Articles with "cyp2c19 cyp3a4" as a keyword



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PBPK Analysis to Study the Impact of Genetic Polymorphism of NAT2 on Drug-Drug Interaction Potential of Isoniazid.

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Published in 2021 at "Pharmaceutical research"

DOI: 10.1007/s11095-021-03095-9

Abstract: PURPOSE Isoniazid (INH) is prescribed both for the prophylaxis as well as the treatment of tuberculosis. It is primarily metabolized through acetylation by a highly polymorphic enzyme, N-acetyl transferase 2 (NAT2), owing to which significant… read more here.

Keywords: isoniazid; cyp2c19 cyp3a4; study; drug ... See more keywords

Determination of lansoprazole, 5-hydroxylansoprazole, and lansoprazole sulfone in human plasma for CYP2C19 and CYP3A4 phenotyping

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Published in 2019 at "Chemical Papers"

DOI: 10.1007/s11696-019-00682-4

Abstract: A simple and sensitive liquid chromatography method with absorbance or mass spectrometry detection was developed and validated for the determination of lansoprazole, lansoprazole sulfone, and 5-hydroxylansorpazole in human serum with omeprazole as an internal standard.… read more here.

Keywords: lansoprazole sulfone; determination lansoprazole; cyp2c19 cyp3a4;
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Abstract 3035: Phase I study to assess the effect of adavosertib (AZD1775) on the pharmacokinetics of substrates of CYP1A2, CYP2C19 and CYP3A4 in patients with advanced solid tumors

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Published in 2020 at "Cancer Research"

DOI: 10.1158/1538-7445.am2020-3035

Abstract: Background: Adavosertib (AD), a selective WEE1 inhibitor, may alter exposure to compounds metabolized by cytochromes P450 (CYP); this two-period open-label study (NCT03333824) assessed the effect of AD on pharmacokinetics (PK) of probe substrates for CYP1A2… read more here.

Keywords: solid tumors; cyp1a2 cyp2c19; cyp2c19 cyp3a4; substrates cyp1a2 ... See more keywords
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Physiologically Based Pharmacokinetic (PBPK) Modeling of Clopidogrel and Its Four Relevant Metabolites for CYP2B6, CYP2C8, CYP2C19, and CYP3A4 Drug–Drug–Gene Interaction Predictions

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Published in 2022 at "Pharmaceutics"

DOI: 10.3390/pharmaceutics14050915

Abstract: The antiplatelet agent clopidogrel is listed by the FDA as a strong clinical index inhibitor of cytochrome P450 (CYP) 2C8 and weak clinical inhibitor of CYP2B6. Moreover, clopidogrel is a substrate of—among others—CYP2C19 and CYP3A4.… read more here.

Keywords: interaction; based pharmacokinetic; cyp2c19 cyp3a4; physiologically based ... See more keywords