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PubMed code 22642259

Compile data set for download or QSAR
Found 22 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
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392045
PNG
(CHEMBL2152561)
Show SMILES OC(=O)c1cccc(c1)-c1cccc(CCS)c1C(O)=O
Show InChI InChI=1S/C16H14O4S/c17-15(18)12-5-1-4-11(9-12)13-6-2-3-10(7-8-21)14(13)16(19)20/h1-6,9,21H,7-8H2,(H,17,18)(H,19,20)
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n/an/a 2n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392040
PNG
(CHEMBL2152556)
Show SMILES OC(=O)c1cccc(COc2ccc(CS)cc2C(O)=O)c1
Show InChI InChI=1S/C16H14O5S/c17-15(18)12-3-1-2-10(6-12)8-21-14-5-4-11(9-22)7-13(14)16(19)20/h1-7,22H,8-9H2,(H,17,18)(H,19,20)
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n/an/a 2n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392046
PNG
(CHEMBL2152562)
Show SMILES OC(=O)c1ccc(cc1)-c1cccc(CCS)c1C(O)=O
Show InChI InChI=1S/C16H14O4S/c17-15(18)12-6-4-10(5-7-12)13-3-1-2-11(8-9-21)14(13)16(19)20/h1-7,21H,8-9H2,(H,17,18)(H,19,20)
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n/an/a 7n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM17762
PNG
(3-[2-carboxy-2-(3-sulfanylpropyl)ethyl]benzoic aci...)
Show SMILES OC(=O)C(CCCS)Cc1cccc(c1)C(O)=O
Show InChI InChI=1S/C13H16O4S/c14-12(15)10-4-1-3-9(7-10)8-11(13(16)17)5-2-6-18/h1,3-4,7,11,18H,2,5-6,8H2,(H,14,15)(H,16,17)
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n/an/a 15n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392041
PNG
(CHEMBL2152557)
Show SMILES OC(=O)c1ccc(COc2ccc(CS)cc2C(O)=O)cc1
Show InChI InChI=1S/C16H14O5S/c17-15(18)12-4-1-10(2-5-12)8-21-14-6-3-11(9-22)7-13(14)16(19)20/h1-7,22H,8-9H2,(H,17,18)(H,19,20)
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n/an/a 16n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50332228
PNG
(1-(3-Carboxyphenyl)-3-(2-mercapto-ethyl)-1H-indole...)
Show SMILES OC(=O)c1c(CCS)c2ccccc2n1-c1cccc(c1)C(O)=O
Show InChI InChI=1S/C18H15NO4S/c20-17(21)11-4-3-5-12(10-11)19-15-7-2-1-6-13(15)14(8-9-24)16(19)18(22)23/h1-7,10,24H,8-9H2,(H,20,21)(H,22,23)
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n/an/a 22n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392036
PNG
(CHEMBL2152437)
Show SMILES OC(=O)c1cccc(c1)-c1ccc(CS)cc1C(O)=O
Show InChI InChI=1S/C15H12O4S/c16-14(17)11-3-1-2-10(7-11)12-5-4-9(8-20)6-13(12)15(18)19/h1-7,20H,8H2,(H,16,17)(H,18,19)
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n/an/a 38n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392039
PNG
(CHEMBL2152555)
Show SMILES OC(=O)c1ccccc1COc1ccc(CS)cc1C(O)=O
Show InChI InChI=1S/C16H14O5S/c17-15(18)12-4-2-1-3-11(12)8-21-14-6-5-10(9-22)7-13(14)16(19)20/h1-7,22H,8-9H2,(H,17,18)(H,19,20)
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n/an/a 41n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392037
PNG
(CHEMBL2152438)
Show SMILES OC(=O)c1ccc(cc1)-c1ccc(CS)cc1C(O)=O
Show InChI InChI=1S/C15H12O4S/c16-14(17)11-4-2-10(3-5-11)12-6-1-9(8-20)7-13(12)15(18)19/h1-7,20H,8H2,(H,16,17)(H,18,19)
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n/an/a 52n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392049
PNG
(CHEMBL2152565)
Show SMILES OC(=O)c1cccc(COc2cccc(CCS)c2C(O)=O)c1
Show InChI InChI=1S/C17H16O5S/c18-16(19)13-5-1-3-11(9-13)10-22-14-6-2-4-12(7-8-23)15(14)17(20)21/h1-6,9,23H,7-8,10H2,(H,18,19)(H,20,21)
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n/an/a 69n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM17755
PNG
(2-(3-sulfanylpropyl)pentanedioic acid | 2-MPPA | C...)
Show SMILES OC(=O)CCC(CCCS)C(O)=O
Show InChI InChI=1S/C8H14O4S/c9-7(10)4-3-6(8(11)12)2-1-5-13/h6,13H,1-5H2,(H,9,10)(H,11,12)
