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Deglycosylated Ginsenosides Are More Potent Inducers of CYP1A1, CYP1A2 and CYP3A4 Expression in HepG2 Cells than Glycosylated Ginsenosides

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Deglycosylated Ginsenosides Are More Potent Inducers of CYP1A1, CYP1A2 and CYP3A4 Expression in HepG2 Cells than Glycosylated Ginsenosides

資料種別
記事
著者
HAO Miaoほか
出版者
The Japanese Society for the Study of Xenobiotics
出版年
2011
資料形態
デジタル
掲載誌名
Drug Metabolism and Pharmacokinetics 26 2
掲載ページ
p.201-205
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要約等:

Ginseng is one of the most commonly used herbal medicines worldwide. Ginsenosides are believed to be responsible for the therapeutic activities of gin...

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デジタル

資料種別
記事
出版年月日等
2011
出版年(W3CDTF)
2011
タイトル(掲載誌)
Drug Metabolism and Pharmacokinetics
巻号年月日等(掲載誌)
26 2
掲載巻
26
掲載号
2
掲載ページ
201-205
掲載年月日(W3CDTF)
2011
ISSN(掲載誌)
13474367
出版事項(掲載誌)
The Japanese Society for the Study of Xenobiotics
本文の言語コード
en
対象利用者
一般
標準番号(その他)
COI : 1:CAS:528:DC%2BC3MXpvVyjurg%3D
PMID : 21178302
参照
Increased Levels of Fatty Acids Contributed to Induction of Hepatic CYP3A4 Activity Induced by Diabetes : In Vitro Evidence From HepG2 Cell and Fa2N-4 Cell Lines
参照
20(S)-25-methoxyl-dammarane-3β, 12β, 20-triol, a novel natural product for prostate cancer therapy: activity in vitro and in vivo and mechanisms of action
Analysis methods of ginsenosides
In Vitro Inhibition and Induction of Human Hepatic Cytochrome P450 Enzymes by Modafinil
Induction of cytochrome P450 1A1 expression by ginsenoside Rg1 and Rb1 in HepG2 cells
Human Cytochrome P-450 3A4: In Vitro Drug-Drug Interaction Patterns Are Substrate-Dependent
Ginsenoside Metabolites, Rather Than Naturally Occurring Ginsenosides, Lead to Inhibition of Human Cytochrome P450 Enzymes
Ginseng pharmacology
Experimental therapy of prostate cancer with novel natural product anti‐cancer ginsenosides
Interactions of Herbs with Cytochrome P450
Herbal Interactions Involving Cytochrome P450 Enzymes
The Inhibitory Effects of Herbal Components on CYP2C9 and CYP3A4 Catalytic Activities in Human Liver Microsomes
Panax ginseng
Cytochrome P450 enzyme levels in HepG2 cells and cryopreserved primary human hepatocytes and their induction in HepG2 cells
CYP1A Induction and Human Risk Assessment: An Evolving Tale of in Vitro and in Vivo Studies
Novel ginsenosides 25-OH-PPD and 25-OCH 3 -PPD as experimental therapy for pancreatic cancer: anticancer activity and mechanisms of action
Regulation of CYP3A4 Expression in Human Hepatocytes by Pharmaceuticals and Natural Products
IN VITRO AND IN VIVO DRUG INTERACTIONS INVOLVING HUMAN CYP3A
Variability in commercial ginseng products: an analysis of 25 preparations
Cytochrome P450: What Have We Learned and What Are the Future Issues?
Regulation of CYP1A1 by heavy metals and consequences for drug metabolism
Herb-drug interactions
Clinical importance of the cytochromes P450
Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography–mass spectrometry and its application in rat pharmacokinetic studies
Effects of ginseng components on c-DNA-expressed cytochrome P450 enzyme catalytic activity
Pharmacokinetics and bioavailability of ginsenoside Rb1 and Rg1 from Panax notoginseng in rats
Structure-Activity Relationship and Substrate-Dependent Phenomena in Effects of Ginsenosides on Activities of Drug-Metabolizing P450 Enzymes
In vitro anti-cancer activity and structure–activity relationships of natural products isolated from fruits of Panax ginseng
EFFECTS OF INDIVIDUAL GINSENOSIDES, GINKGOLIDES AND FLAVONOIDS ON CYP2C19 AND CYP2D6 ACTIVITY IN HUMAN LIVER MICROSOMES
Cytochrome P450 phenotypic ratios for predicting herb‐drug interactions in humans
In Vitro Effect of Standardized Ginseng Extracts and Individual Ginsenosides on the Catalytic Activity of Human CYP1A1, CYP1A2, and CYP1B1
Cancer prevention and therapeutics: Panax ginseng
Metabolism and pharmacokinetics of ginsenosides
The Inhibitory Effect of Intestinal Bacterial Metabolite of Ginsenosides on CYP3A Activity
Metabolic Activation of Ginsenoside: Deglycosylation by Intestinal Bacteria and Esterification With Fatty Acid
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NII論文ID
130004463178