Results 21 to 30 of about 14,735 (228)

Inhibition of CYP2C8 by Acyl Glucuronides of Gemfibrozil and Clopidogrel: Pharmacological Significance, Progress and Challenges [PDF]

open access: goldBiomolecules, 2022
The lipid-regulating drug gemfibrozil is a useful medication for reducing high cholesterol and triglycerides in the blood. In addition to oxidation, it undergoes extensive glucuronidation to produce gemfibrozil acyl glucuronide, which is a known ...
Manish B. Shah
doaj   +2 more sources

CYP2C8 Status of Patients With Malaria Influences Selection of Plasmodium falciparum pfmdr1 Alleles After Amodiaquine-Artesunate Treatment [PDF]

open access: bronze, 2012
info:eu-repo/semantics ...
Isa Cavaco   +5 more
openalex   +4 more sources

Characterisation of CYP2C8, CYP2C9 and CYP2C19 polymorphisms in a Ghanaian population [PDF]

open access: yesBMC Medical Genetics, 2009
Background Genetic influences on drug efficacy and tolerability are now widely known. Pharmacogenetics has thus become an expanding field with great potential for improving drug efficacy and reducing toxicity.
Dodoo Alexander NO   +2 more
doaj   +3 more sources

Meta-analysis of the global distribution of clinically relevant CYP2C8 alleles and their inferred functional consequences [PDF]

open access: goldHuman Genomics
Background CYP2C8 is responsible for the metabolism of 5% of clinically prescribed drugs, including antimalarials, anti-cancer and anti-inflammatory drugs.
Mahamadou D. Camara   +5 more
doaj   +2 more sources

Global variation in CYP2C8–CYP2C9 functional haplotypes [PDF]

open access: yesPharmacogenomics Journal, 2009
We have studied the global frequency distributions of 10 single nucleotide polymorphisms (SNPs) across 132 kb of CYP2C8 and CYP2C9 in approximately 2500 individuals representing 45 populations. Five of the SNPs were in noncoding sequences; the other five involved the more common missense variants (four in CYP2C8, one in CYP2C9) that change amino acids ...
Kenneth K Kidd
exaly   +3 more sources

Assessing CYP2C8-Mediated Pharmaceutical Excipient-Drug Interaction Potential: A Case Study of Tween 80 and Cremophor EL−35 [PDF]

open access: goldPharmaceutics, 2021
Pharmaceutical excipients (PEs) are substances included in drug formulations. Recent studies have revealed that some PEs can affect the activity of metabolic enzymes and drug transporters; however, the effects of PEs on CYP2C8 and its interaction ...
Chengming Wen   +5 more
doaj   +2 more sources

In Silico Dock of TKIs with CYP3A4 and CYP2C8 and Pharmacophore Generation [PDF]

open access: diamondBIO Web of Conferences
Tyrosine kinase inhibitors (TKIs) serve as targeted anticancer drugs that inhibit the abnormal activity of tyrosine kinase (TK) in cancer treatment. However, when used with other medications, they often result in side effects, such as renal impairment ...
Ma Zhenya
doaj   +2 more sources

Are cytochrome P450 CYP2C8 and CYP2C9 polymorphisms associated with ibuprofen response in very preterm infants?

open access: goldPLoS ONE, 2010
BackgroundPatent ductus arteriosus (PDA) in extremely preterm infants remains a challenging condition with conflicting treatment strategies. Ibuprofen is currently used to treat PDA with ductal closure failure rate up to 40%.
Xavier Durrmeyer   +9 more
doaj   +3 more sources

The Effect of Flavonoid Aglycones on the CYP1A2, CYP2A6, CYP2C8 and CYP2D6 Enzymes Activity

open access: yesMolecules, 2019
Cytochromes P450 are major metabolic enzymes involved in the biotransformation of xenobiotics. The majority of xenobiotics are metabolized in the liver, in which the highest levels of cytochromes P450 are expressed.
Mirza Bojić   +2 more
exaly   +3 more sources

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