Utilization of polymeric carriers for (E)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol- E )-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol- 4-yl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one as anticancer agent

被引:0
作者
Mohamed, Ayda A. [1 ,2 ]
Ayad, D. M. [1 ]
Al-Subbagh, H. [3 ]
Abdelaal, M. Y. [1 ]
机构
[1] Mansoura Univ, Fac Sci, Chem Dept, Mansoura 35516, Egypt
[2] Horus Univ Egypt, Fac Pharm, New Damietta, Egypt
[3] Mansoura Univ, Fac Pharm, Med Chem Dept, Mansoura, Egypt
来源
EGYPTIAN JOURNAL OF CHEMISTRY | 2024年 / 67卷 / 02期
关键词
1; 2; 3-triazole chalcone hybrid; anticancer activity; chitosan; CMC; controlled release; CHALCONE; DERIVATIVES; CHITOSAN;
D O I
10.21608/EJCHEM.2023.214817.8068
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the current work, 4-nitroaniline (1) reacted with sodium azide to produce 4-nitrophenyl azide (2) and converted into the corresponding 1,2,3-triazole derivative (3). . The obtained 1,2,3-triazole derivative (3) converted into (E)-1-[5-methyl-1-(4- E )-1-[5-methyl-1-(4- nitrophenyl)triazol-4-yl]-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one (4) through Claisen-Schmidt condensation with 3,4,5trihydroxybenzaldehyde in ethanolic NaOH. Compound 4 was then characterized with the suitable spectroscopic techniques and investigated for its anticancer activity. Blends of 4 with Chitosan (CS) and carboxymethylcellulose (CMC) were prepared by uploading it into the polymer matrices through physical mixing. The release behavior of 4 from the polymer blends into an aqueous medium at room temperature was investigated and discussed.
引用
收藏
页码:487 / 495
页数:9
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