Cannabinoidi
I cannabinoidi sono una classe di composti chimici diversi derivati dagli acidi grassi o dai polichetoidi, che agiscono sui recettori dei cannabinoidi nelle cellule, alterando il rilascio di neurotrasmettitori nel cervello. Presenti principalmente nelle piante di cannabis, cannabinoidi come il THC e il CBD sono ampiamente studiati per i loro effetti terapeutici, tra cui il sollievo dal dolore, le proprietà anti-infiammatorie e il loro potenziale utilizzo nelle malattie neurodegenerative. Da CymitQuimica troverai una vasta gamma di cannabinoidi per la ricerca in farmacologia, neurobiologia e chimica medica.
Trovati 318 prodotti di "Cannabinoidi"
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S-Methoprene
CAS:<p>S-Methoprene (ZR2458), a juvenile hormone analog, acts as an insecticide influencing redox activity and male sex differentiation.</p>Formula:C19H34O3Purezza:97.05% - 98.55%Colore e forma:SolidPeso molecolare:310.47(-)-Isoperitenone
CAS:Prodotto controllato<p>Applications (-)-Isoperitenone, is a derivative of (-)-Cannabidiol (C175300), a major, non psychotropic constituent of cannabis.<br>References Hanus, L. et al.: Organic & Biomolecular Chemistry, Vol.3, Issue 6 (2005);<br></p>Formula:C10H14OColore e forma:NeatPeso molecolare:150.22CB1/2 agonist 3
CAS:CB1/2 agonist 3 is a competitive and potent CB1/CB2 agonist with high affinity for hCB1 and hCB2 and can be used to study neurological disorders.Formula:C25H41NO2Purezza:98.78%Colore e forma:SolidPeso molecolare:387.6APD 371
CAS:<p>A selective cannabinoid receptor type 2 (CB2) agonist. Commonly, CB2 agonists induce receptor internalization, which results in desensitization and tachyphylaxis. However, APD 371 mediates efficient recycling of internalized receptors back to the plasma membrane and thus sustains analgesic effects, upon subchronic treatment, in an osteoarthritis pain model in vivo.</p>Formula:C18H23N5O3Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:357.41 g/molCannabigerovarinic acid
CAS:Prodotto controllato<p>Cannabigerovarinic acid is a phytocannabinoid and the precursor to tetrahydrocannabivarinic acid, cannabidivarinic acid, and cannabichromevarinic acid1. No in vitro or in vivo pharmacological and toxicological studies have been conducted on cannabigerovarinic acid.</p>Formula:C20H28O4Purezza:Min. 95%Peso molecolare:332.43 g/molrel-(1R,2S)-8-Bromo-1-(3-bromo-4-hydroxy-5-methoxyphenyl)-1,2-dihydro-7-hydroxy-N2,N3-bis[2-(4-hydroxyphenyl)ethyl]-6-methoxy-2,3-na phthalenedicarboxamide
CAS:<p>rel-(1R,2S)-8-Bromo-1-(3-bromo-4-hydroxy-5-methoxyphenyl)-1,2-dihydro-7-hydroxy-N2,N3-bis[2-(4-hydroxyphenyl)ethyl]-6-methoxy-2,3-naphthalenedicarboxamide is a synthetic chemical compound, which is derived through targeted organic synthesis and structural optimization efforts. Its source lies in advanced laboratory methodologies designed to enhance specific pharmacological properties. The mode of action is expected to involve selective interaction with particular molecular targets, potentially modulating distinct pathways related to cellular function or signaling processes.</p>Formula:C36H34Br2N2O8Purezza:Min. 95%Colore e forma:PowderPeso molecolare:782.47 g/molGW 833972A
