First Total Synthesis of Phytoprostanes with Prostaglandin‐Like Configuration, Evidence for Their Formation in Edible Vegetable Oils and Orienting Study of Their Biological Activity. Issue 37 (29th May 2021)
- Record Type:
- Journal Article
- Title:
- First Total Synthesis of Phytoprostanes with Prostaglandin‐Like Configuration, Evidence for Their Formation in Edible Vegetable Oils and Orienting Study of Their Biological Activity. Issue 37 (29th May 2021)
- Main Title:
- First Total Synthesis of Phytoprostanes with Prostaglandin‐Like Configuration, Evidence for Their Formation in Edible Vegetable Oils and Orienting Study of Their Biological Activity
- Authors:
- Smrček, Jakub
Hájek, Miroslav
Hodek, Ondřej
Čížek, Karel
Pohl, Radek
Jahn, Emanuela
Galano, Jean‐Marie
Oger, Camille
Durand, Thierry
Cvačka, Josef
Jahn, Ullrich - Abstract:
- Abstract: Phytoprostanes (PhytoP) are natural products, which form in plants under oxidative stress conditions from α‐linolenic acid. However, their epimers with relative prostaglandin configuration termed phytoglandins (PhytoG) have never been detected in Nature, likely because of the lack of synthetic reference material. Here, the first asymmetric total synthesis of such compounds, namely of PhytoGF1α (9‐ epi ‐16‐F1t ‐PhytoP) and its diastereomer ent ‐16‐ epi ‐PhytoGF1α ( ent ‐9, 16‐ diepi ‐16‐F1t ‐PhytoP), has been accomplished. The synthetic strategy is based on radical anion oxidative cyclization, copper(I)‐mediated alkyl‐alkyl coupling and enantioselective reduction reactions. A UHPLC‐MS/MS study using the synthesized compounds as standards indicates PhytoG formation at significant levels during autoxidation of α‐linolenic acid in edible vegetable oils. Initial testing of synthetic PhytoGs together with F1 ‐PhytoP and 15‐F2t ‐IsoP derivatives for potential interactions with the PGF2α (FP) receptor did not reveal significant activity. The notion that PUFA‐derived oxidatively formed cyclic metabolites with prostaglandin configuration do not form to a significant extent in biological or food matrices has to be corrected. Strong evidence is provided that oxidatively formed PhytoG metabolites may be ingested with plant‐derived food, which necessitates further investigation of their biological profile. Abstract : PhytoP against PhytoG : The first total synthesis ofAbstract: Phytoprostanes (PhytoP) are natural products, which form in plants under oxidative stress conditions from α‐linolenic acid. However, their epimers with relative prostaglandin configuration termed phytoglandins (PhytoG) have never been detected in Nature, likely because of the lack of synthetic reference material. Here, the first asymmetric total synthesis of such compounds, namely of PhytoGF1α (9‐ epi ‐16‐F1t ‐PhytoP) and its diastereomer ent ‐16‐ epi ‐PhytoGF1α ( ent ‐9, 16‐ diepi ‐16‐F1t ‐PhytoP), has been accomplished. The synthetic strategy is based on radical anion oxidative cyclization, copper(I)‐mediated alkyl‐alkyl coupling and enantioselective reduction reactions. A UHPLC‐MS/MS study using the synthesized compounds as standards indicates PhytoG formation at significant levels during autoxidation of α‐linolenic acid in edible vegetable oils. Initial testing of synthetic PhytoGs together with F1 ‐PhytoP and 15‐F2t ‐IsoP derivatives for potential interactions with the PGF2α (FP) receptor did not reveal significant activity. The notion that PUFA‐derived oxidatively formed cyclic metabolites with prostaglandin configuration do not form to a significant extent in biological or food matrices has to be corrected. Strong evidence is provided that oxidatively formed PhytoG metabolites may be ingested with plant‐derived food, which necessitates further investigation of their biological profile. Abstract : PhytoP against PhytoG : The first total synthesis of phytoglandins (PhytoG), phytoprostanes (PhytoP) with prostaglandin configuration was accomplished. They are indeed metabolites of α‐linolenic acid and form at sizeable levels during aging of edible vegetable oils as demonstrated in a UHPLC‐MS/MS study. … (more)
- Is Part Of:
- Chemistry. Volume 27:Issue 37(2021)
- Journal:
- Chemistry
- Issue:
- Volume 27:Issue 37(2021)
- Issue Display:
- Volume 27, Issue 37 (2021)
- Year:
- 2021
- Volume:
- 27
- Issue:
- 37
- Issue Sort Value:
- 2021-0027-0037-0000
- Page Start:
- 9556
- Page End:
- 9562
- Publication Date:
- 2021-05-29
- Subjects:
- oxidative stress -- phytoglandin -- phytoprostane -- total synthesis -- vegetable oil
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.202100872 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17439.xml