Capraldehyde

Capraldehyde is a lipid of Fatty Acyls (FA) class.

Cross Reference

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

Current reference collection contains 1217 references associated with Capraldehyde 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.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for Capraldehyde

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Capraldehyde

MeSH term MeSH ID Detail
Diabetes Mellitus D003920 90 associated lipids
Hemolysis D006461 131 associated lipids
Total 2

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with Capraldehyde

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Authors Title Published Journal PubMed Link
Hollis RP et al. Toxicity of the bacterial luciferase substrate, n-decyl aldehyde, to Saccharomyces cerevisiae and Caenorhabditis elegans. 2001 FEBS Lett. pmid:11591388
Gao S et al. Identification of two late acyltransferase genes responsible for lipid A biosynthesis in Moraxella catarrhalis. 2008 FEBS J. pmid:18795947
Furletti VF et al. Action of Coriandrum sativum L. Essential Oil upon Oral Candida albicans Biofilm Formation. 2011 Evid Based Complement Alternat Med pmid:21660258
Kurfürst M et al. Bioluminescence emission of bacterial luciferase with 1-deaza-FMN. Evidence for the noninvolvement of N(1)-protonated flavin species as emitters. 1989 Eur. J. Biochem. pmid:2714296
Shirley S et al. Chemical-modification studies on rat olfactory mucosa using a thiol-specific reagent and enzymatic iodination. 1983 Eur. J. Biochem. pmid:6852009
Epand RM et al. Curvature properties of novel forms of phosphatidylcholine with branched acyl chains. 2000 Eur. J. Biochem. pmid:10806388
Wube AA et al. Synthesis of N-substituted 2-[(1E)-alkenyl]-4-(1H)-quinolone derivatives as antimycobacterial agents against non-tubercular mycobacteria. 2011 Eur J Med Chem pmid:21429630
Cetkauskaite A et al. Elemental sulfur: toxicity in vivo and in vitro to bacterial luciferase, in vitro yeast alcohol dehydrogenase, and bovine liver catalase. 2004 Environ. Toxicol. pmid:15269910
Weschler CJ Ozone's impact on public health: contributions from indoor exposures to ozone and products of ozone-initiated chemistry. 2006 Environ. Health Perspect. pmid:17035131
Pandey SK and Kim KH An evaluation of volatile compounds released from containers commonly used in circulation of sports beverages. 2011 Ecotoxicol. Environ. Saf. pmid:20832862