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Cytochrome P-450 CYP3A Inhibitors
Known as:
P450 CYP3A Inhibitors
, CYP3A Inhibitors
, Inhibitors, CYP3A
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Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP3A.
National Institutes of Health
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Related topics
Related topics
18 relations
Narrower (14)
Amiodarone
Clarithromycin
Cytochrome P-450 CYP3A5 Inhibitors
Cytochrome P-450 CYP3A7 Inhibitors
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In Blood
aspects of radiation effects
chemical synthesis
standards characteristics
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
UDP‐Glucuronosyltransferase (UGT)‐mediated attenuations of cytochrome P450 3A4 activity: UGT isoform‐dependent mechanism of suppression
Y. Miyauchi
,
Yoshitaka Tanaka
,
+4 authors
Y. Ishii
British Journal of Pharmacology
2020
Corpus ID: 204952292
Cytochrome P450 (CYP, P450) 3A4 is involved in the metabolism of 50% of drugs and its catalytic activity in vivo is not explained…
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2018
2018
Improved Predictions of Drug-Drug Interactions Mediated by Time-Dependent Inhibition of CYP3A.
J. Yadav
,
K. Korzekwa
,
S. Nagar
Molecular Pharmaceutics
2018
Corpus ID: 206688296
Time-dependent inactivation (TDI) of cytochrome P450s (CYPs) is a leading cause of clinical drug-drug interactions (DDIs…
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2017
2017
Clinical Drug–Drug Interactions Through Cytochrome P450 3A (CYP3A) for the Selective ALK Inhibitor Alectinib
P. N. Morcos
,
Y. Cleary
,
+8 authors
A. Phipps
Clinical pharmacology in drug development
2017
Corpus ID: 3513686
The efficacy and safety of alectinib, a central nervous system–active and selective anaplastic lymphoma kinase (ALK) inhibitor…
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2014
2014
Structure-activity relationships of diamine inhibitors of cytochrome P450 (CYP) 3A as novel pharmacoenhancers. Part II: P2/P3 region and discovery of cobicistat (GS-9350).
Lianhong Xu
,
Hongtao Liu
,
+14 authors
M. Desai
Bioorganic & Medicinal Chemistry Letters
2014
Corpus ID: 27414993
2014
2014
Structure-activity relationships of diamine inhibitors of cytochrome P450 (CYP) 3A as novel pharmacoenhancers, part I: core region.
Hongtao Liu
,
Lianhong Xu
,
+12 authors
M. Desai
Bioorganic & Medicinal Chemistry Letters
2014
Corpus ID: 206258859
2012
2012
Evidence of CYP3A Allosterism In Vivo: Analysis of Interaction Between Fluconazole and Midazolam
Jing Yang
,
William M. Atkins
,
N. Isoherranen
,
M. Paine
,
K. Thummel
Clinical pharmacology and therapy
2012
Corpus ID: 115875440
The allosteric effect of fluconazole (effector) on the formation of 1′–hydroxymidazolam (1′–OH–MDZ) and 4–hydroxymidazolam (4–OH…
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Highly Cited
2005
Highly Cited
2005
Cytochrome P450 3A inhibitor itraconazole affects plasma concentrations of risperidone and 9‐hydroxyrisperidone in schizophrenic patients
S. Jung
,
Kyoung-Ah Kim
,
+4 authors
Ji-Young Park
Clinical pharmacology and therapy
2005
Corpus ID: 3165152
Highly Cited
2004
Highly Cited
2004
Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugs.
D. McConn
,
Yvonne S. Lin
,
Kyle E. Allen
,
K. Kunze
,
K. Thummel
Drug Metabolism And Disposition
2004
Corpus ID: 30763604
The objectives of this study were to characterize and compare the reversible inhibition and time-dependent inactivation of…
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1999
1999
Role of CYP3A in bromperidol metabolism in rat in vitro and in vivo.
Minoru Watanabe
,
T. Tateishi
,
Masami Tanaka
,
T. Kumai
,
Shinichi Kobayashi
Xenobiotica; the fate of foreign compounds in…
1999
Corpus ID: 12705546
1. The aim was to identify whether CYP3A metabolizes bromperidol (BP), an antipsychotic drug, to form 4-fluorobenzoyl-propionic…
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Highly Cited
1993
Highly Cited
1993
Evidence for CYP3A-mediated N-deethylation of amiodarone in human liver microsomal fractions.
Drug Metabolism And Disposition
1993
Corpus ID: 25894612
Metabolism of amiodarone to its N-deethylated derivative was investigated on a bank of human hepatic microsomal fractions, two of…
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