Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies
Newly synthesized benzimidazole hydrazone derivatives 1-26 were evaluated for their α-glucosidase inhibitory activity. Compounds 1-26 exhibited varying degrees of yeast α-glucosidase inhibitory activity with IC50 values between 8.40 ± 0.76 and 179.71 ± 1.11 μM when compared with standard acarbose. I...
发表在: | Bioorganic Chemistry |
---|---|
主要作者: | 2-s2.0-84948649641 |
格式: | 文件 |
语言: | English |
出版: |
Academic Press Inc.
2016
|
在线阅读: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84948649641&doi=10.1016%2fj.bioorg.2015.11.006&partnerID=40&md5=93ec464c2d71e54bbd8588cac5d567e0 |
相似书籍
-
Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors
由: 2-s2.0-84937512790
出版: (2015) -
Synthesis, biological evaluation and molecular docking study of benzimidazole derivatives as α-glucosidase inhibitors and anti-diabetes candidates
由: 2-s2.0-85144315169
出版: (2023) -
Novel quinoline derivatives as potent in vitro α-glucosidase inhibitors: In silico studies and SAR predictions
由: 2-s2.0-84943771420
出版: (2015) -
5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes
由: 2-s2.0-85016039331
出版: (2017) -
New benzoxazole-based sulphonamide hybrids analogs as potent inhibitors of α-amylase and α-glucosidase: Synthesis and in vitro evaluation along with in silico study
由: 2-s2.0-85140093344
出版: (2022)