Compound
aceneuramate
An N-acetylneuraminate that is the conjugate base of aceneuramic acid arising from the deprotonation of the carboxy group. Major microspecies at pH 7.3.
Definition from ChEBI (CHEBI:173083), read 2026-09-23. CC BY 4.0.
Structure
Loading the model…
- Class
- Organic compound, anion
- Formula
- C11H18NO9
- Mass
- 308.263 g/mol
- Charge
- -1
- InChIKey
- KBGAYAKRZNYFFG-BOHATCBPSA-M
- SMILES
- CC(=O)N[C@@H]([C@@H](O)[C@H](O)[C@H](O)CO)[C@@H](O)CC(=O)C(=O)[O-]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
1 statement
1 statement · 1 reference database · Subject: aceneuramate · Sources: Rhea
- aceneuramate is a substrate of NPLProteinRhea RHEA:23296Inferred only
Reactions
3 reactions
aceneuramatealdehydo-N-acetyl-D-mannosamine+pyruvate
Catalysed by NPL
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:23296CC BY 4.0Reference data
CHEBI:58770aceneuramate
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:67736CC BY 4.0Reference data
N-acetyl-beta-neuraminic acidaceneuramate
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:67740CC BY 4.0Reference data
Other names
6 names
Resolves to: aceneuramate
- Also called
- (4S,5R,6R,7S,8R)-5-acetamido-4,6,7,8,9-pentahydroxy-2-oxononanoateN-acetyl-keto-neuraminateN-acetylneuraminateNeu5Ac(1-)Neu5Ac(1−)
- Systematic name
- 5-acetamido-3,5-dideoxy-D-glycero-D-galacto-non-2-ulosonate