Ubenimex → L-Leucine

HRID 437009

Reaction equation

HRID 437009 reaction equation
[CH3:1][CH:2]([CH2:4][C@H:5]([NH:9]C([C@@H](O)[C@H](N)CC1C=CC=CC=1)=O)[C:6]([OH:8])=[O:7])[CH3:3]>Cl>[NH2:9][C@H:5]([C:6]([OH:8])=[O:7])[CH2:4][CH:2]([CH3:3])[CH3:1]

Participants

3

Reagents, catalysts & solvents 1

Procedure

The hydrolysis of bestatin in 6N HCl at 100° C. for 18 hours yields L-leucine and an unusual amino acid. The ratio of these amino acids is 1:1. Bestatin gives positive Rydon-Smith and ninhydrin reactions. The amino acid sequence of bestatin shown in the structure was elucidated by fragmentation pattern in mass spectrum of bestatin methyl ester hydrochloride. Thus, the structure of bestatin is (2S,3R)-3-amino-2-hydroxy-4-phenylbutyryl-L-leucine.

Sources & evidence

ORD record
ord-4b35802d46464e9cb7248cada345d15e
Source dataset
uspto-grants-1977_06
Patent number
US04029547

Linked notes

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