Cannabidiol, or CBD, is one of at least 85 active cannabinoids identified within the Cannabis plant. It is a major phytocannabinoid, accounting for up to 40% of the Cannabis plant's extract, that binds to a wide variety of physiological targets of the endocannabinoid system within the body. Although the exact medical implications are currently being investigated, CBD has shown promise as a therapeutic and pharmaceutical drug target. In particular, CBD has shown promise as an analgesic, anticonvulsant, muscle relaxant, anxiolytic, antipsychotic and has shown neuroprotective, anti-inflammatory, and antioxidant activity, among other currently investigated uses A32477, A32469. CBD's exact place within medical practice is still currently hotly debated, however as the body of evidence grows and legislation changes to reflect its wide-spread use, public and medical opinion have changed significantly with regards to its usefulness in a number of medical conditions ranging from anxiety to epilepsy.
From a pharmacological perspective, Cannabis' (and CBD's) 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 endogenous cannabinoid receptors of the body A32584. Cannabinoid receptors are utilized endogenously by the body through the endocannabinoid system, which includes a group of lipid proteins, enzymes, and receptors that are involved in many physiological processes. Through its modulation of neurotransmitter release, the endocannabinoid system regulates cognition, pain sensation, appetite, memory, sleep, immune function, and mood among many other bodily systems. These effects are largely mediated through two members of the G-protein coupled receptor family, cannabinoid receptors 1 and 2 (CB1 and CB2)A32585,A32824. CB1 receptors are found in both the central and peripheral nervous systems, with the majority of receptors localized to the hippocampus and amygdala of the brain. Physiological effects of using cannabis make sense in the context of its receptor activity as the hippocampus and amygdala are primarily involved with regulation of memory, fear, and emotion. In contrast, CB2 receptors are mainly found peripherally in immune cells, lymphoid tissue, and peripheral nerve terminals A32676.
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 that are found throughout the body. Although THC and CBD have been the most studied cannabinoids, there are many others identified to date including cannabinol (CBN), cannabigerol (CBG), DB14050 (CBDV), and DB11755 (THCV) that can be found within the medical cannabis A32830. While both CBD and THC are used for medicinal purposes, they have different receptor activity, function, and physiological effects. If not provided in their activated form (such as through synthetic forms of THC like DB00470 or DB00486), THC and CBD are obtained through conversion from their precursors, tetrahydrocannabinolic acid-A (THCA-A) and cannabidiolic acid (CBDA), through decarboxylation reactions. This can be achieved through heating, smoking, vaporization, or baking of dried unfertilized female cannabis flowers.
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 which is clinically significant as direct agonists (such as THC) are limited by their psychomimetic effects such as changes to mood, memory, and anxietyA32469.
In addition to the well-known activity on CB1 and CB2 receptors, there is further evidence that CBD also activates 5-HT1A/2A/3A serotonergic and TRPV1–2 vanilloid receptors, antagonizes alpha-1 adrenergic and µ-opioid receptors, inhibits synaptosomal uptake of noradrenaline, dopamine, serotonin and gamma-aminobutyric acid (GABA), and cellular uptake of anandamide, acts on mitochondria Ca2+ stores, blocks low-voltage-activated (T-type) Ca2+ channels, stimulates activity of the inhibitory glycine-receptor, and inhibits activity of fatty amide hydrolase (FAAH) A31555, A31574.
CBD is currently available in Canada within a 1:1 formulation with tetrahydrocannbinol (THC) (as the formulation known as "nabiximols") as the brand name product Sativex. It is approved for use as adjunctive treatment for symptomatic relief of spasticity in adult patients with multiple sclerosis (MS). Sativex was also given a conditional Notice of Compliance (NOC/c) for use as adjunctive treatment for the symptomatic relief of neuropathic pain in adult patients with multiple sclerosis and as adjunctive analgesic treatment for moderate to severe pain in adult patients with advanced cancer L886.
In April 2018, a Food and Drug Administration advisory panel unanimously recommended approval of Epidiolex (cannabidiol oral solution) for the treatment of two rare forms of epilepsy - Lennox-Gastaut syndrome and Dravet syndrome, which are among the two most difficult types of epilepsy to treat L2721, L2719. Epidiolex was granted Orphan Drug designation as well as Fast Track Approval from the FDA for further study in these hard to treat conditions. Notably, phase 3 clinical trials of Epidiolex have demonstrated clinically significant improvement in Lennox-Gastaut syndrome and Dravet syndrome L2720. On June 25th, 2018, Epidiolex was approved by the FDA to be the first CBD-based product available on the US market.
