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Cannabinoid Receptor
Cannabinoid Receptor
Cannabinoid Receptor Isoform Specific Products
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Cannabinoid Receptor Inhibitors
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Cannabinoid Receptor Agonists
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Cannabinoid Receptor Antagonists
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Cannabinoid Receptor Ligands
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Productos relacionados con Cannabinoid Receptor (448)
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Antibodies (1)
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Cannabinoid Receptor Isoform Comparison
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GAT229
0 ImagesReferencia número: HY-121600No. CAS: 889860-85-9GAT229 is a CB1 positive allosteric modulator (PAM) that effectively reduces intraocular pressure (IOP) in high IOP mouse models and enhances CB1 receptor-mediated IOP-lowering effects. A 0.2% GAT229 solution or 10 mg/kg of GAT229 alone significantly reduces IOP. GAT229 is promising for research related to glaucoma and elevated intraocular pressure. -
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Otenabant Hydrochloride
0 ImagesReferencia número: HY-10871ANo. CAS: 686347-12-6Synonyms: CP 945598 HydrochlorideOtenabant Hydrochloride is a potent and selective cannabinoid receptor CB1 antagonist with Ki of 0.7 nM, exhibits 10,000-fold greater selectivity against human CB2 receptor. -
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(R)-Zevaquenabant
0 ImagesReferencia número: HY-141411BPureza: 99.15%Synonyms: (R)-MRI-1867(R)-Zevaquenabant ((R)-MRI-1867) is the enantiomer of Zevaquenabant (HY-141411A). Zevaquenabant ((S)-MRI-1867) is a peripherally restricted, orally bioavailable dual cannabinoid CB1 receptor and inducible NOS antagonist. Zevaquenabant ameliorates obesity-induced chronic kidney disease (CKD). -
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SER-601
0 ImagesReferencia número: HY-110065No. CAS: 1048038-90-9SER-601 is a potent and selective peripheral cannabinoid (CB2) receptor agonist with a Ki of 6.3 nM. SER-601 has analgesic and antidiabetic properties and can be used for relevant research. -
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Heptadecanoyl ethanolamide
0 ImagesHeptadecanoyl ethanolamide is an endogenous cannabinoid. Heptadecanoyl ethanolamide is a synthetic analog of PEA which incorporates an odd-numbered (17-carbon) fatty acid chain. -
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AM9405
0 ImagesReferencia número: HY-112707No. CAS: 3032946-55-4AM9405 is a novel peripherally active cannabinoid type 1 (CB1) and serotonin type 3 receptor agonist. AM9405 inhibits twitch contraction of the ileum and the colon with IC50s of 45.71 and 0.076 nM, respectively. -
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Anandamide-d11
0 ImagesSynonyms: AEA-d11 -
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S-Methoprene (Standard)
0 ImagesSynonyms: (+)-Methoprene (Standard); (7S)-Methoprene (Standard)2-Methyl-3-(trifluoromethyl)aniline (Standard) is the analytical standard of 2-Methyl-3-(trifluoromethyl)aniline. This product is intended for research and analytical applications. 2-Methyl-3-(trifluoromethyl)aniline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. -
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β-Caryophyllene-13C,d2
0 ImagesReferencia número: HY-N1415S1No. CAS: 3028869-04-4Synonyms: (-)-(E)-Caryophyllene-13C,d2; (−)-β-caryophyllene-13C,d2; (−)-trans-Caryophyllene-13C,d2β-Caryophyllene-13C,d2 is 13C and deuterated labeled β-Caryophyllene (HY-N1415). β-Caryophyllene is a CB2 receptor agonist. -
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CB2 receptor antagonist 1
0 ImagesReferencia número: HY-147707No. CAS: 2772693-05-5Hexyl resorcinol derivative 29 has been proved to be a CB2 selective competitive antagonist / reverse agonist with good potency. Olivanol and 5- (2-methyloctane-2-yl) resorcinol derivatives 23 and 24 showed significant antinociceptive activity. Compound 24 was shown to activate cannabinoid and TRPV1 receptors. -
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Virodhamine TFA
0 ImagesReferencia número: HY-110194No. CAS: 1415264-56-0Virodhamine TFA is an endocannabinoid, it regulates neurotransmission by activating the cannabinoid (CB) receptors. Virodhamine is an antagonist of CB1 receptor and an agonist of CB2 receptor. Virodhamine TFA induces megakaryocytic differentiation by triggering MAPK signaling and ROS production. Virodhamine TFA can be used for the research of various neurological disorders such as Alzheimer's and Parkinson's diseases. -
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Isopropyl dodec-11-enylfluorophosphonate
0 ImagesReferencia número: HY-148909No. CAS: 623114-64-7Synonyms: IDEFPIsopropyl dodec-11-enylfluorophosphonate (IDEFP) is an organophosphorus ester that antagonizes the central cannabinoid receptor (CB1) and inhibits FAAH with similar potencies (IC50 = 2 nM). -
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(R)-SLV 319
0 ImagesReferencia número: HY-121616No. CAS: 656827-86-0(R)-SLV 319 is a potent and selective cannabinoid receptor 1 (CB1) antagonist with a Ki value of 894 nM. (R)-SLV 319 is a dextrorotatory counterpart of SLV 319 -
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RTICBM-189
0 ImagesRTICBM-189 is a potent, brain-penetrant allosteric modulator of the cannabinoid type-1 (CB1) receptor with a pIC50 of 7.54 in Ca2+ mobilization assay. RTICBM-189 has pIC50s of 5.29 and 6.25 for hCB1 and mCB1, respectively. RTICBM-189 significantly and selectively attenuates the reinstatement of the addictive agent-seeking behavior in rats. -
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CB2 receptor agonist 9
0 ImagesReferencia número: HY-168734No. CAS: 2374894-21-8 -
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(±)5(6)-EET Ethanolamide
0 ImagesReferencia número: HY-172568(±)5(6)-EET Ethanolamide is a metabolite of Anandamide (HY-10863) generated via oxidation by cytochrome P450 enzymes. (±)5(6)-EET Ethanolamide is also a selective cannabinoid receptor 2 (CB2) agonist. (±)5(6)-EET Ethanolamide has Ki values of 11.4 μM and 8.9 nM for human CB1 and CB2, respectively . (±)5(6)-EET Ethanolamide can be used in research on immunomodulation and neuroinflammation. -
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Palmitoyl serinol-d5
0 ImagesReferencia número: HY-125407SNo. CAS: 946524-35-2Synonyms: N-Palmitoyl serinol-d5Palmitoyl serinol-d5 is the deuterium labeled Palmitoyl serinol. Palmitoyl serinol (N-Palmitoyl serinol) is an analog of the endocannabinoid N-palmitoyl ethanolamine (PEA). Palmitoyl serinol improves the epidermal permeability barrier in both normal and inflamed skin. -
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- AChE/BChE-IN-18
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Virodhamine hydrochloride
0 ImagesReferencia número: HY-128040No. CAS: 443129-35-9 -
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LY320135
0 ImagesReferencia número: HY-W011040No. CAS: 176977-56-3LY320135 is a potent and selective antagonist of CB1 receptor, with a Ki of 141 nM. LY320135 also binds to 5-HT2 and muscarinic receptors with Kis of 6.4 μM and 2.1 μM, respectively. LY320135 exhibits neuroprotective effect. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.