CAS:<p>A cannabinoid receptor agonist, which binds more selectively to CB2 than CB1 receptors (1000-fold). GW833972A inhibits vagus nerve depolarization induced by tussive agents, such as hypertonic saline (EC50 = 6.5 μM), capsaicin (EC50 = 33.9 μM) or PGE2 (EC50 = 15.9 μM).</p>Formula:C18H13ClF3N5OPurezza:Min. 95%Colore e forma:White To Off-White SolidPeso molecolare:407.78 g/molGW 833972A hydrochloride
CAS:<p>A cannabinoid receptor agonist, which binds more selectively to CB2 than CB1 receptors (1000-fold). GW833972A inhibits vagus nerve depolarization induced by tussive agents, such as hypertonic saline (EC50 = 6.5 μM), capsaicin (EC50 = 33.9 μM) or PGE2 (EC50 = 15.9 μM).</p>Formula:C18H13ClF3N5O·HClPurezza:Min. 95%Colore e forma:White/Off-White SolidPeso molecolare:444.24 g/molACEA, 5mg/ml solution in ethanol
CAS:<p>Cannabinoid type 1 (CB1) receptor agonist. Anti-depressant activity demonstrated in vivo alone, as well as enhancing the effect of fluoxetine. In the brain, ACEA activates CB1 receptors expressed in the mitochondria of neuronal cells to elicit neuroprotective effects. This is mediated by inducing glycogen synthase kinase-3β (GSK-3β) phosphorylation and inhibiting the opening of mitochondrial permeability transition pore (MPTP).<br>Sold by weight of solid</p>Formula:C22H36ClNOPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:365.98 g/mol1,2,3,9-Tetrahydro-4H-carbazol-4-one
CAS:<p>1,2,3,9-Tetrahydro-4H-carbazol-4-one is a cyclic ketone compound, which can be synthesized through various organic reactions involving appropriate precursors. It is often derived from indole-based substrates through catalytic hydrogenation, allowing the formation of its stable tetrahydro structure with a retained core carbazole skeleton.</p>Formula:C12H11NOPurezza:Min. 95%Colore e forma:PowderPeso molecolare:185.23 g/molC2
CAS:Positive allosteric modulator (PAM) of cannabinoid receptors CB2. The C2 modulator is the first synthetic PAM of CB2 receptors with antinociceptive properties, which were observed in a mouse model of neuropathic pain.Formula:C21H24BrFN2O2Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:435.33 g/molAnandamide
CAS:<p>Anandamide is an endogenous cannabinoid, which is a bioactive lipid mediator primarily found in the brain and peripheral organs. It is synthesized from membrane phospholipid precursors through enzymatic pathways, primarily involving the enzyme N-acyl phosphatidylethanolamine phospholipase D (NAPE-PLD). Anandamide acts as a ligand for cannabinoid receptors, mainly the CB1 receptor located in the central nervous system, and the CB2 receptor found in peripheral tissues.</p>Formula:C22H37NO2Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:347.53 g/molCannabichromenic Acid
CAS:<p>Cannabichromenic acid is a non-psychoactive phytocannabinoid and a precursor of cannabichromene1 which toxicological and pharmacological properties are unknown. Due to its structural similarity to cannabichromene, it is thought to reportedly exert anti-analgesic and anti-inflammatory activity.</p>Formula:C22H30O4Purezza:Min. 95%Peso molecolare:358.47 g/molAbnormal 1''-Hydroxycannabidiol
Prodotto controllatoFormula:C21H30O3Colore e forma:NeatPeso molecolare:330.4615-(4-Hydroxypentyl)-1,3-benzenediol
CAS:Prodotto controllato<p>Applications 5-(4-Hydroxypentyl)-1,3-benzenediol is an intermediate used in the synthesis of 4''-Hydroxycannabidiol (H824830), which is a metabolite of Canabidiol (C175300), a major constituents in marijuana. 4''-Hydroxycannabidiol be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.<br>References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)<br></p>Formula:C11H16O3Colore e forma:NeatPeso molecolare:196.24Cannabigerovarinic acid
