What is the translation of " GLUCURONIDE " in Danish?

• glucuronid
• glukuronid

Examples of using Glucuronide in English and their translations into Danish

Irbesartan is metabolised by the liver via glucuronide conjugation and oxidation.
Irbesartan omdannes i leveren ved konjugering som glucuronid og ved oxidation.

The main metabolic pathway of tolcapone is conjugation to its inactive glucuronide.
Hovedomdannelsesvejen af tolcapon er konjugering til dets inaktive glucuronid.

The glucuronide of the parent compound is the only metabolite that has been identified in humans.
Glucuroniden af det oprindelige stof er den eneste metabolit, der er set hos mennesker.

Telmisartan is metabolised by conjugation to the glucuronide of the parent compound.
Telmisartan metaboliseres ved konjugation til glucuronidet til parent compound.

Renal excretion of the glucuronide(and possibly zidovudine itself) is reduced in the presence of probenecid.
Renal udskillelse af glucuronidet(og muligvis zidovudin) er reduceret ved tilstedeværelse af probenecid.

At 11.0% of urine radioactivity(0.5% of dose) was a glucuronide conjugate of tipranavir.
Af radioaktiviteten(0, 5% af dosis) var et glucuronid- konjugat fra tipranavir.

Baicalin is a flavone glycoside, the glucuronide of baicalein, which is obtained through the binding of glucuronic acid to baicalein.
Baicalin er et flavon glycosid, glucuronidet af baicalein, som opnås gennem binding af glucuronsyre til baicalein.

Raloxifene comprises less than 1% of the combined concentrations of raloxifene and the glucuronide metabolites.
Raloxifen udgør mindre end 1% af den samlede koncentration af raloxifen og glukuronid metabolitter.

Peak serum concentrations of the glucuronide occur 2 to 3 hours after administration of deferiprone.
Spidskoncentrationer i serum for glucuronid forekommer 2 til 3 timer efter indgivelse af deferiprone.

Ethinyl estradiol is also metabolised to various hydroxylated products and their glucuronide and sulfate conjugates.
Ethinylestradiol nedbrydes også til forskellige hydroxylerede produkter og deres glucoronid- og sulfatkonjugater.

The principal urinary metabolites were glucuronide products derived from leflunomide(mainly in 0 to 24 hour samples) and an oxanilic acid derivative of A771726.
De væsentligste metabolitter i urinen var glukoronidprodukter afledt af leflunomid(især opsamlet i tiden 0- 24 timer) og et oxanilderivat af A771726.

Greater than 80% of the radioactivity in urine was made up of glucuronide conjugates of hydroxylated metabolites.
Mere end 80% af radioaktiviteten i urinen består af glucuronid konjugater af hydroxylerede metabolitter.

Ambrisentan is glucuronidated via several UGT isoenzymes(UGT1A9S, UGT2B7S and UGT1A3S) to form ambrisentan glucuronide 13.
Ambrisentan bliver glukuronideret via adskillige UGT- isoenzymer(UGT1A9S, UGT2B7S og UGT1A3S), og derved dannes ambrisentan- glukuronid 13.

Concentrations of the M2 metabolite(glucuronide) increase by up to a factor of 2.5 with a creatinine clearance of< 30 ml/ min/ 1.73 m2.
I takt med at nyrefunktionens clearance nedsættes, øges koncentrationen af M2- metabolitten(glucuronid) med op til en faktor 2, 5 ved kreatin clearance på< 30 ml/ min/ 1, 73 m2.

Withdrawal by a system of the kidneys and intestines intact and in the form of sulpho compounds and inactive glucuronide. Metabolites detected in plasma.
Tilbagetrækning af et system af nyrerne og tarmene intakte og i form af sulfongrupper forbindelser og inaktive glucuronid. Metabolitter påvist i plasma.

Raloxifene undergoes extensive first pass metabolism to the glucuronide conjugates: raloxifene-4'- glucuronide, raloxifene-6-glucuronide, and raloxifene-6, 4′-diglucuronide.
Metabolisme Raloxifen undergår omfattende first pass metabolisme til glukuronid- konjugater: raloxifen- 4'- glukuronid, raloxifen- 6- glukuronid og raloxifen- 6, 4'- diglukuronid.

Following administration of 14C-entecavir, no oxidative or acetylated metabolites and minor amounts of the phase II metabolites, glucuronide and sulfate conjugates.
Efter administration af 14C- entecavir sås ingen oxidative eller acetylerede metabolitter og der sås mindre mængder af fase II metabolitterne, glucuronid- og sulfatkonjugater.

Thus cytochrome P450 metabolism, glucuronide conjugation, and urinary excretion of glucuronidated metabolites represent the primary route of nevirapine biotransformation and elimination in humans.
Cytokrom P450- metabolismen, glucuronide konjugater og den urinære ekskretion af glucuronide metabolitter repræsenterer således den primære rute for nevirapins biotransformation og elimination hos mennesket.

