CHEBI:192259 - fluoxytioconazole (thione)

ChEBI IDCHEBI:192259
ChEBI Namefluoxytioconazole (thione)
Stars
DefinitionA racemate comprising equimolar amounts of (R)- and (S)-fluoxytioconazole (thione).
Last Modified13 September 2022
SubmitterAdnan
FormulaC23H15F4N5O2S
Net Charge0
Average Mass501.460
Monoisotopic Mass501.08826
Roles Classification
Biological Roles:
fungicide  A substance used to destroy fungal pests.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
ergosterol biosynthesis inhibitor  Any compound that inhibits one or more steps in the pathway leading to the synthesis of ergosterol.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
ergosterol biosynthesis inhibitor  Any compound that inhibits one or more steps in the pathway leading to the synthesis of ergosterol.
Application:
fungicide  A substance used to destroy fungal pests.
ChEBI Ontology
Outgoing Relation(s)
fluoxytioconazole (thione) (CHEBI:192259) has part (R)-fluoxytioconazole (thione) (CHEBI:193116)
fluoxytioconazole (thione) (CHEBI:192259) has part (S)-fluoxytioconazole (thione) (CHEBI:193118)
fluoxytioconazole (thione) (CHEBI:192259) is a conazole fungicide (CHEBI:87067)
fluoxytioconazole (thione) (CHEBI:192259) is a racemate (CHEBI:60911)
fluoxytioconazole (thione) (CHEBI:192259) is tautomer of fluoxytioconazole (thiol) (CHEBI:192258)
Incoming Relation(s)
fluoxytioconazole (thiol) (CHEBI:192258) is tautomer of fluoxytioconazole (thione) (CHEBI:192259)
IUPAC Name 
rac-4-({6-[2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-sulfanylidene-2,5-dihydro-1H-1,2,4-triazol-1-yl)propyl]pyridin-3-yl}oxy)benzonitrile
Synonyms  Source
racemic fluoxytioconazole (thione)ChEBI
4-({6-[(2RS)-2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-sulfanylidene-2,5-dihydro-1H-1,2,4-triazol-1-yl)propyl]pyridin-3-yl}oxy)benzonitrileIUPAC
Manual XrefsDatabases
WO2016187201Patent
Registry NumbersSources
Reaxys:30536868Reaxys
CAS:2046300-61-0ChemIDplus