Fluorinated Mechanism-Based Inhibitors: Common Themes and Recent Developments

被引:24
作者
Tysoe, Christina [1 ]
Withers, Stephen G. [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Amine oxidases; drug design; enzyme inhibition; enzyme mechanisms; fluorine; glycosidases; mechanism-based inhibition; ACTIVATED IRREVERSIBLE INHIBITORS; S-ADENOSYLHOMOCYSTEINE HYDROLASE; MICROBIAL TYRAMINE OXIDASE; L-HOMOCYSTEINE HYDROLASE; COENZYME-BINDING-SITES; SERINE O-SULFATE; MONOAMINE-OXIDASE; ENZYME INACTIVATORS; ORNITHINE-DECARBOXYLASE; SIALIDASE INHIBITORS;
D O I
10.2174/1568026614666140202204602
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Mechanism-based inhibitors are relatively chemically inert compounds that become activated when processed by their target enzyme, leading to covalent enzyme inactivation. Fluorine substitution confers a number of properties that are beneficial to the chemistry of such inhibitors and to their potential use as pharmaceuticals, and indeed several fluorinated mechanism-based inhibitors have made it to clinical usage over the past 50 years. Well-known examples are the 5-fluorouracil metabolite, 5-fluoro-2'-deoxyuridine-5'-monophosphate, which is used in the treatment of cancer, and alpha-difluoromethylornithine for the treatment of African sleeping sickness. As the prevalence of fluorine in medicinal chemistry continues to rise, more and more medically relevant fluorinated mechanism-based inhibitors are being developed with a variety of interesting properties and uses.
引用
收藏
页码:865 / 874
页数:10
相关论文
共 83 条
[1]   INACTIVATION OF GAMMA-CYSTATHIONASE BY GAMMA-FLUORINATED AMINO-ACIDS [J].
ALSTON, TA ;
MURAMATSU, H ;
UEDA, T ;
BRIGHT, HJ .
FEBS LETTERS, 1981, 128 (02) :293-297
[2]   Insight into the Mechanism of Inactivation of Ribonucleotide Reductase by Gemcitabine 5′-Diphosphate in the Presence or Absence of Reductant [J].
Artin, Erin ;
Wang, Jun ;
Lohman, Gregory J. S. ;
Yokoyama, Kenichi ;
Yu, Guixue ;
Griffin, Robert G. ;
Bar, Galit ;
Stubbe, JoAnne .
BIOCHEMISTRY, 2009, 48 (49) :11622-11629
[3]  
Baker GB, 2007, J PSYCHIATR NEUROSCI, V32, P313
[4]   Use of fluorinated functionality in enzyme inhibitor development: Mechanistic and analytical advantages [J].
Berkowitz, David B. ;
Karukurichi, Kannan R. ;
de la Salud-Bea, Roberto ;
Nelson, David L. ;
McCune, Christopher D. .
JOURNAL OF FLUORINE CHEMISTRY, 2008, 129 (09) :731-742
[5]  
Bie HY, 2013, NAT CHEM BIOL, V9, P739, DOI [10.1038/NCHEMBIO.1357, 10.1038/nchembio.1357]
[6]   The polar hydrophobicity of fluorinated compounds [J].
Biffinger, JC ;
Kim, HW ;
DiMagno, SG .
CHEMBIOCHEM, 2004, 5 (05) :622-627
[7]  
Bijnsdorp IV, 2007, ONCOL REP, V18, P287
[8]   MECHANISM-BASED INHIBITION OF YEAST ALPHA-GLUCOSIDASE AND HUMAN PANCREATIC ALPHA-AMYLASE BY A NEW CLASS OF INHIBITORS - 2-DEOXY-2,2-DIFLUORO-ALPHA-GLYCOSIDES [J].
BRAUN, C ;
BRAYER, GD ;
WITHERS, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26778-26781
[9]   A new generation of specific Tryponosoma cruzi trans-sialidase inhibitors [J].
Buchini, Sabrina ;
Buschiazzo, Alejandro ;
Withers, Stephen G. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (14) :2700-2703
[10]   The mechanism of MIO-based aminomutases in β-amino acid biosynthesis [J].
Christianson, Carl V. ;
Montavon, Timothy J. ;
Festin, Grace M. ;
Cooke, Heather A. ;
Shen, Ben ;
Bruner, Steven D. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (51) :15744-+