CHEBI:16216 - 3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid
ChEBI ID CHEBI:16216
Definition A dicarboxylic acid that is succinic acid substituted at position 2 by an acetamidomethylidene group and at position 3 by a hydroxymethyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:11472, CHEBI:11475, CHEBI:972, CHEBI:19412
Supplier Information
Download Molfile XML SDF
Formula C8H11NO6
Net Charge 0
Average Mass 217.17608
Monoisotopic Mass 217.05864
InChI InChI=1S/C8H11NO6/c1-4(11)9-2-5(7(12)13)6(3-10)8(14)15/h2,6,10H,3H2,1H3,(H,9,11)(H,12,13)(H,14,15)
InChIKey BHXUWJPOOLFBAP-UHFFFAOYSA-N
SMILES CC(=O)NC=C(C(CO)C(O)=O)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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216) has functional parent succinic acid (CHEBI:15741)
3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216) is a 3-hydroxy carboxylic acid (CHEBI:61355)
3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216) is a dicarboxylic acid (CHEBI:35692)
3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216) is a primary alcohol (CHEBI:15734)
3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216) is conjugate acid of 3-(acetamidomethylene)-2-(hydroxymethyl)succinate(2−) (CHEBI:19418)
Incoming 3-(acetamidomethylene)-2-(hydroxymethyl)succinate(2−) (CHEBI:19418) is conjugate base of 3-(acetamidomethylidene)-2-(hydroxymethyl)succinic acid (CHEBI:16216)
IUPAC Name
2-(acetamidomethylidene)-3-(hydroxymethyl)butanedioic acid
Synonyms Sources
2-(Acetamidomethylene)-3-(hydroxymethyl)succinate KEGG COMPOUND
2-(Hydroxymethyl)-3-(acetamidomethylene)succinate KEGG COMPOUND
Manual Xref Database
C04690 KEGG COMPOUND
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Last Modified
04 August 2014