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3-Ureidopropionic acid
CAS No. 462-88-4
3-Ureidopropionic acid( Ureidopropionic acid | Carbamoyl-b-alanine )
Catalog No. M19721 CAS No. 462-88-4
Ureidopropionic acid is an intermediate in the metabolism of uracil. More specifically it is a breakdown product of dihydrouracil and is produced by the enzyme dihydropyrimidase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 43 | In Stock |
|
| 100MG | 65 | In Stock |
|
| 200MG | 88 | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name3-Ureidopropionic acid
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NoteResearch use only, not for human use.
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Brief DescriptionUreidopropionic acid is an intermediate in the metabolism of uracil. More specifically it is a breakdown product of dihydrouracil and is produced by the enzyme dihydropyrimidase.
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DescriptionUreidopropionic acid is an intermediate in the metabolism of uracil. More specifically it is a breakdown product of dihydrouracil and is produced by the enzyme dihydropyrimidase. It is further decomposed to beta-alanine via the enzyme beta-ureidopropionase. Ureidopropionic acid is essentially a urea derivative of beta-alanine. High levels of Ureidopropionic acid are found in individuals with beta-ureidopropionase (UP) deficiency. Enzyme deficiencies in pyrimidine metabolism are associated with a risk for severe toxicity against the antineoplastic agent 5-fluorouracil.
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In Vitro——
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In Vivo——
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SynonymsUreidopropionic acid | Carbamoyl-b-alanine
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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RecptorHuman Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number462-88-4
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Formula Weight132.12
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Molecular FormulaC4H8N2O3
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESNC(=O)NCCC(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Brown D G Rao S Weir T L et al. Metabolomics and metabolic pathway networks from human colorectal cancers adjacent mucosa and stool[J]. Cancer & Metabolism 2016 4(1):11.
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