Results 21 to 30 of about 4,302 (241)

A Bacterial Pterin Deaminase

open access: hybridJournal of Biological Chemistry, 1959
Publisher Summary This chapter describes the bacterial pterin deaminase. In the standard assay, the mixture contains 0.05 ml of pterin carboxylic acid, 0.8 ml of phosphate buffer, and 0.02 to 0.15 ml of enzyme in a final volume of 1.0 ml. Incubation is carried out at 23° in a 1-ml Beckman quartz cuvette with a light path of 1.00 cm. Reaction is begun
Bruce Levenberg, Osamu Hayaishi
openalex   +4 more sources

A contribution to the chemistry of pterins [PDF]

open access: bronzeProceedings of the Royal Society of London. Series B - Biological Sciences, 1942
The experiments in this paper have been chiefly concerned with a derivative from pterins, the wing pigments of pierid butterflies. These pigments have become prominent of recent years, partly on account of the prolonged efforts (1925-41) of continental workers to determine their nature.
Frederick Gowland Hopkins
openalex   +3 more sources

Pterins in Human Urine

open access: yesJournal of Biological Chemistry, 1972
Abstract Qualitative and quantitative analyses for pterins (derivatives of 2-amino-4-hydroxypteridine) in human urine were carried out by an improved procedure which involved the use of two new weak ion exchangers, ECTEOLA-Sephadex and phospho-Sephadex.
Tetsuo Shiota, Takeshi Fukushima
openaire   +3 more sources

Direct coordination of pterin to Fe II enables neurotransmitter biosynthesis in the pterin-dependent hydroxylases [PDF]

open access: yesProceedings of the National Academy of Sciences, 2021
Significance The mononuclear pterin-dependent nonheme iron enzymes catalyze the rate-limiting step in neurotransmitter biosynthesis and are essential in maintaining proper brain function. These enzymes utilize molecular oxygen, a redox active pterin cofactor, and a ferrous active site to generate an Fe IV -
Shyam R. Iyer   +13 more
openaire   +4 more sources

Exploring the scope of DBU-promoted amidations of 7-carboxymethyl-pterin [PDF]

open access: yes, 2020
Pteridines are an important heterocycle often used in the development of pharmaceutically relevant compounds, and in the field of supramolecular chemistry.
Bockman, Anna
core   +3 more sources

Photocarcinogenesis of the skin: Current status and future trends. [PDF]

open access: yesKaohsiung J Med Sci
Abstract Solar radiation is essential for life on Earth but is also a major contributor to skin carcinogenesis. Solar radiation, particularly ultraviolet (UV) B (280–320 nm) and UVA (320–400 nm), induces photocarcinogenesis via various pathways. UV light can directly cause DNA damage, resulting in genetic mutations if not repaired correctly.
Yang TT, Lan CE.
europepmc   +2 more sources

Mapping an atlas of tissue-specific drosophila melanogaster metabolomes by high resolution mass spectrometry [PDF]

open access: yes, 2013
Metabolomics can provide exciting insights into organismal function, but most work on simple models has focussed on the whole organism metabolome, so missing the contributions of individual tissues.
A Kamleh   +47 more
core   +3 more sources

Modulation of Free Radical Formation by Pterin Derivatives

open access: yesPteridines, 2004
All classes of pterins, fully reduced tetrahydropterins, aromatic pterins and dihydropterins have been investigated upon their effects on radical mediated reactions.
Karl Oettl   +2 more
doaj   +1 more source

Comparative routes to 7-carboxymethyl-pterin: A useful medicinal chemistry building block

open access: yesPteridines, 2022
Pterins, such as folate and biopterin, and their derivatives hold significant importance given their biological relevance, as well as the numerous pterin-based inhibitors developed for targeting various biological targets. For this reason, pterins can be
Bennett Zachary   +2 more
doaj   +1 more source

Pterin determination in cerebrospinal fluid: state of the art

open access: yesPteridines, 2017
The analysis of pterins in the cerebrospinal fluid (CSF) is mandatory for the etiologic diagnosis of inborn errors of dopamine and serotonin metabolism.
Guibal Pierre   +3 more
doaj   +1 more source

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