コンテンツへスキップ
Merck
  • Inhibitors of bacterial N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity.

Inhibitors of bacterial N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity.

Bioorganic & medicinal chemistry letters (2009-10-14)
Danuta Gillner, Nicola Armoush, Richard C Holz, Daniel P Becker
要旨

The dapE-encoded N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) is a critical bacterial enzyme for the construction of the bacterial cell wall. A screen biased toward compounds containing zinc-binding groups (ZBG's) including thiols, carboxylic acids, boronic acids, phosphonates and hydroxamates has delivered a number of micromolar inhibitors of DapE from Haemophilus influenzae, including the low micromolar inhibitor L-captopril (IC(50)=3.3 microM, K(i)=1.8 microM). In vitro antimicrobial activity was demonstrated for L-captopril against Escherichia coli.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
フェニルボロン酸, 95%
Sigma-Aldrich
N-フェニルチオ尿素, ≥98%
Sigma-Aldrich
D-ペニシラミン, 98-101%
Sigma-Aldrich
カプトプリル, ≥98% (HPLC), powder
Sigma-Aldrich
アセトヒドロキサム酸, 98%
Sigma-Aldrich
ブチルボロン酸, 97%
Sigma-Aldrich
L-ペニシラミン, 99%
Sigma-Aldrich
N-(Benzyloxycarbonyl)hydroxylamine, 99%
Sigma-Aldrich
カプトプリル, meets USP testing specifications
Supelco
ブチルボロン酸, for GC derivatization, LiChropur, ≥96.0% (T)