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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).
分子量 | 384.59 |
公式 | C26H40O2 |
储存 | Store at +4°C |
纯度 | ≥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 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
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
关键词: L-759,633, L-759,633 supplier, High, affinity, selective, CB2, agonists, cannabinoids, Receptors, cb2r, L759633, 2433, Tocris Bioscience
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