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
pmid:19817640
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Han LL et al. (S)-Perillaldehyde azine. 2010 Acta Crystallogr Sect E Struct Rep Online pmid:21580329
Yuan XY et al. Perillartine. 2009 Acta Crystallogr Sect E Struct Rep Online pmid:21577558
Bumblauskiené L et al. Preliminary analysis on essential oil composition of Perilla L. cultivated in Lithuania. 2009 Jul-Aug Acta Pol Pharm pmid:19702173
Masutani H et al. Fragrant unsaturated aldehydes elicit activation of the Keap1/Nrf2 system leading to the upregulation of thioredoxin expression and protection against oxidative stress. 2009 Antioxid. Redox Signal. pmid:19123792
Ballal NR et al. Perillyl alcohol dehydrogenase from a soil pseudomonad. 1966 Biochem. Biophys. Res. Commun. pmid:4289759
Sato K et al. Antimicrobial effect of trans-cinnamaldehyde, (-)-perillaldehyde, (-)-citronellal, citral, eugenol and carvacrol on airborne microbes using an airwasher. 2006 Biol. Pharm. Bull. pmid:17077531
Bassoli A et al. Taste-guided identification of high potency TRPA1 agonists from Perilla frutescens. 2009 Bioorg. Med. Chem. pmid:19162486
Goretti M et al. Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells. 2011 Bioresour. Technol. pmid:21232941
Liang T and Kuwahara S Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, Rhizoglyphus sp. 2002 Biosci. Biotechnol. Biochem. pmid:12506997
Mizuno M et al. Dominant colonization and inheritance of Methylobacterium sp. strain OR01 on perilla plants. 2013 Biosci. Biotechnol. Biochem. pmid:23832351
Cornelissen S et al. Whole-cell-based CYP153A6-catalyzed (S)-limonene hydroxylation efficiency depends on host background and profits from monoterpene uptake via AlkL. 2013 Biotechnol. Bioeng. pmid:23239244
Brennan DJ et al. Tumour-specific HMG-CoAR is an independent predictor of recurrence free survival in epithelial ovarian cancer. 2010 BMC Cancer pmid:20359358
Seo KA et al. The monoterpenoids citral and geraniol are moderate inhibitors of CYP2B6 hydroxylase activity. 2008 Chem. Biol. Interact. pmid:18611395
McKim JM et al. A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells. 2010 Cutan Ocul Toxicol pmid:20491607
Hobbs CA et al. Genotoxicity assessment of the flavouring agent, perillaldehyde. 2016 Food Chem. Toxicol. pmid:27593899
Cohen SM et al. FEMA expert panel review of p-mentha-1,8-dien-7-al genotoxicity testing results. 2016 Food Chem. Toxicol. pmid:27773699
Dhavalikar RS et al. Microbiological transformations of terpenes. IX. Pathways of degradation of limonene in a soil pseudomonad. 1966 Indian J Biochem pmid:4227571