STUDY ON ISOLATION OF TRITERPENOID SAPONINS FROM THE LEAVES OF WEIGELA FLORIDA “PINK POPPET”
About this article
Received: 12/02/22                Revised: 08/04/22                Published: 13/04/22Abstract
(1→6)-[a-L-rhamnopyranosyl-(1→2)]-b-D-glucopyranosyl ester (2), and 3-O-β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosylhederagenin 28-O-α-L-rhamnopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→6)]-β-D-glucopyranosyl ester (3). Additionally, in this study, the relationship between the chemical structure and biological activities of the saponins was discussed, which is fundamental for evaluating the biological activities of these compounds in the future.
Keywords
Full Text:
PDFReferences
[1] Saini, J. Chauhan, and P. Kaushik, “Medicinal value of domiciliary ornamental plants of the Asteraceae family,” J. Young Pharm., vol. 12, no. 1, p. 3, 2020.
[2] X. Wei, S. Lyu, Y. Yu, Z. Wang, H. Liu, D. Pan, and J. Chen, “Phylloremediation of Air Pollutants: Exploiting the Potential of Plant Leaves and Leaf-Associated Microbes,” Frontiers in Plant Science, vol. 8. p. 1318, 2017.
[3] P. Kaushik, I. Andújar, S. Vilanova, M. Plazas, P. Gramazio, F. J. Herraiz, N. S. Brar, and J. Prohens, “Breeding Vegetables with Increased Content in Bioactive Phenolic Acids,” Molecules, vol. 20, no. 10. 2015, doi: 10.3390/molecules201018464.
[4] A. Rezgui, A.-C. Mitaine-Offer, T. Miyamoto, C. Tanaka, S. Delemasure, P. Dutartre, and M.-A. Lacaille-Dubois, “Oleanolic acid and hederagenin glycosides from Weigela stelzneri,” Phytochemistry, vol. 123, pp. 40-47, 2016, doi: 10.1016/j.phytochem.2015.12.016.
[5] H.-J. Lim, E. Y. Jie, I.-S. Park, S.-J. Kim, W. S. Ahn, S.-I. Jeong, S. W. Kim, and C.-H. Jung, “Anti-Inflammatory Effects of Weigela subsessilis Callus Extract via Suppression of MAPK and NF-κB Signaling,” Plants, vol. 10, no. 8, 2021, doi: 10.3390/plants10081635.
[6] A. N. Sennikov, D. E. Soltis, D. J. Mabberley, J. W. Byng, M. F. Fay, M. J. M. Christenhusz, M. W. Chase, P. F. Stevens, P. S. Soltis, W. S. Judd, “An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV,” Bot. J. Linn. Soc., vol. 181, no. 1, pp. 1-20, Apr. 2016, doi: 10.1111/boj.12385.
[7] A.-S. Champy-Tixier, A.-C. Mitaine-Offer, F. Real Fernández, T. Miyamoto, C. Tanaka, A.-M. Papini, and M.-A. Lacaille-Dubois, “Oleanane-type glycosides from the roots of Weigela florida ‘rumba’ and evaluation of their antibody recognition,” Fitoterapia, vol. 128, pp. 198-203, 2018, doi: 10.1016/j.fitote.2018.04.017.
[8] N. Andriamisaina, A.-C. Mitaine-Offer, B. Pruvot, J. Chluba, T. Miyamoto, C. Tanaka, and M.-A. Lacaille-Dubois, “Phytochemistry of Weigela x ‘kosteriana variegata’ (Caprifoliaceae),” Nat. Prod. Commun., vol. 13, no. 4, pp. 403-406, Jan. 2018, doi: 10.1177/1934578X1801300406.
[9] Y.-M. Won, Z.-K. Seong, J.-L. Kim, H.-S. Kim, H.-H. Song, D.-Y. Kim, J.-H. Kim, S.-R. Oh, H.-W. Cho, J.-H. Cho, “Triterpene glycosides with stimulatory activity on melanogenesis from the aerial parts of Weigela subsessilis,” Arch. Pharm. Res., vol. 38, no. 8, pp. 1541-1551, Aug. 2015, doi: 10.1007/s12272-014-0524-0.
[10] P. T. Thuong, B.-S. Min, W. Jin, M. Na, J. Lee, R. Seong, Y.-M. Lee, K. Song, Y. Seong, H.-K. Lee, “Anti-complementary Activity of Ursane-Type Triterpenoids from Weigela subsessilis,” Biol. Pharm. Bull., vol. 29, no. 4, pp. 830-833, 2006, doi: 10.1248/bpb.29.830.
[11] D. H. Nguyen, A.-C. Mitaine-Offer, S. Maroso, A.-M. Papini, T. Paululat, P.-S. Bellaye, B. Collin, O. Chambin, and M.-A. Lacaille-Dubois, “Cytotoxic glycosides from the roots of Weigela x ‘Bristol Ruby,’” Fitoterapia, vol. 137, p. 104242, Sep. 2019, doi: 10.1016/J.FITOTE.2019.104242.
[12] H. Ishii, I. Kitagawa, K. Matsushita, K. Shirakawa, K. Tori, T. Tozyo, M. Yoshikawa, and Y. Yoshimura, “The configuration and conformation of the arabinose moiety in platycodins, saponins isolated from platycodon grandiflorum, and mi-saponins from madhuca longifolia based on carbon-13 and hydrogen-1 nmr spectroscopic evidence: The total structures of the sa,” Tetrahedron Lett., vol. 22, no. 16, pp. 1529-1532, 1981, doi: 10.1016/S0040-4039(01)90369-7.
[13] K. H. Son, K. Y. Jung, H. W. Chang, H. P. Kim, and S. S. Kang, “Triterpenoid saponins from the aerial parts of Lonicera japonica,” Phytochemistry, vol. 35, no. 4, pp. 1005-1008, 1994, doi: 10.1016/S0031-9422(00)90656-3.
[14] D. H. Nguyen, A.-C. Mitaine-Offer, T. Miyamoto, C. Tanaka, P.-S. Bellaye, B. Collin, O. Chambin, and M.-A. Lacaille-Dubois, “Phytochemical analysis of two Weigela florida cultivars, ‘Pink Poppet’ and ‘Jean’s Gold,’” Phytochem. Lett., vol. 37, pp. 85-89, 2020, doi: 10.1016/j.phytol.2020.04.009.
[15] S.-C. Bang, J.-H. Lee, G.-Y. Song, D.-H. Kim, M.-Y. Yoon, and B.-Z. Ahn, “Antitumor activity of Pulsatilla koreana saponins and their structure-activity relationship.,” Chem. Pharm. Bull. (Tokyo)., vol. 53, no. 11, pp. 1451-1454, Nov. 2005.
[16] S. J. Lee, E. J. Shin, K. H. Son, H. W. Chang, S. S. Kang, and H. P. Kim, “Anti-inflammatory activity of the major constituents of Lonicera japonica,” Arch. Pharm. Res., vol. 18, no. 2, p. 133, 1995, doi: 10.1007/BF02979147.DOI: https://doi.org/10.34238/tnu-jst.5536
Refbacks
- There are currently no refbacks.





