Design, Synthesis, and Biological Evaluation of 1,3,4-Oxadiazole-oxazole-pyrimidine Derivativesas Anticancer Agents

A new series of 1,3,4-oxadiazole-oxazole-pyrimidine compounds (10a–10j) was synthesized and their structures were determined using 1H, 13C NMR and mass spectral data. Further, all compounds were examined for their preliminary anticancer properties towards four types of cancer cell lines such as breast cancer (MCF-7), lung cancer (A549), colon cancer (Colo-205) and ovarian cancer (A2780) by using of MTT method. The obtained IC50 values were compared with the known standard drug etoposide. The investigation of anticancer testing indicated that all derivatives displayed moderate to good anticancer activities. Among them, these compounds 10a, 10b, 10c, 10d, and 10g displayed more potent activity. Predominantly, one compound 10a showed superior activity.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s1070428025601840
Primary Topic
Synthesis and biological activity
Type
article
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article

Design, Synthesis, and Biological Evaluation of 1,3,4-Oxadiazole-oxazole-pyrimidine Derivativesas Anticancer Agents

Naveen Mulakayala, Madhu Raju Veeraboina, Laxminarayana Eppakayala, VeeranjaneyuluPattabi et al.
Russian Journal of Organic Chemistry
Synthesis and biological activity
article

Design, Synthesis, and Biological Evaluation of 1,3,4-Oxadiazole-oxazole-pyrimidine Derivativesas Anticancer Agents

Naveen Mulakayala, Madhu Raju Veeraboina, Laxminarayana Eppakayala, VeeranjaneyuluPattabi, Srinivasu Navuluri
article en

Abstract

A new series of 1,3,4-oxadiazole-oxazole-pyrimidine compounds (10a–10j) was synthesized and their structures were determined using 1H, 13C NMR and mass spectral data. Further, all compounds were examined for their preliminary anticancer properties towards four types of cancer cell lines such as breast cancer (MCF-7), lung cancer (A549), colon cancer (Colo-205) and ovarian cancer (A2780) by using of MTT method. The obtained IC50 values were compared with the known standard drug etoposide. The investigation of anticancer testing indicated that all derivatives displayed moderate to good anticancer activities. Among them, these compounds 10a, 10b, 10c, 10d, and 10g displayed more potent activity. Predominantly, one compound 10a showed superior activity.

Russian Journal of Organic ChemistryVol. 61(S1)
Vignan's Foundation for Science, Technology & Research (IN), Indian Council of Agricultural Research (IN), Indian Institute of Technology Hyderabad (IN)
Good health and well-being
Openalex Percentile: Top 31%
Synthesis and biological activity
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