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
Báez D et al. Floral scent composition of Plumeria tuberculata analyzed by HS-SPME. 2012 Nat Prod Commun pmid:22428259
Subongkot T et al. Ultradeformable liposomes with terpenes for delivery of hydrophilic compound. 2012 J Liposome Res pmid:22663352
Sacks GL et al. Sensory threshold of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN) and concentrations in young Riesling and non-Riesling wines. 2012 J. Agric. Food Chem. pmid:22397689
Juega M et al. Influence of yeast mannoproteins in the aroma improvement of white wines. 2012 J. Food Sci. pmid:22860598
Savage TJ et al. Condensation of the isoprenoid and amino precursors in the biosynthesis of domoic acid. 2012 Toxicon pmid:22041653
Lüddeke F et al. Geraniol and geranial dehydrogenases induced in anaerobic monoterpene degradation by Castellaniella defragrans. 2012 Appl. Environ. Microbiol. pmid:22286981
Balachandra BA et al. Control of stored grain pest, Callosobruchus maculatus (F.) (Coleoptera: Bruchidae) using the essential oil isolated from Plectranthus zeylanicus. 2012 Nat. Prod. Res. pmid:22188569
Dziadas M and Jeleń H Influence of glycosidases addition on selected monoterpenes contents in musts and white wines from two grape varieties grown in Poland. 2011 Jan-Mar Acta Sci Pol Technol Aliment pmid:22232525
Marcuzzi A et al. Geraniol rescues inflammation in cellular and animal models of mevalonate kinase deficiency. 2011 Jan-Feb In Vivo pmid:21282739
Aiemsaard J et al. The effect of lemongrass oil and its major components on clinical isolate mastitis pathogens and their mechanisms of action on Staphylococcus aureus DMST 4745. 2011 Res. Vet. Sci. pmid:21316719
Gonzalez-Audino P et al. Comparative toxicity of oxygenated monoterpenoids in experimental hydroalcoholic lotions to permethrin-resistant adult head lice. 2011 Arch. Dermatol. Res. pmid:21174108
Cruz JC et al. Immobilization of enzymes on fumed silica nanoparticles for applications in nonaqueous media. 2011 Methods Mol. Biol. pmid:21553189
Verma RS et al. Volatile constituents of essential oil and rose water of damask rose (Rosa damascena Mill.) cultivars from North Indian hills. 2011 Nat. Prod. Res. pmid:21711177
Kim SH et al. Geraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways. 2011 Biochem. Biophys. Res. Commun. pmid:21371438
Marcuzzi A et al. The farnesyltransferase inhibitors tipifarnib and lonafarnib inhibit cytokines secretion in a cellular model of mevalonate kinase deficiency. 2011 Pediatr. Res. pmid:21430599
Szendrei Z et al. Identification and field evaluation of attractants for the cranberry weevil, Anthonomus musculus Say. 2011 J. Chem. Ecol. pmid:21445566
Botana A et al. J-modulation effects in DOSY experiments and their suppression: the Oneshot45 experiment. 2011 J. Magn. Reson. pmid:21185209
Paroul N et al. Solvent-free geranyl oleate production by enzymatic esterification. 2011 Bioprocess Biosyst Eng pmid:20981557
Weldon PJ et al. Anointing chemicals and hematophagous arthropods: responses by ticks and mosquitoes to citrus (Rutaceae) peel exudates and monoterpene components. 2011 J. Chem. Ecol. pmid:21409496
Yang T et al. Metabolic engineering of geranic acid in maize to achieve fungal resistance is compromised by novel glycosylation patterns. 2011 Metab. Eng. pmid:21296182