N-Carbamoyl-L-aspartate (BioCAD00000014636)
Metabolite Card
Formula: C5H8N2O5 (176.0433)
SMILES: NC(=O)N[C@@H](CC(O)=O)C(O)=O
Synonyms [en]
N-carbamoyl-L-aspartate; N-carbamoyl-L-aspartic acid; N-(aminocarbonyl)-L-aspartic acid; L-Ureidosuccinic acid; (2S)-2-(carbamoylamino)butanedioic acid; N-carbamoylaspartate
Last reviewed on 2024-06-28.
Cite this Page
N-Carbamoyl-L-aspartate. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000014636). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Ureidosuccinic acid, also known as L-ureidosuccinate or carbamyl-L-aspartate, belongs to the class of organic compounds known as aspartic acids and derivatives. Aspartic acids and derivatives are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Ureidosuccinic acid is also classified as a carbamate derivative. It is a solid that is soluble in water. Ureidosuccinic acid exists in all living species, ranging from bacteria to plants to humans. Ureidosuccinic acid can be biosynthesized from carbamoyl phosphate and L-aspartic acid through the action of the enzyme known as aspartate carbamoyltransferase (ACTase) and serves as an intermediate in pyrimidine biosynthesis. In humans, a drop in the level of urinary ureidosuccinic acid is associated with bladder cancer (PMID: 25562196). It is also involved in the metabolic disorder called Canavan disease.
DBLinks
- CAS Registry Number: 13184-27-5
- PubChem CID: 93072
- ChEBI: 15859
- HMDB: HMDB0000828
- LipidMaps:
- KEGG: C00438
- BioCyc:
- NCBI MeSH: ureidosuccinic acid
- Wikipedia: Carbamoyl_aspartic_acid
Other DBLinks
- CAS Registry Number: 13184-27-5
- CAS Registry Number: 923-37-5
- PubChem: 279
- PubChem: 3727
- PubChem: 93072
- ChEBI: ChEBI:15859
- ChEBI: ChEBI:64850
- HMDB: HMDB0000828
- KEGG: C00438
- NCBI MeSH: ureidosuccinic acid
- Wikipedia: Carbamoyl_aspartic_acid
- DrugBank: DB04252
- RefMet: RM0037601
- RefMet: RM0128765
- MoNA: FiehnLib000406
- MoNA: FiehnLib000407
- MoNA: GLS00112
- MoNA: KO000411
- MoNA: KO000412
- MoNA: KO000413
- MoNA: KO000414
- MoNA: KO000415
- MoNA: OUF00384
- MoNA: PR100879
- MoNA: PS104801
- MoNA: PS104802
- MoNA: PS104803
- MoNA: PS104807
- MoNA: PS104808
- Metlin: METLIN_3304
- Coconut NaturalProduct: CNP0396749.1
Class / Ontology
- WishartLab ClassyFire: [Amino acids, peptides, and analogues] Amino acids, peptides, and analogues
- RefMet: [Amino acids] Amino acids
- ChEBI: [CHEBI:15859] N-carbamoyl-L-aspartic acid
- Coconut NaturalProduct: [Aminoacids] Aminoacids
| ID | EC Number | Name |
|---|---|---|
| KEGG:R00484 | 3.5.1.7 | N-carbamoyl-L-aspartate amidohydrolase |
| KEGG:R01397 | 2.1.3.2 | carbamoyl-phosphate:L-aspartate carbamoyltransferase |
| KEGG:R01993 | 3.5.2.3 | (S)-dihydroorotate amidohydrolase |
| KEGG:R02284 | 3.5.2.4 | L-5-carboxymethylhydantoin amidohydrolase |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:TRYPANO_PRPP-PWY | superpathway of histidine, purine, and pyrimidine biosynthesis |
| BioCyc:LEISH_PWY-5686 | uridine-5'-phosphate biosynthesis |
| BioCyc:TRYPANO_PWY-5686 | uridine-5'-phosphate biosynthesis |
| BioCyc:LEISH_PWY0-162 | pyrimidine ribonucleotides de novo biosynthesis |
| BioCyc:TRYPANO_PWY0-162 | pyrimidine ribonucleotides de novo biosynthesis |
| WikiPathways:WP3604 | Biochemical pathways: part I |
| WikiPathways:WP662 | Amino acid metabolism |
| WikiPathways:WP106 | Alanine and aspartate metabolism |
| WikiPathways:WP4022 | Pyrimidine metabolism |
| WikiPathways:WP3262 | Alanine and aspartate metabolism |
| WikiPathways:WP3925 | Amino acid metabolism |
| PathBank:SMP0120678 | beta-Ureidopropionase Deficiency |
| PathBank:SMP0120722 | Hypoacetylaspartia |
| PathBank:SMP0120750 | MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy) |
| PathBank:SMP0000178 | Dihydropyrimidinase Deficiency |
| PathBank:SMP0087165 | Aspartate Metabolism |
| PathBank:SMP0087426 | Aspartate Metabolism |
| PathBank:SMP0120681 | Canavan Disease |
| PathBank:SMP0120693 | Dihydropyrimidinase Deficiency |
| PathBank:SMP0120507 | UMP Synthase Deficiency (Orotic Aciduria) |