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Type :Article
Subject :Q Science (General)
ISBN :1478-6419
Main Author :Wan Mohd Nuzul Hakimi Wan Salleh
Title :Lepiginosides A-D: Three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
Hits :49
Place of Production :Tanjung Malim
Publisher :Fakulti Sains & Matematik
Year of Publication :2024
Notes :Natural Product Research
Corporate Name :Universiti Pendidikan Sultan Idris
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Abstract : Universiti Pendidikan Sultan Idris
Phytochemical investigation of methanolic extract of L. rubiginosa using modern chromatographic techniques has led to the isolation of three new triterpenoid saponins, lepiginosides A-C (1-3), a new farnesyl glycoside, lepiginoside D (4), together with lepisantheside B (5) and gleditsoside C (6). The characterization and structural elucidation of the isolated compounds were established by extensive spectroscopic data analysis and comparison with literature data. Moreover, the antibacterial activity against seven bacteria, but none is active. © 2022 Informa UK Limited, trading as Taylor & Francis Group.

References

Adesanya SA, Martin MT, Hill B, Dumontet V, Tri MV, Sevenet T, Païs M. 1999. Rubiginoside, a farnesyl glycoside from Lepisanthes rubiginosa. Phytochemistry. 51(8):1039–1041.

Agrawal PK. 1992. NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides. Phytochemistry. 31(10):3307–3330.

Bubb WA. 2003. NMR spectroscopy in the study of carbohydrates: characterizing the structural complexity. Concepts Magn Reson. 19A(1):1–19.

Chen Q, Zhang Y, Zhang W, Chen Z. 2011. Identification and quantification of oleanolic acid and ursolic acid in Chinese herbs by liquid chromatography-ion trap mass spectrometry. Biomed Chromatogr. 25(12):1381–1388.

Duus JO, Gotfredsen CH, Bock K. 2000. Carbohydrate structural determination by NMR spectroscopy: modern methods and limitations. Chem Rev. 100(12):4589–4614.

Hafid AF, Wardiyanto S, Tumewu L, Rahman A, Widyawaruyanti A. 2014. Free-radical scavenging activity screening of some Indonesian plants. Int J Pharm Pharm Sci. 6(6):115–117.

Hasan MM, Hossain A, Shamim A, Rahman MM. 2017. Phytochemical and pharmacological evaluation of ethanolic extract of Lepisanthes rubiginosa leaves. BMC Complement Altern Med. 17(1):1–11.

Mudiana D, Ariyanti EE. 2021. Katilayu (Lepisanthes rubiginosa (Roxb.) Leenh. Population in Mt. Baung Nature Tourism Park. In IOP Conference Series: Earth and Environmental Science, 743(1):12023. IOP Publishing.

Onche EU, Tukura BW, Bako SS. 2013. Nuclear magnetic resonance (NMR) analysis of d- (þ)-glucose: a guide to spectrometric structural elucidation of sugars. IOSR J Appl Chem. 6:45–51.

Rana SMM, Billah MM, Hossain MS, Saifuddin AKM, Islam SA, Banik S, Naim Z, Raju GS. 2014. Susceptibility of microorganism to selected medicinal plants in Bangladesh. Asian Pac J Trop Biomed. 4(11):911–917.

Tran LV, P, Thi, N, Thi L, Van Tran C, Vo NTQ, Ho AN, Tran TTP. 2022. Two new glycosides, farnesyl pentaglycoside and oleanane triglycoside from Lepisanthes rubiginosa, a mangrove plant collected from Thua Thien-Hue province, Vietnam. Nat Prod Res. 36(7):1774–1780.

Zulkifli SZ, A, Ghani N, Ismail NH, Bihud, Rasol NE. 2021. Phytochemistry and pharmacological activities of Lepisanthes genus: a review. Trop J Nat Prod Res. 5(6):994–1005.


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