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(RS)-famoxadone

Structure via PubChem · Public domain (PubChem)

EntityQ412776· pop 11· linked from 4 articles

(RS)-famoxadone

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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.

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

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 sections
Contents
  • 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  • Great Britain approval withdrawn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.

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