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
Moreno PR et al. Induction of ajmalicine formation and related enzyme activities in Catharanthus roseus cells: effect of inoculum density. 1993 Appl. Microbiol. Biotechnol. pmid:7763550
Corsini A et al. Relationship between mevalonate pathway and arterial myocyte proliferation: in vitro studies with inhibitors of HMG-CoA reductase. 1993 Atherosclerosis pmid:8216498
Blanchard L and Karst F Characterization of a lysine-to-glutamic acid mutation in a conservative sequence of farnesyl diphosphate synthase from Saccharomyces cerevisiae. 1993 Gene pmid:8096487
Melnykovych G et al. Growth inhibition of leukemia cell line CEM-C1 by farnesol: effects of phosphatidylcholine and diacylglycerol. 1992 Biochem. Biophys. Res. Commun. pmid:1632790
Moleyar V and Narasimham P Antibacterial activity of essential oil components. 1992 Int. J. Food Microbiol. pmid:1457292
Baraldi PG et al. Geiparvarin analogues. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain. 1992 J. Med. Chem. pmid:1588564
Wang G et al. [Analysis of chemical constituent of essential oil in Lonicera japonnica Thunb. cultivated on the northern plain of Henan Province]. 1992 Zhongguo Zhong Yao Za Zhi pmid:1418559
Van Dessel G et al. Uptake of dolichol by Vero cells. 1992 Biochem. Cell Biol. pmid:1449713
Keung WM Human liver alcohol dehydrogenases catalyze the oxidation of the intermediary alcohols of the shunt pathway of mevalonate metabolism. 1991 Biochem. Biophys. Res. Commun. pmid:1993065
Vilaplana J et al. Contact dermatitis from geraniol in Bulgarian rose oil. 1991 Contact Derm. pmid:1868720
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
Shoff SM et al. Concentration-dependent increase of murine P388 and B16 population doubling time by the acyclic monoterpene geraniol. 1991 Cancer Res. pmid:1988098
Wheeler CJ et al. Uncompetitive inhibition of monoterpene cyclases by an analog of the substrate geranyl pyrophosphate and inhibition of monoterpene biosynthesis in vivo by an analog of geraniol. 1990 Arch. Biochem. Biophys. pmid:2350172
Chambon C et al. Isolation and properties of yeast mutants affected in farnesyl diphosphate synthetase. 1990 Curr. Genet. pmid:2245473
Berger RG et al. Catabolism of geraniol by cell suspension cultures of Citrus limon. 1990 Biochim. Biophys. Acta pmid:2265211
Hausen BM and Kulenkamp D [Geraniol contact allergy]. 1990 Z. Hautkr. pmid:2143044
Matsuoka H et al. Evaluation of antifungal volatile compounds on the basis of the elongation rate of a single hypha. 1990 Appl. Environ. Microbiol. pmid:2082824
Cardullo AC et al. Allergic contact dermatitis resulting from sensitivity to citrus peel, geraniol, and citral. 1989 J. Am. Acad. Dermatol. pmid:2526827
Overbosch P et al. Temporal integration and reaction times in human smell. 1989 Physiol. Behav. pmid:2756054
Kreilgård B and Hansen J Aspects of pharmaceutical and chemical standardization of patch test materials. 1989 J. Am. Acad. Dermatol. pmid:2600208