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Within these requirements, a large number of different lipophilic and leaving groups have been used.
They form a lipophilic bubble that can easily move through the barrier.
The lipophilic end is also referred to as being hydrophobic.
It is fairly lipophilic with a K of 4.65.
The other end is lipophilic - it likes fats.
They are very lipophilic and are stored mainly in body fat.
Most species of corynebacteria are not lipophilic, but some are.
That is usually true for small lipophilic drugs.
It was originally believed that only lipophilic substitution would be tolerated.
Overall the entire body has less lipophilic drug.
It is therefore sometimes employed to crystallize highly lipophilic compounds.
It is a slightly polar, weak base and is lipophilic.
For example for the selective removal of water by using lipophilic membranes.
This shows that it is a lipophilic substance.
The pharmacokinetics of cyproterone are complicated due to its lipophilic nature.
The drug has lipophilic properties, and therefore crosses the blood-brain barrier.
Propranolol is a highly lipophilic drug achieving high concentrations in the brain.
It is a relatively lipophilic and unstable drug.
Examples, with the lipophilic part of the molecule represented by an R, are:
Lipophilic barriers make use of a number of different mechanisms to power motion from one compartment to another.
This hydrophobic or lipophilic end can diffuse across cells that line the stomach wall.
Often, due to their high lipophilic character, these and other metabolites may be detected in the urine up to 18 months.
Its complexes are generally lipophilic and feature metals in low oxidation states.
Etoxadrol is lipophilic and can readily cross the blood-brain barrier.
Ketoconazole is very lipophilic and tends to accumulate in fatty tissues.