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Inhibition of Alpha-glucosidase and Amylase by Luteolin, a Flavonoid

KIM, Jong-Sang, KWON, Chong-Suk, SON, Kun Ho·2000·Bioscience, Biotechnology, and Biochemistry

Abstract

Twenty-one naturally occurring flavonoids were tested for inhibitory activities against alpha-glucosidase (EC 3.2.1.20) and alpha-amylase (EC 3.2.1.1). Luteolin, amentoflavone, luteolin 7-O-glucoside, and daidzein were the strongest inhibitors among the compounds tested. Luteolin inhibited alpha-glucosidase by 36% at the concentration of 0.5 mg/ml and was stronger than acarbose, the most widely prescribed drug, in inhibitory potency, suggesting that it has the possibility to effectively suppress postprandial hyperglycemia in patients with non-insulin dependent diabetes mellitus. Luteolin also inhibited alpha-amylase effectively although it was less potent than acarbose. The clinical value of luteolin needs to be further evaluated.

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Metadata

Authors
KIM, J.-S., KWON, C.-S., & SON, K. H.
Venue
Bioscience, Biotechnology, and Biochemistry
Published
2000-01-01
Volume
64
Issue
11
Pages
2458-2461
ISSN
  • 0916-8451 (ISSN-L)
  • 1347-6947
OpenAlex
W2020411326
Cited by
667
References
0
FWCI
2.36
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Inhibition of Alpha-glucosidase and Amylase by Luteolin, a Flavonoid. https://app.cochat.ai/papers/10.1271/bbb.64.2458
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KIM, J.-S., KWON, C.-S., & SON, K. H. (2000). Inhibition of Alpha-glucosidase and Amylase by Luteolin, a Flavonoid. Bioscience, Biotechnology, and Biochemistry. https://doi.org/10.1271/bbb.64.2458

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.