-30-18-11-19-31(24-30)45-36(26-12-5-2-6-13-26)33(37(47)27-14-7-3-8-15-27)35(44-45)39(49)41-29-20-22-32(23-21-29)52(40,50)51/h2-24,42H,1H3,(H,41,49)(H2,40,50,51)/b43-34+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	521	-35.9	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193744 (tert-Butyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulf...) Show SMILES CC(=O)C(=N\Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(=O)OC(C)(C)C Show InChI InChI=1S/C29H28N12O9S4/c1-14(42)19(24(45)50-29(2,3)4)35-34-16-11-8-12-17(13-16)41-21(15-9-6-5-7-10-15)18(22(43)32-25-36-38-27(51-25)53(30,46)47)20(40-41)23(44)33-26-37-39-28(52-26)54(31,48)49/h5-13,34H,1-4H3,(H2,30,46,47)(H2,31,48,49)(H,32,36,43)(H,33,37,44)/b35-19-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	522	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM238300 (4-benzoyl-1-(3-((2-hydroxy-4-oxopent-2-en-3-yl) di...) Show SMILES [#6]-[#6](=O)-[#6](=[#7]\[#7]-c1cccc(c1)-n1nc(-[#6](=O)-[#7]-c2ccc(cc2)S([#7])(=O)=O)c(-[#6](=O)-c2ccccc2)c1-c1ccccc1)\[#6](-[#6])=O Show InChI InChI=1S/C34H28N6O6S/c1-21(41)30(22(2)42)38-37-26-14-9-15-27(20-26)40-32(23-10-5-3-6-11-23)29(33(43)24-12-7-4-8-13-24)31(39-40)34(44)36-25-16-18-28(19-17-25)47(35,45)46/h3-20,37H,1-2H3,(H,36,44)(H2,35,45,46)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	595	-35.5	n/a	n/a	n/a	n/a	n/a	7.4	25
Dumlupinar University					Assay Description CA activity was assayed in inhibition studies by following the change in absorbance at 348 nm of 4-nitrophenylacetate (NPA) to 4-nitrophenylate ion o...				J Enzyme Inhib Med Chem 28: 328-36 (2013) Article DOI: 10.3109/14756366.2011.651465 BindingDB Entry DOI: 10.7270/Q2V986ZJ
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM193739 (Ethyl 3-oxo-2-(2-(3-(5-phenyl-3,4-bis((5-sulfamoyl...) Show SMILES CCOC(=O)C(=N/Nc1cccc(c1)-n1nc(C(=O)Nc2nnc(s2)S(N)(=O)=O)c(C(=O)Nc2nnc(s2)S(N)(=O)=O)c1-c1ccccc1)\C(C)=O Show InChI InChI=1S/C27H24N12O9S4/c1-3-48-23(43)18(13(2)40)33-32-15-10-7-11-16(12-15)39-20(14-8-5-4-6-9-14)17(21(41)30-24-34-36-26(49-24)51(28,44)45)19(38-39)22(42)31-25-35-37-27(50-25)52(29,46)47/h4-12,32H,3H2,1-2H3,(H2,28,44,45)(H2,29,46,47)(H,30,34,41)(H,31,35,42)/b33-18-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	710	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University					Assay Description CA activity was measured according to the method described by Verpoorte et al. in inhibition studies, spectrophotometrically [Biochem., 242:4221-4229...				Bioorg Chem 68: 64-71 (2016) Article DOI: 10.1016/j.bioorg.2016.07.006 BindingDB Entry DOI: 10.7270/Q2N29VQC
					More data for this Ligand-Target Pair

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