Quinazoline derivatives as potential anticancer agents: a patent review (2007-2010)

被引:115
作者
Marzaro, Giovanni [1 ]
Guiotto, Adriano [1 ]
Chilin, Adriana [1 ]
机构
[1] Univ Padua, Dipartimento Sci Farmaceut, I-35131 Padua, Italy
关键词
anticancer compounds; kinase inhibitors; p53; modulators; quinazolines; GROWTH-FACTOR RECEPTOR; AURORA-B KINASE; THYMIDYLATE SYNTHASE INHIBITOR; POLO-LIKE KINASE; HISTONE DEACETYLASE INHIBITORS; COPPER-CATALYZED SYNTHESIS; PROTEIN-TYROSINE KINASES; ALPHA-FOLATE RECEPTOR; BREAST-CANCER CELLS; PANCREATIC-CANCER;
D O I
10.1517/13543776.2012.665876
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Due to the increase in knowledge about cancer pathways, there is a growing interest in finding novel potential drugs. Quinazoline is one of the most widespread scaffolds amongst bioactive compounds. A number of patents and papers appear in the literature regarding the discovery and development of novel promising quinazoline compounds for cancer chemotherapy. Although there is a progressive decrease in the number of patents filed, there is an increasing number of biochemical targets for quinazoline compounds. Areas covered: This paper provides a comprehensive review of the quinazolines patented in 2007 - 2010 as potential anticancer agents. Information from articles published in international peer-reviewed journals was also included, to give a more exhaustive overview. Expert opinion: From about 1995 to 2006, the anticancer quinazolines panorama has been dominated by the 4-anilinoquinazolines as tyrosine kinase inhibitors. The extensive researches conducted in this period could have caused the progressive reduction in the ability to file novel patents as shown in the 2007 - 2010 period. However, the growing knowledge of cancer-related pathways has recently highlighted some novel potential targets for therapy, with quinazolines receiving increasing attention. This is well demonstrated by the number of different targets of the patents considered in this review. The structural heterogeneity in the patented compounds makes it difficult to derive general pharmacophores and make comparisons among claimed compounds. On the other hand, the identification of multi-target compounds seems a reliable goal. Thus, it is reasonable that quinazoline compounds will be studied and developed for multi-target therapies.
引用
收藏
页码:223 / 252
页数:30
相关论文
共 208 条
[1]  
ADAMS ND, 2008, Patent No. 2008157191
[2]  
Ahn Y.G., 2007, [No title captured], Patent No. [WO 2007055514 A1, 2007055514, 2007055514A1]
[3]   Dual inhibition of VEGFR and EGFR signaling reduces the incidence and size of intestinal adenomas in ApcMin/+ mice [J].
Alferez, Denis ;
Wilkinson, Robert W. ;
Watkins, Jim ;
Poulsom, Richard ;
Mandir, Nikki ;
Wedge, Stephen R. ;
Pyrah, Ian T. ;
Smith, Neil R. ;
Jackson, Lynsay ;
Ryan, Anderson J. ;
Goodlad, Robert A. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (03) :590-598
[4]   Simultaneous targeting of the epidermal growth factor receptor and cyclooxygenase-2 pathways for pancreatic cancer therapy [J].
Ali, S ;
El-Rayes, BF ;
Sarkar, FH ;
Philip, PA .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (12) :1943-1951
[5]   Polo-like kinase 1 (Plk1) inhibits p53 function by physical interaction and phosphorylation [J].
Ando, K ;
Ozaki, T ;
Yamamoto, H ;
Furuya, K ;
Hosoda, M ;
Hayashi, S ;
Fukuzawa, M ;
Nakagawara, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (24) :25549-25561
[6]  
Angion Biomedica, 2007, Modulators of hepatocyte growth factor/c-Met activity, Patent No. [WO2007081978, 2007081978]
[7]  
[Anonymous], 2012, Clinical Trial of BMS-911543, Patent No. 2010099379
[8]  
[Anonymous], 2008, World Patent, Patent No. [2008086462, WO 2008086462]
[9]   Src kinase potentiates androgen receptor transactivation function and invasion of androgen-independent prostate cancer C4-2 cells [J].
Asim, M. ;
Siddiqui, I. A. ;
Hafeez, B. B. ;
Baniahmad, A. ;
Mukhtar, H. .
ONCOGENE, 2008, 27 (25) :3596-3604
[10]  
Astra Zeneca A.B., 2007, World Patent, Patent No. 2007071963