Synthesis and anticancer activity of novel C6-piperazine substituted purine steroid-nucleosides analogues.

Abstract:

:Novel C6-piperazine substituted purine nucleoside analogues (2-9) bearing a modified pyranose-like D ring of the 4-azasteroid moiety were efficiently synthesized through nucleophilic substitution at C6 position of the steroid-nucleoside precursors (1) with versatile piperazines. All newly-synthesized compounds were evaluated for their anticancer activity in vitro against Hela, PC-3 and MCF-7 cell lines. Among them, compounds 8b and 9b exhibited significant cytotoxicity on PC-3 cell lines.

journal_name

Steroids

journal_title

Steroids

authors

Huang LH,Xu HD,Yang ZY,Zheng YF,Liu HM

doi

10.1016/j.steroids.2013.12.004

subject

Has Abstract

pub_date

2014-04-01 00:00:00

pages

1-6

eissn

0039-128X

issn

1878-5867

pii

S0039-128X(13)00289-4

journal_volume

82

pub_type

杂志文章

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