Aspartame (BioCAD00000006850)

saliva brain

Metabolite Card

Formula: C14H18N2O5 (294.1216)
SMILES: COC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@@H](N)CC(O)=O

Synonyms [en]

aspartame; Aspartamum; Asp-phe-ome; L-Aspartyl-L-phenylalanine methyl ester; 1-Methyl N-L-alpha-aspartyl-L-phenylalanate; Aminosweet

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Aspartame. 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: BioCAD00000006850). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Aspartame is the name for an artificial, non-carbohydrate sweetener, aspartyl-phenylalanine-1-methyl ester; i.e., the methyl ester of the dipeptide of the amino acids aspartic acid and phenylalanine. It is marketed under a number of trademark names, such as Equal, and Canderel, and is an ingredient of approximately 6,000 consumer foods and beverages sold worldwide. It is commonly used in diet soft drinks, and is often provided as a table condiment. It is also used in some brands of chewable vitamin supplements. In the European Union, it is also known under the E number (additive code) E951. Aspartame is also one of the sugar substitutes used by diabetics. Upon ingestion, aspartame breaks down into several constituent chemicals, including the naturally-occurring essential amino acid phenylalanine which is a health hazard to the few people born with phenylketonuria, a congenital inability to process phenylalanine. Aspartic acid is an amino acid commonly found in foods. Approximately 40% of aspartame (by mass) is broken down into aspartic acid. Because aspartame is metabolized and absorbed very quickly (unlike aspartic acid-containing proteins in foods), it is known that aspartame could spike blood plasma levels of aspartate. Aspartic acid is in a class of chemicals known as excitotoxins. Abnormally high levels of excitotoxins have been shown in hundreds of animals studies to cause damage to areas of the brain unprotected by the blood-brain barrier and a variety of chronic diseases arising out of this neurotoxicity.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 22839-47-0
  • CAS Registry Number: 25548-16-7
  • CAS Registry Number: 53906-69-7
  • CAS Registry Number: 7421-84-3
  • PubChem: 134601
  • PubChem: 2242
  • ChEBI: ChEBI:177838
  • ChEBI: ChEBI:2877
  • HMDB: HMDB0001894
  • HMDB: HMDB01894
  • KEGG: C11045
  • KEGG: D02381
  • NCBI MeSH: Aspartame
  • Wikipedia: Aspartame
  • DrugBank: DB00168
  • RefMet: RM0136131
  • MoNA: AU580906
  • MoNA: CCMSLIB00000078403
  • MoNA: EA277001
  • MoNA: EA277002
  • MoNA: EA277003
  • MoNA: EA277004
  • MoNA: EA277005
  • MoNA: EA277006
  • MoNA: EA277007
  • MoNA: EA277008
  • MoNA: EA277009
  • MoNA: EA277010
  • MoNA: EA277011
  • MoNA: EA277012
  • MoNA: EA277013
  • MoNA: EA277014
  • MoNA: EA277051
  • MoNA: EA277052
  • MoNA: EA277053
  • MoNA: EA277054
  • MoNA: EA277055
  • MoNA: EA277056
  • MoNA: EA277057
  • MoNA: EA277058
  • MoNA: EA277059
  • MoNA: EA277060
  • MoNA: EA277061
  • MoNA: EA277062
  • MoNA: EA277064
  • MoNA: HMDB0001894_ms_ms_1807
  • MoNA: HMDB0001894_ms_ms_1808
  • MoNA: HMDB0001894_ms_ms_1809
  • MoNA: MoNA010789
  • MoNA: MoNA010790
  • MoNA: MoNA010791
  • MoNA: MoNA010792
  • MoNA: MoNA010793
  • MoNA: MoNA010794
  • MoNA: MoNA033072
  • MoNA: MoNA033073
  • MoNA: MoNA033074
  • MoNA: MoNA035264
  • MoNA: MoNA035268
  • MoNA: MoNA035269
  • MoNA: MoNA037503
  • MoNA: MoNA038255
  • MoNA: MoNA038789
  • Metlin: METLIN_6377
  • Coconut NaturalProduct: CNP0285417.1

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

  1. Homo sapiens [ncbi taxid: 9606]

Pathway Synthetic

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