Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3170
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dc.contributor.authorJoshi, Mayank-
dc.contributor.authorChoudhury, A.R.-
dc.date.accessioned2020-12-16T07:29:37Z-
dc.date.available2020-12-16T07:29:37Z-
dc.date.issued2020-
dc.identifier.citationMedicinal Chemistry Research, 29(9), pp.1579-1589.en_US
dc.identifier.otherhttps://doi.org/10.1007/s00044-020-02578-5-
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs00044-020-02578-5-
dc.identifier.urihttp://hdl.handle.net/123456789/3170-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractCancer is often associated with chronic inflammation. In order to develop potential anticancer and anti-inflammatory agents a series of 26 diarylidenecyclopentanones (DACPs) Ia–Iv, II, III, and IV were synthesized. Five of the synthesized DACPs are novel (Ih, Ij, Ik, Is, and Iv), derivative Iv was characterized using single-crystal X-ray diffraction study. All the synthesized derivatives were tested for their anti-inflammatory as well as cytotoxicity properties. Compound Is is found to have the highest anti-inflammatory activity (93.67%) by inhibiting PGE2 (prostaglandin E2) production. Three of the DACPs (Io, It, and Iu) were observed to have high cytotoxicity with IC50 value of 8.73 ± 0.06 µM (Io), 12.55 ± 0.31 µM (It), and 11.47 ± 0.15 µM (Iu) against HeLa cells. Further staining and cell cycle analysis was done using these three DACPs to understand their mechanism of action. The G0/G1 phase was observed to be the longest one through which the cells undergo apoptosis.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectAnticancer agentsen_US
dc.subjectAnti-inflammatoryen_US
dc.subjectDiarylidenecyclopentanoneen_US
dc.titleDiarylidenecyclopentanone derivatives as potent anti-inflammatory and anticancer agentsen_US
dc.typeArticleen_US
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