Примери за използване на Circulating metabolite на Английски и техните преводи на Български
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The major circulating metabolites are inactive.
Genotoxicity data on TCC and its main circulating metabolite SL18.0740(M1).
The major circulating metabolites are inactive.
Covalent adducts to proteins were the major circulating metabolites of afatinib.
The major circulating metabolite is the methylcatechol glucuronide.
In a mass balance study, the metabolite M19 was the major circulating metabolite.
The predominant circulating metabolite of sofosbuvir.
Circulating metabolites do not contribute to its pharmacologic activity.
This is the major circulating metabolite of vitamin D.
Circulating metabolites include neratinib pyridine N-oxide(M3), N-desmethyl neratinib(M6), neratinib dimethylamine N-oxide(M7) and traces of.
C dacomitinib, the most abundant circulating metabolite was O-desmethyl dacomitinib.
Other circulating metabolites included fumaric acid, citric acid and monomethyl fumarate.
The initial products of the hydroxylation andN-dealkylation pathways are major circulating metabolites but none contribute significantly to the overall clinical effect of darifenacin.
The major circulating metabolite is irbesartan glucuronide(approximately 6%).
No effects of azithromycin(500 mg daily for 3 days) were observed on AUC, C max, T max, elimination rate constant,and further T½ sildenafil or its main circulating metabolite.
The major circulating metabolite is the methylcatechol glucuronide.
In normal healthy male volunteers, there was no evidence of an effect of azithromycin(500 mg daily for 3 days) on the AUC, Cmax, tmax, elimination rate constant, orsubsequent half-life of sildenafil or its principal circulating metabolite.
The major circulating metabolite is irbesartan glucuronide(approximately 6%).
In normal healthy male volunteers, there was no evidence of an effect of azithromycin(500 mg daily for 3 days) on the AUC, Cmax, tmax, elimination rate constant, orsubsequent half-life of sildenafil or its principal circulating metabolite.
The major circulating metabolite results from N-demethylation of sildenafil.
The elimination half- life of the main circulating metabolite was 8 hours after single and repeated administration.
The major circulating metabolites are not believed to be pharmacologically active.
The primary and only circulating metabolite, GS-563117, is inactive against PI3Kδ.
Minor circulating metabolites include varenicline N-carbamoylglucuronide and N-glucosylvarenicline.
Based upon in vitro studies, the circulating metabolites of duloxetine are considered pharmacologically inactive.
The main circulating metabolite of sorafenib in plasma, the pyridine N-oxide, shows in vitro potency similar to that of sorafenib.
Based upon in vitro studies, the circulating metabolites of duloxetine are considered pharmacologically inactive.
Of the circulating metabolites, the majority are glucuronide conjugates of posaconazole with only minor amounts of oxidative(CYP450 mediated) metabolites observed.
Another minor circulating metabolite, M3-TEZ, is formed by direct glucuronidation of tezacaftor.
The main circulating metabolite is formed by N-demethylation of sildenafil.