The primary pathways of metabolism in man are by alcohol dehydrogenase and by glucuronidation to produce the 5'-carboxylic acid and 5'-glucuronide which account for about 66% of the dose excreted in the urine.
De primære metaboliseringsveje hos mennesker er ved hjælp af alkoholdehydrogenase og glucuronidering at danne 5′- carboxylsyre og 5′- glucuronid, som udgør ca.

Moxifloxacin undergoes Phase II biotransformation and is excreted via renal and biliary/ faecal pathways as unchanged drug as well as in the form of a sulpho-compound(M1) and a glucuronide M2.
Moxifloxacin gennemgår fase II- biotransformation og udskilles dels via renale og galde/ fækale udskillelsesveje som uforandret lægemiddel, dels i form af en sulfoforbindelse(M1) og et glukuronid M2.

Fifty-seven percent(57%) of the dose is recovered in urine in the form of 5-oxo-zaleplon and its glucuronide metabolite, an additional 9% is recovered as 5-oxo-desethylzaleplon and its glucuronide metabolite.
Syvoghalvtreds procent(57%) af dosen genfindes i urinen i form af 5- oxo- zaleplon og dets glukuronide stofskifteprodukt, og yderligere 9% genfindes som 5- oxodesethylzaleplon og dets glukuronide stofskifteprodukt.

In vitro studies with human liver microsomes showed that those oxidative metabolites were formed primarily by CYP1A1, CYP1A2, CYP2C8 or CYP2C9 and febuxostat glucuronide was formed mainly by UGT 1A1, 1A8, and 1A9.
In vitro- undersøgelser med humane levermikrosomer viste, at disse oxidative metabolitter primært blev dannet ved CYP1A1, CYP1A2, CYP2C8 eller CYP2C9, og febuxostat glukuronid blev hovedsagelig dannet ved UGT 1A1, 1A8 og 1A9.

The equivalency studies were performed on the EN ISO 9308-1:2000(designated“EU reference method” in this report) and included in total five other internationally recognized methods: Lauryl Sulphate Agar(LSA), Membrane Lactose Glucuronide Agar(MLGA), Chromogenic agar, Chromocult, Colilert and the Danish national reference method until now: MPN in MacConkey broth DS 2255:2001.
Det danske studium blev udført på EN ISO 9308-1:2000(betegnet“EU reference metode” i denne rapport) og inkluderede i alt fem internationalt anerkendte metoder: Lauryl Sulfat Agar(LSA), Membran Laktose Glucuronid Agar(MLGA), Chromogen agar, Chromocult, Colilert samt den danske referencemetode indtil nu: DS 2255:2001 med MPN i MacConkey-bouillon.

How to use "glucuronide" in an English sentence

Formoterol formed two detectable glucuronide isomers in the enzymatic reaction.

Development of an immunoassay using an anti-wogonin glucuronide monoclonal antibody.

The α-hydroxymidazolam glucuronide conjugate of midazolam is excreted in urine.

Specifically, ethyl glucuronide is recommended when including urine alcohol monitoring.

Virtually all morphine is converted to glucuronide metabolites, particularly morphine-3-glucuronide.

Glucuronide Note: R-group substituents are H if not indicated otherwise.

Clinical (nonforensic) application of ethyl glucuronide measurement: Are we ready?

with low amounts of the glucuronide also appearing in the urine.

The major routes of metabolism are hydroxylation followed by glucuronide conjugation.

Moreover, the metabolite hydroxyemodin glucuronide was first reported in this article.

How to use "glucuronid, glukuronid" in a Danish sentence

Det udvikLing af en BrugBar Biomarkør Hvis GHB-glucuronid skal bruges som biomarkør, er det vigtigt, at stoffet er stabilt og ikke nedbrydes i de indsamlede urinprøver.

En diastereomer af det hydroxylerede derivat, en N-glucuronid af indacaterol og C- og N-dealkylerede stoffer var andre identificerede metabolitter.

Phenol-O-glucuronid af indacaterol og hydroxyleret indacaterol var ligeledes fremtrædende metabolitter.

Sammen med blodet går i leveren, hvor det omdannes til tetrahydroaldosteron-3-glucuronid.

Metaboliseres hovedsageligt i leveren ved konjugering med glucuronsyre til morphin-3- glucuronid og morphin-6-glucuronid.

Silodosin og den tilhørende glukuronid når til steady-state efter henholdsvis 3 dages og 5 dages behandling.

Den overvejende cirkulerende metabolit er 10-N-glucuronid, som ikke passerer blodhjernebarrieren.

Den terminale halveringstid af det oprindelige lægemiddel og dets glukuronid er hhv.

Lorazepam glukuronid, den inaktive metabolit, kan være meget dialysabel.

I tilfælde af udtalt nyresvigt resulterer gentagen administration i ophobning af den aktive metabolit morphin-6-glucuronid, som har en lang halveringstid.