Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375638 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
Previously it was found that 4-hydroxybenzaldehyde is a competitive inhibitor of GABA transaminase. Here 3-chloro-1-(4-hydroxyphenyl)propan-1-one (9), a 4-hydroxybenzaldehyde analogue, was found to inactivate potently the enzyme in a time-dependent manner. α-Ketoglutarate prevented the enzyme from inactivation, suggesting that the inactivation occurs in its active site. Several experiments indicated that the inactivation is irreversible. This study provides a novel strategy for the design of more effective inhibitors.
Graphical abstract3-Chloro-1-(4-hydroxyphenyl)propan-1-one (9) was found to inactivate potently the enzyme in a time-dependent manner.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yun-Hai Tao, Hui-Bi Xu, Xiang-Liang Yang,