Compile Data Set for Download or QSAR

Found 46 hits with Last Name = 'dastan' and Initial = 'a'   

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))	BDBM50266966 (CHEMBL1662 | di(2,6-di-t-butylphenol)) Show SMILES CC(C)(C)c1cc(cc(c1O)C(C)(C)C)-c1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C28H42O2/c1-25(2,3)19-13-17(14-20(23(19)29)26(4,5)6)18-15-21(27(7,8)9)24(30)22(16-18)28(10,11)12/h13-16,29-30H,1-12H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	290	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					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	370	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50240689 (2,6-Di-tert-butyl-4-methoxy-phenol | 2,6-di-tert-b...) Show SMILES COc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C15H24O2/c1-14(2,3)11-8-10(17-7)9-12(13(11)16)15(4,5)6/h8-9,16H,1-7H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	420	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50240431 (2,6-Di-tert-butyl-phenol | 2,6-di-t-butylphenol | ...) Show SMILES CC(C)(C)c1cccc(c1O)C(C)(C)C Show InChI InChI=1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	510	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50079507 (2,6-Bis(1,1-dimethylethyl)-4-methylphenol | 2,6-Di...) Show SMILES Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	630	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50266963 (3-hydroxy-2-methoxybenzaldehyde | CHEMBL507918) Show SMILES COc1c(O)cccc1C=O Show InChI InChI=1S/C8H8O3/c1-11-8-6(5-9)3-2-4-7(8)10/h2-5,10H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	1.25E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50266965 (CHEMBL478518 | di(2,6-diisopropylphenol)) Show SMILES CC(C)c1cc(cc(C(C)C)c1O)-c1cc(C(C)C)c(O)c(c1)C(C)C Show InChI InChI=1S/C24H34O2/c1-13(2)19-9-17(10-20(14(3)4)23(19)25)18-11-21(15(5)6)24(26)22(12-18)16(7)8/h9-16,25-26H,1-8H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	1.87E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019398 (CHEMBL3290059) Show SMILES O=c1cc(ccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-10-3-1-2-4-11(10)12(14)7-9/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.51E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019395 (CHEMBL3290057) Show SMILES O=c1c(cccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-10-6-3-5-9-4-1-2-7-11(9)12(10)14/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.68E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019400 (CHEMBL3290055) Show SMILES N#CC1=Cc2ccccc2CC=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-4-3-7-11-5-1-2-6-12(11)8-10/h1-6,8H,7H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.88E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50240369 (1-Hydroxy-2-methoxybenzene | 2-Hydroxyanisole | 2-...) Show SMILES COc1ccccc1O Show InChI InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	2.94E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair				3D Structure (docked)
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019400 (CHEMBL3290055) Show SMILES N#CC1=Cc2ccccc2CC=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-4-3-7-11-5-1-2-6-12(11)8-10/h1-6,8H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.06E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019399 (CHEMBL3290054) Show SMILES N#CC1=CCc2ccccc2C=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-5-7-11-3-1-2-4-12(11)8-6-10/h1-7H,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.23E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019397 (CHEMBL3290058) Show SMILES O=c1ccc2ccccc2cc1C#N Show InChI InChI=1S/C12H7NO/c13-8-11-7-10-4-2-1-3-9(10)5-6-12(11)14/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.31E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019398 (CHEMBL3290059) Show SMILES O=c1cc(ccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-10-3-1-2-4-11(10)12(14)7-9/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.62E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019397 (CHEMBL3290058) Show SMILES O=c1ccc2ccccc2cc1C#N Show InChI InChI=1S/C12H7NO/c13-8-11-7-10-4-2-1-3-9(10)5-6-12(11)14/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.66E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019394 (CHEMBL3290056) Show SMILES O=c1ccc(cc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-12(14)11-4-2-1-3-10(11)7-9/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.91E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019394 (CHEMBL3290056) Show SMILES O=c1ccc(cc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-12(14)11-4-2-1-3-10(11)7-9/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.93E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019395 (CHEMBL3290057) Show SMILES O=c1c(cccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-10-6-3-5-9-4-1-2-7-11(9)12(10)14/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.01E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50266964 (CHEMBL449983 | di(2,6-dimethylphenol)) Show SMILES Cc1cc(cc(C)c1O)-c1cc(C)c(O)c(C)c1 Show InChI InChI=1S/C16H18O2/c1-9-5-13(6-10(2)15(9)17)14-7-11(3)16(18)12(4)8-14/h5-8,17-18H,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	4.05E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019399 (CHEMBL3290054) Show SMILES N#CC1=CCc2ccccc2C=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-5-7-11-3-1-2-4-12(11)8-6-10/h1-7H,8H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.06E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50058046 (CHEMBL526 | propofol) Show SMILES CC(C)c1cccc(C(C)C)c1O Show InChI InChI=1S/C12H18O/c1-8(2)10-6-5-7-11(9(3)4)12(10)13/h5-9,13H,1-4H3	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	Article PubMed	1.95E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					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	3.62E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair				3D Structure (crystal)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50266966 (CHEMBL1662 | di(2,6-di-t-butylphenol)) Show SMILES