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 IDDB01183
Drug NameNaloxone
Target IDBE0000770
UniProt IDP35372
Regulation Typeantagonist
PubMed IDs12566163; 12799988; 12842269; 12887410; 12909198; 11752352; 18354714; 17918759; 17367258; 17161885; 17097763
CitationsNarita M, Suzuki M, Mizoguchi H, Narita M, Yajima Y, Sakurada S, Tseng LF, Suzuki T: Up-regulation of mu-opioid receptor-mediated G-protein activation in protein kinase Cgamma knockout mice following repeated naloxone treatment. Neurosci Lett. 2003 Feb 27;338(2):103-6.@@Freye E, Latasch L, Von Bredow G, Neruda B: [The opioid tramadol demonstrates excitatory properties of non-opioid character--a preclinical study using alfentanil as a comparison]. Schmerz. 1998 Feb 28;12(1):19-24.@@Neal CR Jr, Owens CE, Taylor LP, Hoversten MT, Akil H, Watson SJ Jr: Binding and GTPgammaS autoradiographic analysis of preproorphanin precursor peptide products at the ORL1 and opioid receptors. J Chem Neuroanat. 2003 Jul;25(4):233-47.@@Spetea M, Toth F, Schutz J, Otvos F, Toth G, Benyhe S, Borsodi A, Schmidhammer H: Binding characteristics of [3H]14-methoxymetopon, a high affinity mu-opioid receptor agonist. Eur J Neurosci. 2003 Jul;18(2):290-5.@@Marek GJ: Behavioral evidence for mu-opioid and 5-HT2A receptor interactions. Eur J Pharmacol. 2003 Aug 1;474(1):77-83.@@Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5.@@Helm S, Trescot AM, Colson J, Sehgal N, Silverman S: Opioid antagonists, partial agonists, and agonists/antagonists: the role of office-based detoxification. Pain Physician. 2008 Mar-Apr;11(2):225-35.@@Goodman AJ, Le Bourdonnec B, Dolle RE: Mu opioid receptor antagonists: recent developments. ChemMedChem. 2007 Nov;2(11):1552-70.@@van Dorp E, Yassen A, Dahan A: Naloxone treatment in opioid addiction: the risks and benefits. Expert Opin Drug Saf. 2007 Mar;6(2):125-32.@@Nazzaro C, Rizzi A, Salvadori S, Guerrini R, Regoli D, Zeilhofer HU, Calo G: UFP-101 antagonizes the spinal antinociceptive effects of nociceptin/orphanin FQ: behavioral and electrophysiological studies in mice. Peptides. 2007 Mar;28(3):663-9. doi: 10.1016/j.peptides.2006.11.004. Epub 2006 Dec 11.@@Economidou D, Fedeli A, Fardon RM, Weiss F, Massi M, Ciccocioppo R: Effect of novel nociceptin/orphanin FQ-NOP receptor ligands on ethanol drinking in alcohol-preferring msP rats. Peptides. 2006 Dec;27(12):3299-306. doi: 10.1016/j.peptides.2006.09.007.
GroupsApproved; Vet_approved
Direct ClassificationPhenanthrenes and derivatives
SMILESOC1=CC=C2C[C@H]3N(CC=C)CC[C@@]45[C@@H](OC1=C24)C(=O)CC[C@@]35O
PathwaysNaloxone Action Pathway
PharmGKBPA450586
ChEMBLCHEMBL80