Nabiximols

DB14011

small molecule investigational

Deskripsi

Nabiximols (tradename Sativex®) is a whole plant extract from the Cannabis species Cannabis sativa L. that has been purified into the active components CBD (cannabidiol) and THC (delta-9-tetrahydrocannabinol). For trademark purposes, purified CBD is branded as Nabidiolex®, while THC is purified as the product Tetrabinex®. Sativex® is available in a 1:1 formulation of THC:CBD as an oro-mucosal pump spray used for treatment of neuropathic pain from Multiple Sclerosis (MS) and for intractable cancer pain. Although still largely debated, Cannabis has been shown to have analgesic, anticonvulsant, muscle relaxant, anxiolytic, neuroprotective, anti-oxidant, and anti-psychotic activity A32477, A32469.

From a pharmacological perspective, Cannabis' diverse receptor profile explains its potential application for such a wide variety of medical conditions. Cannabis contains more than 400 different chemical compounds, of which 61 are considered cannabinoids, a class of compounds that act upon cannabinoid receptors of the body A32584. Tetrahydrocannabinol (THC) and cannabidiol (CBD) are two types of cannabinoids found naturally in the resin of the marijuana plant, both of which interact with the cannabinoid receptors found in the human body. While both CBD and THC are used for medicinal purposes, they have different receptor activity, function, and physiological effects. While cannabis in its natural plant form is currently used "off-label" for the management of many medical conditions, THC is currently commercially available in synthetic form as DB00486, as purified isomer as DB00470, or in a 1:1 formulation with CBD from purified plant extract as DB14011.

The primary psychoactive component of Cannabis, delta 9-tetrahydrocannabinol (?9-THC), demonstrates its effects through weak partial agonist activity at Cannabinoid-1 (CB1R) and Cannabinoid-2 (CB2R) receptors. This activity results in the well-known effects of smoking cannabis such as increased appetite, reduced pain, and changes in emotional and cognitive processes. In contrast to THC's weak agonist activity, CBD has been shown to act as a negative allosteric modulator of the cannabinoid CB1 receptor, the most abundant G-Protein Coupled Receptor (GPCR) in the body A32469. Allosteric regulation is achieved through the modulation of receptor activity on a functionally distinct site from the agonist or antagonist binding site. The negative allosteric modulatory effects of CBD are therapeutically important as direct agonists are limited by their psychomimetic effects while direct antagonists are limited by their depressant effects A32469.

In Canada, Sativex® has received a Notice of Compliance (NOC) for use as an as adjunctive treatment for symptomatic relief of spasticity in patients with multiple sclerosis (MS) who have not responded adequately to other therapy and who demonstrate meaningful improvement during an initial trial of therapy.

Sativex® has also received a Notice of Compliance with Conditions (NOC/c) for use as an adjunctive treatment for the symptomatic relief of neuropathic pain in adult patients with multiple sclerosis (MS) and as adjunctive analgesic treatment in adult patients with advanced cancer who experience moderate to severe pain during the highest tolerated dose of strong opioid therapy for persistent background pain.

Struktur Molekul 2D

Berat 628.938
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) Elimination from plasma is bi-exponential with an initial half-life of one to two hours. The terminal elimination half-lives are of the order of 24 to 36 hours or longer.
Volume Distribusi Cannabinoids are distributed throughout the body; they are highly lipid soluble and accumulate in fatty tissue. The release of cannabinoids from fatty tissue is responsible for the prolonged terminal elimination half-life.
Klirens (Clearance) -

Absorpsi

Individual subject plasma concentration data and pharmacokinetic parameters show a high degree of inter-subject variability. Following a single buccal administration, maximum plasma concentrations of both CBD and THC typically occur within two to four hours. When administered buccally, blood levels of THC and other cannabinoids are lower compared with inhalation of smoked cannabis. The resultant concentrations in the blood are lower than those obtained by inhaling the same dose because absorption is slower, redistribution into fatty tissues is rapid and additionally some of the THC undergoes hepatic first-pass metabolism to 11-OH-THC, a psycho-active metabolite.

