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大环桦木醇衍生物作为新型抗HIV-1成熟抑制剂的合成及生物学评价

Synthesis and Biological Evaluation of Macrocyclized Betulin Derivatives as a Novel Class of Anti-HIV-1 Maturation Inhibitors.

作者信息

Tang Jun, Jones Stacey A, Jeffery Jerry L, Miranda Sonia R, Galardi Cristin M, Irlbeck David M, Brown Kevin W, McDanal Charlene B, Han Nianhe, Gao Daxin, Wu Yongyong, Shen Bin, Liu Chunyu, Xi Caiming, Yang Heping, Li Rui, Yu Yajun, Sun Yufei, Jin Zhimin, Wang Erjuan, Johns Brian A

机构信息

GlaxoSmithKline Research & Development, Research Triangle Park, NC 27709, USA.

ShangPharma Discovery Chemistry Services, Zhangjiang High-tech Park, Pudong, Shanghai 201203, China.

出版信息

Open Med Chem J. 2014 Sep 3;8:23-7. doi: 10.2174/1874104501408010023. eCollection 2014.

Abstract

A macrocycle provides diverse functionality and stereochemical complexity in a conformationally preorganized ring structure, and it occupies a unique chemical space in drug discovery. However, the synthetic challenge to access this structural class is high and hinders the exploration of macrocycles. In this study, efficient synthetic routes to macrocyclized betulin derivatives have been established. The macrocycle containing compounds showed equal potency compared to bevirimat in multiple HIV-1 antiviral assays. The synthesis and biological evaluation of this novel series of HIV-1 maturation inhibitors will be discussed.

摘要

大环化合物在构象预组织的环状结构中提供了多样的功能和立体化学复杂性,并且在药物发现中占据独特的化学空间。然而,获得这类结构的合成挑战很大,阻碍了对大环化合物的探索。在本研究中,已建立了通往大环化桦木醇衍生物的有效合成路线。在多种HIV-1抗病毒试验中,含大环化合物显示出与贝维拉马相当的效力。将讨论这一系列新型HIV-1成熟抑制剂的合成及生物学评价。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14f8/4157350/aa87d8e76898/TOMCJ-8-23_F1.jpg

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