glucuronic acid conjugation pathway

phate (UDP)-glucuronic acid to finally discharge them through urine or bile In general con‐ jugation dramatically improves solubility which then promotes rapid excretion Among the several types of conjugation reactions which are present in the body including glucuronida‐ tion sulfation and glutathione and amino acid conjugation glutathione which is catalyzed by glutathione S en The major routes of metabolism are N-demethylation and hydroxylation followed by conjugation with sulphate and glucuronic acid da Konjugation — aktiv overfrsel af DNA fra en vrtsorganisme til en anden EurLex-2 en Conjugation — the active transfer of DNA from one host to another da Telmisartan metaboliseres ved konjugation til glucuronidet til parent compound EMEA0 3 en

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(4) Sulfate conjugation eg Phenolic compounds (chromphenicol) and Adrenal and steroids (5) Glycine conjugation — eg salicylates and drugs having carboxylic acid groups 2 The answer is (D) (Ribose) The pentose phosphate cycle is a side pathway whose primary purpose is to produce ribose and NADPH Little ribose is present in the

The Udp-glucuronic Acid Transport Pathway complements our catalog of research reagents including antibodies and ELISA kits against GOLPH3 Udp-glucuronic Acid Transport Bioinformatics Tool Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes diseases and pathways based on co-citations Explore more on Udp-glucuronic Acid Transport below! For more

Glutamine conjugation of phenylacetate Functional group Enzyme Cosubstrate Glucuronic acid UDP-glucuronosyltransferases UDP-glucuronide Sulfate Sulfotransferases 3?-Phosphoadenosine-5?- phosphosulfate (PAPS) Glutathione Glutathione-S-transferases / spontaneous Free glutathione Acetate N-acetyltransferases Acetyl-CoA Methyl N- S- and O-methyl-transferases S

Since the conjugation of drugs to glucose generally represents a minor metabolic pathway when glucuronidation is possible and the newly detected metabolite was formed only by microsomes and has not been generally observed in plasma samples of patients under MMF therapy (Shipkova et al 1999) this metabolic pathway may be of minor importance in vivo However we have recently observed this

After induction with arochlor (PCB) or 3-MC the major pathway was ring-hydroxylation (cytochrome P450 dependent) followed by conjugation to β-glucuronic or sulfuric acid The presence of the glucuronide conjugate of N-hydroxyMeIQx a mutagenic metabolite suggested an induction of P450 CYP1A2 The metabolism of MeIQx by liver cell aggregates is very similar to that observed in vivo and


of benzoic acid is 4 2 and that of benzoyl glycine (hippuric acid) is 3 7 Sig- nificant species differences occur in these phase II reactions largely related to the type of compound used for conjugation For example common brushtail possums (Trichosurus vulpecula) conjugate phenol with glucuronic acid

Known metabolic pathways of MDMC include N-demethylation to normethylone (3 4-methylenedioxycathinone MDC) aliphatic chain hydroxylation and oxidative demethylenation followed by monomethylation and conjugation with glucuronic acid and/or sulphate 2 Three new phase II metabolites amidic conjugates of MDC with succinic glutaric and adipic acid were identified in the

Pathway Responsible for • Glucuronic acid found in agar agra gel and apples • Milk thistle • Green tea • SAMe supplement PHASE II ACETYLATION Acetyl Co-A is attached to toxins to make them less harmful and easy to excrete • Primary way to eliminate sulfa drugs • Low vitamins B2 B5 and C • Cigarette smoking • Acetol-CoA derived from normal metabolism PHASE II AMINO ACID

After induction with arochlor (PCB) or 3-MC the major pathway was ring-hydroxylation (cytochrome P450 dependent) followed by conjugation to β-glucuronic or sulfuric acid The presence of the glucuronide conjugate of N-hydroxyMeIQx a mutagenic metabolite suggested an induction of P450 CYP1A2 The metabolism of MeIQx by liver cell aggregates is very similar to that observed in vivo and

As elucidated by mass spectrometry enzymatic hydrolysis and 1H 13C nuclear magnetic resonance it appears to be a conjugate of o-hydroxybenzoic acid with glucuronic acid Its presence in urine of healthy subjects indicates its physiological character

glucuronic acid [gloo″ku-ronik] a uronic acid formed by oxidation of C-6 of glucose to a carboxy group it occurs in proteoglycans (mucopolysaccharides) and is important in the conjugation of xenobiotics it is conjugated to many poisons and drugs by the liver forming glucuronides which markedly decreases their toxicity and enhances their

with glucuronic acid sulfuric acid or glycine and excreted with urine [14 19] Fig 7 presents a scheme of glucuroni-des formation as an example of conjugation proceeded in the reactions of the second phase The reactions of the second phase of biotransformations of N-nitrosocompounds are characterized by the stereospe- cific attack of an electron pair of the xenobiotic on the carbocation of

Glucuronic acid conjugation occurs in the liver Primary metabolism pathway Non-hepatic metabolism Mitochondrial Beta-oxidation (40%) Primary and preferred non-hepatic pathway Valproate undergoes Fatty Acid beta-oxidation in the mitochondria Requires acetyl-coA to enter mitichondria Requires carnitine to cross Mitochondrial innder-membrane Microsomal omega hydroxylation (5%

Oxidation of glucose

Pathway: 1-Production of UDP-glucuronic acid which is the metabolically active form of glucuronic acid which enters in: Synthesis of mucopolysaccharides Detoxification by conjugation: UDP-glucuronic acid is used to detoxify steroid hormones drugs and toxins Formation of conjugated bilirubin 2-Formation of pentoses 3-Formation of vitamin C in plants and animal 4-formation of

Urinary glucuronic acid conjugate after administration of aliphatic secondary alcohols and ketones to rabbits by gavage Substance: Dose (mg/kg bw) a: Urinary glucuronic acid conjugate (%) 2-Pentanol : 740: 45: 2-Heptanone: 950: 41: 2-Heptanol: 960: 55: 3-Heptanol: 960: 62: 2-Octanol: 1100: 16: a Calculated on the basis of a dose of 25 mmol/3 kg bw alpha beta-Unsaturated ketones are also

English term or phrase: hepatic glucuronic acid conjugation: The drug is mainly excreted through the kidney after hepatic glucuronic acid conjugation essef ((Local time: 16:39: conjugacin heptica CON cido glucurnico : Explanation: 1) Se metaboliza por conjugacin heptica con el cido glucurnico (aproximadamente

Conjugation with glucuronic acid is a major pathway in the biotransformation and elimination of a wide variety of lipophilic compounds of both endogenous and exogenous origin (Coughtrie 1992 Dutton 1980) The glucuronides formed are in general less biologically active and more polar than their aglycone substrates and are hence more readily excreted in the urine Cloning studies using cDNA

Conjugation reactions: Usually detoxification reaction Conjugates: are o more polar o easily excreted o typically inactive Conjugation: o Involves high-energy intermediates and specific transfer enzymes (microsomal or cytosolic transferases) o Conjugation with glucuronic acid requires cytochrome P450 enzymes ? glucuronic acid: available from glucose

Glucuronic acid is available from glucose and its conjugation with lipid-soluble drugs results in a lipophilic glucuronic acid derivative which is typically pharmacologically inactive and more water-soluble compared to the parent compound Therefore the glucuronic acid derivative molecule is more readily excreted in both urine or bile Transferases are enzymes which catalyzes the coupling of

Q 17- UDP-Glucuronic acid the glucuronyl donor in the Glucuronidation reactions is formed in the pathway of Glycolysis Hexose monophosphate Uronic acid Gluconeogenesis Glycogenolysis Q 18- Aspirin has antipyretic analgesic and anti-atherogenic properties It is detoxified by: Oxidation Reduction Hydrolysis Methylation Glucuronidation

The major metabolic pathway is via conjugation with glucuronic acid sometimes preceded by oxidation and hydroxylation Ibuprofen has been recommended in dogs at 5 mg/kg However prolonged use at this dosage may cause gastric ulcers and perforations GI irritation or ulceration GI hemorrhage and renal damage are the most commonly reported toxic effects of ibuprofen ingestion in dogs In

The data obtained from these outcomes recommends that the major pathway of FA metabolism is the conjugation reaction with glucuronic acid and/or sulfate The conjugation of FA takes place mainly in the liver through the activities of sulfotransferases and uridine diphosphate (UDP) glucuronosyl transferases while small amount of conjugation

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