Metabolisme

THC and CBD are metabolized in the liver by a number of cytochrome P450 isoenzymes, including CYP2C9, CYP2C19, CYP2D6 and CYP3A4. They may be stored for as long as four weeks in the fatty tissues from which they are slowly released at sub-therapeutic levels back into the blood stream and metabolized via the renal and biliary systems.

Rute Eliminasi

Nabiximols is excreted in the urine and faeces.

Interaksi Obat

1435 Data
Cocaine Cocaine may increase the tachycardic activities of Nabiximols.
Trospium The risk or severity of Tachycardia and drowsiness can be increased when Trospium is combined with Nabiximols.
Oxyphenonium The risk or severity of Tachycardia and drowsiness can be increased when Oxyphenonium is combined with Nabiximols.
Benzatropine The risk or severity of Tachycardia and drowsiness can be increased when Benzatropine is combined with Nabiximols.
Disopyramide The risk or severity of Tachycardia and drowsiness can be increased when Disopyramide is combined with Nabiximols.
Ipratropium The risk or severity of Tachycardia and drowsiness can be increased when Ipratropium is combined with Nabiximols.
Metixene The risk or severity of Tachycardia and drowsiness can be increased when Metixene is combined with Nabiximols.
Buclizine The risk or severity of Tachycardia and drowsiness can be increased when Buclizine is combined with Nabiximols.
Trihexyphenidyl The risk or severity of Tachycardia and drowsiness can be increased when Trihexyphenidyl is combined with Nabiximols.
Oxyphencyclimine The risk or severity of Tachycardia and drowsiness can be increased when Oxyphencyclimine is combined with Nabiximols.
Procyclidine The risk or severity of Tachycardia and drowsiness can be increased when Procyclidine is combined with Nabiximols.
Profenamine The risk or severity of Tachycardia and drowsiness can be increased when Profenamine is combined with Nabiximols.
Hyoscyamine The risk or severity of Tachycardia and drowsiness can be increased when Hyoscyamine is combined with Nabiximols.
Methscopolamine bromide The risk or severity of Tachycardia and drowsiness can be increased when Methscopolamine bromide is combined with Nabiximols.
Tridihexethyl The risk or severity of Tachycardia and drowsiness can be increased when Tridihexethyl is combined with Nabiximols.
Anisotropine methylbromide The risk or severity of Tachycardia and drowsiness can be increased when Anisotropine methylbromide is combined with Nabiximols.
Atropine The risk or severity of Tachycardia and drowsiness can be increased when Atropine is combined with Nabiximols.
Pirenzepine The risk or severity of Tachycardia and drowsiness can be increased when Pirenzepine is combined with Nabiximols.
Homatropine methylbromide The risk or severity of Tachycardia and drowsiness can be increased when Homatropine methylbromide is combined with Nabiximols.
Benzquinamide The risk or severity of Tachycardia and drowsiness can be increased when Benzquinamide is combined with Nabiximols.
Propantheline The risk or severity of Tachycardia and drowsiness can be increased when Propantheline is combined with Nabiximols.
Dicyclomine The risk or severity of Tachycardia and drowsiness can be increased when Dicyclomine is combined with Nabiximols.
Biperiden The risk or severity of Tachycardia and drowsiness can be increased when Biperiden is combined with Nabiximols.
Methantheline The risk or severity of Tachycardia and drowsiness can be increased when Methantheline is combined with Nabiximols.
Cycrimine The risk or severity of Tachycardia and drowsiness can be increased when Cycrimine is combined with Nabiximols.
Glycopyrronium The risk or severity of Tachycardia and drowsiness can be increased when Glycopyrronium is combined with Nabiximols.
Tolterodine The risk or severity of Tachycardia and drowsiness can be increased when Tolterodine is combined with Nabiximols.
Oxybutynin The risk or severity of Tachycardia and drowsiness can be increased when Oxybutynin is combined with Nabiximols.
Flavoxate The risk or severity of Tachycardia and drowsiness can be increased when Flavoxate is combined with Nabiximols.
