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苯并喹唑啉类支架的重要药理学活性。

Significant pharmacological activities of benzoquinazolines scaffold.

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, PO Box 2457, Riyadh, 11451, Saudi Arabia.

出版信息

Pharmacol Rep. 2023 Apr;75(2):223-235. doi: 10.1007/s43440-023-00453-9. Epub 2023 Feb 6.

DOI:10.1007/s43440-023-00453-9
PMID:36740656
Abstract

Benzoquinazolines, the essential constituents of numerous well-known heterocyclic systems, have occupied a prominent position and played a significant part in the synthesis of various pharmaceutical compounds. The wide range of pharmacological effects attributed to benzoquinazolines has been the subject of extensive study. These include their roles as anticancer, antimicrobial, anti-monoamine oxidase, anticonvulsant, antiviral, antinociceptive, antioxidant, antineoplastic, antituberculosis, antiplatelet, and antiphlogistic agents. This work provides an attempt at a literature review of the pharmacological activities of benzoquinazoline derivatives, including an up-to-date account of recent research findings, and suggests avenues for future exploration in the pursuit of more potent and specific analogues for a wide range of biological targets using this platform.

摘要

苯并喹唑啉是许多著名杂环体系的基本组成部分,在各种药物化合物的合成中占有重要地位。苯并喹唑啉具有广泛的药理作用,这一直是广泛研究的主题。这些作用包括抗癌、抗菌、抗单胺氧化酶、抗惊厥、抗病毒、镇痛、抗氧化、抗肿瘤、抗结核、抗血小板和抗炎作用。这项工作试图对苯并喹唑啉衍生物的药理活性进行文献综述,包括最近研究结果的最新报道,并提出了利用这一平台为广泛的生物靶标寻找更有效和更特异的类似物的未来探索途径。

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Investigation of some benzoquinazoline and quinazoline derivatives as novel inhibitors of HCV-NS3/4A protease: biological, molecular docking and QSAR studies.一些苯并喹唑啉和喹唑啉衍生物作为丙型肝炎病毒NS3/4A蛋白酶新型抑制剂的研究:生物学、分子对接和定量构效关系研究
RSC Adv. 2020 Sep 30;10(59):35820-35830. doi: 10.1039/d0ra05604a. eCollection 2020 Sep 28.
2
Synthesis and biological evaluation of 4-(1-1,2,4-triazol-1-yl)benzoic acid hybrids as anticancer agents.4-(1-1,2,4-三唑-1-基)苯甲酸杂合物作为抗癌剂的合成及生物学评价
RSC Adv. 2019 Jun 17;9(33):19065-19074. doi: 10.1039/c9ra03151k. eCollection 2019 Jun 14.
3
Discovery and mechanistic study of thiazole-4-acylsulfonamide derivatives as potent and orally active ChemR23 inhibitors with a long-acting effect in cynomolgus monkeys.
噻唑-4-酰基磺酰胺衍生物的发现及作用机制研究:作为有效的 ChemR23 抑制剂,在食蟹猴体内具有长效作用。
Bioorg Med Chem. 2022 Feb 15;56:116587. doi: 10.1016/j.bmc.2021.116587. Epub 2022 Jan 10.
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In silico study and biological screening of benzoquinazolines as potential antimicrobial agents against methicillin-resistant Staphylococcus aureus, carbapenem-resistant Klebsiella pneumoniae, and fluconazole-resistant Candida albicans.计算机研究与苯并喹唑啉类化合物的生物筛选及其作为抗耐甲氧西林金黄色葡萄球菌、耐碳青霉烯类肺炎克雷伯菌和氟康唑耐药白色假丝酵母菌的潜在抗菌剂。
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