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  • Synthesis of a novel series of L-isoserine derivatives as aminopeptidase N inhibitors.

Synthesis of a novel series of L-isoserine derivatives as aminopeptidase N inhibitors.

Journal of enzyme inhibition and medicinal chemistry (2011-07-21)
Kanghui Yang, Jinghong Fen, Hao Fang, Lei Zhang, Jianzhi Gong, Wenfang Xu
ABSTRACT

A series of novel L-isoserine derivatives were synthesised and evaluated for their ability to inhibit aminopeptidase N (APN)/CD13. In our preliminary biological results, some of these compounds possessed a potent inhibitory activity against the APN. Within this series, compound 14b not only showed similar enzyme inhibition (IC₅₀ of 12.2 μM) compared with the positive control bestatin (half maximal inhibitory concentration (IC₅₀) of 7.3 μM), but also had a potent antiproliferative activity against human cancer cell lines cells.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
N-[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl]-L-leucine, 97%
Sigma-Aldrich
DL-Isoserine, 98%
Sigma-Aldrich
Bestatin hydrochloride, ≥98% (HPLC)