1,8-Cineol

1,8-cineol is a lipid of Prenol Lipids (PR) class. The involved functions are known as Amplification, enzyme activity and inhibitors. 1,8-cineol often locates in subsynaptic reticulum. The related lipids are palmitoleic acid, pentadecanoic acid, stearic acid and erucic acid.

Cross Reference

Introduction

To understand associated biological information of 1,8-Cineol, 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 1,8-Cineol?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with 1,8-Cineol

MeSH term MeSH ID Detail
Arthritis, Experimental D001169 24 associated lipids
Olfaction Disorders D000857 17 associated lipids
Alzheimer Disease D000544 76 associated lipids
Per page 10 20 | Total 13

PubChem Associated disorders and diseases

What pathways are associated with 1,8-Cineol

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 1,8-Cineol?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with 1,8-Cineol?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with 1,8-Cineol?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with 1,8-Cineol?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with 1,8-Cineol?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with 1,8-Cineol

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Per page 10 20 50 100 | Total 895
Authors Title Published Journal PubMed Link
pmid:
De-Oliveira AC et al. In vitro inhibition of liver monooxygenases by beta-ionone, 1,8-cineole, (-)-menthol and terpineol. 1999 Toxicology pmid:10454222
Zufall F et al. Amplification of odor-induced Ca(2+) transients by store-operated Ca(2+) release and its role in olfactory signal transduction. 2000 J. Neurophysiol. pmid:10634891
Abate P et al. Fetal associative learning mediated through maternal alcohol intoxication. 2000 Alcohol. Clin. Exp. Res. pmid:10656191
Buonviso N and Chaput M Olfactory experience decreases responsiveness of the olfactory bulb in the adult rat. 2000 Neuroscience pmid:10658611
Romagni JG et al. Inhibition of plant asparagine synthetase by monoterpene cineoles. 2000 Plant Physiol. pmid:10859202
Lorenzo D et al. Achyrocline satureioides essential oils from southern Brazil and Uruguay. 2000 Planta Med. pmid:10909273
Vilaplana J and Romaguera C Allergic contact dermatitis due to eucalyptol in an anti-inflammatory cream. 2000 Contact Derm. pmid:10945757
Boyle R et al. Biotransformation of 1,8-cineole in the brushtail possum (Trichosurus vulpecula). 2000 Xenobiotica pmid:11055269
Nikitin ES and Balaban PM Optical recording of odor-evoked responses in the olfactory brain of the naïve and aversively trained terrestrial snails. 2000 Nov-Dec Learn. Mem. pmid:11112801
Hart PH et al. Terpinen-4-ol, the main component of the essential oil of Melaleuca alternifolia (tea tree oil), suppresses inflammatory mediator production by activated human monocytes. 2000 Inflamm. Res. pmid:11131302
Reisert J and Matthews HR Response properties of isolated mouse olfactory receptor cells. 2001 J. Physiol. (Lond.) pmid:11136863
Miyazawa M et al. Oxidation of 1,8-cineole, the monoterpene cyclic ether originated from eucalyptus polybractea, by cytochrome P450 3A enzymes in rat and human liver microsomes. 2001 Drug Metab. Dispos. pmid:11159812
Wilson ND et al. A near-infrared method for the assay of cineole in eucalyptus oil as an alternative to the official BP method. 2001 J. Pharm. Pharmacol. pmid:11206198
Salisová M et al. Comparison of conventional and ultrasonically assisted extractions of pharmaceutically active compounds from Salvia officinalis. 1997 Ultrason Sonochem pmid:11237030
Fang H et al. Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens. 2001 Chem. Res. Toxicol. pmid:11258977
pmid:11270730
Santos FA and Rao VS 1,8-cineol, a food flavoring agent, prevents ethanol-induced gastric injury in rats. 2001 Dig. Dis. Sci. pmid:11281182
Ilmberger J et al. The influence of essential oils on human attention. I: alertness. 2001 Chem. Senses pmid:11287383
Santos FA et al. 1,8-cineole protects against liver failure in an in-vivo murine model of endotoxemic shock. 2001 J. Pharm. Pharmacol. pmid:11341367