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GW 405833

Catalog No. T7705   CAS 180002-83-9
Synonyms: L-768242

GW 405833 (L-768242) is an agonist of cannabinoid-2 (CB(2)) receptor-selective

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GW 405833 Chemical Structure
GW 405833, CAS 180002-83-9
Pack Size Availability Price/USD Quantity
1 mg In stock $ 34.00
2 mg In stock $ 48.00
5 mg In stock $ 80.00
10 mg In stock $ 122.00
25 mg In stock $ 222.00
50 mg In stock $ 347.00
100 mg In stock $ 516.00
1 mL * 10 mM (in DMSO) In stock $ 98.00
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Purity: 99.93%
Purity: 99.82%
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Biological Description
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Description GW 405833 (L-768242) is an agonist of cannabinoid-2 (CB(2)) receptor-selective
In vivo GW405833 (3, 10, and 30 mg/kg i.p.) dose dependently reversed established mechanical allodynia in both pain models in WT mice;?however, the antiallodynic effects of GW405833 were fully preserved in CB2KO mice and absent in CB1KO mice.?Furthermore, the antiallodynic efficacy of GW405833 (30 mg/kg i.p.) was completely blocked by the CB1 antagonist rimonabant (10 mg/kg i.p.) but not by the CB2 antagonist SR144528 (10 mg/kg i.p.).?Thus, the antinociceptive properties of GW405833 are dependent on CB1 receptors.?GW405833 (30 mg/kg i.p.) was also inactive in a tetrad of tests measuring cardinal signs of CB1 activation.?Additionally, unlike rimonabant (10 mg/kg i.p.), GW405833 (10 mg/kg, i.p.) did not act as a CB1 antagonist in vivo to precipitate withdrawal in mice treated chronically with Δ9-tetrahydrocannabinol[1].
Animal Research Baseline mechanical paw withdrawal thresholds were measured in each paw for each animal before performing either PSNL or injecting CFA.?Another predrug baseline was then taken after painful peripheral neuropathy or inflammatory pain was fully established.?GW405833 was administered (i.p.) 30 minutes before evaluation of the impact of drug manipulations on mechanical paw withdrawal thresholds.?Different doses of GW405833 were injected (i.p.) within subjects in the order of vehicle (0), 3, 10, and 30 mg/kg.?Sufficient time was allowed to lapse between each dose to verify that mechanical paw withdrawal thresholds returned to the predrug levels before dose escalation. .?In the groups where CB1 or CB2 antagonists were tested, rimonabant or SR144528 (10 mg/kg i.p.) was administered 20 minutes before GW405833 injection[1].
Synonyms L-768242
Molecular Weight 447.35
Formula C23H24Cl2N2O3
CAS No. 180002-83-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 10 mg/mL (22.35 mM)

TargetMolReferences and Literature

1. Li A L , Carey L M , Mackie K , et al. The cannabinoid CB 2 agonist GW405833 suppresses inflammatory and neuropathic pain through a CB 1 mechanism that is independent of CB 2 receptors in mice[J]. Journal of Pharmacology and Experimental Therapeutics, 2017, 362(2):jpet.117.241901. 2. Parlar A , Arslan S , Doğan, Muhammed, et al. The exogenous administration of CB2 specific agonist, GW405833, inhibits inflammation by reducing cytokine production and oxidative stress[J]. Experimental and Therapeutic Medicine, 2018. 3. Huang Z , Wang H , Wang J , et al. Cannabinoid receptor subtype 2 (CB2R) agonist, GW405833 reduces agonist-induced Ca2+ oscillations in mouse pancreatic acinar cells[J]. Scientific Reports, 2016, 6(1):29757.

Related compound libraries

This product is contained In the following compound libraries:
GPCR Compound Library Neuronal Signaling Compound Library Bioactive Compound Library Anti-Fibrosis Compound Library NO PAINS Compound Library Bioactive Compounds Library Max

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Keywords

GW 405833 180002-83-9 GPCR/G Protein Cannabinoid Receptor GW-405833 L768242 L-768242 L 768242 GW405833 anti-inflammatory Inhibitor neuropathic pain inhibit inhibitor

 

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