Rational Design and Synthesis of 1,2,3-Triazole Incorporated Oxazolo[5,4-d] Pyrimidine Derivatives: In-Vitro Cytotoxicity and In-Silico Molecular Docking Simulations

Name: Rational Design and Synthesis of 1,2,3-Triazole Incorporated Oxazolo[5,4- d ] Pyrimidine Derivatives: In-Vitro Cytotoxicity and In-Silico Molecular Docking Simulations
Creator: Taylor & Francis
Published: 2025-03-30T05:00:08+08:00

DataCite Commons2025-09-26 更新2025-05-07 收录

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https://tandf.figshare.com/articles/dataset/Rational_Design_and_Synthesis_of_1_2_3-Triazole_Incorporated_Oxazolo_5_4-_i_d_i_Pyrimidine_Derivatives_i_In-Vitro_i_Cytotoxicity_and_i_In-Silico_i_Molecular_Docking_Simulations/28691634/1 数据链接链接失效反馈

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资源简介：

A new series of 1,2,3-Triazole incorporated oxazolo[5,4-d]pyrimidine derivatives 24a-j were designed, synthesized and evaluated for their anticancer activity against MCF-7, A549, Colo-205, & A2780 cell lines by using MTT reduction protocol with Etoposide as positive control. Among the screened derivatives, the compound 24a showed potent anticancer activities against MCF-7, and A549 cell lines with IC50 values of 0.11 ± 0.086 and 0.13 ± 0.094 µM, whereas another compound 24h also showed potent anticancer activities against MCF-7, and A549 cell lines with IC50 values of 0.18 ± 0.071 and 0.33 ± 0.067 µM. These activities are more potent than standard drug, Etoposide activities. Hence, these two derivatives are allowed for further investigations in cancer chemotherapy. This anticancer data also supported by the docking score of both the potent derivatives, 24a and 24h. The compounds 24a and 24h showed molecular interactions with human topoisomerase IIβ protein and having binding energies are −5.7 and −5.8 kcal/mole, respectively.

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Taylor & Francis

创建时间：

2025-03-30