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Merck

Synthesis and anticancer evaluation of alpha-lipoic acid derivatives.

Bioorganic & medicinal chemistry letters (2010-04-21)
Shi-Jie Zhang, Qiu-Fu Ge, Dian-Wu Guo, Wei-Xiao Hu, Hua-Zhang Liu
摘要

alpha-Lipoic acid derivatives were synthesized and evaluated for their in vitro anticancer activities against NCI-460, HO-8910, KB, BEL-7402, and PC-3 cell lines. The results, for most compounds exhibited dose-dependent inhibitory property and several compounds had good inhibitions at the dose of 100 microg/mL. Compound 17 m was further selected for in vivo evaluation against S180 xenograft in ICR mice, which had 24.7% tumor-weight inhibition through intragastric administration of 200mg/kg of body weight. Moreover, the LD(50) in mice for 17 m through ig exceeded 1000 mg/kg of body weight.

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Sigma-Aldrich
(±)-α-硫辛酸, ≥98.0%
Sigma-Aldrich
(±)-α-硫辛酸, suitable for cell culture, BioReagent, ≥99%
Sigma-Aldrich
(±)-α-硫辛酸, synthetic, ≥99% (titration), powder