Examples of using Parent compound in English and their translations into Swedish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
renal impairment would not be expected to affect clearance of the parent compound or its metabolite.
appears to have the same pharmacokinetic profile as the parent compound.
all modified from the parent compound Piracetam, which was discovered in the 1960s.
Biotransformation: In man, about 80% of the circulating memantine-related material is present as the parent compound.
The acid metabolite is a potent, active cyclooxygenase inhibitor and prolongs the activity of the parent compound.
with a longer half-life than the parent compound.
leflunomide is not recommended, as leflunomide is the parent compound of teriflunomide.
with the highest levels of unchanged parent compound and hydrolysed product appearing in liver and kidneys.
It is likely that only a small fraction of the caspofungin taken up into tissues later returns to plasma as parent compound.
the N-desmethylated derivative(S 18982) with an exposure about 40% of that of the parent compound.
The parent compound is widely distributed in the tissues with the highest concentrations found in the lungs,
This metabolite has one-tenth to one-fortieth the HMG-CoA reductase inhibitor activity of the parent compound.
Meloxicam is predominantly found in plasma and is also a major biliary excretion product whereas urine contains only traces of the parent compound.
This metabolite has one-tenth to one-fortieth the HMG-CoA reductase inhibitor activity of the parent compound.
Urine comprised mostly of a number of metabolites with minimal renal excretion of parent compound.
is used as a prefix to name a structural analog that can be derived from a parent compound by the removal of one carbon atom along with the accompanying hydrogen atoms.
The parent compound afatinib accounted for 88% of the recovered dose.
In vitro metabolism studies have confirmed that the parent compound is rapidly metabolised to 3-O- acetyltylosin.
owes its in vivo bactericidal activity to the parent compound cefuroxime.
in vivo studies indicated that bosutinib(parent compound) undergoes predominantly hepatic metabolism in humans.