References
- Alexandri E, Ahmed R, Siddiqui H, Choudhary MI, Tsiafoulis CG, Gerothanassis IP. 2017. High-resolution NMR spectroscopy as a structural and analytical tool for unsaturated lipids in solution. Molecules. 22(10):1663.
- Bero J, Ganfon H, Jonville M-C, Frédérich M, Gbaguidi F, DeMol P, Moudachirou M, Quetin-Leclercq J. 2009. In vitro antiplasmodial activity of plants used in Benin in traditional medicine to treat malaria. J Ethnopharmacol. 122(3):439–444.
- Coelho C, Bocca AL, Casadevall A. 2014. The tools for virulence of Cryptococcus neoformans. Adv Appl Microbiol. 87:1–41.
- Di Pietro ME, Mannu A, Mele A. 2020. NMR determination of free fatty acids in vegetable oils. Processes. 8(4):410.
- Ejov M, Dagne D. 2014. Strategic framework for leishmaniasis control in the WHO European Region 2014–2020.
- Field MC, Horn D, Fairlamb AH, Ferguson MAJ, Gray DW, Read KD, De Rycker M, Torrie LS, Wyatt PG, Wyllie S, et al. 2017. Anti-trypanosomatid drug discovery: an ongoing challenge and a continuing need. Nat Rev Microbiol. 15(4):217–231.
- Gazim ZC, Rezende CM, Fraga SR, Svidzinski TIE, Cortez DAG. 2008. Antifungal activity of the essential oil from Calendula officinalis L. (Asteraceae) growing in Brazil. Braz J Microbiol. 39(1):61–63.
- Greenwood B, Mutabingwa T. 2002. Malaria in 2002. Nature. 415(6872):670–672.
- Gunstone F. 1990. The 13C-NMR spectra of oils containing γ-linolenic acid. Chem Phys Lipids. 56(2–3):201–207.
- Iauk L, Lo Bue A, Milazzo I, Rapisarda A, Blandino G. 2003. Antibacterial activity of medicinal plant extracts against periodontopathic bacteria. Phytother Res. 17(6):599–604.
- Imieje V, Falodun A, Zaki A, Ali Z, Imieje V, Khan I, Tekwani B, Khan S, Tekwani B, Egiebor N, et al. 2017. Antiprotozoal and cytotoxicity studies of fractions and compounds from enantia chlorantha. TJNPR. 1(2):89–94.
- Jain S, Jacob M, Walker L, Tekwani B. 2016. Screening North American plant extracts in vitro against Trypanosoma brucei for discovery of new antitrypanosomal drug leads. BMC Complement Altern. Med. 16:1–6.
- Jain SK, Sahu R, Walker LA, Tekwani BL. 2012. A parasite rescue and transformation assay for antileishmanial screening against intracellular Leishmania donovani amastigotes in THP1 human acute monocytic leukemia cell line. J Vis Exp. pii: 4054.
- Latgé J-P. 1999. Aspergillus fumigatus and aspergillosis. Clin Microbiol Rev. 12(2):310–350.
- Muley B, Khadabadi S, Banarase N. 2009. Phytochemical constituents and pharmacological activities of Calendula officinalis Linn (Asteraceae): a review. Trop J Pharm Res. 8:455–465.
- Rigane G, Younes SB, Ghazghazi H, Salem RB. 2013. Investigation into the biological activities and chemical composition of Calendula officinalis L. growing in Tunisia. Int Food Res J. 20:3001–3004.
- Santalova EA, Denisenko VA. 2017. Analysis of the configuration of an isolated double bond in some lipids by selective homonuclear decoupling. Nat Prod Commun. 12(12):1934578X1701201.
- Soberon JR, Sgariglia MA, Sampietro DA, Quiroga EN, Vattuone MA. 2007. Antibacterial activity of plant extracts from northwestern Argentina. J Appl Microbiol. 102(6):1450–1461.
- Tuha A, Bekhit AA, Seid Y. 2017. Screening of some pyrazole derivatives as promising antileishmanial agent. Afr J Pharm Pharmacol. 11:32–37.
- Vidal-Ollivier E, Balansard G, Faure R, Babadjamian A. 1989. Revised structures of triterpenoid saponins from the flowers of Calendula officinalis. J Nat Prod. 52(5):1156–1159.
- Wang X-Y, Yang D, Gan L-J, Zhang H, Shin J-A, Park SH, Lee K-T. 2014. Degree of oxidation depending on the positional distribution of linolenic acid in perilla oil and interesterified products. Food Sci Biotechnol. 23(6):1733–1740.
- Zaki A, Ashour A, Mira A, Kishikawa A, Nakagawa T, Zhu Q, Shimizu K. 2016. Biological activities of oleanolic acid derivatives from Calendula officinalis seeds. Phytother Res. 30(5):835–841.
- Zaki AA, Ashour AA, Qiu L. 2020. New sesquiterpene glycoside ester with antiprotozoal activity from the flowers of Calendula officinalis L. Nat Prod Res.35(23):5250–5254.
- Zaki AA, Qiu L. 2020. Machaerinic acid 3-O-β-D-glucuronopyranoside from Calendula officinalis. Nat Prod Res. 34(20):2938–2944.