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PubMed code 26073005

Compile data set for download or QSAR
Found 18 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM10880
PNG
(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)
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Article
PubMed
370n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM26187
PNG
(α-CA inhibitor, 11 | CHEMBL14060 | US9688816,...)
Show SMILES Oc1ccccc1
Show InChI InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H
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Article
PubMed
5.50E+3n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM26189
PNG
(α-CA inhibitor, 13 | 1,3-Dihydroxybenzene, XI...)
Show SMILES Oc1cccc(O)c1
Show InChI InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H
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PubMed
7.70E+3n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM26188
PNG
(α-CA inhibitor, 12 | 1,2-Dihydroxybenzene, XI...)
Show SMILES Oc1ccccc1O
Show InChI InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H
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PubMed
9.90E+3n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM26187
PNG
(α-CA inhibitor, 11 | CHEMBL14060 | US9688816,...)
Show SMILES Oc1ccccc1
Show InChI InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H
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PubMed
1.02E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106395
PNG
(CHEMBL3601880)
Show SMILES Cc1ccc(cc1)S(=O)(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C11H9BrN2O4S/c1-7-2-4-8(5-3-7)19(17,18)14-6-9(12)10(15)13-11(14)16/h2-6H,1H3,(H,13,15,16)
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1.08E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50106395
PNG
(CHEMBL3601880)
Show SMILES Cc1ccc(cc1)S(=O)(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C11H9BrN2O4S/c1-7-2-4-8(5-3-7)19(17,18)14-6-9(12)10(15)13-11(14)16/h2-6H,1H3,(H,13,15,16)
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2.89E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM10880
PNG
(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)
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3.62E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106411
PNG
(CHEBI:16964 | CHEMBL1233360)
Show SMILES OCc1c[nH]c(=O)[nH]c1=O
Show InChI InChI=1S/C5H6N2O3/c8-2-3-1-6-5(10)7-4(3)9/h1,8H,2H2,(H2,6,7,9,10)
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4.95E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106396
PNG
(CHEBI:74733 | CHEMBL1650614)
Show SMILES Cc1cc(O)nc(O)n1
Show InChI InChI=1S/C5H6N2O2/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)
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PubMed
5.78E+4n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50106397
PNG
(CHEBI:74763 | CHEMBL11470)
Show SMILES Cn1ccc(=O)n(C)c1=O
Show InChI InChI=1S/C6H8N2O2/c1-7-4-3-5(9)8(2)6(7)10/h3-4H,1-2H3
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PubMed
1.66E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106397
PNG
(CHEBI:74763 | CHEMBL11470)
Show SMILES Cn1ccc(=O)n(C)c1=O
Show InChI InChI=1S/C6H8N2O2/c1-7-4-3-5(9)8(2)6(7)10/h3-4H,1-2H3
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PubMed
3.16E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106392
PNG
(CHEMBL3601878)
Show SMILES CS(=O)(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C5H5BrN2O4S/c1-13(11,12)8-2-3(6)4(9)7-5(8)10/h2H,1H3,(H,7,9,10)
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4.28E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50106394
PNG
(CHEMBL3601879)
Show SMILES CC(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C6H5BrN2O3/c1-3(10)9-2-4(7)5(11)8-6(9)12/h2H,1H3,(H,8,11,12)
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4.64E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50106392
PNG
(CHEMBL3601878)
Show SMILES CS(=O)(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C5H5BrN2O4S/c1-13(11,12)8-2-3(6)4(9)7-5(8)10/h2H,1H3,(H,7,9,10)
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PubMed
6.45E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50106394
PNG
(CHEMBL3601879)
Show SMILES CC(=O)n1cc(Br)c(=O)[nH]c1=O
Show InChI InChI=1S/C6H5BrN2O3/c1-3(10)9-2-4(7)5(11)8-6(9)12/h2H,1H3,(H,8,11,12)
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7.79E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA2 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM26189
PNG
(α-CA inhibitor, 13 | 1,3-Dihydroxybenzene, XI...)
Show SMILES Oc1cccc(O)c1
Show InChI InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H
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PubMed
7.95E+5n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM26188
PNG
(α-CA inhibitor, 12 | 1,2-Dihydroxybenzene, XI...)
Show SMILES Oc1ccccc1O
Show InChI InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H
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4.00E+6n/an/an/an/an/an/an/an/a



AgriIbrahim£e£en University

Curated by ChEMBL


Assay Description
Inhibition of human erythrocytes CA1 using 4-nitrophenylacetate as substrate by esterase assay


Bioorg Med Chem Lett 25: 3261-3 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.073
BindingDB Entry DOI: 10.7270/Q2W37Z39
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%