Récepteur cannabinoïde
Les récepteurs cannabinoïdes sont des GPCR qui médiatisent les effets des cannabinoïdes endogènes (endocannabinoïdes) et des phytocannabinoïdes, tels que ceux trouvés dans le cannabis. Les deux principaux types de récepteurs cannabinoïdes, CB1 et CB2, sont impliqués dans la régulation d'une large gamme de processus physiologiques, y compris la perception de la douleur, l'appétit, l'humeur et la fonction immunitaire. Les modulateurs des récepteurs cannabinoïdes ont un potentiel thérapeutique dans le traitement de conditions telles que la douleur chronique, l'épilepsie et la sclérose en plaques. Chez CymitQuimica, nous offrons une large gamme de modulateurs de récepteurs cannabinoïdes de haute qualité pour soutenir vos recherches en neuropharmacologie, gestion de la douleur et immunologie.
196 produits trouvés pour "Récepteur cannabinoïde"
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EHP-101
CAS :<p>EHP-101 is a PPARγ/CB2 dual agonist with anti-inflammatory properties, inhibits fat formation, and combats diet-related obesity.</p>Formule :C28H35NO3Degré de pureté :98.36%Couleur et forme :SolidMasse moléculaire :433.58Rimonabant
CAS :<p>Rimonabant (SR141716) is an inverse agonist for the cannabinoid receptor CB1.</p>Formule :C22H21Cl3N4ODegré de pureté :98% - 99.91%Couleur et forme :White Or Almost White Crystalline PowderMasse moléculaire :463.79JHU 75528
CAS :<p>JHU 75528 (JHU-75528) is a novel PET tracer with inhibitory effects on CB that can be used to study the cannabinoid system in schizophrenic patients.</p>Formule :C23H21Cl2N5O2Degré de pureté :99.79%Couleur et forme :SolidMasse moléculaire :470.35Pregnenolone
CAS :<p>Pregnenolone (Arthenolone) is an endogenous steroid hormone synthesized from cholesterol, used in the treatment of Alzheimer's disease.</p>Formule :C21H32O2Degré de pureté :99.5% - >99.99%Couleur et forme :SolidMasse moléculaire :316.48Anandamide
CAS :<p>Anandamide ((5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide), an immune modulator, acts via not only cannabinoid receptors (CB1 and CB2) but also</p>Formule :C22H37NO2Degré de pureté :95.037% - 99.22%Couleur et forme :Light Yellow OilMasse moléculaire :347.53Rimonabant hydrochloride
CAS :<p>Rimonabant hydrochloride (SR 141716A) 是中心大麻素受体 1 的高效选择性反向激动剂， Ki 值为1.8 nM。它也能够抑制分枝杆菌膜蛋白3。</p>Formule :C22H22Cl4N4ODegré de pureté :98.24% - 99.5%Couleur et forme :Off-White To White Crystalline PowderMasse moléculaire :500.25CB1 antagonist 2
CAS :<p>CB1 antagonist 2 (AM4113) is caimabinoid 1 (CB1) antagonist which inhibits CB1 in vivo with an IC50 of 25.5 nM.</p>Formule :C17H12Cl3N3ODegré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :380.666-Iodopravadoline
CAS :<p>6-Iodopravadoline (AM630) is an antagonist of CB2 (Ki: 31.2 nM). And it shows 165-fold selectivity more than CB1 receptors.</p>Formule :C23H25IN2O3Degré de pureté :99.29%Couleur et forme :Off-White SolidMasse moléculaire :504.36exo-Tetrahydrocannabivarin
CAS :<p>exo-Tetrahydrocannabivarin (Compound 12) is an analog of Δ9,11-THC. It weakly binds to cannabinoid receptors (CB) with an IC50 of 1.4 μM. In mice, exo-Tetrahydrocannabivarin exhibits activity related to both motor function and analgesia.</p>Formule :C19H26O2Couleur et forme :SolidMasse moléculaire :286.41Hemopressin(human, mouse) TFA
