Toward the development of chemoprevention agents. Part II: Chemo-enzymatic synthesis and anti-inflammatory activities of a new class of 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes

被引:21
作者
Gu, Keli
Bi, Lanrong
Zhao, Ming [1 ]
Wang, Chao
Ju, Jingfang
Peng, Shiqi
机构
[1] Capital Med Univ, Coll Pharmaceut Sci, Beijing 100054, Peoples R China
[2] Peking Univ, Coll Pharmaceut Sci, Beijing 100083, Peoples R China
[3] Univ S Alabama, Mitchell Canc Inst, Mobile, AL 36688 USA
关键词
chemoprevention; chemo-enzymatic synthesis; 2,5-disubstituted-dioxacycloalkanes; anti-inflammatory activity; structure-activity; relationship study;
D O I
10.1016/j.bmc.2007.06.018
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
A new series of optically pure 5-amino-2-substitutedphenyl-1,3-dioxacyclozilkanes were designed and synthesized via a chemo-enzymatic combined method to develop new chemoprevention agents. Twenty-four of newly synthesized compounds significantly inhibited xylene-induced rat ear edema and exhibited comparable or better anti-inflammatory activities than the reference drug aspirin. Treatment of these anti-inflammatory agents did not prolong the tail bleeding time in rat. In addition, 5-amino-2-substitutedphenyl- I 3-dioxacycloalkanes exhibited good membrane permeability based on in vitro Caco-2 cell monolayer permeability assay. Furthermore, some preliminary structure-activity relationships were further analyzed among these compounds. Taken together, 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes may represent a new class of anti-inflammatory drugs with safer pharmacological profile. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6273 / 6290
页数:18
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