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Two New Benzoquinone Derivatives from Vietnamese Knema globularia Stems.
Truong Nguyen, Huy; Duong, Thuc-Huy; Dang, Minh-Khai; Pham, Mai-Dang-Truong; Pham, Nguyen-Kim-Tuyen; Tri Mai, Dinh; Son Dang, Van; Nguyen, Ngoc-Hong; Sichaem, Jirapast.
  • Truong Nguyen H; Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City, 700000, Vietnam.
  • Duong TH; Department of Chemistry, Ho Chi Minh City University of Education, 280 An Duong Vuong Street, District 5, Ho Chi Minh City, 748342, Vietnam.
  • Dang MK; Department of Chemistry, Ho Chi Minh City University of Education, 280 An Duong Vuong Street, District 5, Ho Chi Minh City, 748342, Vietnam.
  • Pham MD; Department of Chemistry, Ho Chi Minh City University of Education, 280 An Duong Vuong Street, District 5, Ho Chi Minh City, 748342, Vietnam.
  • Pham NK; Faculty of Environment, Sai Gon University, 273 An Duong Vuong, Ward 3, District 5, Ho Chi Minh City, 70000, Vietnam.
  • Tri Mai D; Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 11300, Vietnam.
  • Son Dang V; Institute of Chemical Technology, Vietnam Academy of Science and Technology, 1 A TL29 Street, Thanh Loc ward, District 12, Ho Chi Minh City, 700000, Vietnam.
  • Nguyen NH; Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 11300, Vietnam.
  • Sichaem J; Institute of Tropical Biology, Vietnam Academy of Science and Technology, 85 Tran Quoc Toan Street, District 3, Ho Chi Minh City, 700000, Vietnam.
Chem Biodivers ; 21(5): e202400380, 2024 May.
Article en En | MEDLINE | ID: mdl-38498616
ABSTRACT
The chemical investigation of the stems of Knema globularia led to the isolation of two new benzoquinones derivatives, embenones A and B (1 and 2), along with three known compounds (3-5). The structures of the isolated compounds were determined using spectroscopic techniques, including HRESIMS, 1D and 2D NMR, in conjunction with comparison to existing literature data. Compounds 1 and 2 represent new carbon skeletons in nature. Furthermore, all isolated compounds were evaluated for their α-glucosidase inhibitory activity, with compounds 1-3 exhibiting superior potency relative to the positive control (acarbose, IC50 331 µM). Their IC50 values ranged from 1.40 to 96.1 µM.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Benzoquinonas / Tallos de la Planta / Myristicaceae País como asunto: Asia Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Benzoquinonas / Tallos de la Planta / Myristicaceae País como asunto: Asia Idioma: En Año: 2024 Tipo del documento: Article