Compile Data Set for Download or QSAR

Found 87 hits with Last Name = 'saramet' and Initial = 'i'   

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))	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 Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair				3D Structure (crystal)
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 PubMed	12	-45.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85563 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H14BrN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	16	-44.5	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85566 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H13BrN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	21	-43.8	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85562 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H14ClN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	24	-43.5	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					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 Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85561 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H15N3O4S3/c17-26(22,23)18-10-13-11-24-16(19-13)12-6-8-15(9-7-12)25(20,21)14-4-2-1-3-5-14/h1-9,11,18H,10H2,(H2,17,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	28	-43.1	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85565 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H13ClN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	30	-42.9	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM85564 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H14N2O5S3/c17-26(21,22)23-10-13-11-24-16(18-13)12-6-8-15(9-7-12)25(19,20)14-4-2-1-3-5-14/h1-9,11H,10H2,(H2,17,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	33	-42.7	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM10868 (1,3,4-Thiadiazole-2-sulfonamide, 6 | 1,3,4-thiadia...) Show SMILES Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C2H4N4O2S2/c3-1-5-6-2(9-1)10(4,7)8/h(H2,3,5)(H2,4,7,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents	Article PubMed	41	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85563 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H14BrN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	50	-41.7	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85566 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H13BrN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	54	-41.5	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM10868 (1,3,4-Thiadiazole-2-sulfonamide, 6 | 1,3,4-thiadia...) Show SMILES Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C2H4N4O2S2/c3-1-5-6-2(9-1)10(4,7)8/h(H2,3,5)(H2,4,7,8)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents	PDB Article PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85562 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H14ClN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	65	-41.0	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85565 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H13ClN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	66	-41.0	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	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)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	70	-40.8	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85561 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H15N3O4S3/c17-26(22,23)18-10-13-11-24-16(19-13)12-6-8-15(9-7-12)25(20,21)14-4-2-1-3-5-14/h1-9,11,18H,10H2,(H2,17,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	83	-40.4	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Bos taurus (bovine))	BDBM85564 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H14N2O5S3/c17-26(21,22)23-10-13-11-24-16(18-13)12-6-8-15(9-7-12)25(19,20)14-4-2-1-3-5-14/h1-9,11H,10H2,(H2,17,21,22)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	87	-40.3	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165742 (CHEMBL194016 | Pyridine-2-carboxylic acid (5-merca...) Show SMILES Sc1nnc(NC(=O)c2ccccn2)s1 Show InChI InChI=1S/C8H6N4OS2/c13-6(5-3-1-2-4-9-5)10-7-11-12-8(14)15-7/h1-4H,(H,12,14)(H,10,11,13)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	97	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (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	DrugBank PDB Article PubMed	250	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 1 (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	