Chemical constituents from the stem barks of Polyscias serrata Balf
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https://doi.org/10.15625/2525-2518/16656Keywords:
Polyscias serrata, stem barks, phytochemistryAbstract
Plants of the genus Polyscias (the family Araliaceae) are represented as perennial shrubs and are commonly cultivated in southeastern Asia and the Pacific regions. Pharmacological studies revealed that Polyscias crude extracts and their isolated compounds exhibited a variety of biological activity, such as antibacterial, antifungal, cytotoxic, immuno-stimulant, wound healing and anti-asthmatic activities. For the first time, phytochemical study on the methanol (MeOH) extract of the stem barks of Vietnamese species Polyscias serrata Balf. (locally named Dinh lang rang) resulted in the isolation and NMR (Nuclear Magnetic Resonance)-determination of six compounds 1-6. They include one nucleobase uracil (1), two nucleosides uridine (2) and adenosine (3), one alkaloid indole-3-carboxylic acid (4), one mono-phenol glucoside koaburside (5), and one saponin randianin (6). The chemical structures of these phytochemicals were elucidated by physicochemical, the 1D-NMR [1H, 13C-NMR, and DEPT (Distortionless Enhancement by Polarization Transfer)], the 2D-NMR [HSQC (heteronuclear single quantum coherence), HMBC (Heteronuclear Multiple Bond Correlation), and COSY (correlation spectroscopy)] spectral, and ESI-MS (Electron Spray Ionization-Mass Spectrum) data. This is the first time that compounds 2-6 have been obtained from the genus Polyscias. In agreement with various reports, the nitrogenous compounds and triterpene saponins can be seen as characteristic metabolites of genus Polyscia
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Naglaa S. A., Haidy A. G., Mohamed L. A., Sherweit H. E., Abdel N. B. S. -The genus Polyscias (Araliaceae): A phytochemical and biological review, J. Herb. Med. 23 (2020) 100377. https://doi.org/10.1016/j.hermed.2020.100377. DOI: https://doi.org/10.1016/j.hermed.2020.100377
Prakash Chaturvedula V. S., Schilling J. K., Miller J. S., Andriantferana R., Rasamison V. E., Kingston D. G. I. –New cytotoxic oleanane saponins from the infructescences of Polyscias amplifolia from the Madagascar rainforest. Plant. Med. 69 (2003) 440-444. DOI: 10.1055/s-2003-39711. DOI: https://doi.org/10.1055/s-2003-39711
Guy S. S. N., Zhizhi D., Donatien G., Arno R. N. D., Michel F. T., Hippolyte K. W., Pierre T., Raymond S. D., Xiaodong L., Jules R. K. -Antifungal properties of a new terpernoid saponin and other compounds from the stem bark of Polyscias fulva Hiern (Araliaceae). BMC Complement. Altern. Med. 15 (2015) 25. DOI 10.1186/s12906-015-0541-7. DOI: https://doi.org/10.1186/s12906-015-0541-7
Divakar C. M., Sheela S., Sandhya S., Vinod K. R., Pillai N. R., Rao S. B. -Anti-inflammatory and antioxidant activities of Polyscias filicifolia saponins, Pharm. Lett. 2 (2010) 41-47.
Malcolm S. B., Anthony R. C., Annette E., John P., Rama A., Ronald J. Q. -Tyrosine kinase inhibitors from the rainforest tree Polyscias murrayi, Phytochemistry 66 (2005) 481-485. DOI: 10.1016/j.phytochem.2004.12.022. DOI: https://doi.org/10.1016/j.phytochem.2004.12.022
Giuseppina C., Antonio V., Laura L., Fabio V., Fabrizio D. P., Nunziatina D. T. -Antiproliferative oleanane saponins from Polyscias guilfoylei, Nat. Prod. Commun. 3 (2008) 1667-2670. https://doi.org/10.1177/1934578X080030101.
Paphassarang S., Raynaud J., Lussignol M., Becchi M. -Triterpenic glycosides from Polyscias scutellaria, Phytochemistry 28 (1989) 1539-1541. https://doi.org/10.1016/S0031-9422(00)97786-0 DOI: https://doi.org/10.1016/S0031-9422(00)97786-0
Huan V. D., Yamamura S., Ohtani K., Kasai R., Yamasaki K., Nham N. T., Chau H. M. -Oleanane saponins from Polyscias fruticosa, Phytochemistry 47 (1998) 45-457. DOI: https://doi.org/10.1016/S0031-9422(97)00618-3
Tuyet N. T. A., Phung N. K. P. -Chemical examination of Polyscias serrata Balf. family Araliaceae, Vietnam J. Chem. 45 (2007) 102-105. DOI: https://doi.org/10.15625/4718.
