General Information of This Metabolic Reaction (MR) (ID: MR007847)
Formula
SVG example
Unclear
Reactant Formic acid Product CO2
Reactant Info Product Info
Metabolic Type Unclear - Unclear
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
MR003256 Fospropofol Formic acid Unclear Fospropofol [1]
MR006016 INS-260 Formic acid Unclear INS-260 [2]
MR001402 Lactulose Formic acid Oxidation - N-Dealkylation Lactulose [3]
MR004296 N,N-dimethylformamide Formic acid Unclear N,N-dimethylformamide [4]
MR007846 Formaldehyde Formic acid Unclear - Unclear Fospropofol disodium [5]
Other MR(s) That Metabolize The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR007848 Formic acid H2O Unclear - Unclear Fospropofol disodium [5]
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 [6]
MR009216 Acetylcarnitine CO2 Oxidation - Oxidation Acetylcarnitine [7]
MR004185 D-lactic acid Carbon dioxide Oxidation - Oxidationn D-lactic acid [8]
MR003888 DB-053072 Carbon dioxide Unclear DB-053072 [9]
MR006290 Diethylenetriamine Carbon dioxide Unclear Diethylenetriamine [10]
MR002714 Eszopiclone Carbon dioxide Oxidation - Oxidative Decarboxylation Eszopiclone [11]
MR005861 L-tyrosine Carbon dioxide Unclear L-tyrosine [12]
MR001579 Liraglutide Carbon dioxide Unclear Liraglutide [13]
MR004251 Methylamine Carbon dioxide Unclear Methylamine [14]
MR006821 Sodium acetate Carbon dioxide Hydrolysis - Hydrolysis Sodium acetate [15]
MR005892 Stigmasterol Carbon dioxide Unclear Stigmasterol [16]
MR006225 Urethane Carbon dioxide Unclear Urethane [17]
MR009650 Zopiclone Carbon dioxide Oxidation - Oxidative decarboxylation Zopiclone [18]
MR006838 Glucose Carbon dioxide Unclear Sorbitol [19]
MR006825 Succinic Acid Carbon dioxide Oxidation - Oxidationn Sodium oxybate [20]
MR004036 Urea Carbon dioxide Unclear Xanthine [21]
MR007512 Allantoic acid Carbon dioxide Unclear Inosine [22]
⏷ 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 [9]
MR006822 Carbon dioxide Bicarbonate Reduction - Hydrogenation Sodium acetate [15]
References
1 DrugBank(Pharmacology-Metabolism)Fospropofol
2 pubchem:INS-260
3 LABEL:ACTULOSE- lactulose solution
4 Anaerobic treatment of N, N-dimethylformamide-containing wastewater by co-culturing two sources of inoculum
5 Metabolic Profiles of Propofol and Fospropofol: Clinical and Forensic Interpretative Aspects
6 Disposition of 14C-acetohydroxamic acid and 14C-acetamide in the rat
7 Partial purification and characterization of an acetylcarnitine hydrolase from bovine epididymal spermatozoa
8 [D(-)Lactic acid--a metabolism problem]
9 Detection of Bacteria-Specific Metabolism Using Hyperpolarized [2-(13)C]Pyruvate
10 Pharmacokinetics and material balance studies of diethylenetriamine trihydrochloride in the Fischer 344 rat following oral, endotracheal or intravenous dosing
11 IMOVANE (Zopiclone) Product Monograph
12 Potent inhibitory effects of tyrosine metabolites on dihydropteridine reductase from human and sheep liver
13 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.
14 Microbial metabolism of methanol and methylamine in the Gulf of Mexico: insight into marine carbon and nitrogen cycling
15 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.
16 Degradation of phytosterols in tobacco waste extract by a novel Paenibacillus sp. Biotechnol Appl Biochem. 2017 Nov;64(6):843-850.
17 Cytochrome P450 2E1 (CYP2E1) is the principal enzyme responsible for urethane metabolism: comparative studies using CYP2E1-null and wild-type mice
18 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.
19 An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 1498
20 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.
21 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
22 Metabolism of nicotinamide, adenine and inosine in developing microspore-derived canola (Brassica napus) embryos

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