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 563 prodotti per "Cannabinoidi".
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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.Formula:C23H21Cl2N5O2Purezza:99.79%Colore e forma:White SolidPeso molecolare:470.35Rimonabant
CAS:Rimonabant (SR141716) is an inverse agonist for the cannabinoid receptor CB1.Formula:C22H21Cl3N4OPurezza:98% - 99.91%Colore e forma:White SolidPeso molecolare:463.787Pregnenolone
CAS:Pregnenolone (Arthenolone) is an endogenous steroid hormone synthesized from cholesterol, used in the treatment of Alzheimer's disease.Formula:C21H32O2Purezza:99.5% - 99.84%Colore e forma:SolidPeso molecolare:316.4776SODIUM ARSENATE, HEPTAHYDRATE
CAS:Formula:AsH15Na2O11Purezza:98%Colore e forma:SolidPeso molecolare:312.0136EHP-101
CAS:EHP-101 is a PPARγ/CB2 dual agonist with anti-inflammatory properties, inhibits fat formation, and combats diet-related obesity.Formula:C28H35NO3Purezza:98.36%Colore e forma:SolidPeso molecolare:433.5824CB2R/FAAH modulator-3
CAS:CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH.Formula:C22H31NO2Purezza:99.81%Colore e forma:SolidPeso molecolare:341.487Anandamide
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 alsoFormula:C22H37NO2Purezza:95.03% - 99.22%Colore e forma:Light Yellow OilPeso molecolare:347.53Rimonabant 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。Formula:C22H22Cl4N4OPurezza:98.24% - 99.88%Colore e forma:Off-White To White Crystalline PowderPeso molecolare:500.25CB1 antagonist 2
CAS:CB1 antagonist 2 (AM4113) is caimabinoid 1 (CB1) antagonist which inhibits CB1 in vivo with an IC50 of 25.5 nM.Formula:C17H12Cl3N3OPurezza:99.75%Colore e forma:SolidPeso molecolare:380.6566-Iodopravadoline
CAS:6-Iodopravadoline (AM630) is an antagonist of CB2 (Ki: 31.2 nM). And it shows 165-fold selectivity more than CB1 receptors.Formula:C23H25IN2O3Purezza:99.29%Colore e forma:SolidPeso molecolare:504.36OMDM-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)Formula:C27H45NO3Purezza:99.57%Colore e forma:SolidPeso molecolare:431.6511Zevaquenabant
CAS:Zevaquenabant (S-MRI-1867): oral CB1/iNOS antagonist combatting obesity-induced CKD.Formula:C25H21ClF3N5O2SColore e forma:SolidPeso molecolare:547.98Hemopressin(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.Formula:C53H77N13O12Purezza:98%Colore e forma:SolidPeso molecolare:1088.27N-(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.Formula:C27H45NO3Colore e forma:SolidPeso molecolare:431.661(R)-Zevaquenabant
(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.Colore e forma:Odour SolidHemopressin (human, mouse)
CAS: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.Formula:C50H79N13O12Purezza:98%Colore e forma:SolidPeso molecolare:1054.26RVD-Hpα
CAS:N-terminally extended form of human hemopressin that acts as a selective CB1 receptor agonist.Formula:C65H105N19O17Purezza:98%Colore e forma:SolidPeso molecolare:1424.66Tocrifluor T1117
CAS:Fluorescent form of AM 251, CB1 receptor antagonistFormula:C56H53Cl2N7O5Purezza:98%Colore e forma:SolidPeso molecolare:974.97Docosahexaenoyl glycerol
CAS:Docosahexaenoyl glycerol, an analog of endocannabinoid, stimulates glucose uptake and exhibits anti-inflammatory efficacy [1] [2].Formula:C25H38O4Colore e forma:SolidPeso molecolare:402.57TRPM8 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.
