| Literature DB >> 15081344 |
Renata Fringuelli1, M Pilar Utrilla Navarro, Lara Milanese, Stefano Bruscoli, Fausto Schiaffella, Carlo Riccardi, Claudio De Simone.
Abstract
Two series of derivatives were synthesised. In one series (R)-4-hydroxy-2-pyrrolidinone was used as a mimic of cyclic L-carnitine analogue and in the second series 3-amino-2-piperidinone was used as a cyclic ornithine analogue. N-Benzyloxycarbonyl derivatives of some amino acids were also prepared. The newly synthesised compounds were tested for their ability to inhibit Fas-activated apoptosis of human Jurkatt T-cell line. The results confirm the previously described anti-apoptotic activity of carnitine and indicate new carnitine and amino acid analogues (1, 3, 6, 7, 20) that inhibit Fas-induced apoptosis.Entities:
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Year: 2004 PMID: 15081344 DOI: 10.1016/j.farmac.2004.01.004
Source DB: PubMed Journal: Farmaco ISSN: 0014-827X