Current perspectives on benzoflavone analogues with potent biological activities: A review

被引:1
作者
Liu, Guangxin [1 ]
Zhao, Zefeng [3 ]
Li, Mengjia [1 ]
Zhao, Mingrui [2 ]
Xu, Tong [1 ]
Wang, Shaohui [2 ]
Zhang, Yi [1 ,2 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, State Key Lab Southwestern Chinese Med Resources, Chengdu 611137, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Ethn Med Acad Heritage Innovat Res Ctr, State Key Lab Southwestern Chinese Med Resources, Chengdu, Peoples R China
[3] Shanxi Univ Chinese Med, Coll Acupuncture & Massage, Xixian New Area 712046, Shaanxi, Peoples R China
基金
国家重点研发计划;
关键词
Benzoflavone; Cytochrome P450; Antitumor; Central nervous system; Anti-inflammatory; SAR; Derivatives; CELL-CYCLE ARREST; CHALCONE DERIVATIVES; SYNTHETIC CHALCONES; AH RECEPTOR; INHIBITORS; APOPTOSIS; FLAVONOIDS; ALPHA; 7,8-BENZOFLAVONE; CYTOTOXICITY;
D O I
10.1016/j.arabjc.2022.104109
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Medicinal chemistry investigators have isolated and synthesized benzoflavone analogues with diverse bioactivities including enzyme inhibitory activity, central nervous system (CNS) activity, anti-inflammatory activity, anti-microorganism activity, hypoglycemic activity, and receptor modulating potential. SAR (Structure-Activity Relationship) studies have been conducted extensively and plenty of benzoflavone analogues have been prepared for potential targets. Herein, we review the pharmacology properties and SAR for benzoflavone analogues, and provide a brief summarization of synthetic strategies, wishing to give perspective on the research and development of benzoflavone derivatives. (C) 2022 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页数:20
相关论文
共 58 条
[1]   2'-SUBSTITUTED CHALCONE DERIVATIVES AS INHIBITORS OF INTERLEUKIN-1 BIOSYNTHESIS [J].
BATT, DG ;
GOODMAN, R ;
JONES, DG ;
KERR, JS ;
MANTEGNA, LR ;
MCALLISTER, C ;
NEWTON, RC ;
NURNBERG, S ;
WELCH, PK ;
COVINGTON, MB .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (10) :1434-1442
[2]   SAR-Guided Development and Characterization of a Potent Antitumor Compound toward B-Cell Neoplasms with No Detectable Cytotoxicity toward Healthy Cells [J].
Brunhofer-Bolzer, Gerda ;
Trang Le ;
Dyckmanns, Nils ;
Knaus, Hanna A. ;
Pausz, Clemens ;
Freund, Patricia ;
Jaeger, Ulrich ;
Erker, Thomas ;
Vanura, Katrina .
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (03) :1244-1253
[3]   Discovery, Structure-Activity Relationship, and Antiparkinsonian Effect of a Potent and Brain-Penetrant Chemical Series of Positive Allosteric Modulators of Metabotropic Glutamate Receptor 4 [J].
Charvin, Delphine ;
Pomel, Vincent ;
Ortiz, Millan ;
Frauli, Melanie ;
Scheffler, Sophie ;
Steinberg, Edith ;
Baron, Luc ;
Deshons, Laurene ;
Rudigier, Rachel ;
Thiarc, Delphine ;
Morice, Christophe ;
Manteau, Baptiste ;
Mayer, Stanislas ;
Graham, Danielle ;
Giethlen, Bruno ;
Brugger, Nadia ;
Hedou, Gael ;
Conquet, Francois ;
Schann, Stephan .
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (20) :8515-8537
[4]   Multi-Layer Identification of Highly-Potent ABCA1 Up-Regulators Targeting LXRβ Using Multiple QSAR Modeling, Structural Similarity Analysis, and Molecular Docking [J].
Chen, Meimei ;
Yang, Fafu ;
Kang, Jie ;
Yang, Xuemei ;
Lai, Xinmei ;
Gao, Yuxing .
MOLECULES, 2016, 21 (12)
[5]   Synthetic chalcones as efficient inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase PtpA [J].
Chiaradia, Louise Domeneghini ;
Mascarello, Alessandra ;
Purificacao, Marcela ;
Vernal, Javier ;
Sechini Cordeiro, Marlon Norberto ;
Zenteno, Maria Emilia ;
Villarino, Andrea ;
Nunes, Ricardo Jose ;
Yunes, Rosendo Augusto ;
Terenzi, Hernan .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (23) :6227-6230
[6]   Synthesis and pharmacological activity of chalcones derived from 2,4,6-trimethoxyacetophenone in RAW 264.7 cells stimulated by LPS: Quantitative structure-activity relationships [J].
Chiaradia, Louise Domeneghini ;
Dos Santos, Rodrigo ;
Vitor, Carlos Eduardo ;
Vieira, Andre Alexandre ;
Leal, Paulo Cesar ;
Nunes, Ricardo Jose ;
Calixto, Joao Batista ;
Yunes, Rosendo Augusto .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (02) :658-667
[7]   Synthesis, Biological Evaluation, And Molecular Modeling of Chalcone Derivatives As Potent Inhibitors of Mycobacterium tuberculosis Protein Tyrosine Phosphatases (PtpA and PtpB) [J].
Chiaradia, Louise Domeneghini ;
Alves Martins, Priscila Graziela ;
Sechini Cordeiro, Marlon Norberto ;
Carvalho Guido, Rafael Victorio ;
Ecco, Gabriela ;
Andricopulo, Adriano Defini ;
Yunes, Rosendo Augusto ;
Vernal, Javier ;
Nunes, Ricardo Jose ;
Terenzi, Hernan .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (01) :390-402
[8]   Chemical Modification of the Multitarget Neuroprotective Compound Fisetin [J].
Chiruta, Chandramouli ;
Schubert, David ;
Dargusch, Richard ;
Maher, Pamela .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (01) :378-389
[9]   Design and Synthesis of New α-Naphthoflavones as Cytochrome P450 (CYP) 1B1 Inhibitors To Overcome Docetaxel-Resistance Associated with CYP1B1 Overexpression [J].
Cui, Jiahua ;
Meng, Qingqing ;
Zhang, Xu ;
Cui, Qing ;
Zhou, Wen ;
Li, Shaoshun .
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (08) :3534-3547
[10]   Discovery of heterocycle-containing α-naphthoflavone derivatives as water-soluble, highly potent and selective CYP1B1 inhibitors [J].
Dong, Jinyun ;
Huang, Guang ;
Cui, Qing ;
Meng, Qingqing ;
Li, Shaoshun ;
Cui, Jiahua .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2021, 209