Synthesis and biological activities of novel structural analogues of 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand.
Y Suhara, S Nakane, S Arai, H Takayama, K Waku, Y Ishima, T Sugiura
Index: Bioorg. Med. Chem. Lett. 11(15) , 1985-8, (2001)
Full Text: HTML
Abstract
Novel analogues of 2-arachidonoylglycerol (2-AG), an endogenous cannabinoid receptor ligand, were developed. Chemical synthesis of these analogues (2-AGA105 and 2-AGA109) was accomplished starting from 2-octyn-1-ol and diethyl malonate and employing Wittig coupling of triene phosphonate with an aldehyde intermediate in a convergent and stereoselective manner. These analogues should be useful lead compounds for the development of novel 2-AG mimetics.
Related Compounds
Related Articles:
1981-01-01
[Prep. Biochem. 11(3) , 339-50, (1981)]
2000-04-28
[J. Hazard. Mater. 73(3) , 237-44, (2000)]
2002-01-24
[Org. Lett. 4(2) , 269-72, (2002)]
1986-03-01
[Can. J. Microbiol. 32(3) , 254-8, (1986)]
1983-02-01
[Indian J. Biochem. Biophys. 20(1) , 39-42, (1983)]