Indolyl carboxylic acids by condensation of indoles with alpha-keto acids

Citation
Tr. Garbe et al., Indolyl carboxylic acids by condensation of indoles with alpha-keto acids, J NAT PROD, 63(5), 2000, pp. 596-598
Citations number
10
Categorie Soggetti
Agricultural Chemistry","Pharmacology & Toxicology
Journal title
JOURNAL OF NATURAL PRODUCTS
ISSN journal
01633864 → ACNP
Volume
63
Issue
5
Year of publication
2000
Pages
596 - 598
Database
ISI
SICI code
0163-3864(200005)63:5<596:ICABCO>2.0.ZU;2-5
Abstract
The novel indole derivatives 2,2-bis(3,3'-indolyl)propionic acid (1); 1,1,1 ,-tris(3,3',3 "-indolyl)ethane (2); and 2,2-bis(3,3'-indolyl)isocaproic aci d (3) were isolated from solvent extracts of indole-supplemented supernatan ts of Escherichia coli and corynebacteria. The compounds were also obtained by chemical synthesis: compounds 1 and 2 from indole and pyruvic acid and compound 3 from indole and alpha-ketoisocaproic acid, following incubation at 37 degrees C in aqueous medium. Tryptophan and pyruvic acid gave the nov el 2-(2-tryptophanyl)lactic acid (4). The condensation reaction between ind oles and alpha-keto acids was of general nature, and the mild reaction cond itions suggested it may proceed in vivo. Examples for endogenous occurrence may be the neuro-degenerative diseases phenylketonuria and maple syrup uri ne disease, both characterized by elevated blood levels of alpha-keto acids .