Synthesis and In Vitro Evaluation of Azole‐Based 1H Benzo(c)Isoxazole‐3‐one Derivatives for Antiproliferative and Immunomodulatory Activities

ABSTRACT Azoles represent a significant group of compounds used as nonsteroidal anti‐inflammatory drugs and have additionally demonstrated their potential in combating cancer. In this work, eight synthetic derivatives of 1H Benzo(c)isoxazole‐3‐one have been tested for their anticancer effects to develop them as candidate drugs for cancer. 1H Benzo(c)isoxazole‐3‐one was previously isolated from a marine bacterium, planococcus maritimus , which exhibited antiproliferative activity against proliferating PBMCs and a few cancerous cell lines. Eight derivatives were synthesized from the parent compound and the results represent the initial attempt to assess the antiproliferative effects of synthetic compounds on a cancerous cell line (HeLa) through the SRB assay and on mitogen‐induced using the MTT assay. All the compounds showed anticancer and anti‐inflammatory potential. Moreover, the results of in vitro DNA cleavage demonstrated that these compounds can be effective nucleases, as they completely degrade template DNA. In conclusion, the synthetic derivatives can be used as candidate drugs against cancer and inflammation.

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Journal
ChemistrySelect
Published
2026-02-01
DOI
https://doi.org/10.1002/slct.202501122
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis and In Vitro Evaluation of Azole‐Based 1H Benzo(c)Isoxazole‐3‐one Derivatives for Antiproliferative and Immunomodulatory Activities

Rathika Regurajan, Asha Santhi, Venkatesh Subramanian, Krishnaveni Muthan
ChemistrySelect
Synthesis and biological activity
article

Synthesis and In Vitro Evaluation of Azole‐Based 1H Benzo(c)Isoxazole‐3‐one Derivatives for Antiproliferative and Immunomodulatory Activities

Rathika Regurajan, Asha Santhi, Venkatesh Subramanian, Krishnaveni Muthan
article en

Abstract

ABSTRACT Azoles represent a significant group of compounds used as nonsteroidal anti‐inflammatory drugs and have additionally demonstrated their potential in combating cancer. In this work, eight synthetic derivatives of 1H Benzo(c)isoxazole‐3‐one have been tested for their anticancer effects to develop them as candidate drugs for cancer. 1H Benzo(c)isoxazole‐3‐one was previously isolated from a marine bacterium, planococcus maritimus , which exhibited antiproliferative activity against proliferating PBMCs and a few cancerous cell lines. Eight derivatives were synthesized from the parent compound and the results represent the initial attempt to assess the antiproliferative effects of synthetic compounds on a cancerous cell line (HeLa) through the SRB assay and on mitogen‐induced using the MTT assay. All the compounds showed anticancer and anti‐inflammatory potential. Moreover, the results of in vitro DNA cleavage demonstrated that these compounds can be effective nucleases, as they completely degrade template DNA. In conclusion, the synthetic derivatives can be used as candidate drugs against cancer and inflammation.

ChemistrySelectVol. 11(6)
Manonmaniam Sundaranar University (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Science and Engineering Research Board
Life below water
Openalex Percentile: Top 59%
Synthesis and biological activity
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Synthesis and In Vitro Evaluation of Azole‐Based 1H Benzo(c)Isoxazole‐3‐one Derivatives for Antiproliferative and Immunomodulatory Activities — Rathika Regurajan, Asha Santhi, et al. · ChemistrySelect (2026) | TGRS Research Map | TGRS