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
Chemical and Drug Induced Liver Injury D056486 39 associated lipids
Vaginosis, Bacterial D016585 10 associated lipids
Seizures D012640 87 associated lipids
Scalp Dermatoses D012536 11 associated lipids
Lice Infestations D010373 9 associated lipids
Dyspnea D004417 10 associated lipids
Dermatitis D003872 30 associated lipids
Colitis D003092 69 associated lipids
Candidiasis, Vulvovaginal D002181 8 associated lipids
Body Weight D001835 333 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
van Schie CC et al. Tomato linalool synthase is induced in trichomes by jasmonic acid. 2007 Plant Mol. Biol. pmid:17440821
Fähnrich A et al. Characteristic alatoid 'cineole cassette' monoterpene synthase present in Nicotiana noctiflora. 2014 Plant Mol. Biol. pmid:24493662
Goodger JQ et al. Isolation of intact sub-dermal secretory cavities from Eucalyptus. 2010 Plant Methods pmid:20807444
Serreli G et al. Phenolic Compounds, Volatiles and Antioxidant Capacity of White Myrtle Berry Liqueurs. 2017 Plant Foods Hum Nutr pmid:28447255
Kampranis SC et al. Rational conversion of substrate and product specificity in a Salvia monoterpene synthase: structural insights into the evolution of terpene synthase function. 2007 Plant Cell pmid:17557809
Ohara K et al. Monoterpene engineering in a woody plant Eucalyptus camaldulensis using a limonene synthase cDNA. 2010 Plant Biotechnol. J. pmid:20055958
Karlsson JO et al. Effects of odorants on pigment aggregation and cAMP in fish melanophores. 1994 Pigment Cell Res. pmid:8072946
Franco CR et al. Bioassay-guided evaluation of antinociceptive properties and chemical variability of the essential oil of Hyptis fruticosa. 2011 Phytother Res pmid:21442672
Satou T et al. Organ accumulation in mice after inhalation of single or mixed essential oil compounds. 2013 Phytother Res pmid:22581512
Efferth T et al. Cytotoxic activity of secondary metabolites derived from Artemisia annua L. towards cancer cells in comparison to its designated active constituent artemisinin. 2011 Phytomedicine pmid:21831619