Israel Barajas-Mendoza, Teresa Ramírez-Ápan, Marcos Martínez-García
{"title":"Ugi reaction in the synthesis of Janus dendrimers as nanocarriers of chlorambucil and ibuprofen","authors":"Israel Barajas-Mendoza, Teresa Ramírez-Ápan, Marcos Martínez-García","doi":"10.1016/j.rechem.2025.102361","DOIUrl":null,"url":null,"abstract":"<div><div>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 (IC<sub>50</sub> 8.88 ± 0.7) and mammary adenocarcinoma MCF-7 (IC<sub>50</sub> 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.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"16 ","pages":"Article 102361"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715625003443","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.