Identification of alkaloids; the condensation products of biogenic amines with formaldehyde, enzymatically formed from 5-methyltetrahydrofolic acid

Lauwers, W; Leysen, J; Verhoeven, H; Laduron, P

HERO ID

1514087

Reference Type

Journal Article

Year

1975

Language

English

PMID

1131388

HERO ID 1514087
In Press No
Year 1975
Title Identification of alkaloids; the condensation products of biogenic amines with formaldehyde, enzymatically formed from 5-methyltetrahydrofolic acid
Authors Lauwers, W; Leysen, J; Verhoeven, H; Laduron, P
Journal Biomedical Mass Spectrometry
Volume 2
Issue 1
Page Numbers 15-22
Abstract The use of thin-layer chromatography has demonstrated that incubations of indoleamines with 5-methyl[14-C]tetrahydrofolic acid and an enzyme previously described as an N-methyltransferase, do not yield Nw, N1, or O-methylated products. Further elucidation by thin-layer chromatography, gas chromatography, mass spectrometry and selected ion monitoring enabled us to identify the reaction products as tetrahydroisoquinolines and tetrahydro-beta-carbolines in mixtures incubated respectively with catecholamines and indoleamines in the presence of 5-methyl[14-C]tetrahydrofolic acid and enzyme. The alkaloids have been shown to originate from a spontaneous condensation of the corresponding amines with formaldehyde, this latter being formed in the first stage of the reaction by enzymatic conversion from 5-methyltetrahydrofolic acid.
Pmid 1131388
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Alkaloids/ chemical synthesis; Animals; Biogenic Amines; Brain/enzymology; Carbolines/chemical synthesis; Chemical Phenomena; Chemistry; Chromatography, Gas; Chromatography, Thin Layer; Folic Acid/ analogs & derivatives; Formaldehyde; Isoquinolines/chemical synthesis; Kidney/enzymology; Mass Spectrometry; Methyltransferases