Evaluation and Comparison of the Inhibition Effect of Astragaloside IV and Aglycone Cycloastragenol on Various UDP-Glucuronosyltransferase (UGT) Isoforms.

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Evaluation and Comparison of the Inhibition Effect of Astragaloside IV and Aglycone Cycloastragenol on Various UDP-Glucuronosyltransferase (UGT) Isoforms.

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Evaluation and Comparison of t ...... syltransferase (UGT) Isoforms.

@en

Evaluation and Comparison of t ...... us UDP-Glucuronosyltransferase

@nl

type

Item

label

Evaluation and Comparison of t ...... syltransferase (UGT) Isoforms.

@en

Evaluation and Comparison of t ...... us UDP-Glucuronosyltransferase

@nl

prefLabel

Evaluation and Comparison of t ...... syltransferase (UGT) Isoforms.

@en

Evaluation and Comparison of t ...... us UDP-Glucuronosyltransferase

@nl

P1476

Evaluation and Comparison of t ...... osyltransferase (UGT) Isoforms

@en

P2093

Bowei Chen

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Chunze Zhang

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Rongshan Li

http://www.w3.org/2001/XMLSchema#string

Ruixue Ran

http://www.w3.org/2001/XMLSchema#string

Weihua Zhang

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Xiaolang Du

http://www.w3.org/2001/XMLSchema#string

Xiaolong Yang

http://www.w3.org/2001/XMLSchema#string

Zhenying Zhao

http://www.w3.org/2001/XMLSchema#string

Zhiwei Fu

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Zhongze Fang

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P2860

Review of the botanical characteristics, phytochemistry, and pharmacology of Astragalus membranaceus (Huangqi).

Disposition of Astragaloside IV via Enterohepatic Circulation Is Affected by the Activity of the Intestinal Microbiome.

Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios.

Drug-Drug Interactions Potential of Icariin and Its Intestinal Metabolites via Inhibition of Intestinal UDP-Glucuronosyltransferases.

Structure, mechanism and engineering of plant natural product glycosyltransferases.

Progress in the research of Radix Astragali in treating chronic heart failure: effective ingredients, dose-effect relationship and adverse reaction.

The UDP-glucuronosyltransferases: their role in drug metabolism and detoxification.

A comprehensive review of UDP-glucuronosyltransferase and esterases for drug development.

Evaluating the in vitro inhibition of UGT1A1, OATP1B1, OATP1B3, MRP2, and BSEP in predicting drug-induced hyperbilirubinemia.

Investigation into UDP-glucuronosyltransferase (UGT) enzyme kinetics of imidazole- and triazole-containing antifungal drugs in human liver microsomes and recombinant UGT enzymes.

P31

scholarly article

P356

10.3390/MOLECULES21121616

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2016-11-29T00:00:00Z

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P698

27916843

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P932

6274106

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