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Compile Data Set for Download or QSAR

Found 57 hits with Last Name = 'frycia' and Initial = 'a'   
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
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422558
PNG
(CHEMBL434705)
Show SMILES CC[C@H](N1C[C@H](CN=[N+]=[N-])CC1=O)C(N)=O
Show InChI InChI=1S/C9H15N5O2/c1-2-7(9(10)16)14-5-6(3-8(14)15)4-12-13-11/h6-7H,2-5H2,1H3,(H2,10,16)/t6-,7-/m0/s1
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n/an/a 79.4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422517
PNG
(CHEMBL149348)
Show SMILES CC[C@H](N1C[C@H](CO[N+]([O-])=O)CC1=O)C(N)=O
Show InChI InChI=1S/C9H15N3O5/c1-2-7(9(10)14)11-4-6(3-8(11)13)5-17-12(15)16/h6-7H,2-5H2,1H3,(H2,10,14)/t6-,7+/m1/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422531
PNG
(BRIVARACETAM | UCB-34714)
Show SMILES CCC[C@H]1CN([C@@H](CC)C(N)=O)C(=O)C1 |r|
Show InChI InChI=1S/C11H20N2O2/c1-3-5-8-6-10(14)13(7-8)9(4-2)11(12)15/h8-9H,3-7H2,1-2H3,(H2,12,15)/t8-,9+/m1/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422518
PNG
(CHEMBL358242)
Show SMILES CC[C@H](N1C[C@H](CSC)CC1=O)C(N)=O
Show InChI InChI=1S/C10H18N2O2S/c1-3-8(10(11)14)12-5-7(6-15-2)4-9(12)13/h7-8H,3-6H2,1-2H3,(H2,11,14)/t7-,8+/m1/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422548
PNG
(CHEMBL150241)
Show SMILES CC[C@H](N1CC(CC2CC2)CC1=O)C(N)=O
Show InChI InChI=1S/C12H20N2O2/c1-2-10(12(13)16)14-7-9(6-11(14)15)5-8-3-4-8/h8-10H,2-7H2,1H3,(H2,13,16)/t9?,10-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422525
PNG
(CHEMBL348187)
Show SMILES CC[C@H](N1C[C@H](CI)CC1=O)C(N)=O
Show InChI InChI=1S/C9H15IN2O2/c1-2-7(9(11)14)12-5-6(4-10)3-8(12)13/h6-7H,2-5H2,1H3,(H2,11,14)/t6-,7-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422519
PNG
(CHEMBL358393)
Show SMILES CC[C@H](N1C[C@H](CCl)CC1=O)C(N)=O
Show InChI InChI=1S/C9H15ClN2O2/c1-2-7(9(11)14)12-5-6(4-10)3-8(12)13/h6-7H,2-5H2,1H3,(H2,11,14)/t6-,7-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384300
PNG
(CHEMBL2030661)
Show SMILES CC(=O)N1c2ccccc2CC1(Cc1ccccc1)C(=O)OCc1ccccc1
Show InChI InChI=1S/C25H23NO3/c1-19(27)26-23-15-9-8-14-22(23)17-25(26,16-20-10-4-2-5-11-20)24(28)29-18-21-12-6-3-7-13-21/h2-15H,16-18H2,1H3
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384302
PNG
(CHEMBL2030663)
Show SMILES CC(=O)N1CCCC1(Cc1ccc(F)cc1)C(=O)CCc1ccc(F)cc1
Show InChI InChI=1S/C22H23F2NO2/c1-16(26)25-14-2-13-22(25,15-18-5-10-20(24)11-6-18)21(27)12-7-17-3-8-19(23)9-4-17/h3-6,8-11H,2,7,12-15H2,1H3
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422522
PNG
(CHEMBL347071)
Show SMILES CC[C@H](N1C[C@H](CBr)CC1=O)C(N)=O
Show InChI InChI=1S/C9H15BrN2O2/c1-2-7(9(11)14)12-5-6(4-10)3-8(12)13/h6-7H,2-5H2,1H3,(H2,11,14)/t6-,7-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422540
PNG
(CHEMBL152911)
Show SMILES CCC[C@@H]1CN([C@@H](CC)C(N)=O)C(=O)C1
