Synthesis of oxadiazole-morpholine derivatives and manifestation of the repressed CD31 Microvessel Density (MVD) as tumoral angiogenic parameters in Dalton's Lymphoma

被引:30
作者
Al-Ghorbani, Mohammed [1 ]
Vigneshwaran, V. [2 ]
Ranganatha, V. Lakshmi [1 ,3 ]
Prabhakar, B. T. [2 ]
Khanum, Shaukath Ara [1 ]
机构
[1] Univ Mysore, Yuvarajas Coll, Dept Chem, Mysore 570005, Karnataka, India
[2] Kuvempu Univ, Sahyadri Sci Coll Autonomous, Postgrad Dept Studies & Res Biotechnol, Mol Biomed Lab, Shimoga 577203, Karnataka, India
[3] St Philomenas Coll, PG Dept Chem, Mysore 570015, Karnataka, India
关键词
Oxadiazole-morpholine; Microvessel Density (MVD); CD31; Angiogenesis; Dalton's Lymphoma; 1,3,4-OXADIAZOLE DERIVATIVES; BIOLOGICAL EVALUATION; ANTITUMOR-ACTIVITY; MOLECULAR DOCKING; ANTICANCER; GROWTH; INHIBITION; EXPRESSION; MODELS; MOIETY;
D O I
10.1016/j.bioorg.2015.04.008
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 series of oxadiazole derivatives possessing morpholine 6a-l were synthesized by nucleophilic substitution reaction of key intermediates [1,3,4]-oxadiazole-2-thiol derivatives 5a-l with 4-(2-chloroethyl) morpholine. Compounds 6a-l were evaluated for their in vitro and in vivo antitumor potential in Dalton's Lymphoma Ascites (DLA) tumor cells. Among 6a-l series, compound 6a with concentration similar to 8.5 mu M have shown extensive cytotoxicity in vitro and 85% reduction in tumor volume in vivo, attributing an excellent anti-proliferative capability towards the cancer cells. Compound 6a has extensively inhibited the Microvessel Density (MVD) or tumoral neovasculature which was evident from the CD31 immuno staining and peritoneal H&E staining. The major reason for the antiproliferative activity of compound 6a was due to the repression of tumor vasculature. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:136 / 146
页数:11
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