CHEBI:60312 - 2-amino-2-deoxy-D-galactopyranose

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ChEBI Name 2-amino-2-deoxy-D-galactopyranose
ChEBI ID CHEBI:60312
ChEBI ASCII Name 2-amino-2-deoxy-D-galactopyranose
Definition The pyranose form of D-galactosamine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H13NO5
Net Charge 0
Average Mass 179.17110
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-GASJEMHNSA-N
SMILES N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): toxin
Poisonous substance produced by a biological organism such as a microbe, animal or plant.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via D-galactosamine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-amino-2-deoxy-D-galactopyranose (CHEBI:60312) has functional parent D-galactopyranose (CHEBI:4139)
2-amino-2-deoxy-D-galactopyranose (CHEBI:60312) has role toxin (CHEBI:27026)
2-amino-2-deoxy-D-galactopyranose (CHEBI:60312) is a D-galactosamine (CHEBI:28328)
2-amino-2-deoxy-D-galactopyranose (CHEBI:60312) is a primary amino compound (CHEBI:50994)
2-amino-2-deoxy-D-galactopyranose (CHEBI:60312) is conjugate base of 2-ammonio-2-deoxy-D-galactopyranose (CHEBI:144817)
Incoming α-D-galactosamine (CHEBI:148869) is a 2-amino-2-deoxy-D-galactopyranose (CHEBI:60312)
2-ammonio-2-deoxy-D-galactopyranose (CHEBI:144817) is conjugate acid of 2-amino-2-deoxy-D-galactopyranose (CHEBI:60312)
IUPAC Name
2-amino-2-deoxy-D-galactopyranose
Synonyms Sources
2-Amino-2-deoxy-D-galactose KEGG COMPOUND
Chondrosamine ChemIDplus
D-2-Amino-2-deoxygalactose ChemIDplus
D-Chondrosamine KEGG COMPOUND
D-Galactosamine KEGG COMPOUND
D-GalN JCBN
Galactosamine ChemIDplus
Manual Xref Database
C02262 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
2042269 Beilstein Registry Number Beilstein
2042269 Reaxys Registry Number Reaxys
7535-00-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17456244 PubMed citation Europe PMC
19913595 PubMed citation Europe PMC
28709622 PubMed citation Europe PMC
28752362 PubMed citation Europe PMC
28821814 PubMed citation Europe PMC
28921968 PubMed citation Europe PMC
Last Modified
22 April 2020