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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22541 (Clobenpropit | N''-[(4-chlorophenyl)methyl]{[3-(1H...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase PC cid PC sid UniChem Patents Similars | Article PubMed | 0.339 | -54.1 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22542 (4-(1H-imidazol-4-ylmethyl)piperidine | 4-(1H-imida...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem Patents Similars | Article PubMed | 0.407 | -53.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22548 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-4,4,6-trimeth...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 1 | -51.4 | n/a | n/a | 2 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22538 (4-Benzyl-1H-imidazole derivative, 19 | 4-{[3-(2-ph...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 2 | -49.7 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22540 (4-Benzyl-1H-imidazole derivative, 21 | 4-{[3-(pent...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 3 | -48.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22537 (4-Benzyl-1H-imidazole derivative, 18 | 4-{[3-(3,3-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 4 | -47.9 | n/a | n/a | 8 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22529 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-4,4-dimethyl-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 4 | -47.9 | n/a | n/a | 16 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H4 receptor (Homo sapiens (Human)) | BDBM22537 (4-Benzyl-1H-imidazole derivative, 18 | 4-{[3-(3,3-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 6 | -46.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH4R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H4 receptor (Homo sapiens (Human)) | BDBM22536 (1-[3-(1H-imidazol-4-ylmethyl)phenyl]-3,3-dimethylb...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 6 | -46.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH4R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H4 receptor (Homo sapiens (Human)) | BDBM22548 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-4,4,6-trimeth...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 8 | -46.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH4R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22536 (1-[3-(1H-imidazol-4-ylmethyl)phenyl]-3,3-dimethylb...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 32 | -42.8 | n/a | n/a | 79 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22533 (4-Benzyl-1H-imidazole derivative, 14 | 4-[(3-pheny...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Patents Similars | Article PubMed | 33 | -42.7 | n/a | n/a | 200 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22549 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-3-oxa-1-azasp...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 40 | -42.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22534 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]pyridine | 4-B...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | 41 | -42.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22550 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-1-oxa-3-azasp...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 56 | -41.4 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22552 ((4R)-4-benzyl-2-[3-(1H-imidazol-4-ylmethyl)phenyl]...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 89 | -40.2 | n/a | n/a | 79 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22531 (3-(1H-imidazol-4-ylmethyl)benzonitrile | 4-Benzyl-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 155 | -38.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22532 (4-Benzyl-1H-imidazole derivative, 13 | 4-benzyl-1H...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase PC cid PC sid UniChem Patents Similars | Article PubMed | 162 | -38.8 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22547 (4-(1H-imidazol-4-ylmethyl)aniline | 4-Benzyl-1H-im...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase PC cid PC sid UniChem Patents Similars | Article PubMed | 257 | -37.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22545 (4-Benzyl-1H-imidazole derivative, 23 | 4-[(4-bromo...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 417 | -36.4 | n/a | n/a | 631 | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22535 (4-Benzyl-1H-imidazole derivative, 16 | 4-[3-(1H-im...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 427 | -36.4 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22546 (4-Benzyl-1H-imidazole derivative, 24 | 4-{[4-(3,3-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 537 | -35.8 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22551 (4-(cyclohexylmethyl)-2-[3-(1H-imidazol-4-ylmethyl)...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 708 | -35.1 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22544 (4-(1H-imidazol-4-ylmethyl)benzonitrile | 4-Benzyl-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Patents Similars | Article PubMed | 813 | -34.8 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22539 (4-({3-[2-(naphthalen-1-yl)ethynyl]phenyl}methyl)-1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 1.74E+3 | -32.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22553 (2-[3-(1H-imidazol-4-ylmethyl)phenyl]-5,5-dimethyl-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 2.51E+3 | -32.0 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H3 receptor (Homo sapiens (Human)) | BDBM22543 (2-[4-(1H-imidazol-4-ylmethyl)phenyl]-4,4-dimethyl-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | Article PubMed | 2.51E+3 | -32.0 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
VU University Amsterdam | Assay Description Ligand displacement assays were performed on CHO cells membranes expressing hH3R. Retained radioactivity was determined by liquid scintillation count... | J Med Chem 51: 2944-53 (2008) Article DOI: 10.1021/jm7014149 BindingDB Entry DOI: 10.7270/Q24F1P2W | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Synaptic vesicle glycoprotein 2A (Rattus norvegicus) | BDBM50422558 (CHEMBL434705) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 79.4 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422531 (BRIVARACETAM | UCB-34714) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL149348) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422548 (CHEMBL150241) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 125 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422518 (CHEMBL358242) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 125 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422525 (CHEMBL348187) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 158 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422519 (CHEMBL358393) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 199 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422522 (CHEMBL347071) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 251 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422540 (CHEMBL152911) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 251 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422526 (CHEMBL359062) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 398 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL150331) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 398 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422556 (CHEMBL358161) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 501 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422542 (Keppra | Keppra Xr | LEVETIRACETAM | Levetiracetam...) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 794 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL358239) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 794 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL149400) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.25E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL346223) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 1.25E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL154983) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.25E+3 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422545 (CHEMBL345318) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.25E+3 | n/a | n/a | n/a | n/a | n/a | n/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) | BDBM50422549 (CHEMBL150791) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 1.58E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL421785) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 1.58E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL358877) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.99E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL153282) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.99E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (CHEMBL153264) | PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.99E+3 | n/a | n/a | n/a | n/a | n/a | n/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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