6630-90-6Relevant articles and documents
Synthesis and biological evaluation of pentanedioic acid derivatives as farnesyltransferase inhibitors
Yang, Liuqing,Liu, Wei,Mei, Hanbing,Zhang, Yuan,Yu, Xiaojuan,Xu, Yufang,Li, Honglin,Huang, Jin,Zhao, Zhenjiang
supporting information, p. 671 - 676 (2015/04/27)
Structure-based virtual screening of a commercial library identified pentanedioic acid derivatives (6 and 13b) as a kind of novel scaffold farnesyltransferase inhibitors (FTIs). Chemical modifications of the lead compounds, biological assays and analysis of the structure-activity relationships (SAR) were conducted to discover more potent FTIs. Some of them displayed excellent inhibition against FTase, and among them, the most active compound 13n with an IC50 value of 0.0029 μM and SAR analysis might be helpful to the discovery of more potent FTIs. This journal is
Syntheses of bryophyte constituents. 8. Sphagnum acid and its degradation products
Eicher,Wobido,Speicher
, p. 706 - 710 (2007/10/03)
For Sphagnum acid (1) and its enzymatic degradation product 5-hydroxy-4-(4-hydroxyphenyl)-5H-furan-2-on (2) efficient syntheses on preparative scale were developed. For the (4-hydroxyphenyl)butenolide 2 some characteristic chemical transformations are observed in acidic and basic medium. Johann Ambrosius Barth 1996.