STUDY ON ISOLATION AND STRUCTURAL DETERMINATION OF STEROIDAL SAPONIN FROM THE LEAVES OF Dracaena fragrans | Hùng | TNU Journal of Science and Technology

STUDY ON ISOLATION AND STRUCTURAL DETERMINATION OF STEROIDAL SAPONIN FROM THE LEAVES OF Dracaena fragrans

About this article

Received: 14/12/23                Revised: 05/03/24                Published: 11/03/24

Authors

1. Nguyen Duc Hung Email to author, TNU - University of Education
2. Tu Quang Tan, TNU - University of Education
3. Chu Hoang Mau, TNU - University of Education

Abstract


Saponins is a chemical compound which could be found in almost every part of plant. Some saponins such as protodioscin and protoneodioscin have been chosen for the National Cancer Institute’s anticancer drug screen program. Currently, pharmaceutical companies in the world are focusing on searching for new drugs derived from plants, and also finding how to isolate single compounds in order to remove toxic compounds from initial material and collect compounds possessing biological activity including saponins. In this study, a steroidal saponin with a spirostanol aglycone has been isolated from the leaves of Dracaena fragrans. Chemical structure of this compound has been characterized as spirost-5,25(27)-dien-1β,3β-diol-1-O-α-L-rhamnopyranosy-(1→2)-[β-D-xylopyranosyl-(1→3)]-α-L-arabinopyranoside, which previously isolated from the stems of Nolina recurvata belonging to the Nolina genus, thus the Asparagaceae family distributed in Japan. A short review on saponins isolated from the Dracaena genus as well as their biological activities has been discussed which further could be used to carry out more experiments on biological activities of spirost-5,25(27)-dien-1β,3β-diol-1-O-α-L-rhamnopyranosy-(1→2)-[β-D-xylopyranosyl-(1→3)]-α-L-arabinopyranoside, in order to complete database on chemical composition and biological activity of D. fragrans and the Dracaena genus.

Keywords


Chemical structure; Dracaena fragrans; NMR; Saponin; Spirostane-type

Full Text:

PDF

References


[1] E. Moghimipour and S. Handali, “Saponin: Properties, methods of evaluation and applications,” Annual Research & Review in Biology, vol. 5, pp. 207-220, 2015.

[2] D. Gupta, B. Bleakley, and R. K. Gupta, “Dragon’s blood: Botany, chemistry and therapeutic uses,” J. Ethnopharmacol., vol. 115, no. 3, pp. 361-380, 2008.

[3] N. T. Do, Flora of Vietnam, volume 8, Liliales Perleb. Sci. Tech. Publ. Hanoi, 2007.

[4] H. Jiang, Y. Kang, X. Chen, X. Yang, and X. Yang, “The complete plastid genome sequence of Dracaena fragrans (L.) Ker Gawl. (Asparagaceae),” Mitochondrial DNA Part B, vol. 6, no. 2, pp. 653-655, 2021.

[5] D. Lacroix, S. Prado, D. Kamoga, J. Kasenene, J. Namukobe, S. Krief, V. Dumontet, E. Mouray, B. Bodo, and F. Brunois, “Antiplasmodial and cytotoxic activities of medicinal plants traditionally used in the village of Kiohima, Uganda,” J. Ethnopharmacol., vol. 133, no. 2, pp. 850-855, 2011.

[6] M. J. Moshi, D. F. Otieno, and A. Weisheit, “Ethnomedicine of the Kagera Region, north western Tanzania. Part 3: plants used in traditional medicine in Kikuku village, Muleba District,” J. Ethnobiol. Ethnomed., vol. 8, no. 1, p. 14, 2012.

[7] M. Kamatenesi-Mugisha and H. Oryem-Origa, “Medicinal plants used to induce labour during childbirth in western Uganda,” J. Ethnopharmacol., vol. 109, no. 1, pp. 1-9, 2007.

[8] D. H. Nguyen and Q. T. Tu, “Study on phytochemical composition and isolation steroidal saponin from the leaves of Dracaena fragrans (L.) Ker Gawl.,” TNU Journal of Science and Technology, vol. 227, no. 14, pp. 93-99, 2022.

[9] Q. T. Tu and D. H. Nguyen, “Study on isolation and structure elucidation of steroidal saponins from the leaves of Dracaena fragrans (L.) Ker Gawl.,” TNU Journal of Science and Technology, vol. 228, no. 5, pp. 3-10, 2023.

[10] T. T. Quang, M. C. Hoang, and H. D. Nguyen, “Isolation and Structure Elucidation of a New Spirostane Glycoside from the Leaves of Dracaena fragrans,” Chem. Nat. Compd., vol. 59, no. 2, pp. 520-523, 2023.

[11] Y. Mimaki, Y. Takaashi, M. Kuroda, Y. Sashida, and T. Nikaido, “Steroidal saponins from Nolina recurvata stems and their inhibitory activity on cyclic AMP phosphodiesterase,” Phytochemistry, vol. 42, no. 6, pp. 1609-1615, 1996.

[12] S. L. Fries, F. G. Standaert, E. R. Whitcomb, R. F. Nigrelli, J. D. Chanley, and H. Sobotka, “Some pharmacologic properties of holothurin a, a glycosidic mixture from the sea cucurmber,” Ann. N. Y. Acad. Sci., vol. 90, no. 3, pp. 893-901, 1960.

[13] G. R. Pettit, D. L. Doubek, D. L. Herald, A. Numata, C. Takahasi, R. Fujiki, and T. Miyamoto, “Isolation and structure of cytostatic steroidal saponins from the african medicinal plant Balanites aegyptica,” J. Nat. Prod., vol. 54, no. 6, pp. 1491-1502, 1991.

[14] A. V Rao and M.-K. Sung, “Saponins as Anticarcinogens,” J. Nutr., vol. 125, no. 3, pp. 717S-724S, 1995.

[15] K. S. Reddy, M. S. Shekhani, D. E. Berry, D. G. Lynn, and S. M. Hecht, “Afromontoside. A new cytotoxic principle from Dracaena afromontana,” J. Chem. Soc. Perkin Trans., no. 1, pp. 987-992, 1984.

[16] L. Tang, Z. Wang, H. Wu, A. Yokosuka, and Y. Mimaki, “Steroidal glycosides from the underground parts of Dracaena thalioides and their cytotoxic activity,” Phytochemistry, vol. 107, no. C, pp. 102-110, 2014.

[17] R. B. Teponno, J. P. Dzoyem, R. N. Nono, U. Kauhl, L. P. Sandjo, L. A. Tapondjou, U. Bakowsky, and T. Opatz, “Cytotoxicity of secondary metabolites from Dracaena viridiflora Engl & Krause and their semisynthetic analogues,” Rec. Nat. Prod., vol. 11, no. 5, pp. 421-430, 2017.




DOI: https://doi.org/10.34238/tnu-jst.9402

Refbacks

  • There are currently no refbacks.
TNU Journal of Science and Technology
Rooms 408, 409 - Administration Building - Thai Nguyen University
Tan Thinh Ward - Thai Nguyen City
Phone: (+84) 208 3840 288 - E-mail: jst@tnu.edu.vn
Based on Open Journal Systems
©2018 All Rights Reserved