Show InChI InChI=1S/C11H20N2O2/c1-3-5-8-6-10(14)13(7-8)9(4-2)11(12)15/h8-9H,3-7H2,1-2H3,(H2,12,15)/t8-,9-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384301
PNG
(CHEMBL2030662)
Show SMILES CC(=O)N1CCCC1(Cc1ccccc1)C(=O)CCc1ccccc1
Show InChI InChI=1S/C22H25NO2/c1-18(24)23-16-8-15-22(23,17-20-11-6-3-7-12-20)21(25)14-13-19-9-4-2-5-10-19/h2-7,9-12H,8,13-17H2,1H3
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384298
PNG
(CHEMBL2030659)
Show SMILES CC(=O)N1CCC[C@@]1(Cc1ccccc1)C(=O)OCc1ccccc1 |r|
Show InChI InChI=1S/C21H23NO3/c1-17(23)22-14-8-13-21(22,15-18-9-4-2-5-10-18)20(24)25-16-19-11-6-3-7-12-19/h2-7,9-12H,8,13-16H2,1H3/t21-/m1/s1
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422526
PNG
(CHEMBL359062)
Show SMILES CCCCC1CN(C(CC)C(N)=O)C(=O)C1
Show InChI InChI=1S/C12H22N2O2/c1-3-5-6-9-7-11(15)14(8-9)10(4-2)12(13)16/h9-10H,3-8H2,1-2H3,(H2,13,16)
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n/an/a 398n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422533
PNG
(CHEMBL150331)
Show SMILES CCCC1(C)CN([C@@H](CC)C(N)=O)C(=O)C1
Show InChI InChI=1S/C12H22N2O2/c1-4-6-12(3)7-10(15)14(8-12)9(5-2)11(13)16/h9H,4-8H2,1-3H3,(H2,13,16)/t9-,12?/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422556
PNG
(CHEMBL358161)
Show SMILES CCC(N(S)C(=S)C1CC1)C(N)=O
Show InChI InChI=1S/C8H14N2OS2/c1-2-6(7(9)11)10(13)8(12)5-3-4-5/h5-6,13H,2-4H2,1H3,(H2,9,11)
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384307
PNG
(CHEMBL2030669)
Show SMILES Brc1ccc2oc(=O)c(cc2c1)C(=O)N1CCN(Cc2ccccc2)CC1
Show InChI InChI=1S/C21H19BrN2O3/c22-17-6-7-19-16(12-17)13-18(21(26)27-19)20(25)24-10-8-23(9-11-24)14-15-4-2-1-3-5-15/h1-7,12-13H,8-11,14H2
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422542
PNG
(Keppra | Keppra Xr | LEVETIRACETAM | Levetiracetam...)
Show SMILES CC[C@H](N1CCCC1=O)C(N)=O |r|
Show InChI InChI=1S/C8H14N2O2/c1-2-6(8(9)12)10-5-3-4-7(10)11/h6H,2-5H2,1H3,(H2,9,12)/t6-/m0/s1
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n/an/a 794n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422523
PNG
(CHEMBL358239)
Show SMILES CC[C@H](N1CC(CC(C)(C)C)CC1=O)C(N)=O
Show InChI InChI=1S/C13H24N2O2/c1-5-10(12(14)17)15-8-9(6-11(15)16)7-13(2,3)4/h9-10H,5-8H2,1-4H3,(H2,14,17)/t9?,10-/m0/s1
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UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50315350
PNG
((+)-benzyl 1-acetyl-2-benzylpyrrolidine-2-carboxyl...)
Show SMILES CC(=O)N1CCCC1(Cc1ccccc1)C(=O)OCc1ccccc1
Show InChI InChI=1S/C21H23NO3/c1-17(23)22-14-8-13-21(22,15-18-9-4-2-5-10-18)20(24)25-16-19-11-6-3-7-12-19/h2-7,9-12H,8,13-16H2,1H3
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UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384305
PNG
(CHEMBL2030667)
Show SMILES O=C(OCc1ccccc1)C1(Cc2ccccc2)CCC2CCCC(=O)N12
Show InChI InChI=1S/C23H25NO3/c25-21-13-7-12-20-14-15-23(24(20)21,16-18-8-3-1-4-9-18)22(26)27-17-19-10-5-2-6-11-19/h1-6,8-11,20H,7,12-17H2
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n/an/a 1.00E+3n/an/an/an/an/an/a



UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422545
PNG
(CHEMBL345318)
Show SMILES CC[C@H](N1CC(CC)CC1=O)C(N)=O
Show InChI InChI=1S/C10H18N2O2/c1-3-7-5-9(13)12(6-7)8(4-2)10(11)14/h7-8H,3-6H2,1-2H3,(H2,11,14)/t7?,8-/m0/s1
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n/an/a 1.25E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422541
PNG
(CHEMBL149400)
Show SMILES CC[C@H](N1C[C@H](C)CC1=O)C(N)=O
Show InChI InChI=1S/C9H16N2O2/c1-3-7(9(10)13)11-5-6(2)4-8(11)12/h6-7H,3-5H2,1-2H3,(H2,10,13)/t6-,7+/m1/s1
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n/an/a 1.25E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422544
PNG
(CHEMBL154983)
Show SMILES CCCCCC1CN(C(CC)C(N)=O)C(=O)C1
Show InChI InChI=1S/C13H24N2O2/c1-3-5-6-7-10-8-12(16)15(9-10)11(4-2)13(14)17/h10-11H,3-9H2,1-2H3,(H2,14,17)
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n/an/a 1.25E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422555
PNG
(CHEMBL346223)
Show SMILES CC[C@H](N1C[C@H](CF)CC1=O)C(N)=O
Show InChI InChI=1S/C9H15FN2O2/c1-2-7(9(11)14)12-5-6(4-10)3-8(12)13/h6-7H,2-5H2,1H3,(H2,11,14)/t6-,7-/m0/s1
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n/an/a 1.25E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384304
PNG
(CHEMBL2030665)
Show SMILES CC(=O)N1CCCC1(Cc1ccccc1)C1=N[C@@H](CO1)c1ccccc1 |r,t:17|
Show InChI InChI=1S/C22H24N2O2/c1-17(25)24-14-8-13-22(24,15-18-9-4-2-5-10-18)21-23-20(16-26-21)19-11-6-3-7-12-19/h2-7,9-12,20H,8,13-16H2,1H3/t20-,22?/m0/s1
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n/an/a 1.30E+3n/an/an/an/an/an/a



UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422549
PNG
(CHEMBL150791)
Show SMILES CCC(N1CC(COC)CC1=O)C(N)=O
Show InChI InChI=1S/C10H18N2O3/c1-3-8(10(11)14)12-5-7(6-15-2)4-9(12)13/h7-8H,3-6H2,1-2H3,(H2,11,14)
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n/an/a 1.58E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422536
PNG
(CHEMBL421785)
Show SMILES CC[C@H](N1CC(CC1=O)NC(=O)OC)C(N)=O
Show InChI InChI=1S/C10H17N3O4/c1-3-7(9(11)15)13-5-6(4-8(13)14)12-10(16)17-2/h6-7H,3-5H2,1-2H3,(H2,11,15)(H,12,16)/t6?,7-/m0/s1
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n/an/a 1.58E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422551
PNG
(CHEMBL358877)
Show SMILES CCCCCN(C(CC)C(N)=O)C(=O)CC
Show InChI InChI=1S/C12H24N2O2/c1-4-7-8-9-14(11(15)6-3)10(5-2)12(13)16/h10H,4-9H2,1-3H3,(H2,13,16)
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n/an/a 1.99E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422534
PNG
(CHEMBL153282)
Show SMILES CCC(N1CC2(CCC2)CC1=O)C(N)=O
Show InChI InChI=1S/C11H18N2O2/c1-2-8(10(12)15)13-7-11(4-3-5-11)6-9(13)14/h8H,2-7H2,1H3,(H2,12,15)
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n/an/a 1.99E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422543
PNG
(CHEMBL153264)
Show SMILES CCCCCCCCN(C(CC)C(N)=O)C(=O)Cc1ccc(Cl)cc1
Show InChI InChI=1S/C20H31ClN2O2/c1-3-5-6-7-8-9-14-23(18(4-2)20(22)25)19(24)15-16-10-12-17(21)13-11-16/h10-13,18H,3-9,14-15H2,1-2H3,(H2,22,25)
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n/an/a 1.99E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422553
PNG
(CHEMBL151650)
Show SMILES CC[C@H](N1CCCC1=O)C(=O)NO
Show InChI InChI=1S/C8H14N2O3/c1-2-6(8(12)9-13)10-5-3-4-7(10)11/h6,13H,2-5H2,1H3,(H,9,12)/t6-/m0/s1
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n/an/a 1.99E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422532
PNG
(CHEMBL150281)
Show SMILES CCCCCCCN(C(CC)C(N)=O)C(=O)Cc1ccc(OC)cc1
Show InChI InChI=1S/C20H32N2O3/c1-4-6-7-8-9-14-22(18(5-2)20(21)24)19(23)15-16-10-12-17(25-3)13-11-16/h10-13,18H,4-9,14-15H2,1-3H3,(H2,21,24)
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n/an/a 2.51E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422552
PNG
(CHEMBL153690)
Show SMILES CC[C@H](N1C(C)CCC1=O)C(N)=O
Show InChI InChI=1S/C9H16N2O2/c1-3-7(9(10)13)11-6(2)4-5-8(11)12/h6-7H,3-5H2,1-2H3,(H2,10,13)/t6?,7-/m0/s1
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n/an/a 2.51E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422538
PNG
(CHEMBL154863)
Show SMILES CCC(N1CC(Cc2ccccc2)CC1=O)C(N)=O
Show InChI InChI=1S/C15H20N2O2/c1-2-13(15(16)19)17-10-12(9-14(17)18)8-11-6-4-3-5-7-11/h3-7,12-13H,2,8-10H2,1H3,(H2,16,19)
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n/an/a 2.51E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422529
PNG
(CHEMBL150393)
Show SMILES C[C@H](N1CCCC1=O)C(N)=O
Show InChI InChI=1S/C7H12N2O2/c1-5(7(8)11)9-4-2-3-6(9)10/h5H,2-4H2,1H3,(H2,8,11)/t5-/m0/s1
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n/an/a 3.16E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422527
PNG
(CHEMBL151072)
Show SMILES CCCCCCCCN(C(CC)C(N)=O)C(=O)CC
Show InChI InChI=1S/C15H30N2O2/c1-4-7-8-9-10-11-12-17(14(18)6-3)13(5-2)15(16)19/h13H,4-12H2,1-3H3,(H2,16,19)
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n/an/a 3.98E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422524
PNG
(CHEMBL440539)
Show SMILES CCC(N1CC(CC1=O)C(C)C)C(N)=O
Show InChI InChI=1S/C11H20N2O2/c1-4-9(11(12)15)13-6-8(7(2)3)5-10(13)14/h7-9H,4-6H2,1-3H3,(H2,12,15)
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n/an/a 3.98E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384306
PNG
(CHEMBL2030668)
Show SMILES O=C(N1CCN(Cc2ccccc2)CC1)c1cc2ccccc2oc1=O
Show InChI InChI=1S/C21H20N2O3/c24-20(18-14-17-8-4-5-9-19(17)26-21(18)25)23-12-10-22(11-13-23)15-16-6-2-1-3-7-16/h1-9,14H,10-13,15H2
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n/an/a 4.00E+3n/an/an/an/an/an/a



UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422550
PNG
(CHEMBL2111197)
Show SMILES CCC[C@H](N1CCCC1=O)C(N)=O |r|
Show InChI InChI=1S/C9H16N2O2/c1-2-4-7(9(10)13)11-6-3-5-8(11)12/h7H,2-6H2,1H3,(H2,10,13)/t7-/m0/s1
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n/an/a 5.01E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422557
PNG
(CHEMBL607346)
Show SMILES CCC(N1CCCC1=O)C(=O)NN
Show InChI InChI=1S/C8H15N3O2/c1-2-6(8(13)10-9)11-5-3-4-7(11)12/h6H,2-5,9H2,1H3,(H,10,13)
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n/an/a 6.30E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422554
PNG
(CHEMBL607297)
Show SMILES CCC(N(O)CC1CCC1)C(N)=O
Show InChI InChI=1S/C9H18N2O2/c1-2-8(9(10)12)11(13)6-7-4-3-5-7/h7-8,13H,2-6H2,1H3,(H2,10,12)
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n/an/a 6.30E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422520
PNG
(CHEMBL150903)
Show SMILES CCCCN([C@@H](CC)C(N)=O)C(=O)CC
Show InChI InChI=1S/C11H22N2O2/c1-4-7-8-13(10(14)6-3)9(5-2)11(12)15/h9H,4-8H2,1-3H3,(H2,12,15)/t9-/m0/s1
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n/an/a 9.99E+3n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422521
PNG
(CHEMBL607343)
Show SMILES CC[C@H](N1CCCC1=O)C(N)=N |r|
Show InChI InChI=1S/C8H15N3O/c1-2-6(8(9)10)11-5-3-4-7(11)12/h6H,2-5H2,1H3,(H3,9,10)/t6-/m0/s1
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n/an/a 1.25E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422537
PNG
(CHEMBL153180)
Show SMILES CC[C@H](N1CCCC1=O)C(=O)NC
Show InChI InChI=1S/C9H16N2O2/c1-3-7(9(13)10-2)11-6-4-5-8(11)12/h7H,3-6H2,1-2H3,(H,10,13)/t7-/m0/s1
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n/an/a 1.25E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Solute carrier family 12 member 5


(Rattus norvegicus)
BDBM50384308
PNG
(CHEMBL2030666)
Show SMILES CC(=O)N1CCCC1(Cc1ccccc1)c1nc(co1)-c1ccccc1
Show InChI InChI=1S/C22H22N2O2/c1-17(25)24-14-8-13-22(24,15-18-9-4-2-5-10-18)21-23-20(16-26-21)19-11-6-3-7-12-19/h2-7,9-12,16H,8,13-15H2,1H3
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n/an/a 1.26E+4n/an/an/an/an/an/a



UCB Pharma

Curated by ChEMBL


Assay Description
Inhibition of rat KCC2 expressed in human Sk-Hep cells assessed as induction off Rb+ flux by atomic absorption spectroscopic analysis


Bioorg Med Chem Lett 22: 3978-82 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.097
BindingDB Entry DOI: 10.7270/Q27P90FX
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422530
PNG
(CHEMBL346199)
Show SMILES CC[C@H](N(C)C(C)=O)C(N)=O
Show InChI InChI=1S/C7H14N2O2/c1-4-6(7(8)11)9(3)5(2)10/h6H,4H2,1-3H3,(H2,8,11)/t6-/m0/s1
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n/an/a 1.58E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422546
PNG
(CHEMBL153729)
Show SMILES CC(C)C(N1CCCC1=O)C(N)=O
Show InChI InChI=1S/C9H16N2O2/c1-6(2)8(9(10)13)11-5-3-4-7(11)12/h6,8H,3-5H2,1-2H3,(H2,10,13)
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n/an/a 1.99E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422539
PNG
(CHEMBL153619)
Show SMILES CC[C@H](N1CCC(C)C1=O)C(N)=O
Show InChI InChI=1S/C9H16N2O2/c1-3-7(8(10)12)11-5-4-6(2)9(11)13/h6-7H,3-5H2,1-2H3,(H2,10,12)/t6?,7-/m0/s1
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n/an/a 1.99E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
Synaptic vesicle glycoprotein 2A


(Rattus norvegicus)
BDBM50422535
PNG
(CHEMBL607399)
Show SMILES CCC(N1CCCC1=O)C(=O)N(C)O
Show InChI InChI=1S/C9H16N2O3/c1-3-7(9(13)10(2)14)11-6-4-5-8(11)12/h7,14H,3-6H2,1-2H3
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n/an/a 1.99E+4n/an/an/an/an/an/a



UCB S.A.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against [3H](2S)-2-[4-(3-azidophenyl)-2-oxopyrrolidin-1-yl]butanamide binding to levetiracetam binding site


J Med Chem 47: 530-49 (2004)

Checked by Author
Article DOI: 10.1021/jm030913e
BindingDB Entry DOI: 10.7270/Q2GF0VQ6
More data for this
Ligand-Target Pair
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