Perillaldehyde

Perillaldehyde is a lipid of Prenol Lipids (PR) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 260 references associated with Perillaldehyde in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
Sugaya A et al. [Pharmacological studies on Perillae Herba. I. Neuropharmacological action of water extract and perillaldehyde (author's transl)]. 1981 Yakugaku Zasshi pmid:7320836
Boon PJ et al. Cytotoxicity and biotransformation of the anticancer drug perillyl alcohol in PC12 cells and in the rat. 2000 Toxicol. Appl. Pharmacol. pmid:10936079
Tattje DH and Bos R Composition of essential oil of Ledum palustre. 1981 Planta Med. pmid:17401851
Takagi S et al. Vasodilative effect of perillaldehyde on isolated rat aorta. 2005 Phytomedicine pmid:15957366
Ji WW et al. Effects of perillaldehyde on alternations in serum cytokines and depressive-like behavior in mice after lipopolysaccharide administration. 2014 Pharmacol. Biochem. Behav. pmid:24201050
Inouye S et al. Inhibitory activity of hydrosols, herbal teas and related essential oils against filament formation and the growth of Candida albicans. 2009 Nihon Ishinkin Gakkai Zasshi pmid:19942796
Esmaeili MA et al. Oxidative stress protective effect of Dracocephalum multicaule essential oil against human cancer cell line. 2014 Nat. Prod. Res. pmid:24484273
Sonboli A et al. Antibacterial activity of the essential oil and main components of two Dracocephalum species from Iran. 2012 Nat. Prod. Res. pmid:22007732
Elegbede JA et al. Perillyl alcohol and perillaldehyde induced cell cycle arrest and cell death in BroTo and A549 cells cultured in vitro. 2003 Life Sci. pmid:14511768
Tiefenbacher K and Mulzer J A nine-step total synthesis of (-)-platencin. 2009 J. Org. Chem. pmid:19260660