Synthesis and biological evaluation of S-acyl-3-thiopropyl prodrugs of N-phosphonoacetyl-?-aspartate (PALA)
作者:V Gagnard
DOI:10.1016/j.ejmech.2003.07.002
日期:2003.10
The synthesis of new prodrugs of PALA characterised by the presence of S-acyl-3-thiopropyl, as enzyme-labile groups on the phosphonate moiety of PALA, is reported. The cytotoxic activities of PALA prodrugs were determined against human cell line (SW1573 lung carcinoma cells). A number of prodrugs bearing S-pivaloyl as acyl groups displayed cytotoxic activity in the same order of magnitude of PALA. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
Goodson, John J.; Wharton, Clifford J.; Wrigglesworth, Roger, Journal of the Chemical Society. Perkin transactions I, 1980, p. 2721 - 2727
作者:Goodson, John J.、Wharton, Clifford J.、Wrigglesworth, Roger
DOI:——
日期:——
Montero; Imbach, European Journal of Medicinal Chemistry, 1982, vol. 17, # 1, p. 97 - 99
作者:Montero、Imbach
DOI:——
日期:——
An Improved Synthesis of<i>N</i>(Phosphonoacetyl)-amino Acids