CAS :<p>Hemopressin TFA: nonapeptide from hemoglobin, oral CB1 inverse agonist, eases inflammatory pain.</p>Formule :C52H80F3N13O14Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1168.278β-Hydroxy-exo-THC
CAS :<p>8β-Hydroxy-exo-THC, a cannabinoid ether analog, exhibits weak affinity for receptor sites with an IC50 of 1.2 μM.</p>Formule :C21H30O3Couleur et forme :SolidMasse moléculaire :330.46Δ8-THC methyl ether
CAS :<p>Δ8-THC methyl ether (compound 3) demonstrates a strong docking score of -10.167 kcal/mol for the CB2 receptor. Additionally, Δ8-THC methyl ether exhibits antinociceptive activity in mice.</p>Formule :C22H32O2Couleur et forme :SolidMasse moléculaire :328.49CB2 PET Radioligand 1
<p>CB2 PET Radioligand 1 (compound [18F]9) is a positron emission tomography (PET) radioligand with high affinity for the human cannabinoid receptor 2 (hCB2, Ki=7.</p>Formule :C20H19F3N4ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :388.39CB2R agonist 3
<p>CB2R agonist 3, a potent activator of cannabinoid receptor 2 (CB2R), exhibits an EC50 value of 0.37μM, indicative of its significant role in the immune system [</p>Degré de pureté :98%Couleur et forme :Odour Solidδ8-THC acetate
CAS :<p>Delta8-THC acetate (Delta8-tetrahydrocannabinol) is a psychoactive cannabinoid that binds to the cannabinoid receptor 1 (CB1 receptor) and exhibits anti-nausea, appetite-stimulating, and anti-inflammatory effects. It may also offer neuroprotective benefits and has potential applications in research on anxiety and depression.</p>Formule :C23H32O3Couleur et forme :SolidMasse moléculaire :356.5Afubiata
CAS :<p>ADB-FUBIATA is a synthetic cannabinoid studied for its metabolic profile, along with AFUBIATA, CH-FUBIATA, and CH-PIATA. This in vitro analysis by Watanabe S, et al., examines these compounds, as published in "Arch Toxicol," 2023 Dec;97(12):3085-3094.</p>Formule :C27H29FN2OCouleur et forme :SolidMasse moléculaire :416.53CB2R/FAAH modulator-1
CAS :<p>CB2R/FAAH modulator-1: agonizes CB2R, inhibits FAAH (IC50=4 μM), alters cytokine production; used in inflammation research. Ki: CB2R=14.8 nM, CB1R=241.3 nM.</p>Formule :C24H27NO2Degré de pureté :99.77%Couleur et forme :SoildMasse moléculaire :361.48Tocrifluor T1117
CAS :<p>Fluorescent form of AM 251, CB1 receptor antagonist</p>Formule :C56H53Cl2N7O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :974.97APP-FUBINACA
CAS :<p>APP-FUBINACA is a cannabinoid receptor agonist, classified as a phenylalanine amide-based indazole-3-carboxamide derivative. It exhibits neurostimulatory effects.</p>Formule :C24H21FN4O2Couleur et forme :SolidMasse moléculaire :416.45CB2R/FAAH modulator-2
CAS :<p>CB2R/FAAH modulator-2 (compound 26) is a dual modulator targeting at CB2R and FAAH.</p>Formule :C24H33NO2Degré de pureté :99.15%Couleur et forme :SoildMasse moléculaire :367.52TRPV1/CB2 agonist 1
<p>TRPV1/CB2 agonist 1 (compound 41) is a dual agonist targeting hTRPV1 and CB2 receptors, with an EC50 value of 26.8 μM for hTRPV1. It is applicable in research related to the nervous system.</p>Couleur et forme :Odour SolidΔ8-THC-C8
CAS :<p>Δ8-THC-C8 is a semi-synthetic cannabinoid. It acts as an agonist for the cannabinoid receptor 1 (CB1) with an EC50 value of 13.8 nM.</p>Formule :C24H36O2Couleur et forme :SolidMasse moléculaire :356.54CB1R antagonist 2