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n/an/a 90n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392048
PNG
(CHEMBL2152564)
Show SMILES OC(=O)c1ccccc1COc1cccc(CCS)c1C(O)=O
Show InChI InChI=1S/C17H16O5S/c18-16(19)13-6-2-1-4-12(13)10-22-14-7-3-5-11(8-9-23)15(14)17(20)21/h1-7,23H,8-10H2,(H,18,19)(H,20,21)
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n/an/a 140n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392050
PNG
(CHEMBL2152566)
Show SMILES OC(=O)c1ccc(COc2cccc(CCS)c2C(O)=O)cc1
Show InChI InChI=1S/C17H16O5S/c18-16(19)13-6-4-11(5-7-13)10-22-14-3-1-2-12(8-9-23)15(14)17(20)21/h1-7,23H,8-10H2,(H,18,19)(H,20,21)
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n/an/a 200n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392047
PNG
(CHEMBL2152563)
Show SMILES OC(=O)c1c(CCS)cccc1OCc1ccccc1
Show InChI InChI=1S/C16H16O3S/c17-16(18)15-13(9-10-20)7-4-8-14(15)19-11-12-5-2-1-3-6-12/h1-8,20H,9-11H2,(H,17,18)
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n/an/a 200n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392044
PNG
(CHEMBL2152560)
Show SMILES OC(=O)c1ccccc1-c1cccc(CCS)c1C(O)=O
Show InChI InChI=1S/C16H14O4S/c17-15(18)13-6-2-1-5-11(13)12-7-3-4-10(8-9-21)14(12)16(19)20/h1-7,21H,8-9H2,(H,17,18)(H,19,20)
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n/an/a 230n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392035
PNG
(CHEMBL2152436)
Show SMILES OC(=O)c1ccccc1-c1ccc(CS)cc1C(O)=O
Show InChI InChI=1S/C15H12O4S/c16-14(17)12-4-2-1-3-10(12)11-6-5-9(8-20)7-13(11)15(18)19/h1-7,20H,8H2,(H,16,17)(H,18,19)
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n/an/a 340n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392038
PNG
(CHEMBL2152439)
Show SMILES OC(=O)c1cc(CS)ccc1OCc1ccccc1
Show InChI InChI=1S/C15H14O3S/c16-15(17)13-8-12(10-19)6-7-14(13)18-9-11-4-2-1-3-5-11/h1-8,19H,9-10H2,(H,16,17)
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n/an/a 420n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392042
PNG
(CHEMBL2152558)
Show SMILES OC(=O)c1ccccc1CCS
Show InChI InChI=1S/C9H10O2S/c10-9(11)8-4-2-1-3-7(8)5-6-12/h1-4,12H,5-6H2,(H,10,11)
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n/an/a 930n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392051
PNG
(CHEMBL2152434)
Show SMILES OC(=O)c1cccc(CS)c1
Show InChI InChI=1S/C8H8O2S/c9-8(10)7-3-1-2-6(4-7)5-11/h1-4,11H,5H2,(H,9,10)
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n/an/a 1.30E+3n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392043
PNG
(CHEMBL2152559)
Show SMILES OC(=O)c1c(CCS)cccc1-c1ccccc1
Show InChI InChI=1S/C15H14O2S/c16-15(17)14-12(9-10-18)7-4-8-13(14)11-5-2-1-3-6-11/h1-8,18H,9-10H2,(H,16,17)
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n/an/a 1.40E+3n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50127619
PNG
(5-Mercapto-pentanoic acid | CHEMBL294565)
Show SMILES OC(=O)CCCCS
Show InChI InChI=1S/C5H10O2S/c6-5(7)3-1-2-4-8/h8H,1-4H2,(H,6,7)
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n/an/a 1.40E+3n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
Glutamate carboxypeptidase 2


(Homo sapiens (Human))		BDBM50392034
PNG
(CHEMBL2152435)
Show SMILES OC(=O)c1cc(CS)ccc1-c1ccccc1
Show InChI InChI=1S/C14H12O2S/c15-14(16)13-8-10(9-17)6-7-12(13)11-4-2-1-3-5-11/h1-8,17H,9H2,(H,15,16)
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n/an/a 5.70E+3n/an/an/an/an/an/a



Eisai Inc.

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GCP2 using N-acetyl-L-aspartyl-[3H]-L-glutamate as substrate by microplate assay

J Med Chem 55: 5922-32 (2012)


Article DOI: 10.1021/jm300488m
BindingDB Entry DOI: 10.7270/Q21J9BWN
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%