urothion

Known as: 2-amino-7-(1,2-dihydroxyethyl)-6-(methylthio)thieno(3,2-g)pteridin-4(3H)one, urothione 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2018
0119822018

Papers overview

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2018
2018
Molybdenum cofactor deficiency is an autosomal recessive inborn error of metabolism, which results from mutations in genes… (More)
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1997
1997
The field of molybdopterin-containing enzymes has experienced an infusion of excitement as a result of several reports of high… (More)
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1995
1995
A patient with molybdenum cofactor deficiency (producing the biochemical abnormalities associated with deficiencies of sulphite… (More)
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1995
1995
In order to determine the absolute configuration of urothion (1), the CD spectra of tri-4-chlorobenzoyl derivatives of 2-amino-6… (More)
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1994
1994
Urothione was isolated as an excretion product of Hydrogenophaga pseudoflava and other bacteria at amounts approaching 253… (More)
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1990
1990
A girl aged eight months, who presented with developmental delay and dislocated optic lenses, was diagnosed as having combined… (More)
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1988
1988
The oxidation of trimethylamine to trimethylamine N-oxide in animals is catalyzed by an enzyme which has not yet been fully… (More)
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1985
1985
Genetic and biochemical studies have established that in all molybdenum-containing enzymes, with the exception of nitrogenase… (More)
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1984
1984
Two stable fluorescent derivatives of molybdopterin have been structurally characterized. Form A is an oxidized pterin with a 6… (More)
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1982
1982
The molybdenum cofactor isolated from sulfite oxidase (sulfite: ferricytochrome c oxidoreductase, EC 1.8.2.1) and xanthine… (More)
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