Canabinóides
Os canabinoides são uma classe de compostos químicos diversos derivados de ácidos graxos ou poliquetídeos que atuam sobre os receptores canabinoides nas células, alterando a liberação de neurotransmissores no cérebro. Encontrados principalmente em plantas de cannabis, canabinoides como THC e CBD são amplamente estudados por seus efeitos terapêuticos, incluindo alívio da dor, propriedades anti-inflamatórias e uso potencial em doenças neurodegenerativas. Na CymitQuimica, você encontrará uma ampla variedade de canabinoides para pesquisa em farmacologia, neurobiologia e química medicinal.
Foram encontrados 368 produtos para "Canabinóides".
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Cannabigerol
CAS:Cannabigerol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C21H32O2Pureza:(HPLC) ≥98%Cor e Forma:PowderPeso molecular:316.49Cannabidiolic acid
CAS:Cannabidiolic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C22H30O4Pureza:(HPLC) ≥98%Cor e Forma:PowderPeso molecular:358.48Cannabigerolic acid
CAS:Cannabigerolic acid analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C22H32O4Pureza:(HPLC) ≥98%Cor e Forma:PowderPeso molecular:360.5Cannabidiol
CAS:Cannabidiol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Fórmula:C21H30O2Pureza:(HPLC) ≥98%Cor e Forma:PowderPeso molecular:314.47EHP-101
CAS:EHP-101 is a PPARγ/CB2 dual agonist with anti-inflammatory properties, inhibits fat formation, and combats diet-related obesity.Fórmula:C28H35NO3Pureza:98.36%Cor e Forma:SolidPeso molecular:433.58Ref: TM-T13289
1mg101,00€5mg178,00€1mL*10mM (DMSO)203,00€10mg295,00€25mg485,00€50mg677,00€100mg888,00€OMDM-1
CAS:OMDM-1 ((Z)-N-[(2S)-1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl]octadec-9-enamide) is a selective and metabolically stable anandamide cellular uptake (ACU)Fórmula:C27H45NO3Pureza:99.57%Cor e Forma:SolidPeso molecular:431.65Pregnenolone
CAS:Pregnenolone (Arthenolone) is an endogenous steroid hormone synthesized from cholesterol, used in the treatment of Alzheimer's disease.Fórmula:C21H32O2Pureza:99.5% - 99.84%Cor e Forma:SolidPeso molecular:316.486-Iodopravadoline
CAS:6-Iodopravadoline (AM630) is an antagonist of CB2 (Ki: 31.2 nM). And it shows 165-fold selectivity more than CB1 receptors.Fórmula:C23H25IN2O3Pureza:99.29%Cor e Forma:SolidPeso molecular:504.36Ref: TM-T14204
1mg38,00€2mg52,00€5mg70,00€10mg90,00€1mL*10mM (DMSO)99,00€25mg198,00€50mg326,00€100mg520,00€JHU 75528
CAS: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.Fórmula:C23H21Cl2N5O2Pureza:99.79%Cor e Forma:White SolidPeso molecular:470.35Methanone, (1-methyl-1H-indol-3-yl)[(6R)-4,5,6,7-tetrahydro-1H-benzimidazol-6-yl]-, hydrochloride (1:1)
CAS:Fórmula:C17H18ClN3OPureza:98%Cor e Forma:SolidPeso molecular:315.79733,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
CAS:Fórmula:C15H10O8Pureza:98%Cor e Forma:SolidPeso molecular:318.2351Ref: IN-DA0035A3
1g23,00€5g37,00€10g52,00€25g66,00€50g106,00€100g126,00€250g179,00€500g311,00€1kg662,00€5kg1.072,00€10kg2.130,00€CB2R/FAAH modulator-3
CAS:CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH.Fórmula:C22H31NO2Pureza:99.81%Cor e Forma:SolidPeso molecular:341.49SODIUM ARSENATE, HEPTAHYDRATE
CAS:Fórmula:AsH15Na2O11Pureza:98%Cor e Forma:SolidPeso molecular:312.01361H-Pyrazole-3-carboxamide, 1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-N-4-morpholinyl-
CAS:Fórmula:C21H19Cl2IN4O2Pureza:98%Cor e Forma:SolidPeso molecular:557.2116Borate(1-), tetrafluoro-, sodium (1:1)
CAS:Fórmula:BF4NaPureza:99%Cor e Forma:SolidPeso molecular:109.7944CB1 antagonist 2
CAS:CB1 antagonist 2 (AM4113) is caimabinoid 1 (CB1) antagonist which inhibits CB1 in vivo with an IC50 of 25.5 nM.Fórmula:C17H12Cl3N3OPureza:99.75%Cor e Forma:SolidPeso molecular:380.66Rimonabant hydrochloride
CAS: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。Fórmula:C22H22Cl4N4OPureza:98.24% - 99.88%Cor e Forma:Off-White To White Crystalline PowderPeso molecular:500.25Anandamide
CAS: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 alsoFórmula:C22H37NO2Pureza:95.03% - 99.22%Cor e Forma:Light Yellow OilPeso molecular:347.53Ref: TM-T14046
1mg34,00€2mg46,00€5mg67,00€1mL*10mM (DMSO)73,00€10mg117,00€25mg221,00€50mg330,00€100mg485,00€Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)-
CAS:Fórmula:C23H23ClN2O4Pureza:99%Cor e Forma:SolidPeso molecular:426.8927Rimonabant
CAS:Rimonabant (SR141716) is an inverse agonist for the cannabinoid receptor CB1.Fórmula:C22H21Cl3N4OPureza:98% - 99.91%Cor e Forma:White SolidPeso molecular:463.79Nervonoyl ethanolamide
