Science · 1974 · 82 citations · 15 references
Life SciencesBiochemistryPharmacologyEnzymologyMetabolismNeurochemistryAlkaloid BiosynthesisAmino Acid MetabolismAmino Acid NeurochemistryMonoamine NeurochemistryNeurotransmitter BiosynthesisSerotonergic PharmacologyBiosynthesis Of Trace AminesIndole AlkaloidsMonoamine Biosynthetic PathwaysSerotonin BiosynthesisSerotonin SynthesisTryptophan Metabolism
Enzymes from chick and rat tissues catalyze the reaction of N-methyl tryptamine with 5-methyltetrahydrofolic acid to form 2,3,4,9-tetrahydro-2-methyl-1H-pyrido[3,4b] indole. N,N-Dimethyltryptamine was not formed. With tryptamine as substrate the product is 2,3,4,9-tetrahydro-1H-pyrido[3,4b] indole and not N-methyltryptamine. These pyridoindoles were not formed when S-adenosylmethionine was cosubstrare.
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Precambrian Africa and South America as a Single Continent
J. D. A. Piper, J. C. Briden, Keith Lomax · Nature · 1973 · 132 citations
Inhibitors of Monoamine Oxidase
Beng T. Ho, William M. McIsaac, K. E. Walker et al. · Journal of Pharmaceutical Sciences · 1968 · 119 citations