Cyclin-dependent kinase inhibitors closer to market launch?

被引:25
作者
Galons, Herve [1 ]
Oumata, Nassima [2 ]
Gloulou, Olfa [1 ]
Meijer, Laurent [2 ]
机构
[1] Univ Paris 05, INSERM, U 1022, Lab Chim Organ 2, F-75270 Paris 06, France
[2] Ctr Perharidy, F-29680 Roscoff, France
关键词
cancer; cell cycle; cyclin-dependent kinase; PHASE-I; CELL-CYCLE; CDK INHIBITORS; R-ROSCOVITINE; CANCER; POTENT; DISCOVERY; GROWTH;
D O I
10.1517/13543776.2013.789861
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Interest in cyclin-dependent kinase (CDK) inhibitors was stimulated by the demonstration that their pharmacological activities could lead to therapies for numerous diseases. Until now, despite the clinical introduction of a dozen compounds belonging to other classes of kinase inhibitors, no CDK inhibitor has reached the marketplace. Areas covered: This review covers CDK inhibitor patents published between 2009 and September 2012. It presents compounds currently undergoing clinical development, along with our earlier (2010) review of the same topic, as well as descriptions of recently published compounds not disclosed in the patent literature. It provides the reader with an update of all chemical structures of current interest in the CDK inhibitor field. Expert opinion: Though cancer remains the most obvious application for CDK inhibition, other indications, such as HIV infection, could potentially be treated with CDK inhibitors.
引用
收藏
页码:945 / 963
页数:19
相关论文
共 85 条
[1]  
Aggennix, 2011, Patent No. [SG173222, 173222]
[2]  
Amgen, 2012, WO129344, P27, Patent No. 129344
[3]  
Anygen, 2011, P28, Patent No. [WO096676, 096676]
[4]  
Astex, 2011, P33, Patent No. [EP2395000, 2395000]
[5]  
Astex, 2010, Patent No. [US0004243, 0004243]
[6]  
Astex, 2010, P31, Patent No. [US021420, 021420]
[7]  
Bayer, 2010, Patent No. [EP2179993, 2179993]
[8]  
Bayer, 2011, P35, Patent No. [US0251222, 0251222]
[9]  
Bayer, 2011, Patent No. [US0294838, 0294838]
[10]   CR8, a potent and selective, roscovitine-derived inhibitor of cyclin-dependent kinases [J].
Bettayeb, K. ;
Oumata, N. ;
Echalier, A. ;
Ferandin, Y. ;
Endicott, J. A. ;
Galons, H. ;
Meijer, L. .
ONCOGENE, 2008, 27 (44) :5797-5807