Fitur visualisasi ini dikembangkan menggunakan pendekatan Graph Theory untuk memetakan hubungan polifarmasi dan molekuler. Entitas (Obat, Target, Gen) direpresentasikan sebagai Simpul (Nodes), sedangkan hubungan biologisnya sebagai Sisi (Edges).
drugbank-id dan name pada skema XML DrugBank.targets/target yang memuat polipeptida sasaran.gene-name dan varian snp-effects.Tata letak grafik menggunakan algoritma Force-Directed Graph (Barnes-Hut). Model fisika ini menerapkan gaya tolak-menolak antar simpul (Gravitasi: -3000) agar tidak tumpang tindih, serta gaya pegas (Spring: 0.04) pada garis penghubung untuk fleksibilitas interaksi.
| Cilostazol | The serum concentration of Cilostazol can be increased when it is combined with Cannabidiol. |
| Ramipril | Cannabidiol may decrease the antihypertensive activities of Ramipril. |
| Remikiren | Cannabidiol may decrease the antihypertensive activities of Remikiren. |
| Guanadrel | Cannabidiol may decrease the antihypertensive activities of Guanadrel. |
| Olmesartan | Cannabidiol may decrease the antihypertensive activities of Olmesartan. |
| Chlorthalidone | Cannabidiol may decrease the antihypertensive activities of Chlorthalidone. |
| Nitroprusside | Cannabidiol may decrease the antihypertensive activities of Nitroprusside. |
| Minoxidil | Cannabidiol may decrease the antihypertensive activities of Minoxidil. |
| Bendroflumethiazide | Cannabidiol may decrease the antihypertensive activities of Bendroflumethiazide. |
| Fosinopril | Cannabidiol may decrease the antihypertensive activities of Fosinopril. |
| Trandolapril | Cannabidiol may decrease the antihypertensive activities of Trandolapril. |
| Metolazone | Cannabidiol may decrease the antihypertensive activities of Metolazone. |
| Benazepril | Cannabidiol may decrease the antihypertensive activities of Benazepril. |
| Cyclothiazide | Cannabidiol may decrease the antihypertensive activities of Cyclothiazide. |
| Candoxatril | Cannabidiol may decrease the antihypertensive activities of Candoxatril. |
| Mecamylamine | Cannabidiol may decrease the antihypertensive activities of Mecamylamine. |
| Moexipril | Cannabidiol may decrease the antihypertensive activities of Moexipril. |
| Lisinopril | Cannabidiol may decrease the antihypertensive activities of Lisinopril. |
| Nitroglycerin | Cannabidiol may decrease the antihypertensive activities of Nitroglycerin. |
| Hydroflumethiazide | Cannabidiol may decrease the antihypertensive activities of Hydroflumethiazide. |
| Cryptenamine | Cannabidiol may decrease the antihypertensive activities of Cryptenamine. |
| Perindopril | Cannabidiol may decrease the antihypertensive activities of Perindopril. |
| Fenoldopam | Cannabidiol may decrease the antihypertensive activities of Fenoldopam. |
| Eprosartan | Cannabidiol may decrease the antihypertensive activities of Eprosartan. |
| Chlorothiazide | Cannabidiol may decrease the antihypertensive activities of Chlorothiazide. |
| Quinapril | Cannabidiol may decrease the antihypertensive activities of Quinapril. |
| Telmisartan | The metabolism of Cannabidiol can be decreased when combined with Telmisartan. |
| Methyldopa | Cannabidiol may decrease the antihypertensive activities of Methyldopa. |
| Hydrochlorothiazide | Cannabidiol may decrease the antihypertensive activities of Hydrochlorothiazide. |
| Trichlormethiazide | Cannabidiol may decrease the antihypertensive activities of Trichlormethiazide. |
| Deserpidine | Cannabidiol may decrease the antihypertensive activities of Deserpidine. |
| Pentolinium | Cannabidiol may decrease the antihypertensive activities of Pentolinium. |
| Trimethaphan | Cannabidiol may decrease the antihypertensive activities of Trimethaphan. |
| Diazoxide | Cannabidiol may decrease the antihypertensive activities of Diazoxide. |
| Bretylium | Cannabidiol may decrease the antihypertensive activities of Bretylium. |
| Terazosin | Cannabidiol may decrease the antihypertensive activities of Terazosin. |
| Captopril | Cannabidiol may decrease the antihypertensive activities of Captopril. |
| Epoprostenol | Cannabidiol may decrease the antihypertensive activities of Epoprostenol. |
| Polythiazide | Cannabidiol may decrease the antihypertensive activities of Polythiazide. |
| Cilazapril | Cannabidiol may decrease the antihypertensive activities of Cilazapril. |
| Saprisartan | Cannabidiol may decrease the antihypertensive activities of Saprisartan. |
| Spirapril | Cannabidiol may decrease the antihypertensive activities of Spirapril. |
| Dexpropranolol | Cannabidiol may decrease the antihypertensive activities of Dexpropranolol. |
| Diethylnorspermine | Cannabidiol may decrease the antihypertensive activities of Diethylnorspermine. |
| Temocapril | Cannabidiol may decrease the antihypertensive activities of Temocapril. |
| Trimazosin | Cannabidiol may decrease the antihypertensive activities of Trimazosin. |
