Identification and Characterization of CINPA1 Metabolites Facilitates Structure-Activity Studies of the Constitutive Androstane Receptor-Reference-Cited by-同舟云学术

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Identification and Characterization of CINPA1 Metabolites Facilitates Structure-Activity Studies of the Constitutive Androstane Receptor

Published:2016-08-12 Issue:11 Volume:44 Page:1759-1770
ISSN:1521-009X
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metabolism and Disposition

Author:

Cherian M. T.,Yang L.,Chai S. C.,Lin W.,Chen T.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference31 articles.

1. Expression of Hepatic Drug-Metabolizing Cytochrome P450 Enzymes and Their Intercorrelations: A Meta-Analysis

2. Molecular genetics of CYP2D6: Clinical relevance with focus on psychotropic drugs

3. Small-molecule modulators of the constitutive androstane receptor

4. CINPA1 Is an Inhibitor of Constitutive Androstane Receptor That Does Not Activate Pregnane X Receptor

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Regulation of Nuclear Receptors PXR and CAR by Small Molecules and Signal Crosstalk: Roles in Drug Metabolism and Beyond;Drug Metabolism and Disposition;2022-09-18

2. High-content analysis of constitutive androstane receptor (CAR) translocation identifies mosapride citrate as a CAR agonist that represses gluconeogenesis;Biochemical Pharmacology;2019-10

3. Drug discovery technologies to identify and characterize modulators of the pregnane X receptor and the constitutive androstane receptor;Drug Discovery Today;2019-03

4. CINPA1 binds directly to constitutive androstane receptor and inhibits its activity;Biochemical Pharmacology;2018-06

5. Using TR-FRET to Investigate Protein–Protein Interactions: A Case Study of PXR-Coregulator Interaction;Protein-Protein Interactions in Human Disease, Part A;2018

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