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.

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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?

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What functions are associated with Nerol?


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What lipids are associated with Nerol?

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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
Hagvall L et al. Fragrance compound geraniol forms contact allergens on air exposure. Identification and quantification of oxidation products and effect on skin sensitization. 2007 Chem. Res. Toxicol. pmid:17428070
Trusek-Holownia A and Noworyta A An integrated process: ester synthesis in an enzymatic membrane reactor and water sorption. 2007 J. Biotechnol. pmid:17434222
Joseph T et al. Nanometer sized tridecylamine capped Rhodium dispersed on high surface area support: catalytic investigations. 2007 J Nanosci Nanotechnol pmid:17685309
Chambon C et al. Sterol pathway in yeast. Identification and properties of mutant strains defective in mevalonate diphosphate decarboxylase and farnesyl diphosphate synthetase. 1991 Lipids pmid:1779710
Baumstark AL et al. Kinetics of the epoxidation of geraniol and model systems by dimethyldioxirane. 2004 Molecules pmid:18007416
Ricciardi L et al. Fragrances as a cause of food allergy. 2007 Nov-Dec Allergol Immunopathol (Madr) pmid:18047820
Takiguchi N et al. Performance of mice in discrimination of liquor odors: behavioral evidence for olfactory attention. 2008 Chem. Senses pmid:18178544
Mourtzinos I et al. Encapsulation of nutraceutical monoterpenes in beta-cyclodextrin and modified starch. 2008 J. Food Sci. pmid:18211376
Noe MC et al. A short enantioselective synthesis of N-Boc-(2R,3R)-3-methyl-3-hydroxypipecolic acid from geraniol. 2008 J. Org. Chem. pmid:18338902
Ponzoni C et al. Biotransformation of acyclic monoterpenoids by Debaryomyces sp., Kluyveromyces sp., and Pichia sp. strains of environmental origin. 2008 Chem. Biodivers. pmid:18357555