<p>CB1R antagonist 2 (Compound 11g) functions as an antagonist of the cannabinoid receptor 1 (CB1R), inhibiting the MAPK/NF-κB signaling pathway and exhibiting anti-inflammatory properties. In RAW264.7 cells, it suppresses LPS-induced expression of IL-6, IL-1β, and TNF-α. In murine models, it improves OVA-induced allergic rhinitis.</p>Formule :C24H26N4OCouleur et forme :SolidMasse moléculaire :386.49(±)-9-Nor-9α-hydroxy Hexahydrocannabinol
CAS :<p>(±)-9-Nor-9α-hydroxy Hexahydrocannabinol is a cannabinoid-structured compound that exhibits potent cannabinoid-like activity in both dogs and mice.</p>Formule :C20H30O3Couleur et forme :SolidMasse moléculaire :318.45CB2 receptor agonist 9
CAS :<p>CB2 receptor agonist 9 (Compound 33) is an orally active agonist of cannabinoid receptor 2 (CB2 receptor) with an EC50 of 16.2 nM. It inhibits the expression of TNF-α, IL-1β, and IL-6, demonstrating anti-inflammatory activity in a DSS-induced acute colitis model in mice.</p>Formule :C16H23N3O2SCouleur et forme :SolidMasse moléculaire :321.44N-(1-(3,4-Dihydroxyphenyl)propan-2-yl)oleamide
CAS :<p>N-(1-(3,4-Dihydroxyphenyl)propan-2-yl)oleamide: binds CB1 (Ki=365 nM), activates PPARα (EC50=698 nM), reduces rat food intake, no FAAH inhibition.</p>Formule :C27H45NO3Couleur et forme :SolidMasse moléculaire :431.661Cannabidivarinic acid
CAS :<p>Cannabidivarinic acid (CBDVA), the carboxylic acid precursor to cannabidivarin (CBDV), is a non-psychoactive cannabinoid found in Cannabis and known for its anti-inflammatory properties.</p>Formule :C20H26O4Couleur et forme :SolidMasse moléculaire :330.42PSB-SB-1203
CAS :<p>PSB-SB-1203 (Compound 25b) is a dual CB1/CB2 ligand that blocks the CB1 receptor and activates the CB2 receptor with a CB1 Ki of 0.244 μM, a CB2 Ki of 0.210 μM, and an EC50 of 0.054 μM. It shows potential for research in obesity and cancer.</p>Formule :C25H30O4Couleur et forme :SolidMasse moléculaire :394.5CB2R agonist 2
<p>CB2R agonist 2 (cis-17-para) is a CB2R agonist [1].</p>Degré de pureté :98%Couleur et forme :Odour Solid(R)-Zevaquenabant
<p>(R)-Zevaquenabant ((R)-MRI-1867) is the enantiomer of Zevaquenabant. Zevaquenabant ((S)-MRI-1867) is a peripherally restricted, orally bioavailable dual antagonist of the cannabinoid CB1 receptor and inducible nitric oxide synthase (iNOS). It is beneficial in improving chronic kidney disease (CKD) caused by obesity.</p>Couleur et forme :Odour SolidCB2 receptor agonist 2
CAS :<p>CB2 receptor agonist 2 (ZINC72105556): potent, Ki=8.5 nM, high selectivity for CB2.</p>Formule :C30H36N2O4Degré de pureté :99.75%Couleur et forme :SolidMasse moléculaire :488.62Drinabant
CAS :<p>Drinabant (AVE-1625) is an orally active CB1 receptor antagonist.</p>Formule :C23H20Cl2F2N2O2SDegré de pureté :99.8%Couleur et forme :SolidMasse moléculaire :497.38GPR55 agonist 4
<p>GPR55 agonist 4 (Compound 28), with an EC50 of 131 nM for hGPR55 and 1.41 nM for rGPR55, effectively induces β-arrestin recruitment to human GPR55 [1].</p>Formule :C19H16FN5O2Couleur et forme :SolidMasse moléculaire :365.36Zevaquenabant
CAS :<p>Zevaquenabant (S-MRI-1867): oral CB1/iNOS antagonist combatting obesity-induced CKD.</p>Formule :C25H21ClF3N5O2SCouleur et forme :SolidMasse moléculaire :547.98GFB-024
<p>GFB-024 is a humanized antibody targeting CB1, which can be used to study obesity.</p>Couleur et forme :LiquidMasse moléculaire :145.5kDaRVD-Hpα
CAS :<p>N-terminally extended form of human hemopressin that acts as a selective CB1 receptor agonist.</p>Formule :C65H105N19O17Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1424.66Hemopressin(rat)
