Synthesis and in vitro cytotoxicity of novel long chain busulphan analogues
摘要:
Two novel long chain alkanediol dimethanesulphonates, analogues of busulphan, were synthesized. Their in vitro cytotoxicity was evaluated against six solid tumor cell lines (A2780, H322, LL, WiDr, C26-10 and UMSCC-22B). 2-Tetradecylbutane-1,4-diol dimethanesulphonate was proved to be the most active compound exhibiting IC50 values between 20.82 and 26.36 muM. (C) 2001 Elsevier Science Ltd. All rights reserved.
Synthesis and in vitro cytotoxicity of novel long chain busulphan analogues
作者:George Kokotos、Violetta Constantinou-Kokotou、José M Padrón、Godefridus J Peters
DOI:10.1016/s0960-894x(01)00084-1
日期:2001.3
Two novel long chain alkanediol dimethanesulphonates, analogues of busulphan, were synthesized. Their in vitro cytotoxicity was evaluated against six solid tumor cell lines (A2780, H322, LL, WiDr, C26-10 and UMSCC-22B). 2-Tetradecylbutane-1,4-diol dimethanesulphonate was proved to be the most active compound exhibiting IC50 values between 20.82 and 26.36 muM. (C) 2001 Elsevier Science Ltd. All rights reserved.
Unprecedented surface stabilized InP quantum dots with bidentate ligands
作者:Haewoon Seo、Meehee Bang、Yongjin Kim、Chaeyeon Son、Heung Bae Jeon、Sang-Wook Kim
DOI:10.1039/c9ra10933a
日期:——
For InP-based QDs, the current technology does not outperform CdSe-based QDs in many respects, one of which is stability.