Results 21 to 30 of about 11,244 (259)
Optimization of the CYP inhibition assay using LC-MS/MS
The data presented in this article are related to the research article entitled “Cytochrome P450 inhibition activities of non-standardized botanical products” [1], in which the possible CYP inhibitory properties of botanical products were investigated ...
Muhammad Asyraf Abduraman +4 more
doaj +1 more source
Characterization of porcine hepatic and intestinal drug metabolizing CYP450 : comparison with human orthologues from a quantitative, activity and selectivity perspective [PDF]
Over the past two decades, the pig has gained attention as a potential model for human drug metabolism. Cytochrome P450 enzymes (CYP450), a superfamily of biotransformation enzymes, are pivotal in drug metabolism.
Croubels, Siska +7 more
core +1 more source
Thermodynamics of dissolution and infrared-spectroscopy of solid dispersions of phenacetin
In this work enthalpies of dissolution in water of polyethylene glycols (PEGs) having an average molecular weight of 1000 and 1400, Pluronic-F127, phenacetin as well as the composites prepared from them were measured using solution calorimetry at 298.15 ...
Alexander V Gerasimov +6 more
doaj +1 more source
Cytochrome P450-Based Drug-Drug Interactions of Vonoprazan In Vitro and In Vivo
BackgroundVonoprazan fumarate is a potassium-competitive acid blocker that was developed as a novel acid-suppressing drug for multiple indications. As a potential alternative to proton-pump inhibitors, the determination of the drug-drug interactions is ...
Yiran Wang +7 more
doaj +1 more source
Honokiol (2-(4-hydroxy-3-prop-2-enyl-phenyl)-4-prop-2-enyl-phenol) and magnolol (4-Allyl-2-(5-allyl-2-hydroxy-phenyl)phenol) are the major active polyphenol constituents of Magnolia officinalis (Magnoliaceae) bark, which has been widely used in ...
Sang-Bum Kim +7 more
doaj +1 more source
Background: Phenacetin is an analgesic that causes renal diseases and cancers of the upper‐urinary tract (UUT). It was banned in most countries from the late 1960s.
Sebastien Antoni +6 more
doaj +1 more source
Introduction: Pharmacokinetic variability in disease state is common in clinical practice, but its underlying mechanism remains unclear. Recently, gut microbiota has been considered to be pharmacokinetically equivalent to the host liver.
Jing Guo +9 more
doaj +1 more source
Impurity occurrence and removal in crystalline products from process reactions [PDF]
The behavior of impurities when subjected to crystallizations, and related processes such as recrystallization and reslurrying, has been reviewed with a particular focus on the years 2000–2015, but also including significant cases from outside that ...
Horgan, Danielle E. +1 more
core +1 more source
N-(4-Ethoxyphenyl)-3-oxobutanamide
The title compound, C12H15NO3, crystallizes with Z′ = 2 in space group Pca21 with the two independent molecules having almost the same conformation, differing mostly at the end of the butanamide chain.
Sreevandana Yerramsetty +2 more
doaj +1 more source
Surgical management for upper tract transitional cell carcinoma [PDF]
This review is published as a Cochrane Review in the Cochrane Database of Systematic Reviews 2008, Issue 4. Cochrane Reviews are regularly updated as new evidence emerges and in response to comments and criticisms, and the Cochrane Database of Systematic
Cohen, Nicholas P. +5 more
core +3 more sources

