Substituted spirooxindole derivatives as potent anticancer agents through inhibition of phosphodiesterase 1. Issue 26 (17th April 2018)
- Record Type:
- Journal Article
- Title:
- Substituted spirooxindole derivatives as potent anticancer agents through inhibition of phosphodiesterase 1. Issue 26 (17th April 2018)
- Main Title:
- Substituted spirooxindole derivatives as potent anticancer agents through inhibition of phosphodiesterase 1
- Authors:
- Barakat, Assem
Islam, Mohammad Shahidul
Ghawas, Hussien Mansur
Al-Majid, Abdullah Mohammed
El-Senduny, Fardous F.
Badria, Farid A.
Elshaier, Yaseen A. M. M.
Ghabbour, Hazem A. - Abstract:
- Abstract : Spirooxindole is a promising chemo therapeutic agent. Possible targets include cancers of the liver, prostate, lung, stomach, colon, and breast. Abstract : Spirooxindole is a promising chemo therapeutic agent. Possible targets include cancers of the liver, prostate, lung, stomach, colon, and breast. Here, we demonstrate a one-pot three-component reaction via a [3 + 2] cycloaddition/ring contraction sequence of a dipolarophile (activated alkene) with in situ -generated azomethine ylide (1, 3-dipoles) without the use of any catalyst. The reaction provides efficient access to synthetically useful and biologically important spirooxindoles in high yield (69–94%) with high diastereoselectivity. The synthesized compounds were subjected to cytotoxicity evaluation using colorectal cancer (HCT-116), hepatocellular carcinoma (HepG2), and prostate cancer (PC-3) cells. Compounds4i, 4j, and4k showed potent cytotoxic activity and high selectivity against HCT-116 cells when compared to cisplatin. Meanwhile compound4d retained high cytotoxic activity and selectivity against HepG2 and PC-3 cells in comparison to cisplatin. The mechanism of compound4d was further studied using phosphodiesterase 1 enzyme and showed 74.2% inhibitory activity. A possible binding mode for compound4d to PDE-1 was investigated by molecular modeling using OpenEye software. Pose predictions for the active compounds were demonstrated by ROCS alignments. Compound4d has a special geometry and differs fromAbstract : Spirooxindole is a promising chemo therapeutic agent. Possible targets include cancers of the liver, prostate, lung, stomach, colon, and breast. Abstract : Spirooxindole is a promising chemo therapeutic agent. Possible targets include cancers of the liver, prostate, lung, stomach, colon, and breast. Here, we demonstrate a one-pot three-component reaction via a [3 + 2] cycloaddition/ring contraction sequence of a dipolarophile (activated alkene) with in situ -generated azomethine ylide (1, 3-dipoles) without the use of any catalyst. The reaction provides efficient access to synthetically useful and biologically important spirooxindoles in high yield (69–94%) with high diastereoselectivity. The synthesized compounds were subjected to cytotoxicity evaluation using colorectal cancer (HCT-116), hepatocellular carcinoma (HepG2), and prostate cancer (PC-3) cells. Compounds4i, 4j, and4k showed potent cytotoxic activity and high selectivity against HCT-116 cells when compared to cisplatin. Meanwhile compound4d retained high cytotoxic activity and selectivity against HepG2 and PC-3 cells in comparison to cisplatin. The mechanism of compound4d was further studied using phosphodiesterase 1 enzyme and showed 74.2% inhibitory activity. A possible binding mode for compound4d to PDE-1 was investigated by molecular modeling using OpenEye software. Pose predictions for the active compounds were demonstrated by ROCS alignments. Compound4d has a special geometry and differs from other active compounds. … (more)
- Is Part Of:
- RSC advances. Volume 8:Issue 26(2018)
- Journal:
- RSC advances
- Issue:
- Volume 8:Issue 26(2018)
- Issue Display:
- Volume 8, Issue 26 (2018)
- Year:
- 2018
- Volume:
- 8
- Issue:
- 26
- Issue Sort Value:
- 2018-0008-0026-0000
- Page Start:
- 14335
- Page End:
- 14346
- Publication Date:
- 2018-04-17
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8ra02358a ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6570.xml