Gamma-butyrolactone

Gamma-butyrolactone 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 14993 references associated with Gamma-butyrolactone 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-butyrolactone

Possible diseases from mapped MeSH terms on references

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

MeSH term MeSH ID Detail
Gram-Negative Bacterial Infections D016905 16 associated lipids
Weight Loss D015431 56 associated lipids
Stomach Ulcer D013276 75 associated lipids
Pseudomonas Infections D011552 25 associated lipids
Lung Neoplasms D008175 171 associated lipids
Lung Diseases D008171 37 associated lipids
Colonic Neoplasms D003110 161 associated lipids
Ataxia D001259 20 associated lipids
Adenocarcinoma D000230 166 associated lipids
Total 9

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with Gamma-butyrolactone

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Authors Title Published Journal PubMed Link
Shaw PD et al. Detecting and characterizing N-acyl-homoserine lactone signal molecules by thin-layer chromatography. 1997 Proc. Natl. Acad. Sci. U.S.A. pmid:9177164
Lindemann A et al. Isovaleryl-homoserine lactone, an unusual branched-chain quorum-sensing signal from the soybean symbiont Bradyrhizobium japonicum. 2011 Proc. Natl. Acad. Sci. U.S.A. pmid:21949379
Chung J et al. Small-molecule inhibitor binding to an N-acyl-homoserine lactone synthase. 2011 Proc. Natl. Acad. Sci. U.S.A. pmid:21730159
Singh L et al. Enantiomers of HA-966 (3-amino-1-hydroxypyrrolid-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/N-methyl-D-aspartate receptor antagonist, but (-)-HA-966 is a potent gamma-butyrolactone-like sedative. 1990 Proc. Natl. Acad. Sci. U.S.A. pmid:2153294
Pearson JP et al. A second N-acylhomoserine lactone signal produced by Pseudomonas aeruginosa. 1995 Proc. Natl. Acad. Sci. U.S.A. pmid:7878006
Cha SH et al. Hypothalamic malonyl-CoA triggers mitochondrial biogenesis and oxidative gene expression in skeletal muscle: Role of PGC-1alpha. 2006 Proc. Natl. Acad. Sci. U.S.A. pmid:17030788
Gao S and Lane MD Effect of the anorectic fatty acid synthase inhibitor C75 on neuronal activity in the hypothalamus and brainstem. 2003 Proc. Natl. Acad. Sci. U.S.A. pmid:12724522
Cha SH et al. Inhibition of hypothalamic fatty acid synthase triggers rapid activation of fatty acid oxidation in skeletal muscle. 2005 Proc. Natl. Acad. Sci. U.S.A. pmid:16203972
Feigenbaum JJ and Howard SG Gamma hydroxybutyrate is not a GABA agonist. 1996 Prog. Neurobiol. pmid:8931105
Morton MS et al. Lignans and isoflavonoids in plasma and prostatic fluid in men: samples from Portugal, Hong Kong, and the United Kingdom. 1997 Prostate pmid:9215400