urothion

Molybdenum cofactor deficiency is an autosomal recessive inborn error of metabolism, which results from mutations in genes… (More)

The field of molybdopterin-containing enzymes has experienced an infusion of excitement as a result of several reports of high… (More)

A patient with molybdenum cofactor deficiency (producing the biochemical abnormalities associated with deficiencies of sulphite… (More)

In order to determine the absolute configuration of urothion (1), the CD spectra of tri-4-chlorobenzoyl derivatives of 2-amino-6… (More)

Urothione was isolated as an excretion product of Hydrogenophaga pseudoflava and other bacteria at amounts approaching 253… (More)

A girl aged eight months, who presented with developmental delay and dislocated optic lenses, was diagnosed as having combined… (More)

The oxidation of trimethylamine to trimethylamine N-oxide in animals is catalyzed by an enzyme which has not yet been fully… (More)

Genetic and biochemical studies have established that in all molybdenum-containing enzymes, with the exception of nitrogenase… (More)

Two stable fluorescent derivatives of molybdopterin have been structurally characterized. Form A is an oxidized pterin with a 6… (More)

The molybdenum cofactor isolated from sulfite oxidase (sulfite: ferricytochrome c oxidoreductase, EC 1.8.2.1) and xanthine… (More)