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Horner-Wadsworth-Emmons approach to piperlongumine analogues with potent anti-cancer activity.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2016 Aug 21; Vol. 14 (31), pp. 7585-93. Date of Electronic Publication: 2016 Jul 22. - Publication Year :
- 2016
-
Abstract
- Natural products with anti-cancer activity play a vital role in lead and target discovery. We report here the synthesis and biological evaluation of the plant-derived alkaloid, piperlongumine and analogues. Using a Horner-Wadsworth-Emmons coupling approach, a selection of piperlongumine-like compounds were prepared in good overall yield from a novel phosphonoacetamide reagent. A number of the compounds displayed potent anti-cancer activity against colorectal (HCT 116) and ovarian (IGROV-1) carcinoma cell lines, via a mechanism of action which may involve ROS generation. Contrary to previous reports, no selective action in cancer cell (MRC-5) was observed for piperlongumine analogues.
- Subjects :
- Antineoplastic Agents chemical synthesis
Antineoplastic Agents chemistry
Cell Line, Tumor
Cell Proliferation drug effects
Dioxolanes chemical synthesis
Dioxolanes chemistry
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
Humans
Molecular Structure
Reactive Oxygen Species metabolism
Structure-Activity Relationship
Antineoplastic Agents pharmacology
Dioxolanes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1477-0539
- Volume :
- 14
- Issue :
- 31
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 27443386
- Full Text :
- https://doi.org/10.1039/c6ob01160h