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Synthesis and pharmacology of a very potent cannabinoid lacking a phenolic hydroxyl with high affinity for the CB2 receptor.
Department of Chemistry, Clemson University, South Carolina 29634-1905, USA.
PMID: 8831752 [PubMed - indexed for MEDLINE]
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Cited by 8 PubMed Central articles
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ReviewTargeting the cannabinoid CB2 receptor: modelling and structural determinants of CB2 selective ligands.
Poso A, Huffman JW.
Br J Pharmacol. 2008 Jan; 153(2):335-46. Epub 2007 Nov 5.
[Br J Pharmacol. 2008]
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Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940.
Huffman JW, Thompson AL, Wiley JL, Martin BR.
Bioorg Med Chem. 2008 Jan 1; 16(1):322-35. Epub 2007 Sep 22.
[Bioorg Med Chem. 2008]
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The role of fluorine substitution in the structure-activity relationships (SAR) of classical cannabinoids.
Crocker PJ, Mahadevan A, Wiley JL, Martin BR, Razdan RK.
Bioorg Med Chem Lett. 2007 Mar 15; 17(6):1504-7. Epub 2007 Jan 13.
[Bioorg Med Chem Lett. 2007]
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