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.

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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
Colitis D003092 69 associated lipids
Body Weight D001835 333 associated lipids
Arthritis, Experimental D001169 24 associated lipids
Chemical and Drug Induced Liver Injury D056486 39 associated lipids
Alzheimer Disease D000544 76 associated lipids
Olfaction Disorders D000857 17 associated lipids
Seizures D012640 87 associated lipids
Dermatitis D003872 30 associated lipids
Dyspnea D004417 10 associated lipids
Vaginosis, Bacterial D016585 10 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

Download all related citations
Per page 10 20 50 100 | Total 895
Authors Title Published Journal PubMed Link
McLean S et al. Pharmacokinetics of 1,8-cineole, a dietary toxin, in the brushtail possum (Trichosurus vulpecula): significance for feeding. 2007 Xenobiotica pmid:17896321
Miyazawa M et al. Roles of cytochrome P450 3A enzymes in the 2-hydroxylation of 1,4-cineole, a monoterpene cyclic ether, by rat and human liver microsomes. 2001 Xenobiotica pmid:11695850
Pass GJ et al. Microsomal metabolism of the terpene 1,8-cineole in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus), rat and human. 2001 Xenobiotica pmid:11465406
Boyle R et al. Biotransformation of 1,8-cineole in the brushtail possum (Trichosurus vulpecula). 2000 Xenobiotica pmid:11055269
Pass GJ and McLean S Inhibition of the microsomal metabolism of 1,8-cineole in the common brushtail possum (Trichosurus vulpecula) by terpenes and other chemicals. 2002 Xenobiotica pmid:12593759
Pass GJ et al. Microsomal metabolism and enzyme kinetics of the terpene p-cymene in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus) and rat. 2002 Xenobiotica pmid:12065061
Machado M et al. Activity of Thymus capitellatus volatile extract, 1,8-cineole and borneol against Leishmania species. 2014 Vet. Parasitol. pmid:24365244
Santos SR et al. Toxic effects on and structure-toxicity relationships of phenylpropanoids, terpenes, and related compounds in Aedes aegypti larvae. 2010 Vector Borne Zoonotic Dis. pmid:20455777
Salisová M et al. Comparison of conventional and ultrasonically assisted extractions of pharmaceutically active compounds from Salvia officinalis. 1997 Ultrason Sonochem pmid:11237030
De-Oliveira AC et al. In vitro inhibition of liver monooxygenases by beta-ionone, 1,8-cineole, (-)-menthol and terpineol. 1999 Toxicology pmid:10454222