Compile Data Set for Download or QSAR

Found 100 hits Enz. Inhib. hit(s) with all data for entry = 50003009   

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 9 (Homo sapiens (Human))	BDBM50465679 (CHEMBL4279796) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(F)cc2)c1 Show InChI InChI=1S/C13H12FN3O4S/c14-8-1-3-9(4-2-8)16-13(19)17-11-7-10(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465674 (CHEMBL4294946) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2[N+]([O-])=O)c1 Show InChI InChI=1S/C13H12N4O6S/c14-24(22,23)8-5-6-12(18)10(7-8)16-13(19)15-9-3-1-2-4-11(9)17(20)21/h1-7,18H,(H2,14,22,23)(H2,15,16,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465678 (CHEMBL4287685) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2cccc(Cl)c2)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-8-2-1-3-9(6-8)16-13(19)17-11-7-10(22(15,20)21)4-5-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465663 (CHEMBL4292591) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2Cl)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-9-3-1-2-4-10(9)16-13(19)17-11-7-8(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50334354 (4-(3-(4-fluorophenyl)ureido)benzenesulfonamide | 4...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)Nc2ccc(F)cc2)cc1 Show InChI InChI=1S/C13H12FN3O3S/c14-9-1-3-10(4-2-9)16-13(18)17-11-5-7-12(8-6-11)21(15,19)20/h1-8H,(H2,15,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	4.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465664 (CHEMBL4293437) Show SMILES CCCCc1ccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)cc1 Show InChI InChI=1S/C17H21N3O4S/c1-2-3-4-12-5-7-13(8-6-12)19-17(22)20-15-11-14(25(18,23)24)9-10-16(15)21/h5-11,21H,2-4H2,1H3,(H2,18,23,24)(H2,19,20,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465668 (CHEMBL4292271) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)NCc2ccccc2)c1 Show InChI InChI=1S/C14H15N3O4S/c15-22(20,21)11-6-7-13(18)12(8-11)17-14(19)16-9-10-4-2-1-3-5-10/h1-8,18H,9H2,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465667 (CHEMBL4290328) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)NC2CCCC2)c1 Show InChI InChI=1S/C12H17N3O4S/c13-20(18,19)9-5-6-11(16)10(7-9)15-12(17)14-8-3-1-2-4-8/h5-8,16H,1-4H2,(H2,13,18,19)(H2,14,15,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465669 (CHEMBL4294703) Show SMILES Cc1ccc(CNC(=O)Nc2cc(ccc2O)S(N)(=O)=O)cc1 Show InChI InChI=1S/C15H17N3O4S/c1-10-2-4-11(5-3-10)9-17-15(20)18-13-8-12(23(16,21)22)6-7-14(13)19/h2-8,19H,9H2,1H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	5.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM10880 (AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...) Show SMILES CC(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	5.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465658 (CHEMBL4284307) Show SMILES Cc1cc(C)cc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C15H17N3O4S/c1-9-5-10(2)7-11(6-9)17-15(20)18-13-8-12(23(16,21)22)3-4-14(13)19/h3-8,19H,1-2H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465666 (CHEMBL4289589) Show SMILES Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C6H8N2O3S/c7-5-3-4(12(8,10)11)1-2-6(5)9/h1-3,9H,7H2,(H2,8,10,11)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465660 (CHEMBL4288405) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(Cl)cc2)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-8-1-3-9(4-2-8)16-13(19)17-11-7-10(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465677 (CHEMBL4292967) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)NCCc2ccccc2)c1 Show InChI InChI=1S/C15H17N3O4S/c16-23(21,22)12-6-7-14(19)13(10-12)18-15(20)17-9-8-11-4-2-1-3-5-11/h1-7,10,19H,8-9H2,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465678 (CHEMBL4287685) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2cccc(Cl)c2)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-8-2-1-3-9(6-8)16-13(19)17-11-7-10(22(15,20)21)4-5-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465675 (CHEMBL4282828) Show SMILES COc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C14H15N3O5S/c1-22-13-5-3-2-4-10(13)16-14(19)17-11-8-9(23(15,20)21)6-7-12(11)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	7.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465679 (CHEMBL4279796) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(F)cc2)c1 Show InChI InChI=1S/C13H12FN3O4S/c14-8-1-3-9(4-2-8)16-13(19)17-11-7-10(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465674 (CHEMBL4294946) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2[N+]([O-])=O)c1 Show InChI InChI=1S/C13H12N4O6S/c14-24(22,23)8-5-6-12(18)10(7-8)16-13(19)15-9-3-1-2-4-11(9)17(20)21/h1-7,18H,(H2,14,22,23)(H2,15,16,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465662 (CHEMBL4287699) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C13H12N4O6S/c14-24(22,23)10-5-6-12(18)11(7-10)16-13(19)15-8-1-3-9(4-2-8)17(20)21/h1-7,18H,(H2,14,22,23)(H2,15,16,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465657 (CHEMBL4282079) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2cccc3ccccc23)c1 Show InChI InChI=1S/C17H15N3O4S/c18-25(23,24)12-8-9-16(21)15(10-12)20-17(22)19-14-7-3-5-11-4-1-2-6-13(11)14/h1-10,21H,(H2,18,23,24)(H2,19,20,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	8.