Description
L-759,633 is a cannabinoid receptor 2 (CB2) selective agonist. It mimics CP 55,940 in a forskolin-induced cyclic AMP production assay by inhibiting the amount of cyclic AMP produced.
| Product Unit Size | Cost | Quantity | Stock |
|---|
L-759,633 is a cannabinoid receptor 2 (CB2) selective agonist. It mimics CP 55,940 in a forskolin-induced cyclic AMP production assay by inhibiting the amount of cyclic AMP produced.
| Cas No. | 174627-50-0 |
|---|---|
| Purity | ≥98% |
| Formula | C26H40O2 |
| Formula Wt. | 384.60 |
| Chemical Name | (6aR,10aR)-1-methoxy-6,6,9-trimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromene |
| IUPAC Name | (6aR,10aR)-1-methoxy-6,6,9-trimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromene |
| Solubility | 50mM in ethanol 25mM in DMSO |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Ross RA, Brockie HC, Stevenson LA, et al. Agonist-inverse agonist characterization at CB1 and CB2 cannabinoid receptors of L759633, L759656 and AM630. Br J Pharmacol. 1999 Feb;126(3):665-72. PMID: 10188977.
RIP1 inhibitor.
Potential voltage-gated Na+ channel blocker.
Endogenous glycoprotein hormone involved in red...
Penicillin derivative, chelating agent; carboxy...
EGFR inhibitor.
KRAS inhibitor
Aminoquinoline, binds heme, causes cell lysis.<...
Mineralocorticoid antagonist.
NSAID; COX-1/2 inhibitor.
Diterpene found in Taxus.
Impurity of diclofenac
Anxiolytic-like agent that stimulates angiogene...
c-Raf inhibitor, tyrosine kinase inhibitor.
Polycyclic aromatic hydrocarbon (PAH) found in ...
Lincosamide; ribosomal translocation and protei...
Quaternary base alkaloid found in Phellodendron...
p110α inhibitor.
Taxane found in species of Taxus; potential mic...
Non-depolarizing NMJ blocker; nAChR antagonist....