CAS :<p>Peptide inhibitor for ep24.15, neurolysin & ACE with Ki 27.76, 3.43, 1.87 μM. Lowers blood pressure, modulates CB1 receptor, reduces pain & food intake.</p>Formule :C53H77N13O12Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1088.27Vicasinabin
CAS :<p>Vicasinabin: potent CB2 agonist; researches chronic pain, atherosclerosis, bone mass, neuroinflammation.</p>Formule :C15H22N10OCouleur et forme :SolidMasse moléculaire :358.41Hemopressin (human, mouse)
CAS :<p>Endogenous peptide, inhibits ep24.15/24.16/ACE with Ki of 27.76/3.43/1.87 μM. Lowers blood pressure, CB1 inverse agonist, reduces pain in vivo.</p>Formule :C50H79N13O12Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :1054.26CB2R probe 1
CAS :<p>CB2R Probe 1, a cannabinoid 2 receptor (CB2R) fluorescent probe, exhibits both safety and environmental friendliness, boasting a dissociation constant (K i) of</p>Formule :C36H42N4O4Couleur et forme :SolidMasse moléculaire :594.74NESS 0327
CAS :<p>NESS 0327 is a high selectivity antagonist of the cannabinoid CB1 receptor. NESS 0327 is more than 60,000-fold selective for the CB1 receptor.</p>Formule :C24H23Cl3N4ODegré de pureté :99.78%Couleur et forme :SolidMasse moléculaire :489.82CB2R/FAAH modulator-3
CAS :<p>CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH.</p>Formule :C22H31NO2Degré de pureté :99.81%Couleur et forme :SoildMasse moléculaire :341.49Noladin ether
CAS :<p>Noladin ether (2-AG ether) is a cannabinoid CB1 receptor agonist.</p>Formule :C23H40O3Couleur et forme :SolidMasse moléculaire :364.56CB1R agonist 1
<p>CB1R agonist 1 (Compound '1350) is a potent full agonist of the cannabinoid-1 receptor (CB1R) with a Ki value of 0.95 nM. It demonstrates significant pain-relieving effects in various pain models, including acute thermal pain, inflammatory pain, and neuropathic pain.</p>Formule :C20H18F3N3O3SCouleur et forme :SolidMasse moléculaire :437.435VIP36
<p>VIP36 is an agonist of the cannabinoid type 1 receptor (CB1) with analgesic properties. It reduces the recruitment of inhibitory proteins, thereby exerting its pain-relieving effects, and is applicable in research related to chronic pain.</p>Formule :C27H35FN6O4Couleur et forme :SolidMasse moléculaire :526.603Taranabant racemate
CAS :<p>Taranabant racemate is an antagonist and/or inverse agonist of the Cannabinoid-1 (CB1) receptor.</p>Formule :C27H25ClF3N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :515.95Virodhamine
CAS :<p>Virodhamine (O-arachidonoyl ethanolamine), an endocannabinoid, is an antagonist of CB1 receptor and an agonist of CB2 receptor.</p>Formule :C22H37NO2Degré de pureté :98%Couleur et forme :SoildMasse moléculaire :347.53AM251
CAS :<p>AM251: potent CB1 blocker (IC50: 8 nM), 306x CB2 selective; GPR55 activator (EC50: 39 nM).</p>Formule :C22H21Cl2IN4ODegré de pureté :97.43% - 98.79%Couleur et forme :A Crystalline SolidMasse moléculaire :555.24A-836339
CAS :<p>A-836339: Potent cannabinoid, CB2-focused (Ki=0.64nM), lesser CB1 affinity (Ki=270nM); analgesic, anti-inflammatory in mice.</p>Formule :C16H26N2O2SDegré de pureté :99.94%Couleur et forme :SolidMasse moléculaire :310.45CB1-IN-1
CAS :<p>CB1-IN-1 (DBPR211) is a peripherally restricted CB1R antagonist, for CB1R and CB2R with Ki of 0.3 nM and 21 nM,respectively.</p>Formule :C33H31Cl2F3N6O3S2Degré de pureté :99.08% - 99.76%Couleur et forme :SolidMasse moléculaire :751.67
