iprobenfos
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.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C13H21O3PS |
|---|---|
| Charge | 0 |
| Average mass | 288.349 Da |
| Monoisotopic mass | 288.0949 Da |
| Source | ChEBI |
| InChIKey | FCOAHACKGGIURQ-UHFFFAOYSA-N |
CC(C)OP(=O)(OC(C)C)SCc1ccccc1
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
Also called
- S-benzyl O,O-dipropan-2-yl phosphorothioate
- Kitazin P
- O,O-Bis(1-methylethyl) S-(phenylmethyl)phosphorothioate
- O,O-DIIsopropyl S-benzyl thiophosphate
- O,O-Diisopropyl S-benzyl phosphorothioate
- Phosphorothioic acid, S-benzyl O,O-diisopropyl ester
- S-Benzyl O,O-diisopropyl phosphorothioate
- S-Benzyl O,O-diisopropyl thiophosphate
- S-Benzyl diisopropyl phosphorothioate
Cross-references
Patents and articles
Activity roles
- antifungal agrochemical
CHEBI:86328
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:79737 |
iprobenfos | antibioticmech:chebi-2d8c969f06 |
2026-08-30 |
Mechanism summary
- Mode of action
- CELL_MEMBRANE_SYNTHESIS_INHIBITION host shared target
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories