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
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
Hisamoto K et al. Hydroxy-group effect on the regioselectivity in a photochemical oxetane formation reaction (the Paternò-Büchi Reaction) of geraniol derivatives. 2011 Photochem. Photobiol. Sci. pmid:21541429
Saha P et al. Synthesis of oxabicyclo[3.3.1]nonenes and substituted tetrahydropyrans via (3,5)-oxonium-ene reaction. 2011 Org. Biomol. Chem. pmid:21512689
Rodríguez A et al. Terpene down-regulation in orange reveals the role of fruit aromas in mediating interactions with insect herbivores and pathogens. 2011 Plant Physiol. pmid:21525333
Gamero A et al. Monoterpene alcohols release and bioconversion by Saccharomyces species and hybrids. 2011 Int. J. Food Microbiol. pmid:21176987
Paroul N et al. Erratum to: Solvent-free geranyl oleate production by enzymatic esterification. 2011 Bioprocess Biosyst Eng pmid:21191617
Leonardo T et al. Carbonyl oxides reactions from geraniol-trans-(3,7-dimethylocta-2,6-dien-1-ol), 6-methyl-5-hepten-2-one, and 6-hydroxy-4-methyl-4-hexenal ozonolysis: kinetics and mechanisms. 2011 J Phys Chem A pmid:21609020
Merlini V et al. Biomimetic cyclization of geraniol derivatives, a useful tool in the total synthesis of bioactive monocyclic terpenoids. 2011 Nat Prod Commun pmid:21560759
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
Kuwahara Y et al. Geraniol, E-3,7-dimethyl-2,6-octadien-1-ol, as the alarm pheromone of the sycamore lace bug Corythucha ciliata (Say). 2011 J. Chem. Ecol. pmid:22076683
Vinothkumar V and Manoharan S Chemopreventive efficacy of geraniol against 7,12-dimethylbenz[a]anthracene-induced hamster buccal pouch carcinogenesis. 2011 Redox Rep. pmid:21801490
Frija LM et al. Sigmatropic rearrangements in 5-allyloxytetrazoles. 2011 Org. Biomol. Chem. pmid:21750817
Katiki LM et al. Anthelmintic activity of Cymbopogon martinii, Cymbopogon schoenanthus and Mentha piperita essential oils evaluated in four different in vitro tests. 2011 Vet. Parasitol. pmid:21820807
Riclea R and Dickschat JS The absolute configuration of the pyrrolosesquiterpenoid glaciapyrrol A. 2011 Chemistry pmid:21901770
Ahmad ST et al. Preclinical renal cancer chemopreventive efficacy of geraniol by modulation of multiple molecular pathways. 2011 Toxicology pmid:21907755
Shukla M and Dorai K Resolving overlaps in diffusion encoded spectra using band-selective pulses in a 3D BEST-DOSY experiment. 2011 J. Magn. Reson. pmid:21937251
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