Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS42001512EBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10012006HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10007858HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10008487HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10009685HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10010472HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10010870HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10011363HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10011435HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
TVIS10013160HBVENSG00000112038.18protein_codingOPRM1NoNo4988B8K2Q5
G8XRH4
G8XRH5
L0E130
P35372
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Drug Information
GeneOPRM1
DrugBank IDDB00844
Drug NameNalbuphine
Target IDBE0000770
UniProt IDP35372
Regulation Typeantagonist
PubMed IDs10844102; 8388112; 9084061; 9399970; 18425947; 16517095; 19403853; 15602503; 18810678; 17407276
CitationsKishioka S, Ko MC, Woods JH: Diltiazem enhances the analgesic but not the respiratory depressant effects of morphine in rhesus monkeys. Eur J Pharmacol. 2000 May 26;397(1):85-92.@@Hoehe M, Duka T: Opiates increase plasma catecholamines in humans. Psychoneuroendocrinology. 1993;18(2):141-8.@@Zernig G, Lewis JW, Woods JH: Clocinnamox inhibits the intravenous self-administration of opioid agonists in rhesus monkeys: comparison with effects on opioid agonist-mediated antinociception. Psychopharmacology (Berl). 1997 Feb;129(3):233-42.@@Picker MJ: Discriminative stimulus effects of the mixed-opioid agonist/antagonist dezocine: cross-substitution by mu and delta opioid agonists. J Pharmacol Exp Ther. 1997 Dec;283(3):1009-17.@@McNicol ED, Boyce D, Schumann R, Carr DB: Mu-opioid antagonists for opioid-induced bowel dysfunction. Cochrane Database Syst Rev. 2008 Apr 16;(2):CD006332. doi: 10.1002/14651858.CD006332.pub2.@@Tao PL, Liang KW, Sung WY, Wu YT, Huang EY: Nalbuphine is effective in decreasing the rewarding effect induced by morphine in rats. Drug Alcohol Depend. 2006 Sep 15;84(2):175-81. Epub 2006 Mar 6.@@Smith MA, Greene-Naples JL, Lyle MA, Iordanou JC, Felder JN: The effects of repeated opioid administration on locomotor activity: I. Opposing actions of mu and kappa receptors. J Pharmacol Exp Ther. 2009 Aug;330(2):468-75. doi: 10.1124/jpet.108.150011. Epub 2009 Apr 29.@@Mello NK, Mendelson JH, Sholar MB, Jaszyna-Gasior M, Goletiani N, Siegel AJ: Effects of the mixed mu/kappa opioid nalbuphine on cocaine-induced changes in subjective and cardiovascular responses in men. Neuropsychopharmacology. 2005 Mar;30(3):618-32.@@Meerpohl JJ, Timmer A: [News from the cochrane library: mu opioid antagonists for opioid-induced bowel dysfunction]. Z Gastroenterol. 2008 Sep;46(9):917-21. doi: 10.1055/s-2008-1027720. Epub 2008 Sep 22.@@Peng X, Knapp BI, Bidlack JM, Neumeyer JL: Pharmacological properties of bivalent ligands containing butorphan linked to nalbuphine, naltrexone, and naloxone at mu, delta, and kappa opioid receptors. J Med Chem. 2007 May 3;50(9):2254-8. Epub 2007 Apr 4.
GroupsApproved
Direct ClassificationPhenanthrenes and derivatives
SMILESO[C@H]1CC[C@@]2(O)[C@H]3CC4=CC=C(O)C5=C4[C@@]2(CCN3CC2CCC2)[C@H]1O5
PathwaysNalbuphine Action Pathway
PharmGKBPA164745372
ChEMBLCHEMBL895