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寻找新型抗疟药药效团:一些含喹啉部分的2(3H)-呋喃酮的合成及其抗疟活性

Search for new pharmacophore as antimalarial agent: synthesis and antimalarial activity of some 2(3H)-furanones bearing quinoline moiety.

作者信息

Alam Mohammad Mumtaz, Sarkar Deba Priya, Alam Ozair, Husain Asif, Marella Akranth, Akhtar Mymoona, Shaquiquzzaman Mohammad, Khanna Suruchi

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jamia Hamdard, New Delhi-110062, India.

出版信息

Acta Pol Pharm. 2011 Mar-Apr;68(2):231-6.

Abstract

A series of substituted 3-[(substituted-2-chloroquinolin-3-yl)methylene]-5-(substituted-phenyl)-furan-2(3H)-ones (4a-p) have been synthesized and evaluated for their in vitro antimalarial activity against P. falciparum. The title compounds were synthesized by condensing 3-(substituted-benzoyl)propionic acids (3a-d) with substituted 2-chloroquinoline-3-carbaldehydes (2a-d) following modified Perkin's reaction. Compounds 3-[2-chloro-6-methylquinolin-3-yl)methylene]-5-(2,4-dimethyl-phenyl)-furan-2(3H)-one (4n) and 3-[2-chloro-6-methoxyquinolin-3-yl)methylene]-5-(2,4-dimethyl-phenyl)-furan-2(3H)-one (4p) showed promising antimalarial activity with MIC of 10 microg/mL.

摘要

一系列取代的3-[(取代-2-氯喹啉-3-基)亚甲基]-5-(取代苯基)-呋喃-2(3H)-酮(4a-p)已被合成,并对其针对恶性疟原虫的体外抗疟活性进行了评估。标题化合物是通过按照改进的珀金反应,将3-(取代苯甲酰基)丙酸(3a-d)与取代的2-氯喹啉-3-甲醛(2a-d)缩合而合成的。化合物3-[2-氯-6-甲基喹啉-3-基)亚甲基]-5-(2,4-二甲基苯基)-呋喃-2(3H)-酮(4n)和3-[2-氯-6-甲氧基喹啉-3-基)亚甲基]-5-(2,4-二甲基苯基)-呋喃-2(3H)-酮(4p)显示出有前景的抗疟活性,最低抑菌浓度为10微克/毫升。

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