(+)-borneol

(+)-borneol is a lipid of Prenol Lipids (PR) class.

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

Current reference collection contains 736 references associated with (+)-borneol in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.

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We collected disease MeSH terms mapped to the references associated with (+)-borneol

PubChem Biomolecular Interactions and Pathways

All references with (+)-borneol

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Authors Title Published Journal PubMed Link
Wu C et al. Effect of natural borneol on the pharmacokinetics and distribution of nimodipine in mice. 2014 Eur J Drug Metab Pharmacokinet pmid:23673491
Jiang P et al. The effectiveness of borneol on pharmacokinetics changes of four ginsenosides in Shexiang Baoxin Pill in vivo. 2014 Biomed. Chromatogr. pmid:24123182
Bruder S et al. Use of fuzzy logic models for prediction of taste and odor compounds in algal bloom-affected inland water bodies. 2014 Environ Monit Assess pmid:24242080
Zhang L et al. The use of borneol as an enhancer for targeting aprotinin-conjugated PEG-PLGA nanoparticles to the brain. 2013 Pharm. Res. pmid:23615859
Almeida JR et al. Borneol, a bicyclic monoterpene alcohol, reduces nociceptive behavior and inflammatory response in mice. 2013 ScientificWorldJournal pmid:23710149
Chen ZZ et al. Influence of borneol and muscone on geniposide transport through MDCK and MDCK-MDR1 cells as blood-brain barrier in vitro model. 2013 Int J Pharm pmid:23973509
Chen J et al. Mechanical, rheological and release behaviors of a poloxamer 407/ poloxamer 188/carbopol 940 thermosensitive composite hydrogel. 2013 Molecules pmid:24108402
Su J et al. Natural borneol, a monoterpenoid compound, potentiates selenocystine-induced apoptosis in human hepatocellular carcinoma cells by enhancement of cellular uptake and activation of ROS-mediated DNA damage. 2013 PLoS ONE pmid:23700426
Cheng C et al. Sensitive assay for measurement of volatile borneol, isoborneol, and the metabolite camphor in rat pharmacokinetic study of Borneolum (Bingpian) and Borneolum syntheticum (synthetic Bingpian). 2013 Acta Pharmacol. Sin. pmid:23974515
Prasad B et al. Water oxidation by a cytochrome p450: mechanism and function of the reaction. 2013 PLoS ONE pmid:23634216

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