Literature DB >> 22404097

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

Giovanni Marzaro1, Adriano Guiotto, Adriana Chilin.   

Abstract

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.

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Year:  2012        PMID: 22404097     DOI: 10.1517/13543776.2012.665876

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  17 in total

1.  Synthesis and Structure-Activity Relationship Study of 1-Phenyl-1-(quinazolin-4-yl)ethanols as Anticancer Agents.

Authors:  Kenta Kuroiwa; Hirosuke Ishii; Kenji Matsuno; Akira Asai; Yumiko Suzuki
Journal:  ACS Med Chem Lett       Date:  2015-01-10       Impact factor: 4.345

2.  Aggravated DNA damage as a basis for enhanced glioma cell killing by MJ-66 in combination with minocycline.

Authors:  Mann-Jen Hour; Wei-Ting Liu; I-Chen Lu; Sheng-Chu Kuo; Po-Wu Gean
Journal:  Am J Cancer Res       Date:  2014-09-06       Impact factor: 6.166

3.  Iodine/potassium iodide catalyst for the synthesis of trifluoromethylated quinazolines via intramolecular cyclization of 2,2,2-trifluoro-N-benzyl-N'-arylacetimidamides.

Authors:  Ali Darehkordi; Elham Kazemi
Journal:  Mol Divers       Date:  2019-03-13       Impact factor: 2.943

4.  Discovery of biarylaminoquinazolines as novel tubulin polymerization inhibitors.

Authors:  Giovanni Marzaro; Antonio Coluccia; Alessandro Ferrarese; Paola Brun; Ignazio Castagliuolo; Maria Teresa Conconi; Giuseppe La Regina; Ruoli Bai; Romano Silvestri; Ernest Hamel; Adriana Chilin
Journal:  J Med Chem       Date:  2014-05-14       Impact factor: 7.446

5.  MJ-66 induces malignant glioma cells G2/M phase arrest and mitotic catastrophe through regulation of cyclin B1/Cdk1 complex.

Authors:  Wei-Ting Liu; Ching Chen; I-Chen Lu; Sheng-Chu Kuo; Kuo-Hsiung Lee; Tai-Lin Chen; Ta-Shu Song; Yi-Liang Lu; Po-Wu Gean; Mann-Jen Hour
Journal:  Neuropharmacology       Date:  2014-08-05       Impact factor: 5.250

6.  Synthesis and Antimicrobial Activity of 6-Thioxo-6,7-dihydro-2H-[1,2,4]triazino[2,3-c]-quinazolin-2-one Derivatives.

Authors:  Inna S Nosulenko; Olexii Yu Voskoboynik; Galina G Berest; Sergiy L Safronyuk; Sergiy I Kovalenko; Oleksandr M Kamyshnyi; Nataliya M Polishchuk; Raisa S Sinyak; Andrey V Katsev
Journal:  Sci Pharm       Date:  2014-03-24

7.  Targeting kinases with anilinopyrimidines: discovery of N-phenyl-N'-[4-(pyrimidin-4-ylamino)phenyl]urea derivatives as selective inhibitors of class III receptor tyrosine kinase subfamily.

Authors:  Valentina Gandin; Alessandro Ferrarese; Martina Dalla Via; Cristina Marzano; Adriana Chilin; Giovanni Marzaro
Journal:  Sci Rep       Date:  2015-11-16       Impact factor: 4.379

8.  Synthesis and cytotoxic evaluation of novel quinazolinone derivatives as potential anticancer agents.

Authors:  Safoora Poorirani; Sedighe Sadeghian-Rizi; Ghadamali Khodarahmi; Marzieh Rahmani Khajouei; Farshid Hassanzadeh
Journal:  Res Pharm Sci       Date:  2018-10

9.  A novel multi-component reaction to imidazo[4,5-g]-quinazolines.

Authors:  Li Li; Qianqian Zhang; Bo Liu; Gang Liu
Journal:  Molecules       Date:  2013-05-16       Impact factor: 4.411

10.  Synthesis and cytotoxic evaluation of some derivatives of triazole-quinazolinone hybrids.

Authors:  Farshid Hassanzadeh; Hojjat Sadeghi-Aliabadi; Shadan Nikooei; Elham Jafari; Golnaz Vaseghi
Journal:  Res Pharm Sci       Date:  2019-03-08
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