Phytochemical Constituents of F. Sagittifolia Warburg ex Mildbraed & Burret Leaves with Antimicrobial Activity

Olayombo Margaret Taiwo, Olaoluwa Omosalewa Olaoluwa, Olapeju Oluyemisi Aiyelaagbe, Josphat Clement Matasyoh

Abstract


The leaves and bark of Ficus sagittifolia have been used as a cure for stomach and pulmonary disorders, respectively. The bark is edible and is taken against colic. From the leaves of F. sagittifolia, a steroidal glycoside named Stigmast-5,22-diene-3-O-?-D-glucopyranoside 1 and three isoflavonoids named 5-hydroxy-3-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one 2, 5-hydroxy-3(4-hydroxylphenyl)-8,8-dimethylpyrano[2,3-f]-chromen-4(8H)-one 3 and 5-hydroxy-3-(4-hydroxyphemyl)-8,8-dimethylpyrano[3,2-g}-chromen-4(8H)-one 4 were isolated, and this is the first report of the isolation of these compounds from this plant. The structural elucidation of the compounds was based on 1D and 2D NMR, IR and MS data analyses. Compounds 1 and 2 inhibited the growth of Pseudomonas aeruginosa and Aspergillus Niger at 0.0625 mg/mL, respectively while compounds 2 and 4 were active against Helicobacter pylori at 0.0625 mg/mL. These findings corroborate the ethno-medicinal use of F. sagittifolia leaves as a treatment for stomach disorders.

Keywords


Antimicrobial activity; F. sagittifolia; Isoflavonoids; Natural products; Steroidal glycoside

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References


Ateba, S.B., Mvondo, M.A., Djiogue, S., Zingué, S., Krenn, L. and Njamen, D., 2019. A pharmacological overview of alpinumisoflavone, a natural prenylated isoflavonoid. Frontiers in pharmacology, 952. doi: https://doi.org/10.3389/fphar.2019.00952

Awouafack, M.D., Spiteller, P., Lamshoft, M., Kusari, S., Ivanova, B., Tane, P., & Spiteller M. (2011). Amtimicrobial isopropenyl-dihydrofurano isoflavones from crotalaria lachnophora. Journal of natural products, 74(2), 272-278. doi: https://doi.org/10.1021/np1005218

Bai, H., Li, S., Yin, F., & Hu, L. (2005). Isoprenylated Naphthoquinone Dimers Firmianones A, B, and C from Firmiana p latanifolia. Journal of natural products, 68(8), 1159-1163.

Burkill H.M. (1997). The useful plants of West Tropical Africa. Families M-R Kew: Royal Botanic Garden, Kew, 4(2) 165-167.

Dastidar, S.G., Manna, A., Kumar, K.A., Mazumdar, K., Dutta, N.K., Chakrabarty, A.N., Motohashi, N., & Shirataki, Y. (2004). Studies on the antibacterial potentiality of isoflavones. International journal of antimicrobial agents, 23(1), 99-102. doi: https://doi.org/10.1016/j.ijantimicag.2003.06.003

Edziri, H., Mastouri M., Mohamed, A.M., Zine, M., Aouni M., & Verschaeve L. (2012). Antibacterial, Antifungal and Cytotoxic activities of Two flavonoids from reteam raetam flowers, Molecules, 17(6), 1784-7293.doi: https://doi.org/10.3390/molecules17067284

Gupta, C., & Prakash, D. (2014). Phytonutrients as therapeutic agents. Journal of Complementary and Integrative Medicine, 11(3), 151-169.doi: https://doi.org/10.1515/jcim-2013-0021

Hussain, M.M., Dastagir, M.G., BILLAH, A.M., & Ismail, M. (2011). Alpinum isoflavone from Erythrina stricta Roxb. Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas, 10(1), 88-90.

Ilango, K. (2018). β-sitosterol glucoside from Pisonia grandis R. Br. stem bark in ethyl acetate extract. International Journal of Green Pharmacy, 12(01). doi: http://dx.doi.org/10.22377/ijgp.v12i01.1526

Kopustinskiene, D. M., Jakstas, V., Savickas, A., & Bernatoniene, J. (2020). Flavonoids as anticancer agents. Nutrients, 12(2), 457. doi:https://doi.org/10.3390/nu12020457

Máximoa, P., Lourenço, A., Feio, S.S., & Roseiro, J.C. (2002). A new prenylisoflavone from Ulex jussiaei. Zeitschrift für Naturforschung C, 57(7-8), 609-613. doi: https://doi.org/10.1515/znc-2002-7-810

Nawaz, H., Waheed, R., & Nawaz, M. (2019). Phytochemical Composition, Antioxidant Potential, and Medicinal Significance of Ficus. Modern Fruit Industry.

