Gamma-valerolactone

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

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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.

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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

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Ftouni J et al. Influence of Sulfuric Acid on the Performance of Ruthenium-based Catalysts in the Liquid-Phase Hydrogenation of Levulinic Acid to γ-Valerolactone. 2017 ChemSusChem pmid:28603841
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Borges G et al. A comprehensive evaluation of the [2-C](-)-epicatechin metabolome in rats. 2016 Free Radic. Biol. Med. pmid:27495388
Tabasso S et al. Microwave-Assisted γ-Valerolactone Production for Biomass Lignin Extraction: A Cascade Protocol. 2016 Molecules pmid:27023511
Turrini NG et al. Sequential Enzymatic Conversion of α-Angelica Lactone to γ-Valerolactone through Hydride-Independent C=C Bond Isomerization. 2016 ChemSusChem pmid:27885835
Mülek M et al. Profiling a gut microbiota-generated catechin metabolite's fate in human blood cells using a metabolomic approach. 2015 J Pharm Biomed Anal pmid:26025814
Rodriguez-Mateos A et al. Influence of age on the absorption, metabolism, and excretion of cocoa flavanols in healthy subjects. 2015 Mol Nutr Food Res pmid:25981347
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Zhang L et al. Production of furfural from xylose, xylan and corncob in gamma-valerolactone using FeCl3·6H2O as catalyst. 2014 Bioresour. Technol. pmid:24262845
Luterbacher JS et al. Nonenzymatic sugar production from biomass using biomass-derived γ-valerolactone. 2014 Science pmid:24436415
Xin L et al. Electricity storage in biofuels: selective electrocatalytic reduction of levulinic acid to valeric acid or γ-valerolactone. 2013 ChemSusChem pmid:23457116
Zeng FX et al. Ionic-liquid-catalyzed efficient transformation of γ-valerolactone to methyl 3-pentenoate under mild conditions. 2013 ChemSusChem pmid:23468313
Yang Z et al. RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature. 2013 Chem. Commun. (Camb.) pmid:23648801
Götz K et al. A chemo-enzymatic route to synthesize (S)-γ-valerolactone from levulinic acid. 2013 Appl. Microbiol. Biotechnol. pmid:23296499
Gürbüz EI et al. Conversion of hemicellulose into furfural using solid acid catalysts in γ-valerolactone. 2013 Angew. Chem. Int. Ed. Engl. pmid:23212945
Deng J et al. Conversion of carbohydrate biomass to γ-valerolactone by using water-soluble and reusable iridium complexes in acidic aqueous media. 2013 ChemSusChem pmid:23757330
Bui L et al. Domino reaction catalyzed by zeolites with Brønsted and Lewis acid sites for the production of γ-valerolactone from furfural. 2013 Angew. Chem. Int. Ed. Engl. pmid:23757377
Klossek ML et al. Eco-solvents--cluster-formation, surfactantless microemulsions and facilitated hydrotropy. 2013 Phys Chem Chem Phys pmid:23708062
Andresen-Streichert H et al. Uptake of gamma-valerolactone--detection of gamma-hydroxyvaleric acid in human urine samples. 2013 J Anal Toxicol pmid:23486087
Muzaiyanah AR and Amirul AA Studies on the microbial synthesis and characterization of polyhydroxyalkanoates containing 4-hydroxyvalerate using γ-valerolactone. 2013 Appl. Biochem. Biotechnol. pmid:23649305
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
Du XL et al. Conversion of biomass-derived levulinate and formate esters into γ-valerolactone over supported gold catalysts. 2011 ChemSusChem pmid:22105964
Du XL et al. Hydrogen-independent reductive transformation of carbohydrate biomass into γ-valerolactone and pyrrolidone derivatives with supported gold catalysts. 2011 Angew. Chem. Int. Ed. Engl. pmid:21732502
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
Del Rio D et al. Bioavailability and catabolism of green tea flavan-3-ols in humans. 2010 Nov-Dec Nutrition pmid:20080030
Bozell JJ Chemistry. Connecting biomass and petroleum processing with a chemical bridge. 2010 Science pmid:20671177
Deng L et al. Conversion of levulinic acid and formic acid into γ-valerolactone over heterogeneous catalysts. 2010 ChemSusChem pmid:20872402
Bond JQ et al. γ-Valerolactone ring-opening and decarboxylation over SiO2/Al2O3 in the presence of water. 2010 Langmuir pmid:20513157
Bond JQ et al. Integrated catalytic conversion of gamma-valerolactone to liquid alkenes for transportation fuels. 2010 Science pmid:20185721
Fun HK et al. Absolute configuration of isoeichlerialactone. 2010 Acta Crystallogr Sect E Struct Rep Online pmid:21580698
Deng L et al. Catalytic conversion of biomass-derived carbohydrates into gamma-valerolactone without using an external H2 supply. 2009 Angew. Chem. Int. Ed. Engl. pmid:19630045
Shintani R et al. Palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes. 2009 Org. Lett. pmid:19908855
Aparicio S and Alcalde R Characterization of two lactones in liquid phase: an experimental and computational approach. 2009 Phys Chem Chem Phys pmid:19809678
Bourne RA et al. Maximising opportunities in supercritical chemistry: the continuous conversion of levulinic acid to gamma-valerolactone in CO(2). 2007 Chem. Commun. (Camb.) pmid:17989815
Lange JP et al. Towards 'bio-based' Nylon: conversion of gamma-valerolactone to methyl pentenoate under catalytic distillation conditions. 2007 Chem. Commun. (Camb.) pmid:17700891
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Leonovich SA Phenol and lactone receptors in the distal sensilla of the Haller's organ in Ixodes ricinus ticks and their possible role in host perception. 2004 Exp. Appl. Acarol. pmid:15139275
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Chen GB and Tang KW [Preparation of gas chromatographic capillary columns with beta-cyclodextrin polymer stationary phase modified with methyl phenyl silicone(OV-17)]. 2000 Se Pu pmid:12541514
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Hein S et al. Biosynthesis of poly(4-hydroxybutyric acid) by recombinant strains of Escherichia coli. 1997 FEMS Microbiol. Lett. pmid:9271870