Synthesis and Biological Activity of Several Modified 5α-Androstanolone Derivatives

被引:5
作者
Nadaraia, N. Sh. [1 ]
Barbakadze, N. N. [1 ]
Kakhabrishvili, M. L. [1 ]
Sylla, B. [2 ]
Pichette, A. [2 ]
Makhmudov, U. S. [3 ]
机构
[1] Tbilisi State Med Univ, I Kutateladze Inst Pharmacochem, Tbilisi 0159, Georgia
[2] Univ Quebec Chicoutimi, LASEVE, Chicoutimi, PQ G7H 2B1, Canada
[3] Acad Sci Uzbek, S Yu Yunusov Inst Chem Plant Subst, Tashkent, Uzbekistan
基金
美国国家科学基金会;
关键词
antiviral activity; epiandrosterone; modification; phenylacetic acid; hydrazones; pyrazolines; PHENYLACETIC ACID; STEROIDS; AUXIN;
D O I
10.1007/s10600-018-2330-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several new N-containing epiandrosterone derivatives modified by phenylacetic acid chloride were synthesized for biological activity studies. Compounds with antiviral activity were discovered among them and 3 beta-hydroxy-1'-aryl-3'-methyl-5'-androstano[17,16-d]pyrazolines prepared by us earlier.
引用
收藏
页码:310 / 314
页数:5
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