Design, parallel synthesis of Biginelli 1,4-dihydropyrimidines using PTSA as a catalyst, evaluation of anticancer activity and structure activity relationships via 3D QSAR studies

التفاصيل البيبلوغرافية
العنوان: Design, parallel synthesis of Biginelli 1,4-dihydropyrimidines using PTSA as a catalyst, evaluation of anticancer activity and structure activity relationships via 3D QSAR studies
المؤلفون: Merugumolu Vijay Kumar, Laxmi Adhikary, T. Ashok, Antony Justin, Revanasiddappa Bistuvalli Chandrashekarappa, Syed Faizan, Nulgumnalli Manjunathaiah Raghavendra, Namburu Lalitha Naishima, B. R. Prashantha Kumar, Pradeep Kabadi
المصدر: Bioorganic Chemistry. 117:105462
بيانات النشر: Elsevier BV, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Quantitative structure–activity relationship, Dose-Response Relationship, Drug, Molecular Structure, Cell Survival, Chemistry, Organic Chemistry, Quantitative Structure-Activity Relationship, Antineoplastic Agents, Context (language use), Biochemistry, Combinatorial chemistry, Cell Line, Catalysis, Pyrimidines, Drug Design, Chlorocebus aethiops, Drug Discovery, Animals, Humans, Breast cancer cells, Drug Screening Assays, Antitumor, Efficient catalyst, Cytotoxicity, Molecular Biology, Cell Proliferation
الوصف: Biginelli 1,4-dihydropyrimidines are extensively screened for their potential anticancer activity in the last decade. In this context, a series of Biginelli 1,4-dihydropyrimidines were designed and synthesised using PTSA as an efficient catalyst. The synthesised 1,4-dihydropyrimidines were screened for their anticancer activity against MCF-7 breast cancer cells by measuring cytotoxicity. The compounds exhibited activity ranging from weak to significant in terms of percentage cytotoxicity which is proportional to the anticancer activity. Amongst the screened compounds, compounds 4, 6 and 8 exhibited potential anticancer activity. Furthermore, CoMSIA studies were performed to derive the structure activity relationships in a 3D grid space by plotting experimental vs predicted cytotoxic activities. We have an opinion that, this developed model helps us in future to develop more potential 1,4-dihydropyrimidines for their cytotoxicity or anticancer activity.
تدمد: 0045-2068
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa91262705625217115ecbf0431f793
https://doi.org/10.1016/j.bioorg.2021.105462
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....efa91262705625217115ecbf0431f793
قاعدة البيانات: OpenAIRE