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α-Glucosidase inhibition of sesquiterpenoids from the heartwood of Mansonia gagei.
Le, Huong Thi Thu; Hioki, Yusuke; Danova, Ade; Nguyen, Van-Kieu; Duong, Thuc-Huy; Kita, Masaki; Chavasiri, Warinthorn.
Affiliation
  • Le HTT; Department of Chemistry, Ho Chi Minh City University of Education, 280 an Duong Vuong Street, District 5, Ho Chi Minh City, 700000, Viet Nam. Electronic address: huongltt@hcmue.edu.vn.
  • Hioki Y; Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan.
  • Danova A; Organic Chemistry Division, Faculty of Mathematics and Natural Sciences, Bandung Institute of Technology, JI. Ganesha 10, Bandung, West Java, 40132, Indonesia.
  • Nguyen VK; Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, 700000, Viet Nam; Faculty of Natural Sciences, Duy Tan University, Da Nang, 550000, Viet Nam.
  • Duong TH; Department of Chemistry, Ho Chi Minh City University of Education, 280 an Duong Vuong Street, District 5, Ho Chi Minh City, 700000, Viet Nam.
  • Kita M; Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan.
  • Chavasiri W; Center of Excellence in Natural Products Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand; Nanotec-CU Center of Excellence on Food and Agriculture, Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 103
Phytochemistry ; 213: 113778, 2023 Sep.
Article in En | MEDLINE | ID: mdl-37364707
ABSTRACT
Nine undescribed sesquiterpenoids, along with ten known compounds, were isolated from the ethyl acetate extract of Mansonia gagei heartwood. Their structures were determined by spectroscopic data analysis (FTIR, 1D, 2D NMR, and HRESIMS), and their absolute configurations were established by ECD calculation. The isolated compounds were evaluated for their inhibitory effect against α-glucosidase from yeast. The results showed that mansonone U, mansonialactam, heliclactone and mansonone S exhibited exceptionally potent activities when compared to the positive control, acarbose, with IC50 values of 12.38 ± 0.71, 0.20 ± 0.05, 13.12 ± 2.85, and 12.05 ± 1.91 µM, respectively. Among them, mansonialactam possessed the most potent inhibitory activity against yeast α-glucosidase, and it showed an uncompetitive inhibition mode.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Malvaceae Language: En Journal: Phytochemistry Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sesquiterpenes / Malvaceae Language: En Journal: Phytochemistry Year: 2023 Document type: Article
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