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

EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

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

Take structure to advanced search

ChEBI ID	CHEBI:47977
ChEBI Name	2-amino-2-deoxy-D-glucopyranose
Stars
ASCII Name	2-amino-2-deoxy-D-glucopyranose
Definition	A D-glucosamine whose structure comprises D-glucopyranose having an amino substituent at position 2.
Secondary ChEBI IDs	CHEBI:4162, CHEBI:47972
Last Modified	26 October 2021
Submitter	Kirill Degtyarenko
Downloads	Molfile

Formula	C6H13NO5
Net Charge	0
Average Mass	179.172
Monoisotopic Mass	179.07937
SMILES	N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
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

Species of Metabolite	Component	Source	Comments
Escherichia coli (ncbitaxon:562)	-	PubMed (21988831)
Mus musculus (ncbitaxon:10090)	-	PubMed (19425150)	Source: BioModels - MODEL1507180067

Roles Classification

Biological Roles:	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).
Application:	geroprotector Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.

ChEBI Ontology

Outgoing Relation(s)
	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 Relation(s)
	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-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)
	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	Source
D-Glucosamine	KEGG COMPOUND
Chitosamine	KEGG COMPOUND
2-Amino-2-deoxy-D-glucose	KEGG COMPOUND

Manual Xrefs	Databases
C00329	KEGG COMPOUND
D04334	KEGG DRUG
1307	DrugCentral
G80384UV	GlyTouCan
G80384UV	GlyGen
388352	ChemSpider

Registry Numbers	Sources
Gmelin:397125	Gmelin
Beilstein:1423209	Beilstein
Reaxys:1423209	Reaxys
CAS:3416-24-8	KEGG COMPOUND

Citations