CHEBI:48291 - (R)-3-sulfolactic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (R)-3-sulfolactic acid
ChEBI ID CHEBI:48291
ChEBI ASCII Name (R)-3-sulfolactic acid
Definition The (R)-enantiomer of 3-sulfolactic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:1667, CHEBI:39945, CHEBI:38022, CHEBI:11890, CHEBI:16071
Supplier Information
Download Molfile XML SDF
more structures >>
Formulae C3H6O6S
C3H6O6S
Net Charge 0
Average Mass 170.14100
Monoisotopic Mass 169.98851
InChI InChI=1S/C3H6O6S/c4-2(3(5)6)1-10(7,8)9/h2,4H,1H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
InChIKey CQQGIWJSICOUON-REOHCLBHSA-N
SMILES O[C@@H](CS(O)(=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 (R)-3-sulfolactic acid (CHEBI:48291) is a 3-sulfolactic acid (CHEBI:38023)
(R)-3-sulfolactic acid (CHEBI:48291) is conjugate acid of (R)-3-sulfolactate (CHEBI:58738)
(R)-3-sulfolactic acid (CHEBI:48291) is enantiomer of (S)-3-sulfolactic acid (CHEBI:16712)
Incoming (R)-3-sulfolactate (CHEBI:58738) is conjugate base of (R)-3-sulfolactic acid (CHEBI:48291)
(S)-3-sulfolactic acid (CHEBI:16712) is enantiomer of (R)-3-sulfolactic acid (CHEBI:48291)
IUPAC Names
(2R)-2-hydroxy-3-sulfopropanoate
(2R)-2-hydroxy-3-sulfopropanoic acid
Synonyms Sources
(2R)-3-Sulfolactate KEGG COMPOUND
(2R)-3-SULFOLACTIC ACID PDBeChem
Manual Xrefs Databases
3SL PDBeChem
C11537 KEGG COMPOUND
View more database links
Registry Number Type Source
5506152 Beilstein Registry Number Beilstein
Citation Waiting for Citations Type Source
20150239 PubMed citation Europe PMC
Last Modified
14 January 2011