Okamura W H, Palenzuela J A, Plumet J, Midland M M
Department of Chemistry, University of California, Riverside 92521.
J Cell Biochem. 1992 May;49(1):10-8. doi: 10.1002/jcb.240490104.
There is continuing and emerging new interest in the development of vitamin D analogs resulting from the recognition that analogs of 1 alpha,25-dihydroxyvitamin D3 [1 alpha,25-(OH)2D3] may be therapeutically useful. Side chain analogs of this steroid hormone are of particular interest because a family of lead structures have recently emerged for possible use in the treatment of certain types of cancers and skin diseases. Because of the chaotic array of side chain structures which exhibit useful therapeutic indices for these purposes, a more systematic approach towards developing intelligible structure-function information needs development. Accordingly, a method has been devised to analyze analogs as to their side chain topology based on identifying specific occupancy volumes through conformational analysis. Dot maps have been constructed as an indication of the volume in space which the side chain of 1 alpha,25-(OH)2-D3 or analogs is permitted to occupy. Volume exclusion analyses based on comparison of structural and biological data for 1 alpha,25-(OH)2-D3 and analogs are anticipated to lead to a more cogent model for drug design. A cautionary note on the limitations of this approach is discussed.
由于认识到1α,25 - 二羟基维生素D3[1α,25 - (OH)2D3]的类似物可能具有治疗作用,人们对维生素D类似物的开发持续保持着新的兴趣且兴趣不断涌现。这种类固醇激素的侧链类似物特别受关注,因为最近出现了一系列可能用于治疗某些类型癌症和皮肤病的先导结构。由于用于这些目的的具有有用治疗指数的侧链结构杂乱无章,因此需要开发一种更系统的方法来获取清晰的结构 - 功能信息。相应地,已经设计出一种方法,通过构象分析识别特定的占据体积,从而分析类似物的侧链拓扑结构。已构建点图以表明1α,25 - (OH)2 - D3或其类似物的侧链在空间中允许占据的体积。基于对1α,25 - (OH)2 - D3及其类似物的结构和生物学数据的比较进行的体积排除分析,有望为药物设计带来更有说服力的模型。本文还讨论了该方法局限性的警示说明。