CAS:Carboxylic acid with phenol functionFormula:C20H28O4Purezza:≥ 90.0 % (HPLC)Colore e forma:PowderPeso molecolare:332.43Dehydroabiethylamine
CAS:Dehydroabiethylamine (NSC-2955) boosts liver CYP2B, blocks PDKs & cholesterol transport, and has anti-tumor effects.Formula:C20H31NPurezza:98.79%Colore e forma:Pale Yellow Viscous Liquid /Technical Grade/ Viscous Colorless To Amber LiquidPeso molecolare:285.47UR-144 N-Pentanoic Acid
CAS:Prodotto controllatoFormula:C21H27NO3Colore e forma:NeatPeso molecolare:341.442-[(9Z)-9-Octadecenyloxy]-1,3-propanediol
CAS:Prodotto controllato<p>Applications 2-[(9Z)-9-Octadecenyloxy]-1,3-propanediol, which is an endogenous cannabinoid receptor ligand.<br>References Suhara, Y. et al.: Chem. Pharm. Bull., 48, 903 (2000);<br></p>Formula:C21H42O3Colore e forma:NeatPeso molecolare:342.56(1S,4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol
CAS:Prodotto controllato<p>Applications 1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol is an acetal reagent used in the synthesis of desoxy cannabidiols and THC (T293202) related psychoactive compounds. It is formed from (+)-Limonene using a photosynthesized O2 transfer.<br>References Wilkinson, S. et al.: Tetrahedron Lett., 54, 52 (2013);<br></p>Formula:C10H16OColore e forma:NeatPeso molecolare:152.231-(3,5-Bis(benzyloxy)phenyl)pentan-1-ol
CAS:Prodotto controllatoFormula:C25H28O3Colore e forma:NeatPeso molecolare:376.491-(3,5-Bis(benzyloxy)phenyl)pent-1-en-3-one
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications (Z)-1-(3,5-Bis(benzyloxy)phenyl)pent-1-en-3-one is a reagent in the synthesis of 3''-Hydroxycannabidiol (H824825) which is a major constituents in marijuana. 3''-Hydroxycannabidiol be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.<br>References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)<br></p>Formula:C25H24O3Colore e forma:NeatPeso molecolare:372.46Ethyl 2-Oxopentanoate
CAS:Prodotto controllato<p>Applications Ethyl 2-oxopentanoate is used as a reagent to synthesize selective CB1 cannabinoid receptor antagonists. Ethyl 2-oxopentanoate is also used to synthesize derivatives of iminodiacid, an inhibitor of angiotensin converting enzyme.<br>References Lange, J., et al.: J. Med. Chem., 48, 1823 (2005); Vincent, M., et al.: Tetrahedron Lett., 23, 1677 (2982)<br></p>Formula:C7H12O3Colore e forma:NeatPeso molecolare:144.17Cannabigerorcinic Acid
CAS:Prodotto controllato<p>Stability Light Sensitive<br>Applications Cannabigerorcinic Acid is a compound that takes part in the biosynthesis of daurichromenic acid synthase which is active in anti-HIV biosynthesis.<br>References Iijima, M. et al.: Plant Phys., 174, 2213 (2017);<br></p>Formula:C18H24O4Colore e forma:NeatPeso molecolare:304.382-Arachidonyl glycerol
CAS:<p>2-Arachidonyl glycerol is an endogenous cannabinoid receptor agonist, which is derived from arachidonic acid present in cellular membranes. It functions as a signaling lipid and plays a critical role in the endocannabinoid system, which is a complex network of receptors and ligands involved in maintaining physiological homeostasis.</p>Formula:C23H38O4Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:378.55 g/molOMDM-6
