References
- Choi, S. H., Ahn, J. B., Kozukue, N., Levin, C. E. and Friedman, M. (2011) Distribution of free amino acids, flavonoids, total phenolics, and antioxidative activities of Jujube (Ziziphus jujuba) fruits and seeds harvested from plants grown in Korea. J. Agr. Food Chem. 59, 6594-6604. https://doi.org/10.1021/jf200371r
- Dang, Z., Ho, P., Zhu, L., Qian, K., Lee, K. H., Huang, L. and Chen, C. H. (2013) New betulinic acid derivatives for bevirimat-resistant human immunodeficiency virus type-1. J. Med. Chem. 56, 2029-2037. https://doi.org/10.1021/jm3016969
- Dubey, K. K. and Goel, N. (2013) Evaluation and optimization of downstream process parameters for extraction of betulinic acid from the bark of Ziziphus jujuba L. ScientificWolrdJournal 2013, 469674.
- Guo, S., Duan, J. A., Tang, Y. P., Yang, N. Y., Qian, D. W., Su, S. L. and Shang, E. X. (2010a) Characterization of triterpenic acids in fruits of ziziphus species by HPLC-ELSD-MS. J. Agr. Food Chem. 58, 6285-6289. https://doi.org/10.1021/jf101022p
- Guo, S., Duan, J. A., Tang, Y. P., Zhu, Z. H., Qian, Y. F., Yang, N. Y., Shang, E. X. and Qian, D. W. (2010b) Characterization of nucleosides and nucleobases in fruits of Ziziphus jujuba by UPLC-DADMS. J. Agr. Food Chem. 58, 10774-10780. https://doi.org/10.1021/jf102648q
- Huang, Y. L., Yen, G. C., Sheu, F. and Chau, C. F. (2008) Effects of water-soluble carbohydrate concentrate from Chinese jujube on different intestinal and fecal indices. J. Agr. Food Chem. 56, 1734-1739. https://doi.org/10.1021/jf072664z
- Li, J.-W., Fan, L.-P., Ding, S.-D. and Ding, X.-L. (2007) Nutritional composition of five cultivars of chinese jujube. Food Chem. 103, 454-460. https://doi.org/10.1016/j.foodchem.2006.08.016
- Pawlowska, A. M., Camangi, F., Bader, A. and Braca, A. (2009) Flavonoids of Zizyphus jujuba L. and Zizyphus spina-christi (L.) Willd (Rhamnaceae) fruits. Food Chem. 112, 858-862. https://doi.org/10.1016/j.foodchem.2008.06.053
- Rastogi, S., Pandey, M. M. and Kumar Singh Rawat, A. (2015) Medicinal plants of the genus Betula-Traditional uses and a phytochemical-pharmacological review. J. Ethnopharmacol. 159, 62-83. https://doi.org/10.1016/j.jep.2014.11.010
- Shim, D. H., Chang, S. Y., Park, S. M., Jang, H., Carbis, R., Czerkinsky, C., Uematsu, S., Akira, S. and Kweon, M. N. (2007) Immunogenicity and protective efficacy offered by a ribosomal-based vaccine from Shigella flexneri 2a. Vaccine 25, 4828-4836. https://doi.org/10.1016/j.vaccine.2007.03.050
- Slemons, R. D., Johnson, D. C., Osborn, J. S. and Hayes, F. (1974) Type-A influenza viruses isolated from wild free-flying ducks in California. Avian Dis. 18, 119-124. https://doi.org/10.2307/1589250
- Song, J., Yeo, S. G., Hong, E. H., Lee, B. R., Kim, J. W., Kim, J., Jeong, H., Kwon, Y., Kim, H., Lee, S., Park, J. H. and Ko, H. J. (2014) Antiviral activity of hederasaponin B from Hedera helix against enterovirus 71 Subgenotypes C3 and C4a. Biomol. Ther. 22, 41-46. https://doi.org/10.4062/biomolther.2013.108
- Ward, P., Small, I., Smith, J., Suter, P. and Dutkowski, R. (2005) Oseltamivir (Tamiflu) and its potential for use in the event of an influenza pandemic. J. Antimicrob. Chemother. 55 Suppl 1, i5-i21. https://doi.org/10.1093/jac/dki018
- Webster, R. G., Bean, W. J., Gorman, O. T., Chambers, T. M. and Kawaoka, Y. (1992) Evolution and ecology of influenza A viruses. Microbiol. Rev. 56, 152-179.
- Yili, A., Mutalipu, Aisa, H. A. and Isaev, M. I. (2009) Betulinic acid and sterols from Astragalus altaicus. Chem. Nat. Compd. 45, 592-594. https://doi.org/10.1007/s10600-009-9377-z
- Yogeeswari, P. and Sriram, D. (2005) Betulinic acid and its derivatives: a review on their biological properties. Curr. Med. Chem. 12, 657-666. https://doi.org/10.2174/0929867053202214
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