Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 30, 2024
Язык: Английский
Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 30, 2024
Язык: Английский
Biomedical Chromatography, Год журнала: 2024, Номер unknown
Опубликована: Окт. 4, 2024
Nimbolide is a major furanoid compound isolated from Azadirachta indica. The aim of this study was to characterize the metabolites nimbolide in rats and propose metabolic pathways. were generated by incubating (10 μM) with rat liver microsomes, nicotinamide adenine dinucleotide phosphate (NADPH), nucleophiles (glutathione [GSH] or N-acetyl-lysine [NAL]) at 37°C for 60 min. For vivo study, intravenously administered single dose 10 mg/kg, bile urine collected. identified ultra-high-performance liquid chromatography-quadrupole/orbitrap mass spectrometry (UPLC-Q/Orbitrap-MS) using electrospray ionization positive ion mode. Totally, nine detected, their identities characterized accurate MS MS/MS data. In GSH-supplemented GSH conjugation primary elimination pathway. furan ring bioactivated into cis-butene-1,4-dial that can be trapped GSH. NAL-supplemented two NAL conjugates (M4 M5) derived observed. urine, N-acetyl-cysteine, cysteine-glycine, conjugate also found. current provides an overview metabolism bioactivation profiles rats, which aids understanding its safety activity.
Язык: Английский
Процитировано
1Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 30, 2024
Язык: Английский
Процитировано
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