Structure via PubChem · Public domain (PubChem)
(RS)-famoxadone
Sign in to saveFamoxadone is a fungicide to protect agricultural products against various fungal diseases on fruiting vegetables, tomatoes, potatoes, curcurbits, lettuce and grapes. It is used in combination with cymoxanil. Famoxadone is a QI, albeit with a chemistry different from most QIs. (It is an oxazolidine-dione while most are strobilurins.) It is commonly used against Plasmopara viticola, Alternaria solani, Phytophthora infestans, and Septoria nodorum.
In the Vinony graph
Within Vinony's link graph, (RS)-famoxadone is referenced by 4 other articles, and connects out to fungicide, tomato and potato.
It is catalogued under topics including Chembox image size set, ECHA InfoCard ID from Wikidata and Fungicides.
Its subject is documented across 11 Wikipedia language editions.
Chemical data
- Formula
- C22H18N2O4
- Molecular weight
- 374.4 g/mol
- IUPAC name
- 3-anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 374.127
- Has use
- fungicide
Show 2 more facts
- chemical formula
- C₂₂H₁₈N₂O₄
- canonical SMILES
- CC1(C(=O)N(C(=O)O1)NC2=CC=CC=C2)C3=CC=C(C=C3)OC4=CC=CC=C4
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
5 sectionsContents
- Molecular interaction
- Resistance management
- Great Britain approval withdrawn
- References
- External links
Famoxadone is a fungicide to protect agricultural products against various fungal diseases on fruiting vegetables, tomatoes, potatoes, curcurbits, lettuce and grapes. It is used in combination with cymoxanil. Famoxadone is a QI, albeit with a chemistry different from most QIs. (It is an oxazolidine-dione while most are strobilurins.) It is commonly used against Plasmopara viticola, Alternaria solani, Phytophthora infestans, and Septoria nodorum.
==Molecular interaction== Famoxadone is of lesser interaction strength at the Q pocket than some other QIs, for example, azoxystrobin. This is because azoxystrobin and such interact more centrally in the Q pocket than does famoxadone.
Excerpted from Wikipedia’s “(RS)-famoxadone” article, available under the CC BY-SA 4.0 licence.
Gallery (2)
Available in 11 languages
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