DrugBank PDB PubMed	250	-37.7	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85566 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H13BrN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85565 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H13ClN2O5S3/c17-12-3-7-15(8-4-12)26(20,21)14-5-1-11(2-6-14)16-19-13(10-25-16)9-24-27(18,22)23/h1-8,10H,9H2,(H2,18,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85564 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)OCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H14N2O5S3/c17-26(21,22)23-10-13-11-24-16(18-13)12-6-8-15(9-7-12)25(19,20)14-4-2-1-3-5-14/h1-9,11H,10H2,(H2,17,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85563 (2-[4-(4-Bromophenylsulfonyl)-Phenyl}-thiazole-4-yl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C16H14BrN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85562 (2-[4-(4-Chlorophenylsulfonyl)-Phenyl}-thiazole-4-y...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C16H14ClN3O4S3/c17-12-3-7-15(8-4-12)26(21,22)14-5-1-11(2-6-14)16-20-13(10-25-16)9-19-27(18,23)24/h1-8,10,19H,9H2,(H2,18,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM85561 (2-[4-(Phenylsulfonyl)-Phenyl}-thiazole-4-yl-methyl...) Show SMILES NS(=O)(=O)NCc1csc(n1)-c1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C16H15N3O4S3/c17-26(22,23)18-10-13-11-24-16(19-13)12-6-8-15(9-7-12)25(20,21)14-4-2-1-3-5-14/h1-9,11,18H,10H2,(H2,17,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>1.00E+3	>-34.2	n/a	n/a	n/a	n/a	n/a	7.4	25
Università degli Studi					Assay Description Inhibition assay using human Carbonic anhydrase I and II and bovine carbonic anhydrase IV.				J Enzym Inhib 16: 351-8 (2001) BindingDB Entry DOI: 10.7270/Q2K9363Z
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165739 (5-[4-(4-Bromo-benzenesulfonyl)-phenyl]-4-butyl-4H-...) Show SMILES CCCCn1c(n[nH]c1=S)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C18H18BrN3O2S2/c1-2-3-12-22-17(20-21-18(22)25)13-4-8-15(9-5-13)26(23,24)16-10-6-14(19)7-11-16/h4-11H,2-3,12H2,1H3,(H,21,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165736 (1-(5-sulfanyl-1,3,4-thiadiazol-2-yl)-3-[(5-sulfany...) Show SMILES Sc1nnc(NC(=O)NS(=O)(=O)Nc2nnc(S)s2)s1 Show InChI InChI=1S/C5H5N7O3S5/c13-1(6-2-7-9-4(16)18-2)11-20(14,15)12-3-8-10-5(17)19-3/h(H,8,12)(H,9,16)(H,10,17)(H2,6,7,11,13)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165745 (CHEMBL382111 | N-(5-Mercapto-[1,3,4]thiadiazol-2-y...) Show SMILES CC(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C4H5N3OS2/c1-2(8)5-3-6-7-4(9)10-3/h1H3,(H,7,9)(H,5,6,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	4.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165740 (3-(5-Mercapto-[1,3,4]thiadiazol-2-yl)-1,1-diphenyl...) Show SMILES Sc1nnc(NC(=O)N(c2ccccc2)c2ccccc2)s1 Show InChI InChI=1S/C15H12N4OS2/c20-14(16-13-17-18-15(21)22-13)19(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H,18,21)(H,16,17,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165743 (5-Amino-[1,3,4]thiadiazole-2-thiol | CHEMBL372507) Show SMILES Nc1nnc(S)s1 Show InChI InChI=1S/C2H3N3S2/c3-1-4-5-2(6)7-1/h(H2,3,4)(H,5,6)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	7.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165732 (5-(4-Nitro-phenylsulfanylamino)-[1,3,4]thiadiazole...) Show SMILES [O-][N+](=O)c1ccc(SNc2n[n-]c(=[SH+])s2)cc1 Show InChI InChI=1S/C8H6N4O2S3/c13-12(14)5-1-3-6(4-2-5)17-11-7-9-10-8(15)16-7/h1-4H,(H2,9,10,11,15)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	7.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165748 (5-Dimethylamino-naphthalene-1-sulfonic acid (5-mer...) Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C14H14N4O2S3/c1-18(2)11-7-3-6-10-9(11)5-4-8-12(10)23(19,20)17-13-15-16-14(21)22-13/h3-8H,1-2H3,(H,15,17)(H,16,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	7.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165748 (5-Dimethylamino-naphthalene-1-sulfonic acid (5-mer...) Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C14H14N4O2S3/c1-18(2)11-7-3-6-10-9(11)5-4-8-12(10)23(19,20)17-13-15-16-14(21)22-13/h3-8H,1-2H3,(H,15,17)(H,16,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165736 (1-(5-sulfanyl-1,3,4-thiadiazol-2-yl)-3-[(5-sulfany...) Show SMILES Sc1nnc(NC(=O)NS(=O)(=O)Nc2nnc(S)s2)s1 Show InChI InChI=1S/C5H5N7O3S5/c13-1(6-2-7-9-4(16)18-2)11-20(14,15)12-3-8-10-5(17)19-3/h(H,8,12)(H,9,16)(H,10,17)(H2,6,7,11,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	8.