Diphenidol The risk or severity of Tachycardia and drowsiness can be increased when Diphenidol is combined with Nabiximols.
Tiotropium The risk or severity of Tachycardia and drowsiness can be increased when Tiotropium is combined with Nabiximols.
Solifenacin The risk or severity of Tachycardia and drowsiness can be increased when Solifenacin is combined with Nabiximols.
Isopropamide The risk or severity of Tachycardia and drowsiness can be increased when Isopropamide is combined with Nabiximols.
Mepenzolate The risk or severity of Tachycardia and drowsiness can be increased when Mepenzolate is combined with Nabiximols.
Fesoterodine The risk or severity of Tachycardia and drowsiness can be increased when Fesoterodine is combined with Nabiximols.
Hexocyclium The risk or severity of Tachycardia and drowsiness can be increased when Hexocyclium is combined with Nabiximols.
Dimetindene The risk or severity of Tachycardia and drowsiness can be increased when Dimetindene is combined with Nabiximols.
Aclidinium The risk or severity of Tachycardia and drowsiness can be increased when Aclidinium is combined with Nabiximols.
Dexetimide The risk or severity of Tachycardia and drowsiness can be increased when Dexetimide is combined with Nabiximols.
Umeclidinium The risk or severity of Tachycardia and drowsiness can be increased when Umeclidinium is combined with Nabiximols.
Trimebutine The risk or severity of Tachycardia and drowsiness can be increased when Trimebutine is combined with Nabiximols.
Imidafenacin The risk or severity of Tachycardia and drowsiness can be increased when Imidafenacin is combined with Nabiximols.
Butylscopolamine The risk or severity of Tachycardia and drowsiness can be increased when Butylscopolamine is combined with Nabiximols.
Thonzylamine The risk or severity of Tachycardia and drowsiness can be increased when Thonzylamine is combined with Nabiximols.
Methscopolamine The risk or severity of Tachycardia and drowsiness can be increased when Methscopolamine is combined with Nabiximols.
Oxitropium The risk or severity of Tachycardia and drowsiness can be increased when Oxitropium is combined with Nabiximols.
Propiverine The risk or severity of Tachycardia and drowsiness can be increased when Propiverine is combined with Nabiximols.
Batefenterol The risk or severity of Tachycardia and drowsiness can be increased when Batefenterol is combined with Nabiximols.
Mebeverine The risk or severity of Tachycardia and drowsiness can be increased when Mebeverine is combined with Nabiximols.
Tropatepine The risk or severity of Tachycardia and drowsiness can be increased when Tropatepine is combined with Nabiximols.
Prifinium The risk or severity of Tachycardia and drowsiness can be increased when Prifinium is combined with Nabiximols.
Piperidolate The risk or severity of Tachycardia and drowsiness can be increased when Piperidolate is combined with Nabiximols.
Benzilone The risk or severity of Tachycardia and drowsiness can be increased when Benzilone is combined with Nabiximols.
Difemerine The risk or severity of Tachycardia and drowsiness can be increased when Difemerine is combined with Nabiximols.
Phenglutarimide The risk or severity of Tachycardia and drowsiness can be increased when Phenglutarimide is combined with Nabiximols.
Mazaticol The risk or severity of Tachycardia and drowsiness can be increased when Mazaticol is combined with Nabiximols.
Etybenzatropine The risk or severity of Tachycardia and drowsiness can be increased when Etybenzatropine is combined with Nabiximols.
Otilonium The risk or severity of Tachycardia and drowsiness can be increased when Otilonium is combined with Nabiximols.
Poldine The risk or severity of Tachycardia and drowsiness can be increased when Poldine is combined with Nabiximols.
Bevonium The risk or severity of Tachycardia and drowsiness can be increased when Bevonium is combined with Nabiximols.
Rociverine The risk or severity of Tachycardia and drowsiness can be increased when Rociverine is combined with Nabiximols.
