Synthesis and Cytotoxic Activity of Conjugates of Mitochondrial-Directed Cationic Compound F16 with Ursane-Structure Triterpenic Acids Containing a Polyhydroxylated A-ring
Author:
Affiliation:
1. Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 141 Prospekt Oktyabrya, Ufa 450075, Russia
Publisher
MDPI
Link
https://www.mdpi.com/2673-4583/14/1/43/pdf
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2. Woźniak, L., Szakiel, A., Głowacka, A., Rozpara, E., Marszałek, K., and Skąpska, S. (2023). Triterpenoids of three apple cultivars–biosynthesis, antioxidative and anti-inflammatory properties, and fate during processing. Molecules, 28.
3. Stoner, G.D., and Seeram, N.P. (2011). Berries and Cancer Prevention, Springer Science+Business Media.
4. Pharmacological activities of natural triterpenoids and their therapeutic implications;Dzubak;Nat. Prod. Rep.,2006
5. Ursolic acid derivatives for pharmaceutical use: A patent review (2012–2016);Hussain;Expert. Opin. Ther. Pat.,2017
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