• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

合成α-葡萄糖苷酶抑制剂的最新进展

Recent Advances in Synthetic α-Glucosidase Inhibitors.

作者信息

Liu Zhiyang, Ma Shutao

机构信息

Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, 44 West Culture Road, Jinan, 250012, P.R. China.

出版信息

ChemMedChem. 2017 Jun 7;12(11):819-829. doi: 10.1002/cmdc.201700216. Epub 2017 Jun 1.

DOI:10.1002/cmdc.201700216
PMID:28498640
Abstract

Over the past few years, the number of people diagnosed with type 2 diabetes has increased owing to an unhealthy diet, a limited amount of exercise, and obesity. The search for novel and efficient antidiabetes agents has become an urgent task for scientists. Among the antidiabetes drugs, α-glucosidase inhibitor drugs have been proven to have many advantages over other drugs, and therefore, a large number of new compounds as α-glucosidase inhibitors has recently been reported. In this review, we summarize these newly found α-glucosidase inhibitors and their structure-activity relationships in antidiabetic studies and provide better structures for α-glucosidase inhibitors or even preclinical candidates. Beyond that, some enlightening strategies for the synthesis of relevant compounds are highlighted.

摘要

在过去几年中,由于不健康饮食、运动量有限和肥胖,被诊断出患有2型糖尿病的人数有所增加。寻找新型高效的抗糖尿病药物已成为科学家们的一项紧迫任务。在抗糖尿病药物中,α-葡萄糖苷酶抑制剂药物已被证明比其他药物具有许多优势,因此,最近有大量作为α-葡萄糖苷酶抑制剂的新化合物被报道。在这篇综述中,我们总结了这些新发现的α-葡萄糖苷酶抑制剂及其在抗糖尿病研究中的构效关系,并为α-葡萄糖苷酶抑制剂甚至临床前候选药物提供了更好的结构。除此之外,还强调了一些合成相关化合物的启发性策略。

相似文献

1
Recent Advances in Synthetic α-Glucosidase Inhibitors.合成α-葡萄糖苷酶抑制剂的最新进展
ChemMedChem. 2017 Jun 7;12(11):819-829. doi: 10.1002/cmdc.201700216. Epub 2017 Jun 1.
2
Synthesis and biological evaluation of 3-styrylchromone derivatives as free radical scavengers and α-glucosidase inhibitors.3-苯乙烯基色酮衍生物作为自由基清除剂和α-葡萄糖苷酶抑制剂的合成及生物学评价
Chem Pharm Bull (Tokyo). 2014;62(8):810-5. doi: 10.1248/cpb.c14-00351.
3
Hetarylcoumarins: Synthesis and biological evaluation as potent α-glucosidase inhibitors.海他丁内酯香豆素:作为强效α-葡萄糖苷酶抑制剂的合成与生物评价。
Bioorg Chem. 2017 Aug;73:1-9. doi: 10.1016/j.bioorg.2017.05.009. Epub 2017 May 10.
4
Synthesis and biological evaluation of novel 2,4,5-triarylimidazole-1,2,3-triazole derivatives via click chemistry as α-glucosidase inhibitors.通过点击化学合成新型2,4,5-三芳基咪唑-1,2,3-三唑衍生物作为α-葡萄糖苷酶抑制剂及其生物学评价
Bioorg Med Chem Lett. 2016 Dec 1;26(23):5719-5723. doi: 10.1016/j.bmcl.2016.10.057. Epub 2016 Oct 21.
5
Synthesis & α-glucosidase inhibitory & glucose consumption-promoting activities of flavonoid-coumarin hybrids.黄酮-香豆素杂合化合物的合成及α-葡萄糖苷酶抑制和促进葡萄糖消耗活性。
Future Med Chem. 2018 May 1;10(9):1055-1066. doi: 10.4155/fmc-2017-0293. Epub 2018 Apr 20.
6
A new entry into the portfolio of α-glucosidase inhibitors as potent therapeutics for type 2 diabetes: Design, bioevaluation and one-pot multi-component synthesis of diamine-bridged coumarinyl oxadiazole conjugates.新型 α-葡萄糖苷酶抑制剂作为 2 型糖尿病的有效治疗药物:二胺桥连香豆素噁二唑共轭物的设计、生物评价和一锅多组分合成。
Bioorg Chem. 2018 Apr;77:190-202. doi: 10.1016/j.bioorg.2017.12.022. Epub 2018 Jan 16.
7
Synthesis, biological evaluation and molecular docking studies of chromone hydrazone derivatives as α-glucosidase inhibitors.色酮腙衍生物作为α-葡萄糖苷酶抑制剂的合成、生物学评价及分子对接研究
Bioorg Med Chem Lett. 2017 Jul 1;27(13):2957-2961. doi: 10.1016/j.bmcl.2017.05.007. Epub 2017 May 5.
8
In search of new α-glucosidase inhibitors: Imidazolylpyrazole derivatives.寻找新型α-葡萄糖苷酶抑制剂:咪唑基吡唑衍生物
Bioorg Chem. 2017 Apr;71:102-109. doi: 10.1016/j.bioorg.2017.01.017. Epub 2017 Jan 23.
9
Synthesis, in vitro α-glucosidase inhibitory activity and docking studies of novel chromone-isatin derivatives.新型色酮-异吲哚酮衍生物的合成、体外α-葡萄糖苷酶抑制活性及对接研究
Bioorg Med Chem Lett. 2018 Jan 15;28(2):113-116. doi: 10.1016/j.bmcl.2017.11.047. Epub 2017 Nov 28.
10
Towards multi-target antidiabetic agents: In vitro and in vivo evaluation of 3,5-disubstituted indolin-2-one derivatives as novel α-glucosidase inhibitors.针对多靶点抗糖尿病药物:新型α-葡萄糖苷酶抑制剂 3,5-二取代吲哚啉-2-酮衍生物的体外和体内评价。
Bioorg Med Chem Lett. 2022 Jan 1;55:128449. doi: 10.1016/j.bmcl.2021.128449. Epub 2021 Nov 12.

