Design and synthesis of highly oxygenated furo[3,2-c]pyran-4-ones and furo[3,2-c]chromen-4-ones scaffold as potential anticancer and antimicrobial agent

  1. Suman Rani,
  2. Nisha Kamra,
  3. Sumit Thakral,
  4. Devinder KumarORCID Logo,
  5. Ajeet Singh,
  6. Payare L Sangwan and
  7. Shashank K Singh

Submitting author affiliation: Guru Jambheshwar University of Science and Technology, Hisar, India

Beilstein Arch. 2021, 202137. https://doi.org/10.3762/bxiv.2021.37.v1

Published 17 May 2021

  • Preprint

Abstract

Synthesis of a number of highly oxygenated furo[3,2-c]pyran-4-one (4, 5) and furo[3,2-c]chromen-4-one (8, 9) has been accomplished by a simple one pot reaction from easily available versatile starting materials - dehydroacetic acid and 3-acetyl-4-hydroxycoumarin. All the synthesized molecules were characterized utilizing various spectroscopic techniques and screened for anticancer activity (in vitro) against three Colon (HCT-116, SW-620, HT-24), Lung (A-549), Prostate-(PC-3), Breast-(MCF-7) cell lines. Compounds 5a, 9d, 9f showed good activity against breast MCF-7 cancer cell line having IC50 values 6.9, 2.8, 5.3 µM, respectively. Out of these compound 9d showed better activity against prostate PC-3 cell line with IC50 value 3.8 µM. The synthesized compounds were also studied for potential antibacterial activity (in vitro) using different strains of bacteria (Bacillus subtilis and Staphylococcus aureus -Gram-positive, and Escherichia coli- Gram negative) as well as fungal strains (Aspergillus niger and Candida albicans) using Norfloxacin and Fluconazole as antibacterial and antifungal standard drugs, respectively. The outcome of the antimicrobial screening study showed that compound 9f exhibited promising activity against S. aureus and B. subtilis while 5h showed excellent and 5i and 9b showed better activity against E. coli. The compounds 5c-5e displayed excellent activity against C. albicans and A. niger than Fluconazole.

Keywords: 3-Acetyl-4-hydroxycoumarin, anticancer, antimicrobial, dehydroacetic acid,  furo[3,2-c]pyrone, furo[3,2-c]chromen-4-one

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When a peer-reviewed version of this preprint is available, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Rani, S.; Kamra, N.; Thakral, S.; Kumar, D.; Singh, A.; Sangwan, P. L.; Singh, S. K. Beilstein Arch. 2021, 202137. doi:10.3762/bxiv.2021.37.v1

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