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
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
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