Repair of Oxidizing Hydroxyl Adduct Radicals of DNA Bases by Hydroxyl‐trans‐Stilbenes via Single Electron Transfer. Issue 13 (3rd April 2019)
- Record Type:
- Journal Article
- Title:
- Repair of Oxidizing Hydroxyl Adduct Radicals of DNA Bases by Hydroxyl‐trans‐Stilbenes via Single Electron Transfer. Issue 13 (3rd April 2019)
- Main Title:
- Repair of Oxidizing Hydroxyl Adduct Radicals of DNA Bases by Hydroxyl‐trans‐Stilbenes via Single Electron Transfer
- Authors:
- An, Ping
Wang, Yuyue
Li, Shujin
Zhou, Liping - Abstract:
- Abstract: Repair of oxidizing hydroxyl adduct radicals of DNA bases (base‐OH‐adduct) by eleven hydroxyl‐ trans ‐stilbenes via single electron transfer under physiological conditions are investigated using density functional theory. For eleven hydroxyl‐ trans ‐stilbenes (PSOHs), their anions make all the contributions to repairing oxidizing base‐OH‐adduct radicals. Ten PSOHs show better beneficial antioxidant effect than trans ‐resveratrol. 3, 3′, 4, 4′, 5, 5′‐Hexahydroxy‐ trans ‐stilbene (PSOH d ) performs the best repair activity to oxidizing base‐OH‐adduct radicals, and 3′, 4′, 5, 5′‐tetrahydroxy‐ trans ‐stibene has the smallest p K a value. The rate constants for the reactions of PSOH d with oxidizing base‐OH‐adduct radicals are about 10 5 ∼10 9 dm 3 mol −1 s −1 . Main factors affecting the repair reactions are the vertical ionization potential, the p K a of PSOHs and the vertical electron affinity of oxidizing base‐OH‐adduct radicals. This study gives information on repairing oxidizing base‐OH‐adduct radicals by PSOHs in biological environment for the first time and finds more beneficial antioxidant effect polyphenol than trans ‐resveratrol or piceatannol. Abstract : Repair of oxidizing hydroxyl adduct radicals of DNA base by eleven hydroxyl‐ trans ‐stilbenes via single electron transfer (SET) are investigated using density functional theory for the first time. Their anions make all the contributions to repairing oxidizing base‐OH‐adduct radicals. The rate constants forAbstract: Repair of oxidizing hydroxyl adduct radicals of DNA bases (base‐OH‐adduct) by eleven hydroxyl‐ trans ‐stilbenes via single electron transfer under physiological conditions are investigated using density functional theory. For eleven hydroxyl‐ trans ‐stilbenes (PSOHs), their anions make all the contributions to repairing oxidizing base‐OH‐adduct radicals. Ten PSOHs show better beneficial antioxidant effect than trans ‐resveratrol. 3, 3′, 4, 4′, 5, 5′‐Hexahydroxy‐ trans ‐stilbene (PSOH d ) performs the best repair activity to oxidizing base‐OH‐adduct radicals, and 3′, 4′, 5, 5′‐tetrahydroxy‐ trans ‐stibene has the smallest p K a value. The rate constants for the reactions of PSOH d with oxidizing base‐OH‐adduct radicals are about 10 5 ∼10 9 dm 3 mol −1 s −1 . Main factors affecting the repair reactions are the vertical ionization potential, the p K a of PSOHs and the vertical electron affinity of oxidizing base‐OH‐adduct radicals. This study gives information on repairing oxidizing base‐OH‐adduct radicals by PSOHs in biological environment for the first time and finds more beneficial antioxidant effect polyphenol than trans ‐resveratrol or piceatannol. Abstract : Repair of oxidizing hydroxyl adduct radicals of DNA base by eleven hydroxyl‐ trans ‐stilbenes via single electron transfer (SET) are investigated using density functional theory for the first time. Their anions make all the contributions to repairing oxidizing base‐OH‐adduct radicals. The rate constants for the reactions of PSOH d with oxidizing base‐OH‐adduct radicals are about 10 5 ∼10 9 dm 3 mol −1 s −1 . … (more)
- Is Part Of:
- ChemistrySelect. Volume 4:Issue 13(2019)
- Journal:
- ChemistrySelect
- Issue:
- Volume 4:Issue 13(2019)
- Issue Display:
- Volume 4, Issue 13 (2019)
- Year:
- 2019
- Volume:
- 4
- Issue:
- 13
- Issue Sort Value:
- 2019-0004-0013-0000
- Page Start:
- 3782
- Page End:
- 3790
- Publication Date:
- 2019-04-03
- Subjects:
- Hydroxyl-trans-Stilbenes -- Oxidizing DNA Base-OH-adduct Radicals -- Repair Reaction -- Single Electron Transfer -- Density Functional Theory
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.201803802 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11943.xml