CHEBI:7027 - 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose

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ChEBI Name 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose
ChEBI ID CHEBI:7027
ChEBI ASCII Name 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose
Definition The pyranose form of muramic acid.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C9H17NO7
Net Charge 0
Average Mass 251.23382
Monoisotopic Mass 251.101
InChI InChI=1S/C9H17NO7/c1-3(8(13)14)16-7-5(10)9(15)17-4(2-11)6(7)12/h3-7,9,11-12,15H,2,10H2,1H3,(H,13,14)/t3-,4-,5-,6-,7-,9?/m1/s1
InChIKey MSFSPUZXLOGKHJ-PGYHGBPZSA-N
SMILES C[C@@H](O[C@@H]1[C@@H](N)C(O)O[C@H](CO)[C@H]1O)C(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via muramic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027) has functional parent 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027) is a muramic acid (CHEBI:28118)
Incoming N-acetyl-D-muramic acid (CHEBI:21615) has functional parent 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027)
α-muramic acid (CHEBI:47969) is a 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027)
β-muramic acid (CHEBI:44312) is a 2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027)
IUPAC Name
2-amino-3-O-[(1R)-1-carboxyethyl]-2-deoxy-D-glucopyranose
Synonyms Sources
2-Amino-3-O-D-1-carboxyethyl-2-deoxy-D-glucose KEGG COMPOUND
3-O-alpha-Carboxyethyl-D-glucosamine KEGG COMPOUND
Muramic acid KEGG COMPOUND
Manual Xrefs Databases
C06470 KEGG COMPOUND
Muramic_acid Wikipedia
View more database links
Registry Numbers Types Sources
2334586 Reaxys Registry Number Reaxys
2334586 Beilstein Registry Number Beilstein
484-57-1 CAS Registry Number ChemIDplus
Last Modified
27 August 2014