| Nicorandil | Cannabidiol may decrease the antihypertensive activities of Nicorandil. |
| Rauwolfia serpentina root | Cannabidiol may decrease the antihypertensive activities of Rauwolfia serpentina root. |
| Enalaprilat | Cannabidiol may decrease the antihypertensive activities of Enalaprilat. |
| Angiotensin 1-7 | Cannabidiol may decrease the antihypertensive activities of Angiotensin 1-7. |
| Imidapril | Cannabidiol may decrease the antihypertensive activities of Imidapril. |
| BQ-123 | Cannabidiol may decrease the antihypertensive activities of BQ-123. |
| Cicletanine | Cannabidiol may decrease the antihypertensive activities of Cicletanine. |
| Zofenopril | Cannabidiol may decrease the antihypertensive activities of Zofenopril. |
| Guanoxan | Cannabidiol may decrease the antihypertensive activities of Guanoxan. |
| Delapril | Cannabidiol may decrease the antihypertensive activities of Delapril. |
| Vincamine | Cannabidiol may decrease the antihypertensive activities of Vincamine. |
| Linsidomine | Cannabidiol may decrease the antihypertensive activities of Linsidomine. |
| Guanoxabenz | Cannabidiol may decrease the antihypertensive activities of Guanoxabenz. |
| Tolonidine | Cannabidiol may decrease the antihypertensive activities of Tolonidine. |
| Endralazine | Cannabidiol may decrease the antihypertensive activities of Endralazine. |
| Cadralazine | Cannabidiol may decrease the antihypertensive activities of Cadralazine. |
| Cyclopenthiazide | Cannabidiol may decrease the antihypertensive activities of Cyclopenthiazide. |
| Bietaserpine | Cannabidiol may decrease the antihypertensive activities of Bietaserpine. |
| Guanazodine | Cannabidiol may decrease the antihypertensive activities of Guanazodine. |
| Methoserpidine | Cannabidiol may decrease the antihypertensive activities of Methoserpidine. |
| Guanoclor | Cannabidiol may decrease the antihypertensive activities of Guanoclor. |
| Muzolimine | Cannabidiol may decrease the antihypertensive activities of Muzolimine. |
| Xipamide | Cannabidiol may decrease the antihypertensive activities of Xipamide. |
| Tocopherylquinone | Cannabidiol may decrease the antihypertensive activities of Tocopherylquinone. |
| Benazeprilat | Cannabidiol may decrease the antihypertensive activities of Benazeprilat. |
| Fosinoprilat | Cannabidiol may decrease the antihypertensive activities of Fosinoprilat. |
| Ramiprilat | Cannabidiol may decrease the antihypertensive activities of Ramiprilat. |
| Perindoprilat | Cannabidiol may decrease the antihypertensive activities of Perindoprilat. |
| Quinaprilat | Cannabidiol may decrease the antihypertensive activities of Quinaprilat. |
| Furosemide | Cannabidiol may decrease the antihypertensive activities of Furosemide. |
| Enalapril | Cannabidiol may decrease the antihypertensive activities of Enalapril. |
| Nimodipine | Cannabidiol may decrease the antihypertensive activities of Nimodipine. |
| Bisoprolol | Cannabidiol may decrease the antihypertensive activities of Bisoprolol. |
| Indapamide | Cannabidiol may decrease the antihypertensive activities of Indapamide. |
| Irbesartan | The metabolism of Irbesartan can be decreased when combined with Cannabidiol. |
| Guanethidine | Cannabidiol may decrease the antihypertensive activities of Guanethidine. |
| Hydralazine | Cannabidiol may decrease the antihypertensive activities of Hydralazine. |
| Pinacidil | Cannabidiol may decrease the antihypertensive activities of Pinacidil. |
| Macitentan | Cannabidiol may decrease the antihypertensive activities of Macitentan. |
| Aliskiren | Cannabidiol may decrease the antihypertensive activities of Aliskiren. |
| Efonidipine | Cannabidiol may decrease the antihypertensive activities of Efonidipine. |
| Lacidipine | Cannabidiol may decrease the antihypertensive activities of Lacidipine. |
| Niguldipine | Cannabidiol may decrease the antihypertensive activities of Niguldipine. |
| Selexipag | The metabolism of Selexipag can be decreased when combined with Cannabidiol. |
| Naftopidil | Cannabidiol may decrease the antihypertensive activities of Naftopidil. |
| Dexniguldipine | Cannabidiol may decrease the antihypertensive activities of Dexniguldipine. |
| Amlodipine | The metabolism of Cannabidiol can be decreased when combined with Amlodipine. |
| Buthiazide | Cannabidiol may decrease the antihypertensive activities of Buthiazide. |
| Esmolol | The metabolism of Esmolol can be decreased when combined with Cannabidiol. |
| Betaxolol | The metabolism of Betaxolol can be decreased when combined with Cannabidiol. |
| Metoprolol | The metabolism of Metoprolol can be decreased when combined with Cannabidiol. |
| Atenolol | The metabolism of Atenolol can be decreased when combined with Cannabidiol. |
| Timolol | The metabolism of Timolol can be decreased when combined with Cannabidiol. |
| Guanabenz | The metabolism of Guanabenz can be decreased when combined with Cannabidiol. |