hydromorphone [Ligand Id: 7082] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL398707 (Dilaudid, Dilaudid-HP, Dimorphone, Hydromorphon, Hydromorphone, IDS-NH-004, Jurnista, N02AA03, Novolaudon, NSC-19046, Palladone)
  • δ receptor/Delta opioid receptor in Human [ChEMBL: CHEMBL236] [GtoPdb: 317] [UniProtKB: P41143]
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  • κ receptor/Kappa opioid receptor in Human [ChEMBL: CHEMBL237] [GtoPdb: 318] [UniProtKB: P41145]
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  • μ receptor/Mu opioid receptor in Human [ChEMBL: CHEMBL233] [GtoPdb: 319] [UniProtKB: P35372]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
δ receptor/Delta opioid receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL236] [GtoPdb: 317] [UniProtKB: P41143]
GtoPdb - - 7.42 pKi 38 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-94 [PMID:19282177]
ChEMBL Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO cells after 3 hrs by scintillation counting B 7.42 pKi 38 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-2294 [PMID:19282177]
κ receptor/Kappa opioid receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL237] [GtoPdb: 318] [UniProtKB: P41145]
GtoPdb - - 8.55 pKi 2.8 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-94 [PMID:19282177]
ChEMBL Displacement of [3H]U69,593 from human kappa opioid receptor expressed in CHO cells after 60 mins by scintillation counting B 8.55 pKi 2.8 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-2294 [PMID:19282177]
ChEMBL Agonist activity at human kappa opioid receptor expressed in CHO cells assessed as stimulation of [35S]GTPgammaS binding F 7.96 pEC50 11 nM EC50 Bioorg Med Chem Lett (2009) 19: 2289-2294 [PMID:19282177]
μ receptor/Mu opioid receptor in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL233] [GtoPdb: 319] [UniProtKB: P35372]
GtoPdb - - 9.55 pKi 0.28 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-94 [PMID:19282177]
ChEMBL Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells after 60 mins by scintillation counting B 9.55 pKi 0.28 nM Ki Bioorg Med Chem Lett (2009) 19: 2289-2294 [PMID:19282177]
ChEMBL Agonist activity at human mu opioid receptor expressed in CHO cells assessed as stimulation of [35S]GTPgammaS binding F 8.59 pEC50 2.6 nM EC50 Bioorg Med Chem Lett (2009) 19: 2289-2294 [PMID:19282177]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]