Olawumi, O.O., & Koma, S.O. (2019). Stigmasterol and stigmasterol glycoside: Isolated compounds from Tetrapleura tetraptera extracts. Journal of Biochemistry International, 6(1), 21-48, ISSN: 2454-4760

Orhan, D.D., Özçelik, B., Özgen, S. & Ergun, F. (2010). Antibacterial, antifungal, and antiviral activities of some flavonoids. Microbiological research, 165(6), 496-504. doi: https://doi.org/10.1016/j.micres.2009.09.002

POWO (2022). "Plants of the World Online. Facilitated by the Royal Botanic Gardens, Kew. Published on the Internet; Retrieved 10 January 2022". https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:584046-1

Rahman, M.Z., Sultana, S.J., Faruquee, C.F., Ferdous, F., Rahman, M.S., Islam, M.S., & Rashid, M.A. (2007). Phytochemical and biological investigations of Erythrina variegata. Saudi pharmaceutical journal, 15(2), 140.

Salehi, B., Prakash Mishra, A., Nigam, M., Karazhan, N., Shukla, I., KieÅ‚tykaâ€Dadasiewicz, A& Sharifiâ€Rad, J. (2021). Ficus plants: state of the art from a phytochemical, pharmacological, and toxicological perspective. Phytotherapy Research, 35(3), 1187-1217.doi: https://doi.org/10.1002/ptr.6884

Salem, M.Z., Salem, A.Z.M., Camacho, L.M. and Ali, H.M., 2013. Antimicrobial activities and phytochemical composition of extracts of Ficus species: An over view. Afr. J. Microbiol. Res., 7(33), pp.4207-4219.

Silverstein, R. M., & Bassler, G. C. (1962). Spectrometric identification of organic compounds. Journal of Chemical Education, 39(11), 546.

Sychrová, A., Koláriková, I., ŽemliÄka, M., & Å mejkal, K. (2020). Natural compounds with dual antimicrobial and anti-inflammatory effects. Phytochemistry reviews, 19(6), 1471-1502.

Taiwo, O.M. & Olaoluwa, O.O., (2020). Qualitative and Quantitative Analyses of Phytochemicals and Antioxidant Activity of Ficus sagittifolia (Warburg Ex Mildbraed and Burret). International Journal of Pharmacological and Pharmaceutical Sciences, 14(1), 1-6. https://publications.waset.org/10010968/pdf

Tjahjadarie, T.S., Saputri, R.D., & Tanjung, M. (2016). March. Phenolic compounds from the stem bark Erythrina Orientalis and detection of antimalaria activity by ELISA. In AIP Conference Proceedings AIP Publishing LLC, 1718(1), 060007. doi: https://doi.org/10.1063/1.4943329

Valizadeh, H., Mahmoodi, K.F., Alizadeh, Z. & Bahadori, M.B. (2014). Isolation and structure elucidation of secondary metabolites from Echinophora platyloba DC from Iran. Journal of Medicinal Plants, 1 (49), 15-21.

Wang, J.F., Liu, S.S., Song, Z.Q., Xu, T.C., Liu, C.S., Hou, Y.G., Huang, R. & Wu, S.H. (2020). Naturally occurring flavonoids and isoflavonoids and their microbial transformation: A review. Molecules, 25(21), 5112. doi: https://doi.org/10.3390/molecules25215112




DOI: https://doi.org/10.14421/biomedich.2022.111.75-81

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Copyright (c) 2022 Olayombo Margaret Taiwo, Olaoluwa Omosalewa Olaoluwa, Olapeju Oluyemisi Aiyelaagbe, Josphat Clement Matasyoh



Biology, Medicine, & Natural Product Chemistry
ISSN 2089-6514 (paper) - ISSN 2540-9328 (online)
Published by Sunan Kalijaga State Islamic University & Society for Indonesian Biodiversity.

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