CHEBI:79737 - iprobenfos

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name iprobenfos
ChEBI ID CHEBI:79737
Definition An organic thiophosphate that is the S-benzyl O,O-diisopropyl ester of phosphorothioic acid. Used as a rice fungicide to control leaf and ear blast, stem rot and sheath blight.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C13H21O3PS
Net Charge 0
Average Mass 288.34300
Monoisotopic Mass 288.09490
InChI InChI=1S/C13H21O3PS/c1-11(2)15-17(14,16-12(3)4)18-10-13-8-6-5-7-9-13/h5-9,11-12H,10H2,1-4H3
InChIKey FCOAHACKGGIURQ-UHFFFAOYSA-N
SMILES CC(C)OP(=O)(OC(C)C)SCc1ccccc1
Roles Classification
Biological Role(s): phospholipid biosynthesis inhibitor
Any compound that inhibits the biosynthesis of any phospholipid.
antifungal agrochemical
Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
Application(s): antifungal agrochemical
Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing iprobenfos (CHEBI:79737) has role antifungal agrochemical (CHEBI:86328)
iprobenfos (CHEBI:79737) has role phospholipid biosynthesis inhibitor (CHEBI:83741)
iprobenfos (CHEBI:79737) is a organic thiophosphate (CHEBI:37512)
IUPAC Name
S-benzyl O,O-dipropan-2-yl phosphorothioate
Synonyms Sources
Kitazin P KEGG COMPOUND
O,O-Bis(1-methylethyl) S-(phenylmethyl)phosphorothioate HMDB
O,O-Diisopropyl S-benzyl phosphorothioate HMDB
O,O-DIIsopropyl S-benzyl thiophosphate HMDB
Phosphorothioic acid, S-benzyl O,O-diisopropyl ester NIST Chemistry WebBook
S-Benzyl diisopropyl phosphorothioate ChemIDplus
S-Benzyl O,O-diisopropyl phosphorothioate HMDB
S-Benzyl O,O-diisopropyl phosphorothioate KEGG COMPOUND
S-Benzyl O,O-diisopropyl thiophosphate HMDB
Manual Xrefs Databases
1207 PPDB
C15230 KEGG COMPOUND
CN101569313 Patent
CN101647467 Patent
CN1930986 Patent
HMDB0031768 HMDB
iprobenfos Alan Wood's Pesticides
View more database links
Registry Numbers Types Sources
1974687 Reaxys Registry Number Reaxys
26087-47-8 CAS Registry Number NIST Chemistry WebBook
26087-47-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
16235270 PubMed citation Europe PMC
21674152 PubMed citation Europe PMC
Last Modified
07 July 2015