Synthesis and Biological Evaluation of New Bis-Indolyl (3-O-Benzyl-1,2-O-Isopropylidenexylopentadialdose-α-D-Glucofuranose)

被引:0
|
作者
Shankar, M. [1 ]
Balasubramaniam, A. [2 ]
Gowrishankar, N. L. [3 ]
Mahendran, S. [4 ]
机构
[1] Swami Vivekanandha Inst Pharmaceut Sci, Dept Pharmaceut Chem, Vangapally 508286, AP, India
[2] JKK Munirajah Med Res Fdn Coll Pharm, Dept Pharmaceut Chem, Komarapalayam 638183, TN, India
[3] Swami Vivekanandha Inst Pharmaceut Sci, Dept Pharmacognosy, Vangapally 508286, AP, India
[4] JSS Coll Pharm, Dept Pharmaceut Chem, Ootacamund 643001, TN, India
关键词
3-O-benzyl-1,2-O-isopropylidene-xylopentadialdose; antibacterial activity; anti-inflammatory activity;
D O I
10.1007/s11094-014-1001-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
3-O-benzyl-1,2-O-isopropylidene-xylopentadialdose has emerged as structurally new antibacterial and anti-inflammatory agent. Therefore, various substituted bis-indolyl- (3-O-benzyl-1,2-O-isopropylidene-xylopentadialdose glucofuranose) derivatives were synthesized by addition of substituted xylopentadialdose with various substituted indoles. The structures of the synthesized compounds were characterized by IR, H-1 NMR, C-13 NMR, and mass spectroscopy techniques. All the synthesised compounds showed maximum zone of inhibition againt both Gram-positive and Gram-negative organisms. In the anti-inflammatory activity test, three compounds (1, 3 and 5) produced significant activity in a dose-dependent manner.
引用
收藏
页码:544 / 548
页数:5
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