CHEBI:47977 - 2-amino-2-deoxy-D-glucopyranose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2-amino-2-deoxy-D-glucopyranose
ChEBI ID CHEBI:47977
ChEBI ASCII Name 2-amino-2-deoxy-D-glucopyranose
Definition A D-glucosamine whose structure comprises D-glucopyranose having an amino substituent at position 2.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:47972, CHEBI:4162
Supplier Information ChemicalBook:CB4385569, eMolecules:475176
Download Molfile XML SDF
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Formula C6H13NO5
Net Charge 0
Average Mass 179.17116
Monoisotopic Mass 179.07937
InChI InChI=1S/C6H13NO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1,7H2/t2-,3-,4-,5-,6?/m1/s1
InChIKey MSWZFWKMSRAUBD-IVMDWMLBSA-N
SMILES N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via D-glucosamine )
Application(s): geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) has functional parent D-glucopyranose (CHEBI:4167)
2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) has role Escherichia coli metabolite (CHEBI:76971)
2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) has role geroprotector (CHEBI:176497)
2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) has role mouse metabolite (CHEBI:75771)
2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) is a D-glucosamine (CHEBI:17315)
2-amino-2-deoxy-D-glucopyranose (CHEBI:47977) is conjugate base of 2-ammonio-2-deoxy-D-glucopyranose (CHEBI:58723)
Incoming α-D-GlcpN-(1→6)-D-GlcpN (CHEBI:150211) has functional parent 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
β-D-Galp-(1→3)-D-GlcpN (CHEBI:152182) has functional parent 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
β-D-GlcN-(1→6)-D-GlcN (CHEBI:146542) has functional parent 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
2-amino-3-O-[(R)-1-carboxyethyl]-2-deoxy-D-glucopyranose (CHEBI:7027) has functional parent 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
α-D-glucosamine (CHEBI:44678) is a 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
β-D-glucosamine (CHEBI:28393) is a 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
2-ammonio-2-deoxy-D-glucopyranose (CHEBI:58723) is conjugate acid of 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
[4)-D-GlcpN-(1→] residue (CHEBI:65272) is substituent group from 2-amino-2-deoxy-D-glucopyranose (CHEBI:47977)
IUPAC Name
2-amino-2-deoxy-D-glucopyranose
Synonyms Sources
2-Amino-2-deoxy-D-glucose KEGG COMPOUND
Chitosamine KEGG COMPOUND
D-Glucosamine KEGG COMPOUND
WURCS=2.0/1,1,0/[a2122h-1x_1-5_2*N]/1/ GlyTouCan
Manual Xrefs Databases
1307 DrugCentral
388352 ChemSpider
C00329 KEGG COMPOUND
D04334 KEGG DRUG
G80384UV GlyTouCan
G80384UV GlyGen
View more database links
Registry Numbers Types Sources
1423209 Beilstein Registry Number Beilstein
1423209 Reaxys Registry Number Reaxys
3416-24-8 CAS Registry Number KEGG COMPOUND
397125 Gmelin Registry Number Gmelin
Citations Types Sources
22846255 PubMed citation Europe PMC
24714520 PubMed citation Europe PMC
59831 PubMed citation Europe PMC
Last Modified
26 October 2021