General Information of This Metabolic Reaction (MR) (ID: MR007512)
Formula Reactant Allantoic acid Product Carbon dioxide
Reactant Info Product Info
Other MR(s) Related to The Reactant of This MR
Other MR(s) That Produce The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR004033 Allantoin Allantoic acid Unclear Xanthine [1]
MR007511 Allantion Allantoic acid Unclear Inosine [2]
Other MR(s) That Metabolize The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR004034 Allantoic acid Urea Unclear Xanthine [1]
Other MR(s) Related to The Product of This MR
Other MR(s) That Produce The Product of This MR
MR ID Reactant Product MR Type Related Drug REF
MR013804 Acetohydroxamic Acid CO2 Unclear - Unclear Acetohydroxamic Acid [3]
MR009216 Acetylcarnitine CO2 Oxidation - Oxidation Acetylcarnitine [4]
MR004185 D-lactic acid Carbon dioxide Oxidation - Oxidationn D-lactic acid [5]
MR003888 DB-053072 Carbon dioxide Unclear DB-053072 [6]
MR006290 Diethylenetriamine Carbon dioxide Unclear Diethylenetriamine [7]
MR002714 Eszopiclone Carbon dioxide Oxidation - Oxidative Decarboxylation Eszopiclone [8]
MR005861 L-tyrosine Carbon dioxide Unclear L-tyrosine [9]
MR001579 Liraglutide Carbon dioxide Unclear Liraglutide [10]
MR004251 Methylamine Carbon dioxide Unclear Methylamine [11]
MR006821 Sodium acetate Carbon dioxide Hydrolysis - Hydrolysis Sodium acetate [12]
MR005892 Stigmasterol Carbon dioxide Unclear Stigmasterol [13]
MR006225 Urethane Carbon dioxide Unclear Urethane [14]
MR009650 Zopiclone Carbon dioxide Oxidation - Oxidative decarboxylation Zopiclone [15]
MR007847 Formic acid CO2 Unclear - Unclear Fospropofol disodium [16]
MR006838 Glucose Carbon dioxide Unclear Sorbitol [17]
MR006825 Succinic Acid Carbon dioxide Oxidation - Oxidationn Sodium oxybate [18]
MR004036 Urea Carbon dioxide Unclear Xanthine [1]
⏷ Show the Full List of MR
Other MR(s) That Metabolize The Produtc of This MR
MR ID Reactant Product MR Type Related Drug REF
MR003889 Carbon dioxide Bicarbonate Unclear DB-053072 [6]
MR006822 Carbon dioxide Bicarbonate Reduction - Hydrogenation Sodium acetate [12]
References
1 Xanthine metabolism in Bacillus subtilis: characterization of the xpt-pbuX operon and evidence for purine- and nitrogen-controlled expression of genes involved in xanthine salvage and catabolism
2 Metabolism of nicotinamide, adenine and inosine in developing microspore-derived canola (Brassica napus) embryos
3 Disposition of 14C-acetohydroxamic acid and 14C-acetamide in the rat
4 Partial purification and characterization of an acetylcarnitine hydrolase from bovine epididymal spermatozoa
5 [D(-)Lactic acid--a metabolism problem]
6 Detection of Bacteria-Specific Metabolism Using Hyperpolarized [2-(13)C]Pyruvate
7 Pharmacokinetics and material balance studies of diethylenetriamine trihydrochloride in the Fischer 344 rat following oral, endotracheal or intravenous dosing
8 IMOVANE (Zopiclone) Product Monograph
9 Potent inhibitory effects of tyrosine metabolites on dihydropteridine reductase from human and sheep liver
10 Metabolism and excretion of the once-daily human glucagon-like peptide-1 analog liraglutide in healthy male subjects and its in vitro degradation by dipeptidyl peptidase IV and neutral endopeptidase. Drug Metab Dispos. 2010 Nov;38(11):1944-53.
11 Microbial metabolism of methanol and methylamine in the Gulf of Mexico: insight into marine carbon and nitrogen cycling
12 Sodium acetate induces a metabolic alkalosis but not the increase in fatty acid oxidation observed following bicarbonate ingestion in humans. J Nutr. 2007 Jul;137(7):1750-6.
13 Degradation of phytosterols in tobacco waste extract by a novel Paenibacillus sp. Biotechnol Appl Biochem. 2017 Nov;64(6):843-850.
14 Cytochrome P450 2E1 (CYP2E1) is the principal enzyme responsible for urethane metabolism: comparative studies using CYP2E1-null and wild-type mice
15 Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development. Curr Med Chem. 2009;16(27):3480-675.
16 Metabolic Profiles of Propofol and Fospropofol: Clinical and Forensic Interpretative Aspects
17 An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 1498
18 Kinetic characterization of human hydroxyacid-oxoacid transhydrogenase: relevance to D-2-hydroxyglutaric and gamma-hydroxybutyric acidurias. J Inherit Metab Dis. 2005;28(6):921-30.

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