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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 216 products of "Cannabinoid Receptor"

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  • AM11638

    CAS:
    AM11638 is an endogenous cannabinoid analogue that targets cannabinoid receptors (CB1 and CB2 receptors), exhibiting analgesic properties. It shows potential for research in neurological disorders and inflammation-related diseases.
    Formula:C27H41NO2
    Color and Shape:Solid
    Molecular weight:411.62
  • CB2 receptor antagonist 1

    CAS:
    Compound 29 is a potent, CB2-selective antagonist/reverse agonist. Derivatives 23 & 24 offer antinociception; 24 activates cannabinoid/TRPV1 receptors.
    Formula:C28H47NO3
    Color and Shape:Solid
    Molecular weight:445.68
  • CB1/2 agonist 1


    Potent CB1/2 agonist 1; crosses blood-brain barrier; anti-inflammatory, analgesic; for multiple sclerosis research.
    Formula:C21H24BrFN2O2
    Color and Shape:Solid
    Molecular weight:435.33
  • CBR Agonist-1


    CBR Agonist-1 targets CB1R and CB2R with Ki of 0.18 μM and 1.22 μM, useful for studying cannabinoid-related diseases.
    Formula:C27H27FN4O
    Color and Shape:Solid
    Molecular weight:442.53
  • MDA7

    CAS:
    <p>MDA7 is a selective agonist of the cannabinoid receptor 2 (CB2), demonstrating an EC50 of 128 nM in human CB2 receptors and 67.4 nM in rat CB2 receptors. The compound exhibits good affinity for CB2 receptors, with Ki values of 422 nM for humans and 238 nM for rats. In rat models, MDA7 shows analgesic activity.</p>
    Formula:C22H25NO2
    Color and Shape:Solid
    Molecular weight:335.439
  • Bzo-poxizid

    CAS:
    Bzo-poxizid is a synthetic cannabinoid and a psychoactive substance.
    Formula:C20H21N3O2
    Color and Shape:Solid
    Molecular weight:335.40
  • HU 433

    CAS:
    <p>HU 433, a synthetic cannabinoid, acts as a CB2 receptor agonist and is an enantiomer of HU 308. It provides anti-inflammatory and neuroprotective effects by binding to the CB2 receptor, primarily found on immune cells, thereby modulating immune responses and inflammation. Additionally, HU 433 influences microglial signaling pathways, particularly LPS and IFNγ-mediated routes, affecting the phosphorylation of MAPKs, including ERK1/2, JNK, p38, and Akt. This compound is valuable in researching neuroinflammation and retinal diseases.</p>
    Formula:C27H42O3
    Color and Shape:Solid
    Molecular weight:414.62
  • CB1/2 receptor-1

    CAS:
    CB1/2 receptor-1 (compound 5.3) serves as an agonist for CB1/2 receptors and is utilized in angiogenesis research.
    Formula:C33H48O2
    Color and Shape:Solid
    Molecular weight:476.73
  • GAT564


    GAT564, an allosteric CB1R modulator, shows EC50s of 87 nM (cAMP) & 320 nM (β-arrestin2) and lowers IOP effectively in glaucoma mice.
    Formula:C20H16N2O2S
    Color and Shape:Solid
    Molecular weight:348.42
  • HU-308

    CAS:
    <p>HU-308, a synthetic cannabinoid analogue, is a highly selective agonist of the CB2 receptor. It demonstrates an affinity for the CB2 receptor that is over 440 times greater than its affinity for the CB1 receptor, which are predominantly found in immune cells. This compound plays a crucial role in modulating the immunosuppressive effects of the endocannabinoid system (ECS). Additionally, HU-308 possesses anti-inflammatory and neuroprotective properties, and it regulates the function of microglia. Its potential applications include research into neuroinflammation and retinal diseases.</p>
    Formula:C27H42O3
    Color and Shape:Solid
    Molecular weight:414.62
  • AB-FUBINACA 3-fluorobenzyl isomer

    CAS:
    AB-FUBINACA 3-fluorobenzyl isomer is a synthetic cannabinoid and an indazole derivative, exhibiting high affinity for central CB1 receptors (Ki= 0.9 nM) and possessing anticonvulsant activity.
    Formula:C20H21FN4O2
    Color and Shape:Solid
    Molecular weight:368.41
  • MDA77

    CAS:
    MDA77 is a CB2 agonist with an EC50 value of 5.82 nM and exhibits no activity towards CB1.
    Formula:C21H23N3O3
    Color and Shape:Solid
    Molecular weight:365.43
  • 1'-Naphthoyl-2-methylindole

    CAS:
    1'-Naphthoyl-2-methylindole (Compound 88) acts as a cannabinoid mimic and an inhibitor of Win 55212-2, displaying a 34% inhibition of [3H]Win 55212-2 binding to cannabinoid receptors at a concentration of 3 μM.
    Formula:C20H15NO
    Color and Shape:Solid
    Molecular weight:285.34
  • TM38837

    CAS:
    <p>CB1 antagonist 4 is an inverse agonist of cannabinoid receptor 1 (CB1) with an IC50 of 0.4 nM. It can reduce body weight, improve plasma inflammatory markers, and enhance glucose homeostasis [1].</p>
    Formula:C27H20Cl2F3N7O
    Color and Shape:Solid
    Molecular weight:586.40
  • (Rac)-Zevaquenabant

    CAS:
    (Rac)-Zevaquenabant ((Rac)-MRI-1867, compound 6b) is a potent and selective antagonist of cannabinoid receptor type 1 (CB1R) and inducible nitric oxide synthase (iNOS), with a binding affinity (Ki) of 5.7 nM for CB1R. It holds promise as an investigative tool in liver fibrosis research due to these characteristics.
    Formula:C25H21ClF3N5O2S
    Color and Shape:Solid
    Molecular weight:547.98

    Ref: TM-T39074

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  • AEF0117

    CAS:
    <p>AEF0117 is a signaling inhibitor of CB1-SSi that inhibits cannabinoid self-administration and can be used to study cannabis withdrawal.</p>
    Formula:C29H40O3
    Purity:99.58%
    Color and Shape:Solid
    Molecular weight:436.63

    Ref: TM-T79909

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