Catechin prodrugs and analogs: a new array of chemical entities with improved pharmacological and pharmacokinetic properties

被引:40
作者
Bansal, Sumit [1 ]
Vyas, Sandeep [2 ]
Bhattacharya, Shoumyo [3 ]
Sharma, Manu [1 ]
机构
[1] Jaypee Univ Informat Technol, Dept Chem, Waknaghat, Himachal Prades, India
[2] Panjab Univ, Dept Chem, Chandigarh 160014, India
[3] Shoolini Univ, Sch Pharmaceut Sci, Solan, Himachal Prades, India
关键词
GREEN TEA POLYPHENOL; ACID MONOESTER DERIVATIVES; NEWLY SYNTHESIZED CATECHIN; SQUAMOUS-CELL CARCINOMA; GALLATE EGCG ANALOGS; PHASE-I TRIAL; (-)-EPIGALLOCATECHIN GALLATE; O-METHYLTRANSFERASE; EPIGALLOCATECHIN-3-GALLATE EGCG; PROTEASOME INHIBITORS;
D O I
10.1039/c3np70038k
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
Extensive research on tea catechins, mainly (-)-epigallocatechin gallate, has shown numerous health promoting effects. However, various clinical studies demonstrated several issues associated with tea catechins which account for their poor systemic bioavailability. In order to improve pharmacological activity and bioavailability of natural tea catechins, two major strategies have been adopted to date which include synthesizing catechin analogs/prodrugs and the development of novel drug delivery systems. In this review, we provide a detailed account of novel synthetic analogs/prodrugs as well as novel drug delivery approaches used for natural tea catechins to make them therapeutically potent drug-like molecules.
引用
收藏
页码:1438 / 1454
页数:17
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