Inhibition of Trypanosoma brucei brucei peptidyl transferase activity by sparsomycin analogs and effects on trypanosome protein synthesis and proliferation
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference22 articles.
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Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Schedule-dependent enhancement of antitumor activity of ethyldeshydroxy-sparsomycin in combination with classical antineoplastic agents;Anti-Cancer Drugs;1995-04
2. Concentration and sequence dependent synergism of ethyldeshydroxy-sparsomycin in combination with antitumor agents;Anti-Cancer Drugs;1994-02
3. Dauer larva recovery in the nematode Caenorhabditis elegans—II. The effect of inhibitors of protein synthesis on recovery, growth and pharyngeal pumping;Comparative Biochemistry and Physiology Part B: Comparative Biochemistry;1991-01
4. Lipophilic analogs of sparsomycin as strong inhibitors of protein synthesis and tumor growth: a structure-activity relationship study;Journal of Medicinal Chemistry;1989-08
5. Effects of α-difluoromethylornithine on protein synthesis and synthesis of the variant-specific glycoprotein (VSG) in Trypanosoma brucei brucei;Biochemical Journal;1988-02-15
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