Nerol

Nerol is a lipid of Prenol Lipids (PR) class. The involved functions are known as Odorant, Anabolism, Diastasis, Metabolic Inhibition and Oxidation. Nerol often locates in germ tube. The related lipids are Octanols, Pinene, Hexanols, ethyl butyrate and ethyl hexanoate.

Cross Reference

Introduction

To understand associated biological information of Nerol, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Nerol?

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

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with Nerol

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

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Nerol?

Related references are published most in these journals:

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What functions are associated with Nerol?


Related references are published most in these journals:

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What lipids are associated with Nerol?

Related references are published most in these journals:

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What genes are associated with Nerol?

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

What common seen animal models are associated with Nerol?

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

NCBI Entrez Crosslinks

All references with Nerol

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Authors Title Published Journal PubMed Link
Nowotarska SW et al. Effect of structure on the interactions between five natural antimicrobial compounds and phospholipids of bacterial cell membrane on model monolayers. 2014 Molecules pmid:24914896
de Menezes-Filho JE et al. Geraniol blocks calcium and potassium channels in the mammalian myocardium: useful effects to treat arrhythmias. 2014 Basic Clin. Pharmacol. Toxicol. pmid:24862086
Chen M et al. Use of synthetic isoprenoids to target protein prenylation and Rho GTPases in breast cancer invasion. 2014 PLoS ONE pmid:24587105
Liang D et al. Construction of the 1,2-dialkenylcyclohexane framework via Ireland-Claisen rearrangement and intramolecular Barbier reaction: application to the synthesis of (±)-Geijerone and a diastereoisomeric mixture with its 5-epimer. 2014 Molecules pmid:24448064
Kubo K et al. Synthesis and properties of cholesteryl 4-(Alkanoylamino)benzoates: liquid crystals and organogelators. 2014 J Oleo Sci pmid:24599108
Ramilijaona J et al. Enzymatic modification of palmarosa essential oil: chemical analysis and olfactory evaluation of acylated products. 2013 Chem. Biodivers. pmid:24327448
Paterson A et al. Environmental and seasonal influences on red raspberry flavour volatiles and identification of quantitative trait loci (QTL) and candidate genes. 2013 Theor. Appl. Genet. pmid:22890807
Tian J et al. Investigations on the antifungal effect of nerol against Aspergillus flavus causing food spoilage. 2013 ScientificWorldJournal pmid:24453813
Bouzenna H and Krichen L Pelargonium graveolens L'Her. and Artemisia arborescens L. essential oils: chemical composition, antifungal activity against Rhizoctonia solani and insecticidal activity against Rhysopertha dominica. 2013 Nat. Prod. Res. pmid:22840199
Boukhatem MN et al. Rose geranium essential oil as a source of new and safe anti-inflammatory drugs. 2013 Libyan J Med pmid:24103319