Compound
a CMP-N-acyl-beta-neuraminate
A nucleotide-sugar oxoanion obtained by deprotonation of the phospho and carboxy groups of any CMP-N-acyl-β-neuraminic acid; major species at pH 7.3.
Definition from ChEBI (CHEBI:68671), read 2026-09-23. CC BY 4.0.
Structure
- Class
- Organic compound, anion
- Formula
- C19H26N4O16PR
- Mass
- 597.401 g/mol
- Charge
- -2
- SMILES
- *C(=O)N[C@@H]1[C@@H](O)C[C@@](OP(=O)([O-])OC[C@H]2O[C@@H](n3ccc(N)nc3=O)[C@H](O)[C@@H]2O)(C(=O)[O-])O[C@@]1([H])[C@@H](O)[C@@H](O)CO
- Look it up
- ChEBI
Identity from ChEBI. 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: a CMP-N-acyl-beta-neuraminate · Sources: Rhea
- a CMP-N-acyl-beta-neuraminate is a substrate of CMASProteinRhea RHEA:11344Inferred only
Reactions
2 reactions
an N-acylneuraminate+CTPa CMP-N-acyl-beta-neuraminate+diphosphate(3-)
Catalysed by CMAS
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:11344CC BY 4.0Reference data
a CMP-N-acyl-beta-neuraminate+wateran N-acylneuraminate+CMP+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:20185CC BY 4.0Reference data