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Cannabinoid Receptor

Cannabinoid Receptor

Cannabinoid receptors are GPCRs that mediate the effects of endogenous cannabinoids (endocannabinoids) and phytocannabinoids, such as those found in cannabis. The two main types of cannabinoid receptors, CB1 and CB2, are involved in regulating a wide range of physiological processes, including pain perception, appetite, mood, and immune function. Cannabinoid receptor modulators have therapeutic potential in treating conditions such as chronic pain, epilepsy, and multiple sclerosis. At CymitQuimica, we offer a wide range of high-quality cannabinoid receptor modulators to support your research in neuropharmacology, pain management, and immunology.

Found 196 products of "Cannabinoid Receptor"

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  • Rimonabant

    CAS:
    <p>Rimonabant (SR141716) is an inverse agonist for the cannabinoid receptor CB1.</p>
    Formula:C22H21Cl3N4O
    Purity:98% - 99.91%
    Color and Shape:White Or Almost White Crystalline Powder
    Molecular weight:463.79
  • CB1 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>
    Formula:C17H12Cl3N3O
    Purity:99.75%
    Color and Shape:Solid
    Molecular weight:380.66
  • 6-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>
    Formula:C23H25IN2O3
    Purity:99.29%
    Color and Shape:Off-White Solid
    Molecular weight:504.36
  • 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>
    Formula:C28H35NO3
    Purity:98.36%
    Color and Shape:Solid
    Molecular weight:433.58
  • Anandamide

    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>
    Formula:C22H37NO2
    Purity:95.037% - 99.22%
    Color and Shape:Light Yellow Oil
    Molecular weight:347.53
  • Rimonabant 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>
    Formula:C22H22Cl4N4O
    Purity:98.24% - 99.5%
    Color and Shape:Off-White To White Crystalline Powder
    Molecular weight:500.25
  • Pregnenolone

    CAS:
    <p>Pregnenolone (Arthenolone) is an endogenous steroid hormone synthesized from cholesterol, used in the treatment of Alzheimer's disease.</p>
    Formula:C21H32O2
    Purity:99.5% - >99.99%
    Color and Shape:Solid
    Molecular weight:316.48
  • JHU 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>
    Formula:C23H21Cl2N5O2
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:470.35
  • GPR55 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>
    Formula:C19H16FN5O2
    Color and Shape:Solid
    Molecular weight:365.36
  • CB1R 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>
    Formula:C20H18F3N3O3S
    Color and Shape:Solid
    Molecular weight:437.435
  • Hemopressin(rat)

    CAS:
    <p>Peptide inhibitor for ep24.15, neurolysin &amp; ACE with Ki 27.76, 3.43, 1.87 μM. Lowers blood pressure, modulates CB1 receptor, reduces pain &amp; food intake.</p>
    Formula:C53H77N13O12
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1088.27
  • Vicasinabin

    CAS:
    <p>Vicasinabin: potent CB2 agonist; researches chronic pain, atherosclerosis, bone mass, neuroinflammation.</p>
    Formula:C15H22N10O
    Color and Shape:Solid
    Molecular weight:358.41
  • CB2R/FAAH modulator-3

    CAS:
    <p>CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH.</p>
    Formula:C22H31NO2
    Purity:99.81%
    Color and Shape:Soild
    Molecular weight:341.49
  • NESS 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>
    Formula:C24H23Cl3N4O
    Purity:99.78%
    Color and Shape:Solid
    Molecular weight:489.82
  • (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>
    Color and Shape:Odour Solid
  • RVD-Hpα

    CAS:
    <p>N-terminally extended form of human hemopressin that acts as a selective CB1 receptor agonist.</p>
    Formula:C65H105N19O17
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1424.66
  • Hemopressin (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>
    Formula:C50H79N13O12
    Purity:98%
    Color and Shape:Solid
    Molecular weight:1054.26
  • N-(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>
    Formula:C27H45NO3
    Color and Shape:Solid
    Molecular weight:431.661
  • CB2R/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>
    Formula:C24H27NO2
    Purity:99.77%
    Color and Shape:Soild
    Molecular weight:361.48
  • VIP36


    <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>
    Formula:C27H35FN6O4
    Color and Shape:Solid
    Molecular weight:526.603