コンテンツへスキップ
Merck
  • Structural essentials for β-N-acetylhexosaminidase inhibition by amides of prolines, pipecolic and azetidine carboxylic acids.

Structural essentials for β-N-acetylhexosaminidase inhibition by amides of prolines, pipecolic and azetidine carboxylic acids.

Organic & biomolecular chemistry (2016-10-14)
A F G Glawar, R F Martínez, B J Ayers, M A Hollas, N Ngo, S Nakagawa, A Kato, T D Butters, G W J Fleet, S F Jenkinson
要旨

This paper explores the computer modelling aided design and synthesis of β-N-acetylhexosaminidase inhibitors along with their applicability to human disease treatment through biological evaluation in both an enzymatic and cellular setting. We investigated the importance of individual stereocenters, variations in structure-activity relationships along with factors influencing cell penetration. To achieve these goals we modified nitrogen heterocycles in terms of ring size, side chains present and ring nitrogen derivatization. By reducing the inhibitor interactions with the active site down to the essentials we were able to determine that besides the established 2S,3R trans-relationship, the presence and stereochemistry of the CH2OH side chain is of crucial importance for activity. In terms of cellular penetration, N-butyl side chains favour cellar uptake, while hydroxy- and carboxy-group bearing sidechains on the ring nitrogen retarded cellular penetration. Furthermore we show an early proof of principle study that β-N-acetylhexosaminidase inhibitors can be applicable to use in a potential anti-invasive anti-cancer strategy.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
硫酸銅(II) 溶液, 4 % (w/v) (prepared from copper (II) sulfate pentahydrate)
カタログ番号
容量
在庫状況
単価
数量
Supelco
ビシンコニン酸 溶液
カタログ番号
容量
在庫状況
単価
数量
Sigma-Aldrich
タンパク質標準品, Micro Standard, liquid
カタログ番号
容量
在庫状況
単価
数量