
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/3170
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DC Field | Value | Language |
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dc.contributor.author | Joshi, Mayank | - |
dc.contributor.author | Choudhury, A.R. | - |
dc.date.accessioned | 2020-12-16T07:29:37Z | - |
dc.date.available | 2020-12-16T07:29:37Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Medicinal Chemistry Research, 29(9), pp.1579-1589. | en_US |
dc.identifier.other | https://doi.org/10.1007/s00044-020-02578-5 | - |
dc.identifier.uri | https://link.springer.com/article/10.1007%2Fs00044-020-02578-5 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/3170 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | Cancer 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.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.subject | Anticancer agents | en_US |
dc.subject | Anti-inflammatory | en_US |
dc.subject | Diarylidenecyclopentanone | en_US |
dc.title | Diarylidenecyclopentanone derivatives as potent anti-inflammatory and anticancer agents | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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