Synthesis and vasorelaxant evaluation of novel 7-methoxyl-2,3-disubstituted-quinoxaline derivatives

被引:10
作者
Zheng, Chang-Bo [3 ,4 ]
Gao, Wen-Cong [3 ,4 ]
Pang, Pan-Pan [3 ,4 ]
Ma, Xin [3 ,4 ]
Peng, Li-Chun [3 ,4 ]
Yang, Liang [5 ]
Li, Xun [1 ,2 ]
机构
[1] Shandong First Med Univ, Inst Mat Med, 6699 Qingdao Rd, Jinan 250002, Shandong, Peoples R China
[2] Shandong Acad Med Sci, 6699 Qingdao Rd, Jinan 250002, Shandong, Peoples R China
[3] Kunming Med Univ, Sch Pharmaceut Sci, Kunming, Yunnan, Peoples R China
[4] Kunming Med Univ, Yunnan Key Lab Pharmacol Nat Prod, Kunming, Yunnan, Peoples R China
[5] Shandong Univ, Sch Pharmaceut Sci, Inst Biochem & Biotechnol Drugs, Minist Educ,Key Lab Chem Biol, Jinan 250012, Shandong, Peoples R China
关键词
7-Methoxyl-2,3-disubstituted quinoxaline derivatives; Vasorelaxant; Endothelium-independent;
D O I
10.1016/j.bmcl.2021.127785
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An array of novel 7-methoxyl-2,3-disubstituted quinoxaline derivatives was designed, synthesized and their potential antihypertensive activities were examined, in an attempt to discover potent small molecules with vasorelaxant effects. The vasoactivities of these compounds on vascular tone, as well as underlying mechanisms were hereby explored. Results showed that five compounds (7s, 7t, 7v, 7w, 7 gamma) could induce endothelium-independent relaxation in high extracellular K+- and phenylephrine-precontracted C57 mice aortic rings. These five compounds, unlike other commonly used vasodilators, could slowly but effectively inhibit vasoconstriction.
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页数:6
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