https://orcid.org/0000-0003-1901-3824
References
- Achouri A, Derbre S, Medjroubi K, Laouer H, Seraphin D, Akkal S. 2017. Two new triterpenoid saponins from the leaves of Bupleurum lancifolium (Apiaceae). Nat Prod Res. 31(19):2286–2293.
- Burns D, Reynolds WF, Buchanan G, Reese PB, Enriquez RG. 2000. Assignment of H-1 and C-13 spectra and investigation of hindered side-chain rotation in lupeol derivatives. Magn Reson Chem. 38(7):488–493.
- Chen Q-W, Zhang X, Gong T, Gao W, Yuan S, Zhang P-C, Kong Q. 2019. Structure and bioactivity of cholestane glycosides from the bulbs of Ornithogalum saundersiae Baker. Phytochemistry. 164:206–214.
- Coates Palgrave K, Drummond R. 2002. Trees of Southern Africa. Cape Town: C. Struik Publishers; p. 652.
- Foubert K, Gorella T, Faizal A, Cos P, Maes L, Apers S, Geelen D, Pieters L. 2016. Triterpenoid saponins from Maesa argentea leaves. Planta Med. 82(18):1568–1575.
- Ganbaatar C, Gruner M, Tunsag J, Batsuren D, Ganpurev B, Chuluunnyam L, Sodbayar B, Schmidt AW, Knölker H-J. 2016. Chemical constituents isolated from Zygophyllum melongena Bunge growing in Mongolia. Nat Prod Res. 30(14):1661–1664.
- Hiraga Y, Taino K, Kurokawa M, Takagi R, Ohkata K. 1997. (-)-Loliolide and other germination inhibitory active constituents in Equisetum arvense. Nat. Prod. Lett. 10(3):181–186.
- Hutchings A. 1996. Zulu medicinal plants: An inventory. Pietermaritzburg, South Africa: University of Natal Press; p. 189.
- Kim KH, Lee KH, Choi SU, Kim YH, Lee KR. 2008. Terpene and phenolic constituents of Lactuca indica L. Arch Pharm Res. 31(8):983–988.
- Lee J, Kim NH, Nam JW, Lee YM, Jang DS, Kim YS, Nam SH, Seo E-K, Yang MS, Kim JS. 2010. Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis ex vivo. Arch Pharm Res. 33(9):1317–1323.
- Makler MT, Ries JM, Williams JA, Bancroft JE, Piper RC, Gibbins BL, Hinrichs DJ. 1993. Parasite lactate dehydrogenase as an assay for Plasmodium falciparum drug sensitivity. Am J Trop Med Hyg. 48(6):739–741.
- Martins D, Nunez CV. 2015. Secondary metabolites from Rubiaceae species. Molecules. 20(7):13422–13495.
- Mongrand S, Badoc A, Patouille B, Lacomblez C, Chavent M, Bessoule JJ. 2005. Chemotaxonomy of the Rubiaceae family based on leaf fatty acid composition. Phytochemistry. 66(5):549–559.
- Mostafa AE, El-Hela AA, Mohammad A-EI, Cutler SJ, Ross SA. 2016. New triterpenoidal saponins from Koelreuteria paniculata. Phytochem Lett. 17:213–218.
- Nethengwe M, Opoku A, Dludla P, Madida K, Shonhai A, Smith P, Singh M. 2012. Larvicidal, antipyretic and antiplasmodial activity of some Zulu medicinal plants. J. Med. Plants Res. 6(7):1255–1262.
- Seebacher W, Simic N, Weis R, Saf R, Kunert O. 2003. Complete assignments of 1H and 13C NMR resonances of oleanolic acid, 18α‐oleanolic acid, ursolic acid and their 11‐oxo derivatives. Magn Reson Chem. 41(8):636–638.
- Suttiarporn P, Chumpolsri W, Mahatheeranont S, Luangkamin S, Teepsawang S, Leardkamolkarn V. 2015. Structures of phytosterols and triterpenoids with potential anti-cancer activity in bran of black non-glutinous rice. Nutrients. 7(3):1672–1687.
- Tajuddeen N, Swart T, Hoppe HC, van Heerden FR. 2021a. Antiplasmodial and cytotoxic flavonoids from Pappea capensis (Eckl. & Zeyh.) Leaves. Molecules. 26(13):3875.
- Tajuddeen N, Swart T, Hoppe HC, van Heerden FR. 2021b. Antiplasmodial and cytotoxic activities of extract and compounds from Ozoroa obovata (Oliv.) R. & A. Fern. var. obovata. Chem Biodivers. 18, e2100240.
- Tajuddeen N, Van Heerden FR. 2019. Antiplasmodial natural products: an update. Malar J. 18(1):404.
- Trager W, Jensen JB. 1976. Human malaria parasites in continuous culture. Science. 193(4254):673–675.
- Watt JM, Breyer-Brandwijk MG. 1962. The medicinal and poisonous plants of Southern and Eastern Africa. London: E. and S. Livingstone LTD.