Compile Data Set for Download or QSAR

Found 63 hits with Last Name = 'gencer' and Initial = 'n'   

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
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139137 (CHEMBL3759162) Show SMILES [Cl-].CCCCn1cc[n+](Cc2cc(=O)oc3cc(C)cc(C)c23)c1 Show InChI InChI=1S/C19H23N2O2.ClH/c1-4-5-6-20-7-8-21(13-20)12-16-11-18(22)23-17-10-14(2)9-15(3)19(16)17;/h7-11,13H,4-6,12H2,1-3H3;1H/q+1;/p-1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.39E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Competitive inhibition of human serum PON1 using paraoxon as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM86068 (PPC) Show SMILES Cc1ccc(cc1)-c1cc2cc(O)c(O)cc2oc1=O Show InChI InChI=1S/C16H12O4/c1-9-2-4-10(5-3-9)12-6-11-7-13(17)14(18)8-15(11)20-16(12)19/h2-8,17-18H,1H3	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139137 (CHEMBL3759162) Show SMILES [Cl-].CCCCn1cc[n+](Cc2cc(=O)oc3cc(C)cc(C)c23)c1 Show InChI InChI=1S/C19H23N2O2.ClH/c1-4-5-6-20-7-8-21(13-20)12-16-11-18(22)23-17-10-14(2)9-15(3)19(16)17;/h7-11,13H,4-6,12H2,1-3H3;1H/q+1;/p-1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.37E+3	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246528 (Saccharin derivative, 6b) Show SMILES COc1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C15H13N3O5S/c1-23-11-4-2-3-9(7-11)16-15(20)17-10-5-6-12-13(8-10)24(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.54E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246543 (Saccharin derivative, 6q) Show SMILES Fc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10FN3O3S2/c15-8-1-3-9(4-2-8)16-14(22)17-10-5-6-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50144692 (CHEMBL3759251) Show SMILES [Cl-].O=C(C[n+]1cn(Cn2nnc3ccccc23)c2ccccc12)c1ccc2OCC(=O)Nc2c1 Show InChI InChI=1S/C24H18N6O3.ClH/c31-22(16-9-10-23-18(11-16)25-24(32)13-33-23)12-28-14-29(21-8-4-3-7-20(21)28)15-30-19-6-2-1-5-17(19)26-27-30;/h1-11,14H,12-13,15H2;1H	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.76E+3	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246547 (Saccharin derivative, 6u) Show SMILES Clc1cc(Cl)cc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H9Cl2N3O3S2/c15-7-3-8(16)5-10(4-7)18-14(23)17-9-1-2-11-12(6-9)24(21,22)19-13(11)20/h1-6H,(H,19,20)(H2,17,18,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246539 (Saccharin derivative, 6m) Show SMILES Cc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O3S2/c1-9-2-4-10(5-3-9)16-15(22)17-11-6-7-12-13(8-11)23(20,21)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246546 (Saccharin derivative, 6t) Show SMILES Clc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c(Cl)c1 Show InChI InChI=1S/C14H9Cl2N3O3S2/c15-7-1-4-11(10(16)5-7)18-14(23)17-8-2-3-9-12(6-8)24(21,22)19-13(9)20/h1-6H,(H,19,20)(H2,17,18,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246533 (Saccharin derivative, 6g) Show SMILES Clc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1Cl Show InChI InChI=1S/C14H9Cl2N3O4S/c15-10-4-2-7(5-11(10)16)17-14(21)18-8-1-3-9-12(6-8)24(22,23)19-13(9)20/h1-6H,(H,19,20)(H2,17,18,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.27E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246539 (Saccharin derivative, 6m) Show SMILES Cc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O3S2/c1-9-2-4-10(5-3-9)16-15(22)17-11-6-7-12-13(8-11)23(20,21)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246542 (Saccharin derivative, 6p) Show SMILES Fc1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10FN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246537 (Saccharin derivative, 6k) Show SMILES Fc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10FN3O4S/c15-8-1-3-9(4-2-8)16-14(20)17-10-5-6-11-12(7-10)23(21,22)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.71E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246545 (Saccharin derivative, 6s) Show SMILES Clc1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10ClN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.72E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246531 (Saccharin derivative, 6e) Show SMILES Clc1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10ClN3O4S/c15-8-2-1-3-9(6-8)16-14(20)17-10-4-5-11-12(7-10)23(21,22)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.78E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50144693 (CHEMBL3758983) Show SMILES [Cl-].Cn1cc[n+](Cc2nc3ccccc3[nH]2)c1 Show InChI InChI=1S/C12H13N4.ClH/c1-15-6-7-16(9-15)8-12-13-10-4-2-3-5-11(10)14-12;/h2-7,9H,8H2,1H3,(H,13,14);1H/q+1;/p-1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.91E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246544 (Saccharin derivative, 6r) Show SMILES Ic1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10IN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246527 (Saccharin derivative, 6a) Show SMILES O=C(Nc1ccccc1)Nc1ccc2C(=O)NS(=O)(=O)c2c1 Show InChI InChI=1S/C14H11N3O4S/c18-13-11-7-6-10(8-12(11)22(20,21)17-13)16-14(19)15-9-4-2-1-3-5-9/h1-8H,(H,17,18)(H2,15,16,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139133 (CHEMBL3759178) Show SMILES Cc1ccc2c(CCl)cc(=O)oc2c1C Show InChI InChI=1S/C12H11ClO2/c1-7-3-4-10-9(6-13)5-11(14)15-12(10)8(7)2/h3-5H,6H2,1-2H3	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246532 (Saccharin derivative, 6f) Show SMILES Clc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10ClN3O4S/c15-8-1-3-9(4-2-8)16-14(20)17-10-5-6-11-12(7-10)23(21,22)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139135 (CHEMBL3759775) Show SMILES [Cl-].Cc1cc(C)c2c(C[n+]3ccn(C)c3)cc(=O)oc2c1 Show InChI InChI=1S/C16H17N2O2.ClH/c1-11-6-12(2)16-13(8-15(19)20-14(16)7-11)9-18-5-4-17(3)10-18;/h4-8,10H,9H2,1-3H3;1H/q+1;/p-1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246530 (Saccharin derivative, 6d) Show SMILES Cc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O4S/c1-9-2-4-10(5-3-9)16-15(20)17-11-6-7-12-13(8-11)23(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246547 (Saccharin derivative, 6u) Show SMILES Clc1cc(Cl)cc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H9Cl2N3O3S2/c15-7-3-8(16)5-10(4-7)18-14(23)17-9-1-2-11-12(6-9)24(21,22)19-13(11)20/h1-6H,(H,19,20)(H2,17,18,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.61E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50144739 (CHEMBL3759516) Show SMILES [Cl-].CCCCn1cc[n+](Cc2nc3ccccc3[nH]2)c1 Show InChI InChI=1S/C15H19N4.ClH/c1-2-3-8-18-9-10-19(12-18)11-15-16-13-6-4-5-7-14(13)17-15;/h4-7,9-10,12H,2-3,8,11H2,1H3,(H,16,17);1H/q+1;/p-1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246541 (Saccharin derivative, 6o) Show SMILES Fc1ccccc1NC(=S)Nc1ccc2C(=O)NS(=O)(=O)c2c1 Show InChI InChI=1S/C14H10FN3O3S2/c15-10-3-1-2-4-11(10)17-14(22)16-8-5-6-9-12(7-8)23(20,21)18-13(9)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246540 (Saccharin derivative, 6n) Show SMILES COc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O4S2/c1-22-11-5-2-9(3-6-11)16-15(23)17-10-4-7-12-13(8-10)24(20,21)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.03E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246544 (Saccharin derivative, 6r) Show SMILES Ic1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10IN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.07E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246530 (Saccharin derivative, 6d) Show SMILES Cc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O4S/c1-9-2-4-10(5-3-9)16-15(20)17-11-6-7-12-13(8-11)23(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139132 (CHEMBL1462074) Show SMILES Cc1cc(C)c2c(CCl)cc(=O)oc2c1 Show InChI InChI=1S/C12H11ClO2/c1-7-3-8(2)12-9(6-13)5-11(14)15-10(12)4-7/h3-5H,6H2,1-2H3	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246534 (Saccharin derivative, 6h) Show SMILES [O-][N+](=O)c1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10N4O6S/c19-13-11-5-4-9(7-12(11)25(23,24)17-13)16-14(20)15-8-2-1-3-10(6-8)18(21)22/h1-7H,(H,17,19)(H2,15,16,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.27E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246545 (Saccharin derivative, 6s) Show SMILES Clc1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10ClN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246529 (Saccharin derivative, 6c) Show SMILES COc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O5S/c1-23-11-5-2-9(3-6-11)16-15(20)17-10-4-7-12-13(8-10)24(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246533 (Saccharin derivative, 6g) Show SMILES Clc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1Cl Show InChI InChI=1S/C14H9Cl2N3O4S/c15-10-4-2-7(5-11(10)16)17-14(21)18-8-1-3-9-12(6-8)24(22,23)19-13(9)20/h1-6H,(H,19,20)(H2,17,18,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246534 (Saccharin derivative, 6h) Show SMILES [O-][N+](=O)c1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10N4O6S/c19-13-11-5-4-9(7-12(11)25(23,24)17-13)16-14(20)15-8-2-1-3-10(6-8)18(21)22/h1-7H,(H,17,19)(H2,15,16,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.75E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246529 (Saccharin derivative, 6c) Show SMILES COc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O5S/c1-23-11-5-2-9(3-6-11)16-15(20)17-10-4-7-12-13(8-10)24(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246535 (Saccharin derivative, 6i) Show SMILES [O-][N+](=O)c1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10N4O6S/c19-13-11-6-3-9(7-12(11)25(23,24)17-13)16-14(20)15-8-1-4-10(5-2-8)18(21)22/h1-7H,(H,17,19)(H2,15,16,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.89E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246531 (Saccharin derivative, 6e) Show SMILES Clc1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10ClN3O4S/c15-8-2-1-3-9(6-8)16-14(20)17-10-4-5-11-12(7-10)23(21,22)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Serum paraoxonase/arylesterase 1 (Homo sapiens (Human))	BDBM50139134 (CHEMBL3758686) Show SMILES CC(C)(C)c1ccc2oc(=O)cc(CCl)c2c1 Show InChI InChI=1S/C14H15ClO2/c1-14(2,3)10-4-5-12-11(7-10)9(8-15)6-13(16)17-12/h4-7H,8H2,1-3H3	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
In£n£ University Curated by ChEMBL					Assay Description Inhibition of human serum PON1 using paraoxon as substrate by spectrophotometric analysis				Bioorg Med Chem 24: 1392-401 (2016) Article DOI: 10.1016/j.bmc.2016.02.012 BindingDB Entry DOI: 10.7270/Q2FT8NWG
