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- W2068333298 abstract "Serotonin was chemically reduced to 2,3-dihydro-5-hydroxytryptamine, which is extremely labile to oxidation. This substance is a substituted amino phenol which, when oxidized, presumably proceeds through the formation of an iminoquinone. The 2,3-dihydro-5-hydroxytryptamine was attacked enzymatically by amine oxidase and by ceruloplasmin. Quantitatively, 2,3-dihydro-5-hydroxytryptophan behaved similarly to serotonin with respect to its effect on the chromatophore activity of the guppy, the isolated virgin rat uterus, and the isolated ileum of the rabbit." @default.
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- W2068333298 date "1962-07-01" @default.
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- W2068333298 title "2,3-Dihydro-5-hydroxytryptamine" @default.
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- W2068333298 doi "https://doi.org/10.1016/0006-2952(62)90116-8" @default.
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