Results 1 to 10 of about 287,149 (254)

Characterization of the metabolism of eupalinolide A and B by carboxylesterase and cytochrome P450 in human liver microsomes [PDF]

open access: yesFrontiers in Pharmacology, 2023
Eupalinolide A (EA; Z-configuration) and eupalinolide B (EB; E-configuration) are bioactive cis-trans isomers isolated from Eupatorii Lindleyani Herba that exert anti-inflammatory and antitumor effects.
Yingzi Li   +8 more
doaj   +2 more sources

In vitro modulatory effects of Terminalia arjuna, arjunic acid, arjunetin and arjungenin on CYP3A4, CYP2D6 and CYP2C9 enzyme activity in human liver microsomes

open access: yesToxicology Reports, 2015
Terminalia arjuna is a tree having an extensive medicinal potential in cardiovascular disorders. Triterpenoids are mainly responsible for cardiovascular properties. Alcoholic and aqueous bark extracts of T.
Alice Varghese   +3 more
doaj   +2 more sources

Comparative Proteomics Analysis of Human Liver Microsomes and S9 Fractions. [PDF]

open access: yesDrug Metab Dispos, 2020
Human liver microsomes (HLM) and human liver S9 fractions (HLS9) are commonly used to study drug metabolism in vitro. However, a quantitative comparison of HLM and HLS9 proteomes is lacking, resulting in the arbitrary selection of one hepatic preparation
Wang X, He B, Shi J, Li Q, Zhu HJ.
europepmc   +2 more sources

Tetrahydrofurofuranoid Lignans, Eudesmin, Fargesin, Epimagnolin A, Magnolin, and Yangambin Inhibit UDP-Glucuronosyltransferase 1A1 and 1A3 Activities in Human Liver Microsomes [PDF]

open access: yesPharmaceutics, 2021
Eudesmin, fargesin, epimagnolin A, magnolin, and yangambin are tetrahydrofurofuranoid lignans with various pharmacological activities found in Magnoliae Flos.
Ria Park   +6 more
doaj   +2 more sources

Evaluation of Herb–Drug Interaction Between Danshen and Rivaroxaban in Rat and Human Liver Microsomes [PDF]

open access: yesFrontiers in Pharmacology, 2022
The combination of Salvia miltiorrhiza (Danshen) and rivaroxaban is a promising treatment option in clinical practice in China, but the herb–drug interaction between Danshen and rivaroxaban remains unclear.
Xu Wang   +10 more
doaj   +2 more sources

Structural Identification of Zotarolimus (ABT-578) Metabolites Generated by Human Liver Microsomes Using Ion-Trap and High-Resolution Time-of-Flight Mass Spectrometry in Combination with the Analysis of Fragmentation Patterns [PDF]

open access: yesMetabolites, 2023
Zotarolimus (ABT-578) is a sirolimus derivative that, like sirolimus and everolimus, is an inhibitor of cell growth via inhibition of the mechanistic target of rapamycin (mTOR).
Touraj Shokati   +5 more
doaj   +2 more sources

Human Liver Microsomal Metabolism of (+)-Discodermolide [PDF]

open access: yesJournal of Natural Products, 2009
The polyketide natural product (+)-discodermolide is a potent microtubule stabilizer that has generated considerable interest in its synthetic, medicinal, and biological chemistry. It progressed to early clinical oncology trials, where it showed some efficacy in terms of disease stabilization but also some indications of causing pneumotoxicity ...
Yun, Fan   +2 more
openaire   +2 more sources

Ethoxyresorufin O‐deethylation by human liver microsomes. [PDF]

open access: yesBritish Journal of Clinical Pharmacology, 1986
As a substrate for human liver microsomes, ethoxyresorufin appears to be metabolised by a group of cytochrome P450 isoenzymes which are inducible by cigarette smoking. Kinetic studies in microsomes from four human livers indicate that only one enzyme component is involved over the full substrate range.
F M, Williams   +4 more
openaire   +2 more sources

Biotransformation of (−)-Menthone by Human Liver Microsomes [PDF]

open access: yesBioscience, Biotechnology, and Biochemistry, 2006
The aim of the current study was to investigate the metabolism of (-)-menthone by liver microsomes of humans. (-)-Menthone (1) was metabolized to (+)-neomenthol (2) (3-reduction) and 7-hydroxymenthone (3) by human liver microsomes. The metabolites formed were analyzed on GC and GC-MS.
Mitsuo, Miyazawa, Kyousuke, Nakanishi
openaire   +2 more sources

In vitro metabolism, reaction phenotyping, enzyme kinetics, CYP inhibition and induction potential of ataluren

open access: yesPharmacology Research & Perspectives, 2020
Ataluren promotes ribosomal readthrough of premature termination codons in mRNA which result from nonsense mutations. In vitro studies were performed to characterize the metabolism and enzyme kinetics of ataluren and its interaction potential with CYP ...
Ronald Kong   +9 more
doaj   +1 more source

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