Guggullipid derivatives: synthesis and applications

被引:5
作者
Ahmad, Moghis U. [1 ]
Ali, Shoukath M. [1 ]
Ahmad, Ateeq [1 ]
Sheikh, Saifuddin [1 ]
Ahmad, Imran [1 ]
机构
[1] Jina Pharmaceut Inc, Libertyville, IL 60048 USA
关键词
Guggullipid; Synthesis; Liposome; Drug delivery; IIA SECRETORY PHOSPHOLIPASE-A2; AYURVEDIC CRUDE DRUGS; COMMIPHORA-MUKUL; STEREOCHEMISTRY; DOXORUBICIN; EXPRESSION; CHEMISTRY; LEUKEMIA; CANCER; RESIN;
D O I
10.1016/j.chemphyslip.2010.02.004
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
Two guggullipid derivatives,Z-guggulsulfate [4,17(20)-pregnadiene-3-one-16 beta-sulfate] sodium salt and Z-guggullaurate (4,17(20)-pregnadiene-3-one-16 beta-laurate], have been synthesized and evaluated for liposomal drug delivery system. Its precursor, Z-guggulsterol [4,17(20)-pregnadiene-3-one-16 beta-ol], is also synthesized in gram scale starting from guggulsterone using the novel combination of known reactions in fewer steps and with higher yield than previously reported synthesis. These new synthetic guggullipid derivatives were also used in the preparation of liposomes. This new class of lipid molecules will be a useful tool in the development of nanosomal or liposomal drug delivery system. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:362 / 366
页数:5
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