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3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) and Other Heterocyclic Amines as Inhibitors of Mitochondrial Monoamine Oxidases Separated From Human Brain Synaptosomes

3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) and Other Heterocyclic Amines as Inhibitors of Mitochondrial Monoamine Oxidases Separated From Human Brain Synaptosomes

T Kojima, M Naoi, K Wakabayashi, T Sugimura, T Nagatsu

Neurochem Int. 1990;16(1):51-7.

PMID: 20504539

Abstract:

Effects of a series of heterocyclic amines on type A and B monoamine oxidases were studied using human brain synaptosomal mitochondria as an enzyme source. 3-Amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) was the most potent inhibitor of the heterocyclic amines examined. It inhibited type A monoamine oxidase in competition with the substrate and the K(i) value toward type A was 0.84 +/- 0.06 ?M, which was about 1/50 of its K(m) value toward an amine substrate, kynuramine; 46.4 +/- 11.4 ?M. 3-Amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1) was also a potent inhibitor. 3- or 2-Aminopyridoindoles or -imidazoles inhibited both type A and B monoamine oxidase competitively to substrate, but inhibition of type B monoamine oxidase by amines with 2-amino-3-methylimidazol ring was non-competitive. In general, type A monoamine oxidase was more sensitive to these heterocyclic amines than type B; the K(i) values toward type A were much smaller than those of type B. Inhibition of type A monoamine oxidase by Trp-P-2 proved to be reversible; the enzyme activity inhibited by Trp-P-2 could be fully recovered by removal of Trp-P-2 by column chromatography with Sephadex G-25.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP245089	5H-Pyrido[3,2-b]indole		245-08-9	Price

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