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246538 (Saccharin derivative, 6l) Show SMILES O=C1NS(=O)(=O)c2cc(NC(=S)Nc3ccccc3)ccc12 Show InChI InChI=1S/C14H11N3O3S2/c18-13-11-7-6-10(8-12(11)22(19,20)17-13)16-14(21)15-9-4-2-1-3-5-9/h1-8H,(H,17,18)(H2,15,16,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246536 (Saccharin derivative, 6j) Show SMILES Fc1ccccc1NC(=O)Nc1ccc2C(=O)NS(=O)(=O)c2c1 Show InChI InChI=1S/C14H10FN3O4S/c15-10-3-1-2-4-11(10)17-14(20)16-8-5-6-9-12(7-8)23(21,22)18-13(9)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.16E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246528 (Saccharin derivative, 6b) Show SMILES COc1cccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C15H13N3O5S/c1-23-11-4-2-3-9(7-11)16-15(20)17-10-5-6-12-13(8-10)24(21,22)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246537 (Saccharin derivative, 6k) Show SMILES Fc1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10FN3O4S/c15-8-1-3-9(4-2-8)16-14(20)17-10-5-6-11-12(7-10)23(21,22)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246540 (Saccharin derivative, 6n) Show SMILES COc1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C15H13N3O4S2/c1-22-11-5-2-9(3-6-11)16-15(23)17-10-4-7-12-13(8-10)24(20,21)18-14(12)19/h2-8H,1H3,(H,18,19)(H2,16,17,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.33E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM246548 (Saccharin derivative, 6v) Show SMILES [O-][N+](=O)c1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10N4O5S2/c19-13-11-6-3-9(7-12(11)25(22,23)17-13)16-14(24)15-8-1-4-10(5-2-8)18(20)21/h1-7H,(H,17,19)(H2,15,16,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.35E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246536 (Saccharin derivative, 6j) Show SMILES Fc1ccccc1NC(=O)Nc1ccc2C(=O)NS(=O)(=O)c2c1 Show InChI InChI=1S/C14H10FN3O4S/c15-10-3-1-2-4-11(10)17-14(20)16-8-5-6-9-12(7-8)23(21,22)18-13(9)19/h1-7H,(H,18,19)(H2,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246542 (Saccharin derivative, 6p) Show SMILES Fc1cccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)c1 Show InChI InChI=1S/C14H10FN3O3S2/c15-8-2-1-3-9(6-8)16-14(22)17-10-4-5-11-12(7-10)23(20,21)18-13(11)19/h1-7H,(H,18,19)(H2,16,17,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246538 (Saccharin derivative, 6l) Show SMILES O=C1NS(=O)(=O)c2cc(NC(=S)Nc3ccccc3)ccc12 Show InChI InChI=1S/C14H11N3O3S2/c18-13-11-7-6-10(8-12(11)22(19,20)17-13)16-14(21)15-9-4-2-1-3-5-9/h1-8H,(H,17,18)(H2,15,16,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246548 (Saccharin derivative, 6v) Show SMILES [O-][N+](=O)c1ccc(NC(=S)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10N4O5S2/c19-13-11-6-3-9(7-12(11)25(22,23)17-13)16-14(24)15-8-1-4-10(5-2-8)18(20)21/h1-7H,(H,17,19)(H2,15,16,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50004506 (6-Aminosaccharin | CHEMBL2016952 | Saccharin deriv...) Show SMILES Nc1ccc2C(=O)NS(=O)(=O)c2c1 Show InChI InChI=1S/C7H6N2O3S/c8-4-1-2-5-6(3-4)13(11,12)9-7(5)10/h1-3H,8H2,(H,9,10)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	4.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM246535 (Saccharin derivative, 6i) Show SMILES [O-][N+](=O)c1ccc(NC(=O)Nc2ccc3C(=O)NS(=O)(=O)c3c2)cc1 Show InChI InChI=1S/C14H10N4O6S/c19-13-11-6-3-9(7-12(11)25(23,24)17-13)16-14(20)15-8-1-4-10(5-2-8)18(21)22/h1-7H,(H,17,19)(H2,15,16,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sakarya University					Assay Description For the inhibition studies of saccharin, different concentrations of these compounds were added to the enzyme. Activity percentage values of CA for d...				J Enzyme Inhib Med Chem 29: 118-23 (2014) Article DOI: 10.3109/14756366.2012.757222 BindingDB Entry DOI: 10.7270/Q2WM1C9V
					More data for this Ligand-Target Pair

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