Heptaelliptoic Acid A, a New Betulinic Acid Saponin from the Leaves of Heptapleurum ellipticum

A bstract: One new 3-O-glycoside of betulinic acid, named heptaelliptoic acid A (1), together with one known betulinic acid analogue (2), and four other compounds (3-6) were separated by combinatively chromatographic techniques.For the first time, all of the purified compounds (1-6) were reported from the H. ellipticum species.Their structures were obviously elucidated basing exhaustive and pervasive UV-VIS, FT-IR, HR-MS-ESI, and NMR experiment data.Compounds 2-4 were significantly displayed the in vitro -glucosidase inhibition (IC50 values of 11.53, 28.75, and 10.90 M, respectively) better than the acarbose positive drug (IC50 value of 214.50 M).

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Publication Details

Journal
Records of Natural Products
Published
2024-09-30
DOI
https://doi.org/10.25135/rnp.476.2407.3265
Citations
1
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.23

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article

Heptaelliptoic Acid A, a New Betulinic Acid Saponin from the Leaves of Heptapleurum ellipticum

Nguyễn Quốc Trung, Trong Nghia Ngo, Hoàng Diễm Lý, Kim-dung Hoang et al.
1 citations
Records of Natural Products
Natural product bioactivities and synthesis
0.23
article

Heptaelliptoic Acid A, a New Betulinic Acid Saponin from the Leaves of Heptapleurum ellipticum

Nguyễn Quốc Trung, Trong Nghia Ngo, Hoàng Diễm Lý, Kim-dung Hoang, Văn Sơn Đặng, Tan Phat Nguyen, Thi Hong Tuoi Do, Thi Kim Phung Nguyen, Kim Yen Huynh, Thi Hong Ngoc Dang
article en
1 citations

Abstract

A bstract: One new 3-O-glycoside of betulinic acid, named heptaelliptoic acid A (1), together with one known betulinic acid analogue (2), and four other compounds (3-6) were separated by combinatively chromatographic techniques.For the first time, all of the purified compounds (1-6) were reported from the H. ellipticum species.Their structures were obviously elucidated basing exhaustive and pervasive UV-VIS, FT-IR, HR-MS-ESI, and NMR experiment data.Compounds 2-4 were significantly displayed the in vitro -glucosidase inhibition (IC50 values of 11.53, 28.75, and 10.90 M, respectively) better than the acarbose positive drug (IC50 value of 214.50 M).

Records of Natural Products(5)
Bộ Giáo dục và Ðào tạo
Openalex Percentile: Top 42%
Natural product bioactivities and synthesis
0.23
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