An Updated Overview of Synthetic α-glucosidase Inhibitors: Chemistry and Bioactivities

被引:6
作者
Cai, Yong-Si [1 ]
Xie, Hong-Xu [1 ]
Zhang, Jin-He [1 ]
Li, Yue [1 ]
Zhang, Juan [1 ]
Wang, Kai-Ming [1 ]
Jiang, Cheng-Shi [1 ]
机构
[1] Univ Jinan, Sch Biol Sci & Technol, Jinan 250022, Peoples R China
关键词
alpha-glucosidase inhibitors; Heterocycles; Structure-activity relationship; Molecular docking; Diabetes mellitus; Hypoglycaemic drugs; PPAR-GAMMA AGONISTS; IN-VITRO EVALUATION; MOLECULAR DOCKING; BIOLOGICAL EVALUATION; OLEANOLIC ACID; URSOLIC ACID; BENZIMIDAZOLE DERIVATIVES; ANTIDIABETIC ACTIVITY; DIABETES-MELLITUS; DESIGN;
D O I
10.2174/0115680266260682230921054652
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetes mellitus (DM) is a critical global health issue, affecting nearly half a billion people worldwide, with an increasing incidence rate and mortality. Type 2 diabetes is caused by the body's inability to effectively use insulin, and approximately 95% of patients have type 2 diabetes. alpha-glucosidase has emerged as an important therapeutic target for the treatment of type 2 diabetes. In the past years, three alpha-glucosidase inhibitors have been approved for clinical use, namely acarbose, voglibose, and miglitol. However, the undesirable effects associated with these carbohydrate mimic-based alpha-glucosidase inhibitors have limited their clinical applications. Consequently, researchers have shifted their focus towards the development of non-carbohydrate mimic alpha-glucosidase inhibitors that can safely and effectively manage postprandial hyperglycemia in type 2 diabetes. Herein, this article provides an overview of the synthetic alpha-glucosidase inhibitors, particularly those based on heterocycles, which have been reported from 2018 to 2022. This article aims to provide useful information for medicinal chemists in further developing clinically available anti-type 2 diabetes drugs.
引用
收藏
页码:2488 / 2526
页数:39
相关论文
共 160 条
[1]  
Abbasi MA, 2019, PAK J PHARM SCI, V32, P61
[2]   Design, synthesis, modeling studies and biological evaluation of thiazolidine derivatives containing pyrazole core as potential anti-diabetic PPAR-γ agonists and anti-inflammatory COX-2 selective inhibitors [J].
Abdellatif, Khaled R. A. ;
Fadaly, Wael A. A. ;
Kamel, Gehan M. ;
Elshaier, Yaseen A. M. M. ;
El-Magd, Mohammed A. .
BIOORGANIC CHEMISTRY, 2019, 82 :86-99
[3]   Development of diarylpentadienone analogues as alpha-glucosidase inhibitor: Synthesis, in vitro biological and in vivo toxicity evaluations, and molecular docking analysis [J].
Abdullah, Maryam Aisyah ;
Lee, Yu-Ri ;
Mastuki, Siti Nurulhuda ;
Leong, Sze Wei ;
Ibrahim, Wan Norhamidah Wan ;
Latif, Muhammad Alif Mohammad ;
Ramli, Aizi Nor Mazila ;
Aluwi, Mohd Fadhlizil Fasihi Mohd ;
Faudzi, Siti Munirah Mohd ;
Kim, Cheol-Hee .
BIOORGANIC CHEMISTRY, 2020, 104
[4]   Triazoloquinazolines as a new class of potent α-glucosidase inhibitors: in vitro evaluation and docking study [J].
Abuelizz, Hatem A. ;
Anouar, El Hassane ;
Ahmad, Rohaya ;
Azman, Nor Izzati Iwana Nor ;
Marzouk, Mohamed ;
Al-Salahi, Rashad .
PLOS ONE, 2019, 14 (08)
[5]   Design and synthesis of new fused carbazole-imidazole derivatives as anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and in silico studies [J].
Adib, Mehdi ;
Peytam, Fariba ;
Shourgeshty, Reihaneh ;
Mohammadi-Khanaposhtani, Maryam ;
Jahani, Mehdi ;
Imanparast, Somaye ;
Faramarzi, Mohammad Ali ;
Larijani, Bagher ;
Moghadamnia, Ali Akbar ;
Esfahani, Ensieh Nasli ;
Bandarian, Fatemeh ;
Mahdavi, Mohammad .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2019, 29 (05) :713-718
[6]   Recent Advances of α-Glucosidase Inhibitors: A Comprehensive Review [J].
Agrawal, Neetu ;
Sharma, Manisha ;
Singh, Shikha ;
Goyal, Ahsas .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2022, 22 (25) :2069-2086
[7]   Synthesis, crystal structure and Hirshfeld Surface analysis of benzamide derivatives of thiourea as potent inhibitors of α-glucosidase in-vitro [J].
Akhter, Sidra ;
Ullah, Saeed ;
Yousuf, Sammer ;
Atia-tul-Wahab ;
Siddiqui, Hina ;
Choudhary, M. Iqbal .
BIOORGANIC CHEMISTRY, 2021, 107
[8]   Synthesis and characterisation of thiobarbituric acid enamine derivatives, and evaluation of their α-glucosidase inhibitory and anti-glycation activity [J].
Ali, M. ;
Barakat, Assem ;
El-Faham, Ayman ;
Al-Rasheed, Hessa H. ;
Dahlous, Kholoud ;
Al-Majid, Abdullah Mohammed ;
Sharma, Anamika ;
Yousuf, Sammer ;
Sanam, Mehar ;
Ul-Haq, Zaheer ;
Choudhary, M. Iqbal ;
de la Torre, Beatriz G. ;
Albericio, Fernando .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2020, 35 (01) :692-701
[9]   Synthesis, in vitro and in silico screening of 2-amino-4-aryl-6-(phenylthio) pyridine-3,5-dicarbonitriles as novel ? -glucosidase inhibitors [J].
Ali, Muhammad ;
Khan, Khalid Mohammed ;
Mahdavi, Mohammad ;
Jabbar, Abdul ;
Shamim, Shahbaz ;
Salar, Uzma ;
Taha, Muhammad ;
Perveen, Shahnaz ;
Larijani, Bagher ;
Faramarzi, Mohammad Ali .
BIOORGANIC CHEMISTRY, 2020, 100
[10]   Synthesis of indole-based-thiadiazole derivatives as a potent inhibitor of α-glucosidaseenzyme along with in silico study [J].
Alomari, Munther ;
Taha, Muhammad ;
Rahim, Fazal ;
Selvaraj, Manikandan ;
Iqbal, Naveed ;
Chigurupati, Sridevi ;
Hussain, Shafqat ;
Uddin, Nizam ;
Almandil, Noor Barak ;
Nawaz, Muhammad ;
Farooq, Rai Khalid ;
Khan, Khalid Mohammed .
BIOORGANIC CHEMISTRY, 2021, 108