引用本文的文献

1
Effect of acarbose and vildagliptin on plasma trimethylamine N-oxide levels in patients with type 2 diabetes mellitus: a 6-month, two-arm randomized controlled trial.阿卡波糖和维格列汀对2型糖尿病患者血浆氧化三甲胺水平的影响:一项为期6个月的双臂随机对照试验。
Front Endocrinol (Lausanne). 2025 May 6;16:1575087. doi: 10.3389/fendo.2025.1575087. eCollection 2025.
2
A review on the in vitro and in vivo screening of α-glucosidase inhibitors.α-葡萄糖苷酶抑制剂的体外和体内筛选综述
Heliyon. 2024 Sep 8;10(18):e37467. doi: 10.1016/j.heliyon.2024.e37467. eCollection 2024 Sep 30.
3
Exploring chalcone-sulfonyl piperazine hybrids as anti-diabetes candidates: design, synthesis, biological evaluation, and molecular docking study.
探索查尔酮-磺酰基哌嗪杂化物作为抗糖尿病候选物:设计、合成、生物学评价及分子对接研究
Mol Divers. 2025 Feb;29(1):43-59. doi: 10.1007/s11030-024-10831-x. Epub 2024 May 22.
4
The Role of Selenium Nanoparticles in Addressing Diabetic Complications: A Comprehensive Study.硒纳米粒子在解决糖尿病并发症中的作用:一项综合研究。
Curr Top Med Chem. 2024;24(15):1327-1342. doi: 10.2174/0115680266299494240326083936.
5
Synthesis, Computational Study, and In Vitro α-Glucosidase Inhibitory Action of 1,3,4-Thiadiazole Derivatives of 3-Aminopyridin-2(1)-ones.3-氨基吡啶-2(1)-酮的1,3,4-噻二唑衍生物的合成、计算研究及体外α-葡萄糖苷酶抑制作用
Pharmaceuticals (Basel). 2024 Mar 15;17(3):377. doi: 10.3390/ph17030377.
6
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline-pyrazolopyrimidine hybrids and Quinoline-4-Arylamines.喹啉-吡唑并嘧啶杂合体和喹啉-4-芳胺的合成、抗糖尿病和抗结核评估。
ChemistryOpen. 2024 Sep;13(9):e202400014. doi: 10.1002/open.202400014. Epub 2024 Mar 20.
7
Synthesis and Biological Evaluation of New Dihydrofuro[3,2-]piperidine Derivatives as Potent -Glucosidase Inhibitors.新型二氢呋喃并[3,2-]哌啶衍生物作为强效α-葡萄糖苷酶抑制剂的合成及生物学评价
Molecules. 2024 Mar 6;29(5):1179. doi: 10.3390/molecules29051179.
8
An Update on Dipeptidyl Peptidase-IV Inhibiting Peptides.二肽基肽酶-4 抑制肽的最新研究进展。
Curr Protein Pept Sci. 2024;25(4):267-285. doi: 10.2174/0113892037287976231212104607.
9
Green Synthesis and Characterization of Silver Nanoparticles Using Seeds Extract: In Vitro and In Vivo Evaluation of Anti-Diabetic Activity.利用种子提取物进行银纳米颗粒的绿色合成与表征:抗糖尿病活性的体外和体内评价
Pharmaceuticals (Basel). 2023 Dec 1;16(12):1677. doi: 10.3390/ph16121677.
10
Synthesis and Biological Evaluation of Some New 3-Aryl-2-thioxo-2,3-dihydroquinazolin-4(1)-ones and 3-Aryl-2-(benzylthio)quinazolin-4(3)-ones as Antioxidants; COX-2, LDHA, α-Glucosidase and α-Amylase Inhibitors; and Anti-Colon Carcinoma and Apoptosis-Inducing Agents.一些新型3-芳基-2-硫代-2,3-二氢喹唑啉-4(1)-酮和3-芳基-2-(苄硫基)喹唑啉-4(3)-酮作为抗氧化剂、COX-2、LDHA、α-葡萄糖苷酶和α-淀粉酶抑制剂以及抗结肠癌和凋亡诱导剂的合成与生物学评价
Pharmaceuticals (Basel). 2023 Oct 1;16(10):1392. doi: 10.3390/ph16101392.