WordNet
- street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
- any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
- having the characteristics of an acid; "an acid reaction"
PrepTutorEJDIC
- 酸性の / 酸味のある,すっぱい(sour) / (言葉・態度などが)厳しい,しんらつな / 酸 / すっぱいもの / 《俗》=LSD
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/08/02 16:32:21」(JST)
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Orotic acid
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Systematic (IUPAC) name |
1,2,3,6-Tetrahydro-2,6-dioxo-4-pyrimidinecarboxylic acid
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Clinical data |
AHFS/Drugs.com |
International Drug Names |
Identifiers |
CAS Registry Number |
65-86-1 Y |
ATC code |
None |
PubChem |
CID: 967 |
IUPHAR/BPS |
4690 |
DrugBank |
DB02262 N |
ChemSpider |
942 N |
UNII |
61H4T033E5 N |
KEGG |
C00295 N |
Chemical data |
Formula |
C5H4N2O4 |
Molecular mass |
156.10 g/mol |
SMILES
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O=C(O)\C1=C\C(=O)NC(=O)N1
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InChI
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InChI=1S/C5H4N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h1H,(H,9,10)(H2,6,7,8,11) N
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Key:PXQPEWDEAKTCGB-UHFFFAOYSA-N N
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N (what is this?) (verify) |
Orotic acid is a heterocyclic compound and an acid; it is also known as pyrimidinecarboxylic acid. Historically it was believed to be part of the vitamin B complex and was called vitamin B13, but it is now known that it is not a vitamin.
The compound is manufactured in the body via a mitochondrial enzyme, dihydroorotate dehydrogenase.[1] or a cytoplasmic enzyme of pyrimidine synthesis pathway. It is sometimes used as a mineral carrier in some dietary supplements (to increase their bioavailability), most commonly for lithium orotate.
Contents
- 1 Synthesis
- 2 Safety
- 3 Pathology
- 4 See also
- 5 References
- 6 External links
Synthesis
Dihydroorotate is synthesized to orotic acid by the enzyme dihydroorate dehydrogenase, where it later combines with phosphoribosyl pyrophosphate (PRPP) to form orotidine-5'-monophosphate (OMP). A distinguishing characteristic of pyrimidine synthesis is that the pyrimidine ring is fully synthesized before being attached to the ribose sugar, whereas purine synthesis happens by building the base directly on the sugar.[2]
Safety
Orotic acid can be mutagenic in mammalian somatic cells. It is also mutagenic for bacteria and yeast.[3]
Pathology
A buildup of orotic acid can lead to orotic aciduria and acidemia. It may be a symptom of an increased ammonia load due to a metabolic disorder, such as a urea cycle disorder.
In ornithine transcarbamoylase deficiency, an X-linked inherited and the most common urea cycle disorder, excess carbamoyl phosphate is converted into orotic acid. This leads to an increased serum ammonia level, increased serum and urinary orotic acid levels and a decreased serum blood urea nitrogen level. This also leads to an increased urinary orotic acid excretion, because the orotic acid is not being properly utilized and must be eliminated. The hyperammonemia depletes alpha-ketoglutarate leading to the inhibition of the tricarboxylic acid cycle (TCA) decreasing adenosine triphosphate (ATP) production.
See also
- Magnesium orotate
- Pyrimidine biosynthesis
References
- ^ Rawls, J; Knecht, W; Diekert, K; Lill, R; Löffler, M (2000). "Requirements for the mitochondrial import and localization of dihydroorotate dehydrogenase". European journal of biochemistry / FEBS 267 (7): 2079–87. doi:10.1046/j.1432-1327.2000.01213.x. PMID 10727948.
- ^ Lippincott (2008). Biochemistry (4th ed.).
- ^ Orotic acid MSDS
External links
|
Wikimedia Commons has media related to Category:Orotic acid. |
- Orotic Acid at the US National Library of Medicine Medical Subject Headings (MeSH)
- Greenbaum, Sheldon B. (1954). "Potential Metabolic Antagonists of Orotic Acid: 6-Uracilsulfonamide and 6-Uracil Methyl Sulfone1". Journal of the American Chemical Society 76 (23): 6052. doi:10.1021/ja01652a056.