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165732 (5-(4-Nitro-phenylsulfanylamino)-[1,3,4]thiadiazole...) Show SMILES [O-][N+](=O)c1ccc(SNc2n[n-]c(=[SH+])s2)cc1 Show InChI InChI=1S/C8H6N4O2S3/c13-12(14)5-1-3-6(4-2-5)17-11-7-9-10-8(15)16-7/h1-4H,(H2,9,10,11,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165735 (2-(5-Mercapto-[1,3,4]thiadiazol-2-ylcarbamoyl)-nic...) Show SMILES OC(=O)c1cccnc1C(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C9H6N4O3S2/c14-6(11-8-12-13-9(17)18-8)5-4(7(15)16)2-1-3-10-5/h1-3H,(H,13,17)(H,15,16)(H,11,12,14)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165741 (1-(3,4-Dichloro-phenyl)-3-(5-mercapto-[1,3,4]thiad...) Show SMILES Sc1nnc(NC(=O)Nc2ccc(Cl)c(Cl)c2)s1 Show InChI InChI=1S/C9H6Cl2N4OS2/c10-5-2-1-4(3-6(5)11)12-7(16)13-8-14-15-9(17)18-8/h1-3H,(H,15,17)(H2,12,13,14,16)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM10868 (1,3,4-Thiadiazole-2-sulfonamide, 6 | 1,3,4-thiadia...) Show SMILES Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C2H4N4O2S2/c3-1-5-6-2(9-1)10(4,7)8/h(H2,3,5)(H2,4,7,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents	Article PubMed	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165745 (CHEMBL382111 | N-(5-Mercapto-[1,3,4]thiadiazol-2-y...) Show SMILES CC(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C4H5N3OS2/c1-2(8)5-3-6-7-4(9)10-3/h1H3,(H,7,9)(H,5,6,8)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50165738 (5-[4-(4-Bromo-benzenesulfonyl)-phenyl]-4-(4-methox...) Show SMILES COc1ccc(cc1)-n1c(n[nH]c1=S)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C21H16BrN3O3S2/c1-28-17-8-6-16(7-9-17)25-20(23-24-21(25)29)14-2-10-18(11-3-14)30(26,27)19-12-4-15(22)5-13-19/h2-13H,1H3,(H,24,29)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165741 (1-(3,4-Dichloro-phenyl)-3-(5-mercapto-[1,3,4]thiad...) Show SMILES Sc1nnc(NC(=O)Nc2ccc(Cl)c(Cl)c2)s1 Show InChI InChI=1S/C9H6Cl2N4OS2/c10-5-2-1-4(3-6(5)11)12-7(16)13-8-14-15-9(17)18-8/h1-3H,(H,15,17)(H2,12,13,14,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165735 (2-(5-Mercapto-[1,3,4]thiadiazol-2-ylcarbamoyl)-nic...) Show SMILES OC(=O)c1cccnc1C(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C9H6N4O3S2/c14-6(11-8-12-13-9(17)18-8)5-4(7(15)16)2-1-3-10-5/h1-3H,(H,13,17)(H,15,16)(H,11,12,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165743 (5-Amino-[1,3,4]thiadiazole-2-thiol | CHEMBL372507) Show SMILES Nc1nnc(S)s1 Show InChI InChI=1S/C2H3N3S2/c3-1-4-5-2(6)7-1/h(H2,3,4)(H,5,6)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	9.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165740 (3-(5-Mercapto-[1,3,4]thiadiazol-2-yl)-1,1-diphenyl...) Show SMILES Sc1nnc(NC(=O)N(c2ccccc2)c2ccccc2)s1 Show InChI InChI=1S/C15H12N4OS2/c20-14(16-13-17-18-15(21)22-13)19(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H,18,21)(H,16,17,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50165743 (5-Amino-[1,3,4]thiadiazole-2-thiol | CHEMBL372507) Show SMILES Nc1nnc(S)s1 Show InChI InChI=1S/C2H3N3S2/c3-1-4-5-2(6)7-1/h(H2,3,4)(H,5,6)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	9.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50165745 (CHEMBL382111 | N-(5-Mercapto-[1,3,4]thiadiazol-2-y...) Show SMILES CC(=O)Nc1nnc(S)s1 Show InChI InChI=1S/C4H5N3OS2/c1-2(8)5-3-6-7-4(9)10-3/h1H3,(H,7,9)(H,5,6,8)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	Article PubMed	9.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50165744 (3-(4-(4-chlorophenylsulfonyl)phenyl)-4-propyl-1H-1...) Show SMILES CCCn1c(n[nH]c1=S)-c1ccc(cc1)S(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C17H16ClN3O2S2/c1-2-11-21-16(19-20-17(21)24)12-3-7-14(8-4-12)25(22,23)15-9-5-13(18)6-10-15/h3-10H,2,11H2,1H3,(H,20,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50165739 (5-[4-(4-Bromo-benzenesulfonyl)-phenyl]-4-butyl-4H-...) Show SMILES CCCCn1c(n[nH]c1=S)-c1ccc(cc1)S(=O)(=O)c1ccc(Br)cc1 Show InChI InChI=1S/C18H18BrN3O2S2/c1-2-3-12-22-17(20-21-18(22)25)13-4-8-15(9-5-13)26(23,24)16-10-6-14(19)7-11-16/h4-11H,2-3,12H2,1H3,(H,21,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bucharest Curated by ChEMBL					Assay Description Inhibitory constant against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 2347-52 (2005) Article DOI: 10.1016/j.bmcl.2005.02.088 BindingDB Entry DOI: 10.7270/Q2348JW7
					More data for this Ligand-Target Pair

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