CC(C)(C)c1cc(cc(c1O)C(C)(C)C)-c1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C28H42O2/c1-25(2,3)19-13-17(14-20(23(19)29)26(4,5)6)18-15-21(27(7,8)9)24(30)22(16-18)28(10,11)12/h13-16,29-30H,1-12H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	3.75E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50266965 (CHEMBL478518 | di(2,6-diisopropylphenol)) Show SMILES CC(C)c1cc(cc(C(C)C)c1O)-c1cc(C(C)C)c(O)c(c1)C(C)C Show InChI InChI=1S/C24H34O2/c1-13(2)19-9-17(10-20(14(3)4)23(19)25)18-11-21(15(5)6)24(26)22(12-18)16(7)8/h9-16,25-26H,1-8H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	3.79E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50266963 (3-hydroxy-2-methoxybenzaldehyde | CHEMBL507918) Show SMILES COc1c(O)cccc1C=O Show InChI InChI=1S/C8H8O3/c1-11-8-6(5-9)3-2-4-7(8)10/h2-5,10H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	5.56E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50240369 (1-Hydroxy-2-methoxybenzene | 2-Hydroxyanisole | 2-...) Show SMILES COc1ccccc1O Show InChI InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	6.02E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50240689 (2,6-Di-tert-butyl-4-methoxy-phenol | 2,6-di-tert-b...) Show SMILES COc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C15H24O2/c1-14(2,3)11-8-10(17-7)9-12(13(11)16)15(4,5)6/h8-9,16H,1-7H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	6.37E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50266964 (CHEMBL449983 | di(2,6-dimethylphenol)) Show SMILES Cc1cc(cc(C)c1O)-c1cc(C)c(O)c(C)c1 Show InChI InChI=1S/C16H18O2/c1-9-5-13(6-10(2)15(9)17)14-7-11(3)16(18)12(4)8-14/h5-8,17-18H,1-4H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	9.28E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50058046 (CHEMBL526 | propofol) Show SMILES CC(C)c1cccc(C(C)C)c1O Show InChI InChI=1S/C12H18O/c1-8(2)10-6-5-7-11(9(3)4)12(10)13/h5-9,13H,1-4H3	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	9.89E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50240430 (2,6-Dimethyl phenol | 2,6-Dimethyl-phenol | 2,6-Di...) Show SMILES Cc1cccc(C)c1O Show InChI InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	1.14E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair				3D Structure (docked)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50240430 (2,6-Dimethyl phenol | 2,6-Dimethyl-phenol | 2,6-Di...) Show SMILES Cc1cccc(C)c1O Show InChI InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	1.98E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50079507 (2,6-Bis(1,1-dimethylethyl)-4-methylphenol | 2,6-Di...) Show SMILES Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	2.45E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50240431 (2,6-Di-tert-butyl-phenol | 2,6-di-t-butylphenol | ...) Show SMILES CC(C)(C)c1cccc(c1O)C(C)(C)C Show InChI InChI=1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.75E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ataturk University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate				Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019397 (CHEMBL3290058) Show SMILES O=c1ccc2ccccc2cc1C#N Show InChI InChI=1S/C12H7NO/c13-8-11-7-10-4-2-1-3-9(10)5-6-12(11)14/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.22E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019395 (CHEMBL3290057) Show SMILES O=c1c(cccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-10-6-3-5-9-4-1-2-7-11(9)12(10)14/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019398 (CHEMBL3290059) Show SMILES O=c1cc(ccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-10-3-1-2-4-11(10)12(14)7-9/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.74E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019394 (CHEMBL3290056) Show SMILES O=c1ccc(cc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-12(14)11-4-2-1-3-10(11)7-9/h1-7H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.82E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019400 (CHEMBL3290055) Show SMILES N#CC1=Cc2ccccc2CC=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-4-3-7-11-5-1-2-6-12(11)8-10/h1-6,8H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50019399 (CHEMBL3290054) Show SMILES N#CC1=CCc2ccccc2C=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-5-7-11-3-1-2-4-12(11)8-6-10/h1-7H,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.38E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-2 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019399 (CHEMBL3290054) Show SMILES N#CC1=CCc2ccccc2C=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-5-7-11-3-1-2-4-12(11)8-6-10/h1-7H,8H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.52E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019398 (CHEMBL3290059) Show SMILES O=c1cc(ccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-10-3-1-2-4-11(10)12(14)7-9/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019397 (CHEMBL3290058) Show SMILES O=c1ccc2ccccc2cc1C#N Show InChI InChI=1S/C12H7NO/c13-8-11-7-10-4-2-1-3-9(10)5-6-12(11)14/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.25E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019400 (CHEMBL3290055) Show SMILES N#CC1=Cc2ccccc2CC=C1 |c:12,t:2| Show InChI InChI=1S/C12H9N/c13-9-10-4-3-7-11-5-1-2-6-12(11)8-10/h1-6,8H,7H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.77E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019394 (CHEMBL3290056) Show SMILES O=c1ccc(cc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-9-5-6-12(14)11-4-2-1-3-10(11)7-9/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.96E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50019395 (CHEMBL3290057) Show SMILES O=c1c(cccc2ccccc12)C#N Show InChI InChI=1S/C12H7NO/c13-8-10-6-3-5-9-4-1-2-7-11(9)12(10)14/h1-7H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
AgriIbrahim£e£en University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA-1 assessed as p-nitrophenolate formation after 3 mins using p-nitrophenylacetate as substrate by spectrophotometer				Bioorg Med Chem 22: 3537-43 (2014) Article DOI: 10.1016/j.bmc.2014.04.007 BindingDB Entry DOI: 10.7270/Q2Z60QM4
					More data for this Ligand-Target Pair