Nucleotide metabolic intermediates
|
|
Purine metabolism |
Anabolism |
R5P→IMP: |
- R5P
- PRPP
- PRA
- GAR
- FGAR
- FGAM
- AIR
- CAIR
- SAICAR
- AICAR
- FAICAR
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IMP→AMP: |
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IMP→GMP: |
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Catabolism |
- Hypoxanthine
- Xanthine
- Uric acid
- 5-Hydroxyisourate
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Pyrimidine metabolism |
Anabolism |
- Carbamoyl phosphate
- Carbamoyl aspartic acid
- 4,5-Dihydroorotic acid
- Orotic acid
- Orotidine 5'-monophosphate
- Uridine monophosphate
|
|
Catabolism |
uracil: |
- Dihydrouracil
- 3-Ureidopropionic acid
- β-Alanine
|
|
thymine: |
- Dihydrothymine
- β-Ureidoisobutyric acid
- 3-Aminoisobutyric acid
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Index of inborn errors of metabolism
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Description |
- Metabolism
- Enzymes and pathways: citric acid cycle
- pentose phosphate
- glycoproteins
- glycosaminoglycans
- phospholipid
- cholesterol and steroid
- sphingolipids
- eicosanoids
- amino acid
- urea cycle
- nucleotide
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|
Disorders |
- Citric acid cycle and electron transport chain
- Glycoprotein
- Proteoglycan
- Fatty-acid
- Phospholipid
- Cholesterol and steroid
- Eicosanoid
- Amino acid
- Purine-pyrimidine
- Heme metabolism
- Symptoms and signs
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Treatment |
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Index of biochemical families
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Carbohydrates |
- Alcohols
- Glycoproteins
- Glycosides
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Lipids |
- Eicosanoids
- Fatty acids
- Glycerides
- Phospholipids
- Sphingolipids
- Steroids
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Nucleic acids |
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Proteins |
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Other |
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UpToDate Contents
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English Journal
- Hereditary Orotic Aciduria and the Excretion of Orotidine.
- Nyhan WL1, Gangoiti JA1.
- Neuropediatrics.Neuropediatrics.2016 Aug 30. [Epub ahead of print]
- Objective Orotic aciduria and deficiency of uridine monophosphate synthetase have been observed in a patient, studied over 10 years, who had no megaloblastic anemia. Excretion of orotic acid and orotidine were 8.24 and 0.52 mmol/mol of creatinine. The ratio of 15.85 differed appreciably from that
- PMID 27574833
- Metabolite amyloids: a new paradigm for inborn error of metabolism disorders.
- Gazit E1.
- Journal of inherited metabolic disease.J Inherit Metab Dis.2016 Jul;39(4):483-8. doi: 10.1007/s10545-016-9946-9. Epub 2016 Jun 6.
- The formation of ordered amyloid assemblies is associated with major human degenerative disorders, including Alzheimer's disease, Parkinson's disease, and type 2 diabetes. Amyloid fibrils are elongated nanoscale structures that bind to specific dyes (including thioflavin T and Congo red). Amyloid fi
- PMID 27271695
Japanese Journal
- Fluorescence assay of dihydroorotate dehydrogenase that may become a cancer biomarker
- Production of orotic acid by a Klura3Δ mutant of Kluyveromyces lactis
- Journal of bioscience and bioengineering 121(6), 625-630, 2016-06
- NAID 40020873358
- Ability of Food/Drink to Reduce the Bitterness Intensity of Topiramate as Determined by Taste Sensor Analysis
Related Links
- Orotic acid is a minor dietary constituent. Indeed, until it was realized that it could be synthesized by humans, orotic acid was known as vitamin B-13. The richest dietary sources of orotic acid are cow's milk and other dairy products ...
- Orotic acid (OA) is an intermediate in de novo pyrimidine biosynthesis that may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from
- Orotic acid is very important in the manufacturing of deoxyribonucleic acid (DNA). In fact, it plays a key role in both DNA and RNA synthesis (). Orotic Acid Side Effects Despite the potential benefits of orotic acid there are some
★リンクテーブル★
[★]
- 英
- orotate, orotic acid
- 同
- オロチン酸、ビタミンB13 vitamin B13、6-カルボキシウラシル 6-carboxyuracil
- 関
- オロット酸
[★]
オロト酸、オロチン酸、オロト酸塩、オロチン酸塩
- 関
- orotic acid
[★]
先天性オロト酸尿症