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Structure-Activity and Structure-Mechanism Relationships for the Radical-Scavenging Reaction of Flavonols

https://repo.qst.go.jp/records/75179
https://repo.qst.go.jp/records/75179
6b712458-6863-451e-9aff-df246a5dd19c
Item type 会議発表用資料 / Presentation(1)
公開日 2019-03-15
タイトル
タイトル Structure-Activity and Structure-Mechanism Relationships for the Radical-Scavenging Reaction of Flavonols
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Nakanishi, Ikuo

× Nakanishi, Ikuo

WEKO 742154

Nakanishi, Ikuo

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Ohkubo, Kei

× Ohkubo, Kei

WEKO 742155

Ohkubo, Kei

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Imai, Kohei

× Imai, Kohei

WEKO 742156

Imai, Kohei

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Ken-ichiro, Matsumoto

× Ken-ichiro, Matsumoto

WEKO 742157

Ken-ichiro, Matsumoto

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Ozawa, Toshihiko

× Ozawa, Toshihiko

WEKO 742158

Ozawa, Toshihiko

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Hamada, Hiroki

× Hamada, Hiroki

WEKO 742159

Hamada, Hiroki

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Fukuhara, Kiyoshi

× Fukuhara, Kiyoshi

WEKO 742160

Fukuhara, Kiyoshi

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Nakanishi, Ikuo

× Nakanishi, Ikuo

WEKO 742161

en Nakanishi, Ikuo

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Ohkubo, Kei

× Ohkubo, Kei

WEKO 742162

en Ohkubo, Kei

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Imai, Kohei

× Imai, Kohei

WEKO 742163

en Imai, Kohei

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Matsumoto, Kenichiro

× Matsumoto, Kenichiro

WEKO 742164

en Matsumoto, Kenichiro

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Ozawa, Toshihiko

× Ozawa, Toshihiko

WEKO 742165

en Ozawa, Toshihiko

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抄録
内容記述タイプ Abstract
内容記述 Flavonols show an efficient scavenging activity against reactive oxygen radicals. However, the detailed mechanism has yet to be fully clarified. There are two mechanism for the radical-scavenging reactions of phenolic antioxidants, i.e., one-step hydrogen-atom transfer (HAT) and electron transfer followed by proton transfer (ET-PT). In this study, we discuss the radical-scavenging mechanism for 6 flavonols, which are myricetin (Myr), quercetin (Que), kaempferol (Kae), and 3 methylated quercetin analogs (2’-MeQue, 5’-MeQue, and Me2Que), based on the relationships between the scavenging rate constants (k) against galvinoxyl radical and thermodynamic parameters, such as O-H bond dissociation energies (DHT) and ionization potentials (IP), calculated by the density functional theory (DFT).
The k values were determined in deaerated acetonitrile at 298 K by a stopped-flow technique. DFT calculations were carried out at the B3LYP/6-31G(d) level.
The k value increases in the order: Que < 2’-MeQue ≈ Kae < Me2Que < Myr < 5’-MeQue. The plot of the logarithm of the k values (log k) vs. DHT or IP values revealed that the log k values for 5’-MeQue, Myr, Me2Que, and Que are linearly correlated with their IP values. These results suggest that the radical-scavenging reaction by these 4 flavonols may proceeds via the ET-PT mechanism.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 The 9th Biennial Meeting of Society for Free Radical Research-Asia (SFRR-Asia)
発表年月日
日付 2019-04-06
日付タイプ Issued
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