Planta Medica International Open 2017; 4(S 01): S1-S202
DOI: 10.1055/s-0037-1608220
Poster Session
Georg Thieme Verlag KG Stuttgart · New York

Isomer of bergenin and phytosterol from the stem bark of Mallotus leucodermis

S Mohd Yusoff Aiza
1   Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
,
N Ahmat
1   Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
2   Atta-ur-Rahman Institute for Natural Product Discovery, Universiti Teknologi MARA, Selangor Branch, Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor, Malaysia
,
H Naz
2   Atta-ur-Rahman Institute for Natural Product Discovery, Universiti Teknologi MARA, Selangor Branch, Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor, Malaysia
,
S Kamarozaman Aisyah
1   Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
2   Atta-ur-Rahman Institute for Natural Product Discovery, Universiti Teknologi MARA, Selangor Branch, Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor, Malaysia
3   Centre of Foundation Studies, Universiti Teknologi MARA, Selangor Branch, Dengkil Campus, 43800 Dengkil, Selangor, Malaysia
› Author Affiliations
Further Information

Publication History

Publication Date:
24 October 2017 (online)

 

Mallotus is one of the most diverse and richest genera of the Euphorbiaceae family, and consists of approximately 150 species distributed in tropical and sub-tropical regions of Asia [1]. Mallotus species are well known to possess medicinal properties and has been reported to be rich in flavonoids, terpenoids, phenolic compounds, and phloroglucinol derivatives [2]. Mallotus leucodermis is commonly known as “balik angin bopeng” in Malaysia, and is used to treat skin complaints [3]. A phytochemical study was conducted on the stem bark of M. leucodermis collected from National Park Kuala Keniam, Pahang, Malaysia. The dried powder of the stem bark (1.3 kg) was macerated with acetone to yield 66.0 g of crude extract. The crude extract was fractionated using vacuum liquid chromatography to give six fractions. Fraction 5 was further purified using radial chromatography to afford an isomer of bergenin (1) (23.0 mg). Purification of fraction 1 using radial chromatography gave a mixture of stigmasterol and β-sitosterol (2.9 mg). The structure of compounds was elucidated by spectroscopic methods including 1D and 2D NMR, UV-Vis, FTIR, MS and by comparison with literature data.

Zoom Image
Fig. 1

Greatest appreciation to Society for Medicinal Plant and Natural Product Research for the GA travel grant, MOHE (RAGS/1/2014/SG01/UITM/4) and Faculty of Applied Sciences for the financial support.

[1] Thakur HA, Patil DA. Journal of Experimental Science 2011; 2:37 – 46

[2] Riviere C, Hong VNT, Hong QT, Chataigne G, Hoai NN, Dejaeger B, Tistaert C, Kim TNT, Heyden YV, Van MC and Quetin-leclercq J. Phytochem Rev 2010; 9:217 – 253

[3] Faridah H, Nurulhuda H. J. Trop. Agric. Sci. 1999; 22: 85 – 94