Literature DB >> 17317179

Synthesis and bioactivity of 4-alkyl(aryl)thioquinazoline derivatives.

Song Yang1, Zhi Li, Linhong Jin, Baoan Song, Gang Liu, Jiang Chen, Zhuo Chen, Deyu Hu, Wei Xue, Ruiqing Xu.   

Abstract

Some S'-substituted 4-alkyl(aryl)thioquinazoline derivatives were synthesized through thioetherification reaction of 4-chloroquinazolines 2 and thiol compounds 1 refluxed in acetone in the presence of K(2)CO(3). Their structures were verified by elemental analysis, IR, (1)H NMR, and (13)C NMR. The compounds were evaluated for their anti-proliferative activities against some cancer cells in vitro by MTT method. Among them, 3c, 3a, 3d, 3f, and 3l were highly effective against PC3 cells and 3a-3m showed weak activities against Bcap37 and BGC823 cells. The IC(50) value of 3c, 3a, 3d, 3f, and3l against PC3 cell was 1.8, 5.6, 8.1, 8.7, and 8.9 microM, respectively.

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Year:  2007        PMID: 17317179     DOI: 10.1016/j.bmcl.2007.01.101

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  3,4,5-Trimethoxy-benzohydrazidium chloride.

Authors:  Aamer Saeed; Amara Mumtaz; Hummera Rafique; Kazuma Gotoh; Hiroyuki Ishida
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-13

2.  Rapid synthesis and antiviral activity of (quinazolin-4-ylamino)methyl-phosphonates through microwave irradiation.

Authors:  Hui Luo; Deyu Hu; Jian Wu; Ming He; Linhong Jin; Song Yang; Baoan Song
Journal:  Int J Mol Sci       Date:  2012-06-01       Impact factor: 6.208

3.  Hexachlorocyclotriphosphazene (HCCP)-mediated direct formation of thioethers and ethers from quinazolin-4(3H)-ones.

Authors:  Baoxiang Hu; Xiaochu Zhang; Lili Sheng; Ming Guo; Zhenlu Shen; Xinquan Hu; Nan Sun; Weimin Mo
Journal:  Molecules       Date:  2013-05-15       Impact factor: 4.411

  3 in total

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