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药物分析英文文献3
554 J. Nat. Prod. 2009, 72, 554–565
Recent Advances in the Chemistry and Biology of New Generation Taxoids‡
Iwao Ojima* and Manisha Das
Department of Chemistry and Institute of Chemical Biology Drug Disco Very, State UniVersity of New York at Stony Brook,
Stony Brook, New York 11794-3400
Recei Ved October 15, 2008
Among the numerous chemotherapeutic drugs, paclitaxel and docetaxel are among the most widely used against various
types of cancer. However, these drugs cause undesirable side effects as well as drug resistance. Therefore, it is essential
to develop “taxane” anticancer agents with better pharmacological properties and improved activity especially against
drug-resistant cancers. Several laboratories have performed extensive SAR studies on paclitaxel. Our SAR studies have
led to the development of numerous highly potent novel second- and third-generation taxoids with systematic modifications
at the C-2, C-10, and C-3′ positions. The third-generation taxoids showed virtually no difference in potency against
drug-resistant and drug-sensitive cell lines. Some of the new generation taxoids also exhibited excellent cytotoxicity
against pancreatic cell lines expressing multidrug-resistant genes. We have also designed taxoids with strategic fluorine
incorporation to investigate their effects on the cytotoxicity and the blockage of known metabolic pathways. Furthermore,
we have successfully employed computational biology analysis to design novel macrocyclic taxoids to mimic the bioactive
conformation of paclitaxel. This account describes our work on the design, synthesis, and biological evaluation of these
novel taxoids, which has led to the discovery of very promising candidates for further preclinical studies.
Introduction
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