CHEBI:58123 - (2S)-2-hydroxy monocarboxylic acid anion

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ChEBI Name (2S)-2-hydroxy monocarboxylic acid anion
ChEBI ID CHEBI:58123
ChEBI ASCII Name (2S)-2-hydroxy monocarboxylic acid anion
Definition A hydroxy monocarboxylic acid anion where the hydroxy group is placed at position 2 (α to the carboxy group) and has (S)-stereochemistry; major species at pH 7.3.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter KAX
Secondary ChEBI IDs CHEBI:61394, CHEBI:70794
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Formula C2H2O3R
Net Charge -1
Average Mass (excl. R groups) 74.03550
Monoisotopic Mass (excl. R groups) 74.00039
SMILES O[C@@H]([*])C([O-])=O
ChEBI Ontology
Outgoing (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123) is a hydroxy monocarboxylic acid anion (CHEBI:36059)
(2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123) is conjugate base of (2S)-2-hydroxy monocarboxylic acid (CHEBI:17375)
(2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123) is enantiomer of (2R)-2-hydroxy monocarboxylic acid anion (CHEBI:58314)
Incoming (2S)-2-hydroxyphytanate (CHEBI:58398) is a (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
(2S)-2-hydroxytetradecanoate (CHEBI:85637) is a (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
(S)-3-phenyllactate (CHEBI:32979) is a (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
indolmycenate (CHEBI:131783) is a (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
(2S)-2-hydroxy monocarboxylic acid (CHEBI:17375) is conjugate acid of (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
(2R)-2-hydroxy monocarboxylic acid anion (CHEBI:58314) is enantiomer of (2S)-2-hydroxy monocarboxylic acid anion (CHEBI:58123)
Synonyms Sources
(2S)-2-hydroxy monocarboxylate ChEBI
(2S)-2-hydroxy monocarboxylates ChEBI
(2S)-2-hydroxy monocarboxylic acid anions ChEBI
(2S)-2-hydroxycarboxylate ChEBI
(2S)-α-hydroxy monocarboxylic acid anion ChEBI
(2S)-α-hydroxy monocarboxylic acid anions ChEBI
(S)-2-hydroxyacid anion ChEBI
(S)-2-hydroxyacid anions ChEBI
a (2S)-2-hydroxycarboxylate UniProt
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10850983 PubMed citation SUBMITTER
Last Modified
02 November 2012