4,5-Dihydroorotic acid
4,5-Dihydroorotic acid
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Names |
IUPAC name
2,6-dioxo-1,3-diazinane-4-carboxylic acid |
Identifiers |
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155-54-4 N |
ChEBI |
CHEBI:30865 Y |
ChEMBL |
ChEMBL75782 Y |
ChemSpider |
628 Y |
InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11) YKey: UFIVEPVSAGBUSI-UHFFFAOYSA-N YInChI=1/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11) Key: UFIVEPVSAGBUSI-UHFFFAOYAI
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Jmol-3D images |
Image |
MeSH |
4,5-dihydroorotic+acid |
PubChem |
648 |
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Properties |
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C5H6N2O4 |
Molar mass |
158.112 g/mol |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
N verify (what is: Y/N?) |
Infobox references |
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4,5-Dihydroorotic acid is a derivative of orotic acid which serves as an intermediate in pyrimidine biosynthesis.[1]
References
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| Purine metabolism | |
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| Pyrimidine 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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| 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 |
- Tetrapyrroles
- intermediates
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