CAS:Nervonoyl ethanolamide (NEA), an endogenous cannabinoid, functions as both a presynaptic and postsynaptic neuromodulator. Additionally, it is utilized in inflammation research [1].Fórmula:C26H51NO2Cor e Forma:SolidPeso molecular:409.69Afubiata
CAS: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.Fórmula:C27H29FN2OCor e Forma:SolidPeso molecular:416.53SCOTfluor-89
CAS:SCOTfluor-89 is a small, conjugatable, orthogonal, and multicolor fluorescent group designed for in vivo imaging of cell metabolism.Fórmula:C12H14N4O7SeCor e Forma:SolidPeso molecular:405.22TRPM8 antagonist 4 prodrug
TRPM8 antagonist 4 prodrug (Compound 8b) is an orally active CB2R agonist (EC50: 51.2 nM) and a weak TRPM8 antagonist. It acts as a prodrug of TRPM8 antagonist 4, exhibiting anti-inflammatory and analgesic properties. TRPM8 antagonist 4 prodrug is applicable in studies of inflammation-related pain disorders.Δ8-THC-C8
CAS: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.Fórmula:C24H36O2Cor e Forma:SolidPeso molecular:356.54exo-Tetrahydrocannabivarin
CAS: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.Fórmula:C19H26O2Cor e Forma:SolidPeso molecular:286.41CB2 receptor agonist 2
CAS:CB2 receptor agonist 2 (ZINC72105556): potent, Ki=8.5 nM, high selectivity for CB2.Fórmula:C30H36N2O4Pureza:99.75%Cor e Forma:SolidPeso molecular:488.62CB2R/FAAH modulator-2
CAS:CB2R/FAAH modulator-2 (compound 26) is a dual modulator targeting at CB2R and FAAH.Fórmula:C24H33NO2Pureza:99.15%Cor e Forma:SolidPeso molecular:367.52Noladin ether
CAS:Noladin ether (2-AG ether) is a cannabinoid CB1 receptor agonist.Fórmula:C23H40O3Cor e Forma:SolidPeso molecular:364.562-Arachidonoylglycerol-D5
CAS:2-Arachidonoylglycerol-D5 is the deuterated form of 2-Arachidonoylglycerol (T14011), which acts as an endogenous cannabinoid ligand within the central nervous system.Fórmula:C23H38O4Cor e Forma:SolidPeso molecular:383.58Drinabant
CAS:Drinabant (AVE-1625) is an orally active CB1 receptor antagonist.Fórmula:C23H20Cl2F2N2O2SPureza:99.8%Cor e Forma:SolidPeso molecular:497.388β-Hydroxy-exo-THC
CAS:8β-Hydroxy-exo-THC, a cannabinoid ether analog, exhibits weak affinity for receptor sites with an IC50 of 1.2 μM.Fórmula:C21H30O3Cor e Forma:SolidPeso molecular:330.46Calcitonin-13C6,15N4 trifluoroacetic acid
Calcitonin-13C6,15N4 trifluoroacetic acid is a version of calcitonin (salmon) labeled with carbon-13 and nitrogen-15. This hormone regulates calcium and acts dualistically as an agonist to both amylin and calcitonin receptors, promoting bone formation while inhibiting bone resorption.Fórmula:C1401C5H240N4315NO48S2·5C2HF3O2Cor e Forma:SolidPeso molecular:4007.93CB1R antagonist 2
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.Fórmula:C24H26N4OCor e Forma:SolidPeso molecular:386.49Vicasinabin
CAS:Vicasinabin: potent CB2 agonist; researches chronic pain, atherosclerosis, bone mass, neuroinflammation.Fórmula:C15H22N10OCor e Forma:SolidPeso molecular:358.41Tocrifluor T1117
CAS:Fluorescent form of AM 251, CB1 receptor antagonistFórmula:C56H53Cl2N7O5Pureza:98%Cor e Forma:SolidPeso molecular:974.97GPR55 agonist 4
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].Fórmula:C19H16FN5O2Cor e Forma:SolidPeso molecular:365.36CB1-IN-3
CB1-IN-3 (Compound 6i) is a potent inhibitor of the cannabinoid receptor type 1 (CB1). It holds potential for research in obesity, inflammation, and neurological disorders.Cor e Forma:Odour SolidCB2 receptor antagonist 2
Compound 39, also known as CB2 receptor antagonist 2, is a potent CB2 antagonist exhibiting an IC50 of 0.33 μM.Cor e Forma:Odour SolidN-(1-(3,4-Dihydroxyphenyl)propan-2-yl)oleamide
CAS: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.Fórmula:C27H45NO3Cor e Forma:SolidPeso molecular:431.661CB2R/FAAH modulator-1
CAS: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.Fórmula:C24H27NO2Pureza:99.77%Cor e Forma:SolidPeso molecular:361.48Ref: TM-T67896
1mg50,00€5mg105,00€1mL*10mM (DMSO)108,00€10mg154,00€25mg224,00€50mg314,00€100mg427,00€200mg575,00€Hemopressin(rat)
CAS: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.Fórmula:C53H77N13O12Pureza:98%Cor e Forma:SolidPeso molecular:1088.27NESS 0327
CAS: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.Fórmula:C24H23Cl3N4OPureza:99.78%Cor e Forma:SolidPeso molecular:489.82
![Methanone, (1-methyl-1H-indol-3-yl)[(6R)-4,5,6,7-tetrahydro-1H-benzimidazol-6-yl]-, hydrochloride …](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb-webp%2FDA0011DB.webp&w=3840&q=75)
![Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb-webp%2FDA002VNX.webp&w=3840&q=75)
