Glucuronidation of Antiallergic Drug, Tranilast: Identification of Human UDP-Glucuronosyltransferase Isoforms and Effect of Its Phase I Metabolite-Reference-Cited by-同舟云学术

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Glucuronidation of Antiallergic Drug, Tranilast: Identification of Human UDP-Glucuronosyltransferase Isoforms and Effect of Its Phase I Metabolite

Published:2007-01-12 Issue:4 Volume:35 Page:583-589
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Katoh Miki,Matsui Tomohito,Yokoi Tsuyoshi

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference20 articles.

1. The UGT1A1*28 allele is relatively rare in a Japanese population

2. Pharmacogenetics of irinotecan: A promoter polymorphism of UGT1A1 gene and severe adverse reactions to irinotecan

3. PHARMACOLOGICAL PROPERTIES OF N-(3′,4′-DIMETHOXYCINNAMOYL) ANTHRANILIC ACID (N-5′), A NEW ANTI-ATOPIC AGENT

4. Differential and Special Properties of the Major Human UGT1-encoded Gastrointestinal UDP-glucuronosyltransferases Enhance Potential to Control Chemical Uptake

5. Discovery of new potentially defective alleles of human CYP2C9

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3. Evidence-based strategies for the characterisation of human drug and chemical glucuronidation in vitro and UDP-glucuronosyltransferase reaction phenotyping;Pharmacology & Therapeutics;2021-02

4. Chemical Probes for Human UDP-Glucuronosyltransferases: A Comprehensive Review;Biotechnology Journal;2018-09-27

5. 6-Chloro-5-[4-(1-Hydroxycyclobutyl)Phenyl]-1H-Indole-3-Carboxylic Acid is a Highly Selective Substrate for Glucuronidation by UGT1A1, Relative toβ-Estradiol;Drug Metabolism and Disposition;2018-09-07

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