Stability of acetal and non acetal-type analogs of artemisinin in simulated stomach acid

Stability of acetal and non acetal-type analogs of artemisinin in simulated stomach acid
复制标题

DOI:
10.1016/s0960-894x(98)00160-7
复制
发表时间:
1998-05-05
影响因子:
2.7
通讯作者:
Lee, S
Lee, S
中科院分区:
医学4区
文献类型:
--
作者:
Jung, M;Lee, S

文献摘要

被引文献

相似文献

一系列12位含C-C键的非缩醛型青蒿素类似物在模拟胃酸中的稳定性比缩醛(C-O)型青蒿素前药高15-22倍。(C)1998爱思唯尔科技有限公司。保留所有权利。
A series of non acetal-type analogs of artemisinin containing C-C bond at position-12 have been found to be 15-22 times more stable than acetal(C-O)-type prodrugs of artemisinin in simulated stomach acid. (C) 1998 Elsevier Science Ltd. All rights reserved.