Isolation, biology and chemistry of the disorazoles: new anti-cancer macrodiolides

被引:42
|
作者
Hopkins, Chad D. [1 ]
Wipf, Peter [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
CHONDROMYCES-CROCATUS MYXOBACTERIA; NATURAL-PRODUCTS; ASYMMETRIC-SYNTHESIS; GLIDING BACTERIA; STEREOSELECTIVE-SYNTHESIS; SPECIES MYXOBACTERIA; MULTIDRUG-RESISTANCE; SORANGIUM-CELLULOSUM; EPOTHILONE-B; MICROTUBULE;
D O I
10.1039/b813799b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The disorazoles comprise a family of 29 closely related macrocyclic polyketides isolated in 1994 from the fermentation broth of the gliding myxobacterium Sorangium cellulosum. Disorazoles A(1), E and C-1 have shown exceptional biological activities toward inhibiting the proliferation of human cancer cell lines in picomolar and nanomolar concentrations through the disruption of microtubule polymerization. This review gives a brief introduction describing the biosynthesis and the significance of the disorazoles as a new class of microtubulin disruptors. Another portion of the review focuses on the biology of the disorazoles, specifically disorazole A(1) and C-1, and their antiproliferative efficacy against animal and human tumor cell lines, as well as the available SAR data. The majority of the discussion addresses synthetic efforts, including partial syntheses of various disorazoles and a summary of the total synthesis of disorazole C-1.
引用
收藏
页码:585 / 601
页数:17
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