Gamma-valerolactone

Gamma-valerolactone is a lipid of Fatty Acyls (FA) class.

Cross Reference

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

Current reference collection contains 374 references associated with Gamma-valerolactone 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.


Here are additional resources we collected from PubChem and MeSH for Gamma-valerolactone

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Gamma-valerolactone

MeSH term MeSH ID Detail
Peripheral Nervous System Diseases D010523 33 associated lipids
Total 1

NCBI Entrez Crosslinks

All references with Gamma-valerolactone

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Authors Title Published Journal PubMed Link
Carta F et al. 5- and 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors. 2012 Bioorg. Med. Chem. Lett. pmid:22137345
Zhao Y et al. Production of aromatic hydrocarbons through catalytic pyrolysis of γ-valerolactone from biomass. 2012 Bioresour. Technol. pmid:22507905
Marinetti LJ et al. Gamma butyrolactone (GBL) and gamma valerolactone (GVL): similarities and differences in their effects on the acoustic startle reflex and the conditioned enhancement of startle in the rat. 2012 Pharmacol. Biochem. Behav. pmid:22349589
Wright WR and Palkovits R Development of heterogeneous catalysts for the conversion of levulinic acid to γ-valerolactone. 2012 ChemSusChem pmid:22890968
Geilen FM et al. Selective homogeneous hydrogenation of biogenic carboxylic acids with [Ru(TriPhos)H]+: a mechanistic study. 2011 J. Am. Chem. Soc. pmid:21786816
Takagaki A et al. Antioxidative activity of microbial metabolites of (-)-epigallocatechin gallate produced in rat intestines. 2011 Biosci. Biotechnol. Biochem. pmid:21389610
Gürbüz EI et al. Reactive extraction of levulinate esters and conversion to γ-valerolactone for production of liquid fuels. 2011 ChemSusChem pmid:21394926
Johansen SS and Windberg CN Simultaneous determination of γ-Hydroxybutyrate (GHB) and its analogues (GBL, 1.4-BD, GVL) in whole blood and urine by liquid chromatography coupled to tandem mass spectrometry. 2011 J Anal Toxicol pmid:21219697
Chia M and Dumesic JA Liquid-phase catalytic transfer hydrogenation and cyclization of levulinic acid and its esters to γ-valerolactone over metal oxide catalysts. 2011 Chem. Commun. (Camb.) pmid:22005944
Jo YJ et al. Comparison of fermented soybean paste (Doenjang) prepared by different methods based on profiling of volatile compounds. 2011 J. Food Sci. pmid:21535802