Bornaprine The risk or severity of Tachycardia and drowsiness can be increased when Bornaprine is combined with Nabiximols.
Etanautine The risk or severity of Tachycardia and drowsiness can be increased when Etanautine is combined with Nabiximols.
Tiemonium iodide The risk or severity of Tachycardia and drowsiness can be increased when Tiemonium iodide is combined with Nabiximols.
Dihexyverine The risk or severity of Tachycardia and drowsiness can be increased when Dihexyverine is combined with Nabiximols.
Penthienate The risk or severity of Tachycardia and drowsiness can be increased when Penthienate is combined with Nabiximols.
Diphemanil The risk or severity of Tachycardia and drowsiness can be increased when Diphemanil is combined with Nabiximols.
Camylofin The risk or severity of Tachycardia and drowsiness can be increased when Camylofin is combined with Nabiximols.
Fenpiverinium The risk or severity of Tachycardia and drowsiness can be increased when Fenpiverinium is combined with Nabiximols.
Emetonium iodide The risk or severity of Tachycardia and drowsiness can be increased when Emetonium iodide is combined with Nabiximols.
Pipenzolate The risk or severity of Tachycardia and drowsiness can be increased when Pipenzolate is combined with Nabiximols.
Timepidium The risk or severity of Tachycardia and drowsiness can be increased when Timepidium is combined with Nabiximols.
Quinidine The risk or severity of Tachycardia and drowsiness can be increased when Quinidine is combined with Nabiximols.
Chlorphenoxamine The risk or severity of Tachycardia and drowsiness can be increased when Chlorphenoxamine is combined with Nabiximols.
Midodrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Midodrine.
Norepinephrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Norepinephrine.
Phenylephrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Phenylephrine.
Phenylpropanolamine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Phenylpropanolamine.
Metaraminol The risk or severity of Tachycardia can be increased when Nabiximols is combined with Metaraminol.
Methoxamine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Methoxamine.
Orciprenaline The risk or severity of Tachycardia can be increased when Nabiximols is combined with Orciprenaline.
Phenmetrazine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Phenmetrazine.
Dobutamine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Dobutamine.
Pseudoephedrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Pseudoephedrine.
Ritodrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Ritodrine.
Terbutaline The risk or severity of Tachycardia can be increased when Nabiximols is combined with Terbutaline.
Oxymetazoline The risk or severity of Tachycardia can be increased when Nabiximols is combined with Oxymetazoline.
Dopamine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Dopamine.
Isoprenaline The risk or severity of Tachycardia can be increased when Nabiximols is combined with Isoprenaline.
Fenoterol The risk or severity of Tachycardia can be increased when Nabiximols is combined with Fenoterol.
Ephedrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Ephedrine.
Mephentermine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Mephentermine.
Procaterol The risk or severity of Tachycardia can be increased when Nabiximols is combined with Procaterol.
Clenbuterol The risk or severity of Tachycardia can be increased when Nabiximols is combined with Clenbuterol.
2,5-Dimethoxy-4-ethylamphetamine The risk or severity of Tachycardia can be increased when Nabiximols is combined with 2,5-Dimethoxy-4-ethylamphetamine.
Chlorphentermine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Chlorphentermine.
Tetryzoline The risk or severity of Tachycardia can be increased when Nabiximols is combined with Tetryzoline.
Tyramine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Tyramine.
Isoxsuprine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Isoxsuprine.
Etilefrine The risk or severity of Tachycardia can be increased when Nabiximols is combined with Etilefrine.