CAS:OMDM-6 is a dual agonist of TRPV1(EC50 = 75 nM) and CB1 (Ki = 3.2 μM). OMDM-6 inhibits anandamide cellular uptake with a Ki of 7.0 μM.Formula:C28H42N2O3Purezza:99.66%Colore e forma:SolidPeso molecolare:454.64LEI 101 hydrochloride
CAS:LEI 101 hydrochloride is potent and selective CB2 partial agonist.Formula:C23H26ClFN4O4SColore e forma:SolidPeso molecolare:508.99N-Arachidonyldopamine
CAS:N-Arachidonyldopamine (NADA) is a selective and potent endogenous CB1 receptor agonist (Ki: 250 nM).N-Arachidonyldopamine is also a potent and selective TRPV1Formula:C28H41NO3Purezza:97.65%Colore e forma:SolidPeso molecolare:439.63AM404
CAS:AM404 is a cannabinoid reuptake inhibitor and a TRPV (1) activator with neuroprotective and anticancer activities that blocks anandamide transport.Formula:C26H37NO2Colore e forma:SolidPeso molecolare:395.58CB2R agonist 1
CAS:CB2R agonist 1 selectively binds human CB2R, EC50 of 0.56 µM, modulates inflammatory cytokines.Formula:C22H32N2OColore e forma:SolidPeso molecolare:340.5Virodhamine trifluoroacetate
CAS:Virodhamine trifluoroacetate: full GPR55 & CB2 agonist, partial CB1 antagonist, cannabinoid receptor mixed antagonist.Formula:C24H38F3NO4Purezza:98%Colore e forma:SolidPeso molecolare:461.56Cannabicitran
CAS:Cannabicitran is a cannabinoid that can decrease rabbits intraocular pressure [1] [2].Formula:C21H30O2Colore e forma:SolidPeso molecolare:314.46CID1792197
CAS:CID1792197 is a selective agonist of GPR55.Formula:C24H23N3O4S2Purezza:98%Colore e forma:SolidPeso molecolare:481.59MJ 15
CAS:<p>MJ 15 is a CB1 receptor antagonist with specificity for the study of obesity-induced diseases.</p>Formula:C23H17Cl3N4OPurezza:99.63%Colore e forma:SolidPeso molecolare:471.77GPR55 agonist 3
CAS:<p>Compound 26, a GPR55 agonist, exhibits potent activity with EC50 values of 0.239 nM for hGPR55 and 1.76 nM for rGPR55.</p>Formula:C19H16F4N4Colore e forma:SolidPeso molecolare:376.35PM226
CAS:CB2 agonist with Ki of 12.8 nM; EC50 of 38.67 nM. Negligible CB1 affinity, no GPR55 activity. Anti-inflammatory, neuroprotective, crosses BBB.Formula:C22H31NO3Colore e forma:SolidPeso molecolare:357.49LBP-1
CAS:LBP-1 is a cannabinoid receptor type 1 (CB1) agonist.Formula:C23H29ClN6O3Colore e forma:SolidPeso molecolare:472.97TC-C 14G
CAS:CB1 receptor inverse agonistFormula:C24H17Cl2F2NO4Purezza:98%Colore e forma:SolidPeso molecolare:492.3ZCZ011
CAS:ZCZ011 enhances CB1 receptor effects, crosses blood-brain barrier, and potentiates cannabimimetic behaviors in mice.Formula:C21H18N2O2SPurezza:98%Colore e forma:SolidPeso molecolare:362.44AZD-2207
CAS:AZD-2207 is a cannabinoid receptor CB1 antagonist and highly lipophilic compound for the treatment of type 2 diabetes mellitus and obesity.Formula:C25H25Cl2F3N4O4SColore e forma:SolidPeso molecolare:605.46MM-22
CAS:biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamideFormula:C36H60N4O5SPurezza:98%Colore e forma:SolidPeso molecolare:660.95Palmitoyl serinol
CAS:Anticancer agent 110 is an anticancer compound with cytotoxic, antitumor and antileukemic activities.Formula:C19H39NO3Colore e forma:SolidPeso molecolare:329.52UCM 707
CAS:endocannabinoid transport inhibitorFormula:C25H37NO2Purezza:98%Colore e forma:SolidPeso molecolare:383.57
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