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Two acridones and two coumarins from the roots of Paramignya trimera

Dang P.H. Faculty of Chemistry, VNUHCM–University of Science, 227 Nguyen Van Cu, Ho Chi Minh City, Viet Nam|
Nguyen N.T. | Nguyen M.T.T. | Le P.T.T. | Phan P.K.T. | Le T.H. Cancer Research Laboratory, Vietnam National University Ho Chi Minh City, 227 Nguyen Van Cu, Ho Chi Minh City, Viet Nam|

Tetrahedron Letters Số 16, năm 2017 (Tập 58, trang 1553-1557)

DOI: 10.1016/j.tetlet.2017.02.083

Tài liệu thuộc danh mục: Scopus

Final

English

Từ khóa: 5 hydroxynoracronycin; acarbose; acridone derivative; alpha glucosidase; citrusinine I; coumarin derivative; daedalin A; glycocitrine III; herbaceous agent; ninhvanin; oriciacridone E; ostruthin; pandanusin A; Paramignya trimera extract; paratrimerin C; paratrimerin D; paratrimerin E; paratrimerin F; plant extract; scopoletin; umbelliferone; unclassified drug; vanillic acid; xanthyletin; Article; biosynthesis; carbon nuclear magnetic resonance; IC50; Paramignya trimera; plant root; proton nuclear magnetic resonance; Rutaceae
Tóm tắt tiếng anh
Two acridones, paratrimerins C (1) and D (2), and two coumarins, paratrimerins E (3) and F (4), were isolated from the CHCl3 and EtOAc extracts of Paramignya trimera (Rutaceae), together with twelve known compounds (5–16). Their structures were elucidated on the basis of spectroscopic data. All isolated compounds possessed significant α-glucosidase inhibitory activity in a concentration-dependent manner, and showed more potent inhibitory activity, with IC50 values ranging from 14.6 to 112.2 μM, than the positive control acarbose (IC50, 214.5 μM). The biosynthesis of the isolated coumarins and acridones was proposed. © 2017 Elsevier Ltd

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