Design, synthesis, and biological evaluation of simplified α-Keto heterocycle, trifluoromethyl ketone, and formyl substituted folate analogues as potential inhibitors of GAR transformylase and AICAR transformylase
摘要:
A series of simplified alpha-keto heterocycle, trifluoromethyl ketone, and formyl substituted folate analogues lacking the benzoylglutamate subunit were prepared and examined as potential inhibitors of glycinamide ribonucleotide transformylase (GAR Tfase) and aminoimidazole carboxamide transformylase (AICAR Tfase). (C) 2003 Elsevier Ltd. All rights reserved.
CINCHONINE-DERIVED CATALYSTS AND METHODS OF USING SAME
申请人:BRANDEIS UNIVERSITY
公开号:US20200048243A1
公开(公告)日:2020-02-13
The present invention includes certain conchinine-derived phase-transfer catalysts of formula (I), compositions comprising the same, and methods of promoting asymmetric addition reactions using the same.
Cinchonine-derived catalysts and methods of using same
申请人:BRANDEIS UNIVERSITY
公开号:US10836761B2
公开(公告)日:2020-11-17
The present invention includes certain conchinine-derived phase-transfer catalysts of formula (I), compositions comprising the same, and methods of promoting asymmetric addition reactions using the same.
Design, synthesis, and biological evaluation of simplified α-Keto heterocycle, trifluoromethyl ketone, and formyl substituted folate analogues as potential inhibitors of GAR transformylase and AICAR transformylase
作者:Thomas H Marsilje、Michael P Hedrick、Joel Desharnais、Ali Tavassoli、Yan Zhang、Ian A Wilson、Stephen J Benkovic、Dale L Boger
DOI:10.1016/s0968-0896(03)00456-5
日期:2003.10
A series of simplified alpha-keto heterocycle, trifluoromethyl ketone, and formyl substituted folate analogues lacking the benzoylglutamate subunit were prepared and examined as potential inhibitors of glycinamide ribonucleotide transformylase (GAR Tfase) and aminoimidazole carboxamide transformylase (AICAR Tfase). (C) 2003 Elsevier Ltd. All rights reserved.