Vous avez cherché: comt (Anglais - Croate)

comt inhibitors
inhibitori comt-a

medicinal products metabolised by comt
lijekovi koji se metaboliziraju pomoću comt-a

entacapone inhibits the comt enzyme mainly in peripheral tissues.
entakapon inhibira enzim comt uglavnom u perifernim tkivima.

no effects were seen on the pharmacokinetics of the comt substrate carbidopa.
nisu opaženi učinci na farmakokinetiku comt- ovog supstrata karbidope.

the s- comt activity inhibition was significantly increased in elderly subjects.
inhibicija aktivnosti s-comt bila je značajno povećana u starijih ispitanika.

studies in healthy volunteers have shown that tolcapone reversibly inhibits human erythrocyte comt activity after oral administration.
ispitivanja na zdravim dobrovoljcima pokazala su da tolkapon reverzibilno inhibira aktivnost comt-a ljudskih eritrocita nakon peroralne primjene.

entacapone is a reversible, specific and mainly peripherally acting comt inhibitor designed for concomitant administration with levodopa.
entakapon je reverzibilan, specifičan i uglavnom periferno aktivan comt inhibitor namijenjen za istodobnu primjenu s levodopom.

comt inhibition in red blood cells closely follows the plasma concentrations of entacapone, thus clearly indicating the reversible nature of comt inhibition.
inhibicija comt u eritrocitima vjerno prati koncentracije entakapona u plazmi, što jasno ukazuje na reverzibilnu prirodu inhibicije comt.

tasmar, as a comt inhibitor, is known to increase the bioavailability of the co-adminstered levodopa.
poznato je da tasmar, kao comt inhibitor, povećava bioraspoloživost istodobno primijenjene levodope.

however, tasmar, as a comt inhibitor, is known to increase the bioavailability of the co-administered levodopa.
međutim, poznato je da tasmar, kao comt inhibitor, povećava bioraspoloživost istodobno primijenjene levodope.

2-hydroxy-3-o-methyl naltrexone and 2-hydroxy-3-o-methyl-6-beta-naltrexol, believed to be mediated by catechol-o-methyl transferases (comt), and glucuronidation, thought to be mediated by ugt1a1 and ugt2b7.
2-hidroksi-3-o-metil-6-beta-naltreksola, vjerojatno posredstvom katekol-o-metill transferaze (comt), i glukuronidacijom vjerojatno posredstvom ugt1a1 i ugt2b7.