Synthesis and anticancer properties of mono Mannich bases containing vanillin moiety

被引:0
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作者
Mehtap Tugrak
Halise Inci Gul
Hiroshi Sakagami
Ebru Mete
机构
[1] Faculty of Pharmacy,Department of Pharmaceutical Chemistry
[2] Ataturk University,School of Dentistry, Division of Pharmacology
[3] Meikai University,Department of Organic Chemistry
[4] Faculty of Science,undefined
[5] Ataturk University,undefined
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关键词
Mannich bases; Cytotoxicity; Vanillin; Methoxy group; Selectivity;
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摘要
In this study, Mannich bases 2–8, 2-(3-or-5-aminomethyl-4-hydroxy-3-or-5-methoxybenzylidene)indan-1-one, were designed and synthesized starting from 2-(4-hydroxy-3-methoxybenzylidene)indan-1-one, 1. Synthesized compounds were tested against several tumor cell lines and non-tumor cells to evaluate the cytotoxicities of the compounds and to test whether the sequential cytotoxicity hypothesis works on the studied compounds. The data obtained from cytotoxicity tests pointed out that sequential cytotoxicity hypothesis worked on compounds 3 and 4 since they had higher potency selectivity expression values. The leader compound of the present study is compound 4, 2-(3-dipropylaminomethyl-4-hydroxy-5-methoxy-benzylidene)-indan-1-one, since it has the highest potency selectivity expression value among the compounds studied. This molecule can be the leader compound for further studies and designes.
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页码:1528 / 1534
页数:6
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