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Submit ReviewHigh affinity, selective CB2 receptor agonist (Ki values are 6.4 and 1043 nM for CB2 and CB1 receptors respectively). Potently inhibits forskolin-stimulated cAMP production via CB2 receptors expressed in CHO cells (EC50 = 8.1 nM).
M. Wt | 384.59 |
Formula | C26H40O2 |
Storage | Store at +4°C |
Purity | ≥98% (HPLC) |
CAS Number | 174627-50-0 |
PubChem ID | 5311215 |
InChI Key | SUFMHSFGODDLKI-NHCUHLMSSA-N |
Smiles | CCCCCCC(C)(C)C(C=C3OC)=CC2=[C@@]3[C@H]1[C@H]([C@@](C)(C)O2)CC=C(C)C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Ross et al (1999) Agonist-inverse agonist characterization at CB1 and CB2 cannabinoid receptors of L759633, L759656 and AM630. Br.J.Pharmacol. 126 665 PMID: 10188977
Huffman et al (1999) 3-(1',1'-dimethylbutyl)-1-deoxy-D8-THC and related compounds: synthesis of selective ligands for the CB2 receptor. Bioorg.Med.Chem. 7 2905 PMID: 10658595
Huffman (2000) The search for selective ligands for the CB2 receptor. Curr.Pharmaceut.Des. 6 1323
Keywords: L-759,633, L-759,633 supplier, High, affinity, selective, CB2, agonists, cannabinoids, Receptors, cb2r, L759633, 2433, Tocris Bioscience
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