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 34:

Zdrazil B, Felix E, Hunter F, Manners EJ, Blackshaw J, Corbett S, de Veij M, Ioannidis H, Lopez DM, Mosquera JF, Magarinos MP, Bosc N, Arcila R, Kizilören T, Gaulton A, Bento AP, Adasme MF, Monecke P, Landrum GA, Leach AR. (2024). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Res., 52(D1). DOI: 10.1093/nar/gkad1004. [EPMCID:10767899] [PMID:37933841]
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]