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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293856 (1-(2,2-dimethyl-1,3-dioxan-5-yl)-3-{[1S,3R,6S)-2,1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [125I]Tyr14-nociceptin from human cloned ORL1 receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50083230 (1-((3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-pipe...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [125I]Tyr14-nociceptin from human cloned ORL1 receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [125I]Tyr14-nociceptin from human cloned ORL1 receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293857 (1-(1,3-dihydroxypropan-2-yl)-3-(1-((1R,3S,4S)-spir...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [125I]Tyr14-nociceptin from human cloned ORL1 receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293857 (1-(1,3-dihydroxypropan-2-yl)-3-(1-((1R,3S,4S)-spir...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Antagonist activity at human ORL1 receptor expressed in CHO cells by [35S]GTPgammaS binding assay | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Antagonist activity at human ORL1 receptor expressed in CHO cells by [35S]GTPgammaS binding assay | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Nociceptin receptor (Homo sapiens (Human)) | BDBM50293856 (1-(2,2-dimethyl-1,3-dioxan-5-yl)-3-{[1S,3R,6S)-2,1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 29 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Antagonist activity at human ORL1 receptor expressed in CHO cells by [35S]GTPgammaS binding assay | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Homo sapiens (Human)) | BDBM50293856 (1-(2,2-dimethyl-1,3-dioxan-5-yl)-3-{[1S,3R,6S)-2,1...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]diprenorphine from human cloned mu opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 4.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]diprenorphine from human cloned mu opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Homo sapiens (Human)) | BDBM50293857 (1-(1,3-dihydroxypropan-2-yl)-3-(1-((1R,3S,4S)-spir...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 6.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]diprenorphine from human cloned mu opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Homo sapiens (Human)) | BDBM50293856 (1-(2,2-dimethyl-1,3-dioxan-5-yl)-3-{[1S,3R,6S)-2,1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 6.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]U69593 from human cloned kappa opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Homo sapiens (Human)) | BDBM50293856 (1-(2,2-dimethyl-1,3-dioxan-5-yl)-3-{[1S,3R,6S)-2,1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]naltrindole from human cloned delta opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Homo sapiens (Human)) | BDBM50293857 (1-(1,3-dihydroxypropan-2-yl)-3-(1-((1R,3S,4S)-spir...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]naltrindole from human cloned delta opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]naltrindole from human cloned delta opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]U69593 from human cloned kappa opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Homo sapiens (Human)) | BDBM50293857 (1-(1,3-dihydroxypropan-2-yl)-3-(1-((1R,3S,4S)-spir...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of [3H]U69593 from human cloned kappa opioid receptor expressed in CHO cells | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Inhibition of CYP2D6 in human liver microsomes assessed as inhibition of dextrometorphan O-demethylation | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Displacement of radiolabeled MK-499 from human ERG expressed in HEK293 cells coexpressing IKr channel protein | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2C9 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Inhibition of CYP2C9 in human liver microsomes assessed as inhibition of diclofenac 4'-hydroxylation | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2C8 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Inhibition of CYP2C8 in human liver microsomes assessed as inhibition of paclitaxel 6-alpha-hydroxylation | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 1A2 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Inhibition of CYP1A2 in human liver microsomes assessed as inhibition of acetophenacetin odeethylation | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 3A4 (Homo sapiens (Human)) | BDBM50293855 (4-{3-[(2R)-2,3-dihydroxypropyl]-2-oxo-2,3-dihydro-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Tsukuba Research Institute Curated by ChEMBL | Assay Description Inhibition of CYP3A4 in human liver microsomes assessed as inhibition of testosterone 6-beta-hydroxylation | J Med Chem 52: 4091-4 (2009) Article DOI: 10.1021/jm900581g BindingDB Entry DOI: 10.7270/Q2V98835 | |||||||||||
More data for this Ligand-Target Pair |