Ugi reaction in the synthesis of Janus dendrimers as nanocarriers of chlorambucil and ibuprofen

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
Israel Barajas-Mendoza, Teresa Ramírez-Ápan, Marcos Martínez-García
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引用次数: 0

Abstract

The synthesis and characterization of Janus dendrimers conjugated with two drugs: chlorambucil and ibuprofen are reported. The dendrons by the Ugi reaction were obtained. The 2-aminoethanol, 3-aminopropanol and 5-aminopentanol were used as the amine resources, which allowed obtaining several Ugi adducts with different aliphatic chain lengths. The newly Janus dendrimers compounds were evaluated against human cancer cell lines. The Janus dendrimer from 2-aminoethanol in the length of the aliphatic chain showed potent activity againts prostatic adenocarcinoma PC-3 (IC50 8.88 ± 0.7) and mammary adenocarcinoma MCF-7 (IC50 9.14 ± 1.0) μM. In addition, the feasibility of incorporating different drugs in the reaction was verified, which opens new possibilities for the functionalization of dendrimers in the therapeutic context.
用Ugi反应合成树状大分子作为氯苯和布洛芬的纳米载体
报道了氯丁酸和布洛芬两种药物偶联Janus树状大分子的合成和表征。通过Ugi反应得到树突。以2-氨基乙醇、3-氨基丙醇和5-氨基戊醇为胺源,得到了几种不同脂肪链长度的Ugi加合物。新的Janus树状大分子化合物对人类癌细胞系进行了评价。脂肪链上2-氨基乙醇的Janus树突状分子对前列腺腺癌PC-3 (IC50为8.88±0.7)和乳腺腺癌MCF-7 (IC50为9.14±1.0)μM具有较强的抑制活性。此外,在反应中加入不同药物的可行性得到验证,这为树状大分子在治疗背景下的功能化开辟了新的可能性。
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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