Franck T., Trinh, T. T. Vy N. T., Nghia N. H., Hoa N. D. L., Phung N. K. P., Hanh N. N.,Duong H. H. T. -Antiproliferation activity of Vietnamese medicinal plants on Hela human cervix cancer cell line, Science & Technology Development 11 (2008), 74-81.
Anh L. T. T., Son N. T., Tuyen N. V., Thuy P. T., QuanP. M., Ha N. T. T., Tra N. T. -Antioxidative and α-glucosidase inhibitory constituents of Polyscias guilfoylei: experimental and computational assessments, Mol. Divers. 26 (1) (2021) 229-243. https://doi.org/10.1007/s11030-021-10206-6 DOI: https://doi.org/10.1007/s11030-021-10206-6
Ai D. T. T., Van T. T. T., Huong D. T. M., Litaudon M., Tram L. H., Cuong P. V. -Chemical constituents of Boehmeria holosericea Blume (Urticaceae), Vietnam J. Chem. 56 (2018) 172-175. DOI: 10.1002/vjch.201800008. DOI: https://doi.org/10.1002/vjch.201800008
Wang C. Y., Jang H. J., Han Y. K., Su X. D., Lee S. W., Rho M. C., Wang H. S., Yang S. Y., Kim Y. H. -Alkaloids from Tetrastigma hemsleyanum and their anti-inflammatory effects on LPS-induced RAW264.7 cells, Molecules. 23 (2018) 1445. doi: 10.3390/molecules23061445. DOI: https://doi.org/10.3390/molecules23061445
In S. J., Seo K. H., Song N. Y., Song M. C., Baek N. I. -Identification of secondary metabolites from the stems of Viburnum erosum, J. Appl. Biol. Chem. 57 (2014) 165-170. DOI: 10.3839/jabc.2014.026. DOI: https://doi.org/10.3839/jabc.2014.026
Huong T. T., Son N. T., Cuong N. M., Van D. T., Cuong T. D., Khanh P. N., Ha V. T. -Morinlongosides A-C, two New isoprenylated naphthoquinone glucosides and a new iridoid glucoside from the roots of Morinda longissima, Chem. Pharm. Bull. 64 (2016) 1230-1234. DOI: 10.1248/cpb.c15-01039 DOI: https://doi.org/10.1248/cpb.c15-01039
Cuong N. M., Huong T. T., Khanh P. N., Tai N. V., Ha V. T., Son N. T., Tai B. H., Kim Y. H. -Paratrimerins A and B, two new dimeric monoterpene-linked coumarin glycosides from the roots and stems of Paramignya trimera, Chem. Pharm. Bull., 63 (2015) 945-949. DOI: 10.1248/cpb.c15-00336. DOI: https://doi.org/10.1248/cpb.c15-00336
Son N. T., Kamiji M., Huong T. T., Kubo M., Cuong N. M., Fukuyama Y. -Chemical constituents of the Vietnamese plants Dalbergia tonkinensis Prain and Cratoxylum formosum (Jack) Dyer in Hook and their antioxidative activities, Med. Chem. Res.28 (2019) 1441-1447. DOI: 10.1007/s00044-019-02383-9. DOI: https://doi.org/10.1007/s00044-019-02383-9
Sotheewaran S., Bokel M., Kraus W. -A hemolytic saponin, Randianin, from Randia dumetorum, Phytochemistry 28 (1989) 1544-1546. https://doi.org/10.1016/S0031-9422(00)97788-4. DOI: https://doi.org/10.1016/S0031-9422(00)97788-4
Dai Y., Harinantenaina L., Brodie P. J., Birkinshaw C., Randrianaivo R., Applequist W., Ratsimbason M., Rasamison V. E., Shen Y., TenDyke K., Kingston D. G. I. -Two antiproliferative triterpene saponins from Nematostylis anthophylla from the highlands of central Madagascar, Chem. Biodivers. 10 (2013), 233-240. doi: 10.1002/cbdv.201200156. DOI: https://doi.org/10.1002/cbdv.201200156
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