作者
Amer M Alanazi, Alaa A-M Abdel-Aziz, Taghreed Z Shawer, Rezk R Ayyad, Abdulrahman M Al-Obaid, Mohamed HM Al-Agamy, Azza R Maarouf, Adel S El-Azab
发表日期
2016/9/2
期刊
Journal of Enzyme Inhibition and Medicinal Chemistry
卷号
31
期号
5
页码范围
721-735
出版商
Taylor & Francis
简介
Some new derivatives of substituted-4(3H)-quinazolinones were synthesized and evaluated for their in vitro antitumor and antimicrobial activities. The results of this study demonstrated that compound 5 yielded selective activities toward NSC Lung Cancer EKVX cell line, Colon Cancer HCT-15 cell line and Breast Cancer MDA-MB-231/ATCC cell line, while NSC Lung Cancer EKVX cell line and CNS Cancer SF-295 cell line were sensitive to compound 8. Additionally, compounds 12 and 13 showed moderate effectiveness toward numerous cell lines belonging to different tumor subpanels. On the other hand, the results of antimicrobial screening revealed that compounds 1, 9 and 14 are the most active against Staphylococcus aureus ATCC 29213 with minimum inhibitory concentration (MIC) of 16, 32 and 32 μg/mL respectively, while compound 14 possessed antimicrobial activities against all tested strains with the …
引用总数
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