CHEBI:91021 - S-propyl propanethiosulfinate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name S-propyl propanethiosulfinate
ChEBI ASCII Name S-propyl propanethiosulfinate
Definition A sulfinic acid derivative obtained by formal condensation of propanethiosulfinic acid with propanethiol.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H14OS2
Net Charge 0
Average Mass 166.307
Monoisotopic Mass 166.049
InChI InChI=1S/C6H14OS2/c1-3-5-8-9(7)6-4-2/h3-6H2,1-2H3
Metabolite of Species Details
Rattus norvegicus (NCBI:txid10116) See: PubMed
Mimosa pudica (NCBI:txid76306) Found in root (BTO:0001188). See: PubMed
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
antibacterial agent
A substance that kills or slows the growth of bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing S-propyl propanethiosulfinate (CHEBI:91021) has role antibacterial agent (CHEBI:33282)
S-propyl propanethiosulfinate (CHEBI:91021) has role antioxidant (CHEBI:22586)
S-propyl propanethiosulfinate (CHEBI:91021) has role plant metabolite (CHEBI:76924)
S-propyl propanethiosulfinate (CHEBI:91021) has role rat metabolite (CHEBI:86264)
S-propyl propanethiosulfinate (CHEBI:91021) is a sulfinic acid derivative (CHEBI:37784)
S-propyl propanethiosulfinate (CHEBI:91021) is a sulfoxide (CHEBI:22063)
S-propyl propane-1-sulfinothioate
Synonyms Sources
1-Propanesulfinothioic acid, S-propyl ester ChemIDplus
dipropyl thiosulfinate ChEBI
propyl propanethiosulfinate ChEBI
propyl propylthiosulfinate ChEBI
S-Propyl 1-propanesulfinothioate HMDB
S-propyl propane-1-thiosulfinate ChEBI
Manual Xrefs Databases
EP2110128 Patent
HMDB0034394 HMDB
US2010035984 Patent
View more database links
Registry Numbers Types Sources
1098798 Reaxys Registry Number Reaxys
1948-52-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10820136 PubMed citation Europe PMC
21445384 PubMed citation Europe PMC
26661932 PubMed citation Europe PMC
Last Modified
26 January 2016