Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

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Structure-Activity Relationships of Pentacyclic Triterpenoids as Potent and Selective Inhibitors against Human Carboxylesterase 1 Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics.

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Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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name

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@en

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@nl

type

Item

label

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@en

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@nl

prefLabel

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@en

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@nl

P1476

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

@en

P2093

Claire Juif

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Elizabeth Kigondu

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

Felix Huth

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Gian Camenisch

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Hilmar Schiller

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Ken-Ichi Umehara

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Marc Witschi

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Markus Zollinger

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P2860

Paraoxonase-2 is a ubiquitously expressed protein with antioxidant properties and is capable of preventing cell-mediated oxidative modification of low density lipoprotein

Antiplatelet agents aspirin and clopidogrel are hydrolyzed by distinct carboxylesterases, and clopidogrel is transesterificated in the presence of ethyl alcohol

The emerging role of human esterases.

The role of human carboxylesterases in drug metabolism: have we overlooked their importance?

The paraoxonases: role in human diseases and methodological difficulties in measurement.

Carboxylesterase 1 as a determinant of clopidogrel metabolism and activation.

Characterization of recombinant human carboxylesterases: fluorescein diacetate as a probe substrate for human carboxylesterase 2.

Predicting drug clearance from recombinantly expressed CYPs: intersystem extrapolation factors.

Identification of the human enzymes responsible for the enzymatic hydrolysis of aclidinium bromide.

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scholarly article

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10.3109/00498254.2015.1133867

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English

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Kelly Chibale

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2016-02-18T00:00:00Z

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295077670

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Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

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P2860

P2860

Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.

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type

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P1433

P1476

P2093

P2860

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P356

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P433

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P50

P577

P5875

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P356

P1433

P1476

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P2860

P304

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P407

P433

P478

P50

P577

P5875

P698