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465676 (CHEMBL4278617) Show SMILES CCOc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C15H17N3O5S/c1-2-23-14-6-4-3-5-11(14)17-15(20)18-12-9-10(24(16,21)22)7-8-13(12)19/h3-9,19H,2H2,1H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	9.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM10880 (AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...) Show SMILES CC(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA2 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465657 (CHEMBL4282079) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2cccc3ccccc23)c1 Show InChI InChI=1S/C17H15N3O4S/c18-25(23,24)12-8-9-16(21)15(10-12)20-17(22)19-14-7-3-5-11-4-1-2-6-13(11)14/h1-10,21H,(H2,18,23,24)(H2,19,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465662 (CHEMBL4287699) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C13H12N4O6S/c14-24(22,23)10-5-6-12(18)11(7-10)16-13(19)15-8-1-3-9(4-2-8)17(20)21/h1-7,18H,(H2,14,22,23)(H2,15,16,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465663 (CHEMBL4292591) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2Cl)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-9-3-1-2-4-10(9)16-13(19)17-11-7-8(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465672 (CHEMBL4285851) Show SMILES Cc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C14H15N3O4S/c1-9-4-2-3-5-11(9)16-14(19)17-12-8-10(22(15,20)21)6-7-13(12)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465675 (CHEMBL4282828) Show SMILES COc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C14H15N3O5S/c1-22-13-5-3-2-4-10(13)16-14(19)17-11-8-9(23(15,20)21)6-7-12(11)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465671 (CHEMBL4283637) Show SMILES CSc1cccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C14H15N3O4S2/c1-22-10-4-2-3-9(7-10)16-14(19)17-12-8-11(23(15,20)21)5-6-13(12)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM10880 (AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...) Show SMILES CC(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465658 (CHEMBL4284307) Show SMILES Cc1cc(C)cc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C15H17N3O4S/c1-9-5-10(2)7-11(6-9)17-15(20)18-13-8-12(23(16,21)22)3-4-14(13)19/h3-8,19H,1-2H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465666 (CHEMBL4289589) Show SMILES Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C6H8N2O3S/c7-5-3-4(12(8,10)11)1-2-6(5)9/h1-3,9H,7H2,(H2,8,10,11)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465659 (CHEMBL4291115) Show SMILES CCc1ccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)cc1 Show InChI InChI=1S/C15H17N3O4S/c1-2-10-3-5-11(6-4-10)17-15(20)18-13-9-12(23(16,21)22)7-8-14(13)19/h3-9,19H,2H2,1H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465661 (CHEMBL4289262) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(Oc3ccccc3)cc2)c1 Show InChI InChI=1S/C19H17N3O5S/c20-28(25,26)16-10-11-18(23)17(12-16)22-19(24)21-13-6-8-15(9-7-13)27-14-4-2-1-3-5-14/h1-12,23H,(H2,20,25,26)(H2,21,22,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	31	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465671 (CHEMBL4283637) Show SMILES CSc1cccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C14H15N3O4S2/c1-22-10-4-2-3-9(7-10)16-14(19)17-12-8-11(23(15,20)21)5-6-13(12)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	36	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465672 (CHEMBL4285851) Show SMILES Cc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C14H15N3O4S/c1-9-4-2-3-5-11(9)16-14(19)17-12-8-10(22(15,20)21)6-7-13(12)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	44	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465670 (CHEMBL4286489) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2)c1 Show InChI InChI=1S/C13H13N3O4S/c14-21(19,20)10-6-7-12(17)11(8-10)16-13(18)15-9-4-2-1-3-5-9/h1-8,17H,(H2,14,19,20)(H2,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	44	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465665 (CHEMBL4294527) Show SMILES CC(C)c1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C16H19N3O4S/c1-10(2)12-5-3-4-6-13(12)18-16(21)19-14-9-11(24(17,22)23)7-8-15(14)20/h3-10,20H,1-2H3,(H2,17,22,23)(H2,18,19,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	45	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50334354 (4-(3-(4-fluorophenyl)ureido)benzenesulfonamide | 4...) Show SMILES NS(=O)(=O)c1ccc(NC(=O)Nc2ccc(F)cc2)cc1 Show InChI InChI=1S/C13H12FN3O3S/c14-9-1-3-10(4-2-9)16-13(18)17-11-5-7-12(8-6-11)21(15,19)20/h1-8H,(H2,15,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	45	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465673 (CHEMBL4286620) Show SMILES Cc1ccc(C)c(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C15H17N3O4S/c1-9-3-4-10(2)12(7-9)17-15(20)18-13-8-11(23(16,21)22)5-6-14(13)19/h3-8,19H,1-2H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	48	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465659 (CHEMBL4291115) Show SMILES CCc1ccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)cc1 Show InChI InChI=1S/C15H17N3O4S/c1-2-10-3-5-11(6-4-10)17-15(20)18-13-9-12(23(16,21)22)7-8-14(13)19/h3-9,19H,2H2,1H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	58	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50465661 (CHEMBL4289262) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(Oc3ccccc3)cc2)c1 Show InChI InChI=1S/C19H17N3O5S/c20-28(25,26)16-10-11-18(23)17(12-16)22-19(24)21-13-6-8-15(9-7-13)27-14-4-2-1-3-5-14/h1-12,23H,(H2,20,25,26)(H2,21,22,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	69	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA12 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye ba...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50465673 (CHEMBL4286620) Show SMILES Cc1ccc(C)c(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)c1 Show InChI InChI=1S/C15H17N3O4S/c1-9-3-4-10(2)12(7-9)17-15(20)18-13-8-11(23(16,21)22)5-6-14(13)19/h3-8,19H,1-2H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	94	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA2 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465676 (CHEMBL4278617) Show SMILES CCOc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C15H17N3O5S/c1-2-23-14-6-4-3-5-11(14)17-15(20)18-12-9-10(24(16,21)22)7-8-13(12)19/h3-9,19H,2H2,1H3,(H2,16,21,22)(H2,17,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	134	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50465672 (CHEMBL4285851) Show SMILES Cc1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C14H15N3O4S/c1-9-4-2-3-5-11(9)16-14(19)17-12-8-10(22(15,20)21)6-7-13(12)18/h2-8,18H,1H3,(H2,15,20,21)(H2,16,17,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	137	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA2 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465664 (CHEMBL4293437) Show SMILES CCCCc1ccc(NC(=O)Nc2cc(ccc2O)S(N)(=O)=O)cc1 Show InChI InChI=1S/C17H21N3O4S/c1-2-3-4-12-5-7-13(8-6-12)19-17(22)20-15-11-14(25(18,23)24)9-10-16(15)21/h5-11,21H,2-4H2,1H3,(H2,18,23,24)(H2,19,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	157	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465670 (CHEMBL4286489) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccccc2)c1 Show InChI InChI=1S/C13H13N3O4S/c14-21(19,20)10-6-7-12(17)11(8-10)16-13(18)15-9-4-2-1-3-5-9/h1-8,17H,(H2,14,19,20)(H2,15,16,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	169	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465665 (CHEMBL4294527) Show SMILES CC(C)c1ccccc1NC(=O)Nc1cc(ccc1O)S(N)(=O)=O Show InChI InChI=1S/C16H19N3O4S/c1-10(2)12-5-3-4-6-13(12)18-16(21)19-14-9-11(24(17,22)23)7-8-15(14)20/h3-10,20H,1-2H3,(H2,17,22,23)(H2,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	180	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465660 (CHEMBL4288405) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)Nc2ccc(Cl)cc2)c1 Show InChI InChI=1S/C13H12ClN3O4S/c14-8-1-3-9(4-2-8)16-13(19)17-11-7-10(22(15,20)21)5-6-12(11)18/h1-7,18H,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	206	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465668 (CHEMBL4292271) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)NCc2ccccc2)c1 Show InChI InChI=1S/C14H15N3O4S/c15-22(20,21)11-6-7-13(18)12(8-11)17-14(19)16-9-10-4-2-1-3-5-10/h1-8,18H,9H2,(H2,15,20,21)(H2,16,17,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	216	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50465677 (CHEMBL4292967) Show SMILES NS(=O)(=O)c1ccc(O)c(NC(=O)NCCc2ccccc2)c1 Show InChI InChI=1S/C15H17N3O4S/c16-23(21,22)12-6-7-14(19)13(10-12)18-15(20)17-9-8-11-4-2-1-3-5-11/h1-7,10,19H,8-9H2,(H2,16,21,22)(H2,17,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	231	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florence Curated by ChEMBL					Assay Description Inhibition of human CA9 assessed as enzyme inhibitor complex formation preincubated for 15 mins and measured for 10 to 100 secs by phenol red dye bas...				J Med Chem 61: 6328-6338 (2018) Article DOI: 10.1021/acs.jmedchem.8b00770 BindingDB Entry DOI: 10.7270/Q2639SDT
					More data for this Ligand-Target Pair

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