flupyroxystrobin
A member of the class of pyridines that is pyridine substituted by 2-[(1E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]phenoxy and trifluoromethyl groups at positions 2 and 4, respectively. It is an insecticide developed by Syngenta Crop Protection AG.
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 | C17H14F3NO4 |
|---|---|
| Charge | 0 |
| Average mass | 353.296 Da |
| Monoisotopic mass | 353.08749 Da |
| Source | ChEBI |
| InChIKey | SEEIKOSFZLBRHO-JLHYYAGUSA-N |
CO/C=C(/C(=O)OC)c1ccccc1Oc1cc(C(F)(F)F)ccn1
InChI=1S/C17H14F3NO4/c1-23-10-13(16(22)24-2)12-5-3-4-6-14(12)25-15-9-11(7-8-21-15)17(18,19)20/h3-10H,1-2H3/b13-10+
Also called
- methyl (2E)-3-methoxy-2-(2-{[4-(trifluoromethyl)pyridin-2-yl]oxy}phenyl)prop-2-enoate
- SYN 549888
- SYN549888
- methyl (2E)-3-methoxy-2-(2-{[4-(trifluoromethyl)-2-pyridyl]oxy}phenyl)propenoate
- methyl (E)-3-methoxy-2-(2-{[4-(trifluoromethyl)-2-pyridyl]oxy}phenyl)acrylate
- methyl (E)-α-(methoxymethylene)-2-[[4-(trifluoromethyl)-2-pyridinyl]oxy]benzeneacetate
Cross-references
Patents and articles
Activity roles
- quinone outside inhibitor
CHEBI:141153
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:229760 |
flupyroxystrobin | antibioticmech:chebi-405663d0db |
2026-08-30 |
Mechanism summary
- Mode of action
- ENERGY_METABOLISM_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