Quinazolines and quinazolinones as ubiquitous structural fragments in medicinal chemistry: An update on the development of synthetic methods and pharmacological diversification

被引:254
作者
Khan, Imtiaz [1 ]
Zaib, Sumera [2 ,3 ]
Batool, Sadaf [4 ]
Abbas, Naeem [1 ]
Ashraf, Zaman [5 ]
Iqbal, Jamshed [3 ]
Saeed, Aamer [1 ]
机构
[1] Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
[2] Hazara Univ, Dept Biochem, Garden Campus, Mansehra, Pakistan
[3] COMSATS Inst Informat Technol, Ctr Adv Drug Res, Abbottabad 22060, Pakistan
[4] Int Islamic Univ, Dept Bioinformat & Biotechnol, Islamabad 44000, Pakistan
[5] Allama Iqbal Open Univ, Dept Chem, Islamabad 44000, Pakistan
关键词
Drug discovery; Heterocycles; Quinazolines; Quinazolinones; Enzyme inhibitors; Biological activity; ALKALINE-PHOSPHATASE INHIBITION; ANTIINFLAMMATORY AGENTS; ANTICONVULSANT ACTIVITY; EFFICIENT SYNTHESIS; CRYSTAL-STRUCTURE; HIGHLY POTENT; IN-VIVO; 1,3,4-THIADIAZOLE DERIVATIVES; BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY;
D O I
10.1016/j.bmc.2016.03.031
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
Nitrogen-rich heterocycles, particularly quinazolines and quinazolinones, represent a unique class of diversified frameworks displaying a broad spectrum of biological functions. Over the past several years, intensive medicinal chemistry efforts have generated numerous structurally functionalized quinazoline and quinazolinone derivatives. Interest in expanding the biological effects, demonstrated by these motifs, is growing exponentially, as indicated by the large number of publications reporting the easy accessibility of these skeletons in addition to the diverse nature of synthetic as well as biological applications. Therefore, the main focus of the present review is to provide an ample but condensed overview on various synthetic approaches providing access to quinazoline and quinazolinone compounds with multifaceted biological activities. Furthermore, mechanistic insights, synthetic utilization, structure-activity relationships and molecular modeling inputs for the potent derivatives have also been discussed. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2361 / 2381
页数:21
相关论文
共 106 条
[1]  
Ahmed M F., 2015, Res Chem Intermed, P1
[2]   Design, Synthesis, and Molecular Docking Studies of 2-(Furan-2-yl)quinazolin-4-one Derivatives as Potential Antiproliferative Agents [J].
Ahmed, Marwa F. ;
Belal, Amany .
ARCHIV DER PHARMAZIE, 2015, 348 (07) :487-497
[3]   Synthesis, anticonvulsant activity and molecular modeling study of some new hydrazinecarbothioamide, benzenesulfonohydrazide, and phenacylacetohydrazide analogues of 4(3H)-quinazolinone [J].
Al-Salem, Huda S. A. ;
Hegazy, Gehan H. ;
El-Taher, Kamal E. H. ;
El-Messery, Shahenda M. ;
Al-Obaid, Abdulrahman M. ;
El-Subbagh, Hussein I. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (07) :1490-1499
[4]   3-(3-Ethylphenyl)-2-substituted hydrazino-3H-quinazolin-4-one Derivatives: New Class of Analgesic and Anti-Inflammatory Agents [J].
Alagarsamy, V. ;
Solomon, V. Raja ;
Sheorey, R. V. ;
Jayakumar, R. .
CHEMICAL BIOLOGY & DRUG DESIGN, 2009, 73 (04) :471-479
[5]  
Alagarsamy V, 2008, J ENZYM INHIB MED CH, V23, P839, DOI [10.1080/14756360701746229, 10.1080/14756360701746229 ]
[6]   Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones [J].
Alagarsamy, Veerachamy ;
Pathak, Urvishbhai S. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (10) :3457-3462
[7]  
[Anonymous], 2001, MERCK INDEX, V13th
[8]  
Archana, 2002, EUR J MED CHEM, V37, P873
[9]   Synthesis and anti-oomycete activity of novel quinazolin- and benzothiazol-6-yloxyacetamides: Potent aza-analogs and five-ring analogs of quinoline fungicides [J].
Beaudegnies, Renaud ;
Quaranta, Laura ;
Kessabi, Fiona Murphy ;
Lamberth, Clemens ;
Knauf-Beiter, Gertrud ;
Fraser, Torquil .
BIOORGANIC & MEDICINAL CHEMISTRY, 2016, 24 (03) :444-452
[10]   In vivo antimalarial evaluation of some 2,3-disubstituted-4(3H)-quinazolinone derivatives [J].
Birhan Y.S. ;
Bekhit A.A. ;
Hymete A. .
BMC Research Notes, 8 (1)