Target Protein

Cannabinoid receptor 1 CNR1
Cannabinoid receptor 2 CNR2
G-protein coupled receptor 12 GPR12
Glycine receptor subunit alpha-1 GLRA1
Glycine receptor (alpha-1/beta) GLRA1
Glycine receptor subunit alpha-3 GLRA3
N-arachidonyl glycine receptor GPR18
G-protein coupled receptor 55 GPR55
5-hydroxytryptamine receptor 1A HTR1A
5-hydroxytryptamine receptor 2A HTR2A
Neuronal acetylcholine receptor subunit alpha-7 CHRNA7
Delta-type opioid receptor OPRD1
Mu-type opioid receptor OPRM1
Peroxisome proliferator-activated receptor gamma PPARG
Transient receptor potential cation channel subfamily V member 1 TRPV1
Voltage-dependent T-type calcium channel subunit alpha-1G CACNA1G
Voltage-dependent T-type calcium channel subunit alpha-1H CACNA1H
Voltage-dependent T-type calcium channel subunit alpha-1I CACNA1I
Transient receptor potential cation channel subfamily A member 1 TRPA1
Transient receptor potential cation channel subfamily M member 8 TRPM8
Transient receptor potential cation channel subfamily V member 2 TRPV2
Transient receptor potential cation channel subfamily V member 3 TRPV3
Transient receptor potential cation channel subfamily V member 4 TRPV4
Non-selective voltage-gated ion channel VDAC1 VDAC1
Prostaglandin G/H synthase 1 PTGS1
Prostaglandin G/H synthase 2 PTGS2
Acetyl-CoA acetyltransferase, mitochondrial ACAT1
Steroid 17-alpha-hydroxylase/17,20 lyase CYP17A1
3-hydroxy-3-methylglutaryl-coenzyme A reductase HMGCR
Glutathione reductase, mitochondrial GSR
Glutathione peroxidase 1 GPX1
Indoleamine 2,3-dioxygenase 1 IDO1
Serotonin N-acetyltransferase AANAT
Cytochrome P450 1B1 CYP1B1
Cytochrome P450 3A5 CYP3A5
Cytochrome P450 2D6 CYP2D6
Cytochrome P450 1A2 CYP1A2
Cytochrome P450 1A1 CYP1A1
Cytochrome P450 3A7 CYP3A7
Quinone oxidoreductase CRYZ
Catalase CAT
Fatty-acid amide hydrolase 1 FAAH
Superoxide dismutase [Cu-Zn] SOD1
N-acylethanolamine-hydrolyzing acid amidase NAAA

Referensi & Sumber

Artikel (PubMed)
  • PMID: 17828291
    Pertwee RG: The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: delta9-tetrahydrocannabinol, cannabidiol and delta9-tetrahydrocannabivarin. Br J Pharmacol. 2008 Jan;153(2):199-215. doi: 10.1038/sj.bjp.0707442. Epub 2007 Sep 10.
  • PMID: 26218440
    Laprairie RB, Bagher AM, Kelly ME, Denovan-Wright EM: Cannabidiol is a negative allosteric modulator of the cannabinoid CB1 receptor. Br J Pharmacol. 2015 Oct;172(20):4790-805. doi: 10.1111/bph.13250. Epub 2015 Oct 13.
  • PMID: 26264914
    Ibeas Bih C, Chen T, Nunn AV, Bazelot M, Dallas M, Whalley BJ: Molecular Targets of Cannabidiol in Neurological Disorders. Neurotherapeutics. 2015 Oct;12(4):699-730. doi: 10.1007/s13311-015-0377-3.
  • PMID: 24281562
    Zhornitsky S, Potvin S: Cannabidiol in humans-the quest for therapeutic targets. Pharmaceuticals (Basel). 2012 May 21;5(5):529-52. doi: 10.3390/ph5050529.
  • PMID: 24160757
    Stout SM, Cimino NM: Exogenous cannabinoids as substrates, inhibitors, and inducers of human drug metabolizing enzymes: a systematic review. Drug Metab Rev. 2014 Feb;46(1):86-95. doi: 10.3109/03602532.2013.849268. Epub 2013 Oct 25.
  • PMID: 23408483
    Sharma P, Murthy P, Bharath MM: Chemistry, metabolism, and toxicology of cannabis: clinical implications. Iran J Psychiatry. 2012 Fall;7(4):149-56.

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