THE FORMATION OF O-METHYLATED CATECHOLS BY MICROSOMAL HYDROXYLATION OF PHENOLS AND SUBSEQUENT ENZYMATIC CATECHOL O-METHYLATION. SUBSTRATE SPECIFICITY.
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Alkylation↗
Biomedical subjects
J K INSCOE
Publications and source records attributed to J K INSCOE.
ENZYMATIC FORMATION OF O-METHYLATED DIHYDROXY DERIVATIVES FROM PHENOLIC AMINES AND INDOLES.
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Alkylation↗
THE UPTAKE AND BINDING OF CIRCULATING SEROTONIN AND THE EFFECT OF DRUGS.
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Amphetamine↗
Liver enzymes during hepatic carcinogenesis.
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Animals↗
Glucuronide formation of narcotic drugs in vitro and in vivo.
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Biochemical Phenomena↗
Some factors affecting glucuronide formation in vitro.
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Glucuronates↗
Induced synthesis of liver microsomal enzymes which metabolize foreign compounds.
The administration of 3,4-benzpyrene to rats markedly increases the activities of certain liver microsomal enzymes which metabolize foreign compounds. Evidence based on studies of enzyme induction is presented which suggests the presence in liver microsomes of several enzymes which can catalyze the same type of reaction.
Animals↗
O-methylation, the principal pathway for the metabolism of epinephrine and norepinephrine in the rat.
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Animals↗
Enzymatic synthesis of N-glucosyluronic acid conjugates.
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Amines↗
The fate of papaverine in man and other mammals.
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Animals↗
1-(3'-methoxy-4'-hydroxy benzyl) 6-7 dimethoxy isoquinoline, a major metabolite of papaverine.
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Humans↗
Enzymatic synthesis of N-glucuronic acid conjugates.
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Carbohydrate Metabolism↗
The effect of 6-mercaptopurine on nucleic acid biosynthesis in Escherichia coli.
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Escherichia coli↗