Novel quinoline derivatives as potent in vitro α-glucosidase inhibitors: In silico studies and SAR predictions
A new series of quinoline derivatives 6-30 was identified as potent α-glucosidase inhibitors. These analogs exhibited inhibitory potentials (IC50 values) in the ranges between 2.60 and 102.12 μM. Among the series, compounds 24 (2.60 ± 0.01 μM), 27 (2.60 ± 0.01 μM) and 20 (2.86 ± 0.01 μM) were found...
出版年: | MedChemComm |
---|---|
第一著者: | 2-s2.0-84943771420 |
フォーマット: | 論文 |
言語: | English |
出版事項: |
Royal Society of Chemistry
2015
|
オンライン・アクセス: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84943771420&doi=10.1039%2fc5md00280j&partnerID=40&md5=ee5961423c8fb138efab5ae30ca1e63e |
類似資料
-
Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions
著者:: 2-s2.0-84942794211
出版事項: (2015) -
Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies
著者:: 2-s2.0-84948649641
出版事項: (2016) -
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
著者:: 2-s2.0-85140093344
出版事項: (2022) -
Synthesis and biological evaluation of novel coumarin derivatives bearing sulfonamide moiety as potent α-glucosidase inhibitors
著者:: Alsukor A.; Inayatsyah N.A.; Ridhwan M.J.M.; Kasim N.; Imran S.
出版事項: (2025) -
Novel thiosemicarbazide-oxadiazole hybrids as unprecedented inhibitors of yeast α-glucosidase and in silico binding analysis
著者:: 2-s2.0-84964523904
出版事項: (2016)