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Details

Stereochemistry ACHIRAL
Molecular Formula C3H4O6S
Molecular Weight 168.125
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFOPYRUVATE

SMILES

OC(=O)C(=O)CS(O)(=O)=O

InChI

InChIKey=BUTHMSUEBYPMKJ-UHFFFAOYSA-N
InChI=1S/C3H4O6S/c4-2(3(5)6)1-10(7,8)9/h1H2,(H,5,6)(H,7,8,9)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
The genome sequence of Methanohalophilus mahii SLP(T) reveals differences in the energy metabolism among members of the Methanosarcinaceae inhabiting freshwater and saline environments.
2010-12-23
Racemase activity effected by two dehydrogenases in sulfolactate degradation by Chromohalobacter salexigens: purification of (S)-sulfolactate dehydrogenase.
2010-03
Convergent evolution of coenzyme M biosynthesis in the Methanosarcinales: cysteate synthase evolved from an ancestral threonine synthase.
2009-12-10
Structure and kinetics of phosphonopyruvate hydrolase from Variovorax sp. Pal2: new insight into the divergence of catalysis within the PEP mutase/isocitrate lyase superfamily.
2006-09-26
Dissimilation of C3-sulfonates.
2006-03
Dissimilation of cysteate via 3-sulfolactate sulfo-lyase and a sulfate exporter in Paracoccus pantotrophus NKNCYSA.
2005-03
The phosphonopyruvate decarboxylase from Bacteroides fragilis.
2003-10-17
Dissociative phosphoryl transfer in PEP mutase catalysis: structure of the enzyme/sulfopyruvate complex and kinetic properties of mutants.
2002-08-13
Name Type Language
SULFOPYRUVATE
Systematic Name English
.BETA.-SULFOPYRUVIC ACID
Preferred Name English
PROPANOIC ACID, 2-OXO-3-SULFO-
Common Name English
3-SULFOPYRUVIC ACID
Common Name English
2-OXO-3-SULFOPROPANOIC ACID
Systematic Name English
Code System Code Type Description
DRUG BANK
DB02156
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
PRIMARY
PUBCHEM
440717
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
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CHEBI
16894
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
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CAS
98022-26-5
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
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EPA CompTox
DTXSID60243370
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
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FDA UNII
8D5GA7PEG6
Created by admin on Tue Apr 01 16:58:04 GMT 2025 , Edited by admin on Tue Apr 01 16:58:04 GMT 2025
PRIMARY