CHEBI:131966 - (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid
ChEBI ID CHEBI:131966
ChEBI ASCII Name (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid
Definition A hexonic acid derivative that is (2Z,4S,5R)-4,5,6-trihydroxyhex-2-enoic acid substituted at position 2 by an amino group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H11NO5
Net Charge 0
Average Mass 177.155
Monoisotopic Mass 177.06372
InChI InChI=1S/C6H11NO5/c7-3(6(11)12)1-4(9)5(10)2-8/h1,4-5,8-10H,2,7H2,(H,11,12)/b3-1-/t4-,5+/m0/s1
InChIKey BWCRWWBHRAOURT-VYOXQMNSSA-N
SMILES C(=O)(/C(/N)=C/[C@H](O)[C@H](O)CO)O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966) is a α-amino acid (CHEBI:33704)
(2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966) is a hexonic acid derivative (CHEBI:63442)
(2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966) is tautomer of (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid zwitterion (CHEBI:131706)
(2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966) is tautomer of (4S,5R)-4,5,6-trihydroxy-2-iminohexanoic acid (CHEBI:131967)
Incoming (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid zwitterion (CHEBI:131706) is tautomer of (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966)
(4S,5R)-4,5,6-trihydroxy-2-iminohexanoic acid (CHEBI:131967) is tautomer of (2Z,4S,5R)-2-amino-4,5,6-trihydroxyhex-2-enoic acid (CHEBI:131966)
IUPAC Name
(2Z)-2-amino-2,3-dideoxy-D-erythro-hex-2-enonic acid
Manual Xref Database
CPD-16808 MetaCyc
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Last Modified
20 May 2016