Results 1 to 10 of about 15,221 (207)

Reaction mechanism of the green synthesis of glutaric acid. [PDF]

open access: yesRSC Adv, 2022
In this study, the reaction mechanism underlying the green synthesis of glutaric acid was studiedviajoint test technology.
Hu J   +5 more
europepmc   +4 more sources

Sustainable production of glutaric acid in microbial cell factories: Current advances and future prospects [PDF]

open access: yesSynthetic and Systems Biotechnology
Glutaric acid is a significant C5 dicarboxylic acid, extensively utilized in the chemical industry, medicine, and biomaterials. In recent years, the advancement of synthetic biology and metabolic engineering has rendered microbial production of glutaric ...
Jie Liu   +4 more
doaj   +2 more sources

Mechanochemical Synthesis and Physicochemical Characterization of Isoniazid and Pyrazinamide Co-crystals With Glutaric Acid [PDF]

open access: yesFrontiers in Chemistry, 2020
The present work reports two novel pharmaceutical co-crystals; 2:1 isoniazid-glutaric acid (INHGA) and 2:1 pyrazinamide-glutaric acid (PGA). Isoniazid and pyrazinamide are key first-line drugs used for the treatment of tuberculosis.
Jean Baptiste Ngilirabanga   +3 more
doaj   +2 more sources

Glutaric acid-mediated apoptosis in primary striatal neurons. [PDF]

open access: yesBiomed Res Int, 2014
Glutaric acid (GA) has been implicated in the mechanism of neurodegeneration in glutaric aciduria type I. In the present study, the potential cytotoxic effects of GA (0.1~50 mM for 24~96 h) were examined in cultured primary rat striatal neurons. Results showed increase in the number of cells labeled by annexin-V or with apoptotic features shown by ...
Tian F   +7 more
europepmc   +4 more sources

Crystallisation of 1,2-dimethylimidazole, and 1-methylimidazole with organic acids [PDF]

open access: yesScientific Reports
Crystals of 1-methylimidazole and 1,2-dimethylimidazole with glutaric and succinic acids are described. The crystal structure including 1,2-dimethylimidazole and glutaric acid, has been reported previously, but the molecular salt of 1-methylimidazole ...
Hadeer Q. Waleed   +5 more
doaj   +2 more sources

A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles [PDF]

open access: yesAtmospheric Chemistry and Physics, 2008
Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds.
A. A. Zardini   +7 more
doaj   +2 more sources

Management of Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Pregnancy [PDF]

open access: yesMetabolites
Multiple acyl-CoA dehydrogenase deficiency (MADD), also known as glutaric acidemia/glutaric aciduria type II (GA II), is an inborn error of fatty acid, amino acid, and choline metabolism.
Matthew A. Shear   +4 more
doaj   +2 more sources

Diagnosis of glutaric aciduria type I based on neuroradiological findings: when neonatal screening fails [PDF]

open access: yesItalian Journal of Pediatrics
Background Glutaric aciduria type I (GA-I) is an autosomal recessive disorder affecting the metabolism of lysine, hydroxylysine, and tryptophan. Patients present in the first age of life with an irreversible motor disorder, and neuroradiological imaging ...
Vincenza Gragnaniello   +8 more
doaj   +2 more sources

Organic acids as cloud condensation nuclei: Laboratory studies of highly soluble and insoluble species [PDF]

open access: yesAtmospheric Chemistry and Physics, 2003
The ability of sub-micron-sized organic acid particles to act as cloud condensation nuclei (CCN) has been examined at room temperature using a newly constructed continuous-flow, thermal-gradient diffusion chamber (TGDC). The organic acids studied were:
P. Pradeep Kumar   +3 more
doaj   +3 more sources

Microencephaly in macrocephaly: Rare report of two siblings with glutaric aciduria type 1

open access: yesAnnals of Movement Disorders, 2021
Glutaric aciduria type 1 is an autosomal recessive disorder caused by mutations in GCDH gene on chromosome 19 leading to the deficiency of glutaryl-CoA dehydrogenase which causes an abnormal metabolism of lysine, hydroxylysine and tryptophan with ...
Ayush Agarwal   +2 more
doaj   +1 more source

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