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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088369 (1-{10-[3-(3-Chloro-phenyl)-allyl]-9,10-diaza-tricy...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (3) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50000092 ((-)-(etorphine) | (-)-morphine | (1S,5R,13R,14S)-1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars | PDB PubMed | 2.80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088365 (1-[10-(3-Naphthalen-1-yl-allyl)-9,10-diaza-tricycl...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 4.66 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (3) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088370 (1-{10-[3-(4-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 5.10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (3) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088361 (1-{10-[3-(3-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 9.5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (3) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088361 (1-{10-[3-(3-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (2) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088362 (1-[10-(3-Phenyl-allyl)-9,10-diaza-tricyclo[4.2.1.1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088369 (1-{10-[3-(3-Chloro-phenyl)-allyl]-9,10-diaza-tricy...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 16.3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (2) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088365 (1-[10-(3-Naphthalen-1-yl-allyl)-9,10-diaza-tricycl...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 21.7 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (2) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088370 (1-{10-[3-(4-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 23 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088370 (1-{10-[3-(4-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 25 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (2) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088369 (1-{10-[3-(3-Chloro-phenyl)-allyl]-9,10-diaza-tricy...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 36.6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088361 (1-{10-[3-(3-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088368 (1-[3-(3-Phenyl-allyl)-3,8-diaza-bicyclo[3.2.1]oct-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | PubMed | 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088362 (1-[10-(3-Phenyl-allyl)-9,10-diaza-tricyclo[4.2.1.1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (2) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088362 (1-[10-(3-Phenyl-allyl)-9,10-diaza-tricyclo[4.2.1.1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 160 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor mu 1 was determined in rat brain homogenate using 3- arylpropenyl-8-propionyl-DBO derivative (3) | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088371 (1-[8-(3-Phenyl-allyl)-3,8-diaza-bicyclo[3.2.1]oct-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 160 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mu-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088365 (1-[10-(3-Naphthalen-1-yl-allyl)-9,10-diaza-tricycl...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 180 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Inhibition of [3H]-DAMGO binding to rat brain homogenat Opioid receptor mu 1 | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig)) | BDBM50088361 (1-{10-[3-(3-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 750 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor kappa 1 was determined in guinea pig homogenate using [3H]-U-69,593 as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088362 (1-[10-(3-Phenyl-allyl)-9,10-diaza-tricyclo[4.2.1.1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor delta 1 was determined in rat brain homogenate using [3H]-deltorphin II as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig)) | BDBM50088362 (1-[10-(3-Phenyl-allyl)-9,10-diaza-tricyclo[4.2.1.1...) | PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor kappa 1 was determined in guinea pig homogenate using [3H]-U-69,593 as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088361 (1-{10-[3-(3-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 7.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor delta 1 was determined in rat brain homogenate using [3H]-deltorphin II as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig)) | BDBM50088370 (1-{10-[3-(4-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor kappa 1 was determined in guinea pig homogenate using [3H]-U-69,593 as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Delta-type opioid receptor (Rattus norvegicus (rat)) | BDBM50088370 (1-{10-[3-(4-Nitro-phenyl)-allyl]-9,10-diaza-tricyc...) | PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Istituto di Chimica Farmaceutica e Tossicologica Curated by ChEMBL | Assay Description Binding affinity towards Opioid receptor delta 1 was determined in rat brain homogenate using [3H]-deltorphin II as radioligand | J Med Chem 43: 2115-23 (2000) BindingDB Entry DOI: 10.7270/Q22N51HT | |||||||||||
More data for this Ligand-Target Pair |