84658-37-7

Usage

InChI:InChI=1/C11H11NO4/c13-7-1-2-9-8(4-7)6(5-12-9)3-10(14)11(15)16/h1-2,4-5,10,12-14H,3H2,(H,15,16)

Upstream product

• 85485-02-5 rac-3-(5-Benzyloxy-3-indolyl)milchsaeure 
• 1215-59-4 5-benzyloxy-1H-indole 
• 4350-07-6 5-H-T-P 
• 85485-01-4 rac-3-(5-Benzyloxy-3-indolyl)milchsaeure-methylester 

Relevant academic research and scientific papers

Formations of (5-Hydroxy)indole S-(-)-lactic Acid, N-acetyl-5-hydroxy-L-tryptophan and (5-Hydroxy)indole Carboxylic Acid in the Metabolism of Tryptophan and 5-Hydroxytryptophan by Chromobacterium violaceum

Tryptophan metabolism catalyzing the production of (5-hydroxy)indolelactate, (5-hydroxy)indole carboxylate, and N-acetyl-5-hydroxytryptophan was found in Chromobacterium violaceum.These metabolites have never been reported before.Metabolic pathways from tryptophan and 5-hydroxytryptophan are proposed.