Insights into the chemistry and therapeutic potential of furanones: A versatile pharmacophore

被引:91
作者
Husain, Asif [1 ]
Khan, Shah Alam [2 ,3 ]
Iram, Farah [1 ]
Iqbal, Md Azhar [1 ]
Asif, Mohammad [4 ]
机构
[1] Jamia Hamdard, Sch Pharmaceut Educ & Res, Dept Pharmaceut Chem, New Delhi 110062, India
[2] Oman Med Coll, Dept Pharm, Muscat, Oman
[3] Natl Univ Sci & Technol, Coll Pharm, Muscat, Oman
[4] GRD PG Inst Management & Technol, Dept Pharm, Dehra Dun 248009, UK, India
关键词
Biological activity; Butenolide; Cyclooxygenase; Furanone; Lactone; SAR; REDUCED GASTROINTESTINAL TOXICITY; BICYCLIC BROMINATED FURANONES; RNA SYNTHETASE SYNTHESIS; CELL-CYCLE ARREST; BIOLOGICAL EVALUATION; MOLECULAR DOCKING; BIOFILM FORMATION; IN-VIVO; 2(5H)-FURANONE DERIVATIVES; ANTIBACTERIAL ACTIVITIES;
D O I
10.1016/j.ejmech.2019.03.021
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Furanone, a five-membered heteroaromatic ring containing oxygen atom, is of immense pharmaceutical importance. Presence of this nucleus in biologically active compounds of natural and synthetic origin has made it an indispensable motif for design and development of new therapeutic agents. In recent years synthesis of furanone derivatives and exploring their therapeutic actions has been the prime interest amongst researchers. Furanone containing compounds cover numerous therapeutic categories viz. Analgesic and anti-inflammatory, anticancer, anticonvulsant, antibacterial and antifungal, antioxidant, antiulcer and anti-TB, etc. There is a need to couple recent work done with previously available information on furanone, a well acknowledged scaffold, to help scientists to develop novel and new furanone based therapeutic agents at a faster pace. This updated review highlights the worth of numerous therapeutically active furanone based compounds developed by the medicinal chemists. SAR studies have also been derived which may be useful for rational designing of furanone derivatives with improved therapeutic index. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:66 / 92
页数:27
相关论文
共 192 条
[1]   Synthesis and Antitumor Activity Evaluation of Some Novel-Fused and Spiro Heterocycles Derived from a 2(3H)-Furanone Derivative [J].
Abou-Elmagd, Wael S. I. ;
Hashem, Ahmed I. .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 2016, 53 (01) :202-208
[2]   Synthesis and evaluation of homologous analogs of anticonvulsant 5-substituted 3,3-diethyl-4,5-dihydro-2(3H)-furanones [J].
Ahungena, Alemayyehu ;
Canney, Daniel J. .
MEDICINAL CHEMISTRY RESEARCH, 2005, 14 (07) :404-428
[3]   Synthesis and antimalarial activity of quinoline-substituted furanone derivatives and their identification as selective falcipain-2 inhibitors [J].
Akhter, Mymoona ;
Saha, Rikta ;
Tanwar, Omprakash ;
Alam, Md. Mumtaz ;
Zaman, M. S. .
MEDICINAL CHEMISTRY RESEARCH, 2015, 24 (02) :879-890
[4]   Synthesis and pharmacological evaluation of 2(3H)-furanones and 2(3H)-pyrrolones, combining analgesic and anti-inflammatory properties with reduced gastrointestinal toxicity and lipid peroxidation [J].
Alam, M. M. ;
Husain, Asif ;
Hasan, S. M. ;
Suruchi ;
Anwer, T. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (06) :2636-2642
[5]   Synthesis of quinoline-attached furan-2(3H)-ones having anti-inflammatory and antibacterial properties with reduced gastro-intestinal toxicity and lipid peroxidation [J].
Alam, Mohammad M. ;
Sarkar, Deba Priya ;
Husain, Asif ;
Marella, Akranth ;
Shaquiquzzaman, Mohammad ;
Akhter, Mymoona ;
Shaharyar, Mohammad ;
Alam, Ozair ;
Azam, Faizul .
JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 2011, 76 (12) :1617-1626
[6]   LUFFARIELLOLIDE, AN ANTIINFLAMMATORY SESTERTERPENE FROM THE MARINE SPONGE LUFFARIELLA SP [J].
ALBIZATI, KF ;
HOLMAN, T ;
FAULKNER, DJ ;
GLASER, KB ;
JACOBS, RS .
EXPERIENTIA, 1987, 43 (08) :949-950
[7]   Synthesis and cytotoxic activity of γ-aryl substituted α-alkylidene-γ-lactones and α-alkylidene-γ-lactams [J].
Albrecht, Anna ;
Koszuk, Jacek F. ;
Modranka, Jakub ;
Rozalski, Marek ;
Krajewska, Urszula ;
Janecka, Anna ;
Studzian, Kazimierz ;
Janecki, Tomasz .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (09) :4872-4882
[8]  
[Anonymous], 2017, EUR J MED CHEM
[9]  
[Anonymous], ANTI RES
[10]  
[Anonymous], APPL ENV MICROBIOL