All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| profungicide | CHEBI_136645 | [A compound that, on administration, must undergo chemical conversion by metabolic processes before becoming the pharmacologically active fungicide for which it is a profungicide.] |
| phospholipid biosynthesis inhibitor | CHEBI_83741 | [Any compound that inhibits the biosynthesis of any phospholipid.] |
| ethyl 2-hydroxy-5-methylpyrazolo[1,5-a]pyrimidine-6-carboxylate | CHEBI_141398 | [A member of the class of pyrazolopyrimidines that is pyrazophos in which the the thiophosphate group has been hydrolysed to the corresponding hydroxy group. The active fungicide of the profungicide pyrazophos.] |
| quizalofop | CHEBI_81943 | [A racemate comprising equimolar amounts of quizalofop-P of and (S)-quizalofop. Quizalofop is used (commonly as the corresponding ethyl ester, known as quizalofop-ethyl) as a selective post-emergence herbicide against annual and winter-hard grasses. The active isomer is the R enantiomer, which is known as quizalofop-P.] |
| quinoxaline herbicide | CHEBI_137504 | [A quinoxaline pesticide that has herbicidal activity.] |
| quizalofop-P | CHEBI_137507 | [A 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid that has R configuration. An acetyl-CoA carboxylase inhibitor, it is used (generally as the corresponding ethyl or tefuryl ester proherbicides) for the control of annual and perennial grass weeds in sugar beet.] |
| (S)-quizalofop | CHEBI_137513 | [A 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid that has S configuration. It is the (inactive) enantiomer of the herbicide quizalofop-P.] |
| tralkoxydim | CHEBI_81948 | |
| Alloxydim | CHEBI_81949 | |
| quizalofop-P-tefuryl | CHEBI_81944 | [A tetrahydrofurylmethyl ester resulting from the formyl condensation of the carboxy group of quizalofop-P with the hydroxy group of tetrahydrofurfuryl alcohol.] |
| tetrahydrofurfuryl alcohol | CHEBI_137944 | [A primary alcohol that is methanol in which one of the hydrogens of the methyl group has been replaced by a tetrahydrofuran-2-yl group.] |
| (2S)-3-(7-carbamimidoylnaphthalen-2-yl)-2-[4-({(3R)-1-[(1Z)-ethanimidoyl]pyrrolidin-3-yl}oxy)phenyl]propanoic acid | CHEBI_42259 | |
| sulfluramid | CHEBI_81945 | [A sulfonamide obtained by the formal condensation of perfluorooctane-1-sulfonic acid with ethylamine.] |
| perfluorooctane-1-sulfonic acid | CHEBI_39421 | [A perfluoroalkanesulfonic acid that is octane-1-sulfonic acid in which all seventeen of the hydrogens that are attached to carbons hvae been replaced by fluorines.] |
| 2,3,6-TBA | CHEBI_81946 | [A chlorobenzoic acid that is benzoic acid in which the hydrogens at positions 2, 3, and 6 have been replaced by chlorines. A synthetic auxin, it is used as a post-emergence herbicide to control weeds in various cereal crops. Not approved for use within the European Union.] |
| terbumeton | CHEBI_81947 | [A diamino-1,3,5-triazine that is N-tert-butyl-N'-ethyl-1,3,5-triazine-2,4-diamine substituted by a methoxy group at position 6. It is an agrochemical used as a herbicide.] |
| methoxy-1,3,5-triazine | CHEBI_38177 | [Any member of the class of 1,3,5-triazines substituted by at least one methoxy group.] |
| (-)-epigallocatechin | CHEBI_42255 | [A flavan-3,3',4',5,5',7-hexol having (2R,3R)-configuration.] |
| flavan-3,3',4',5,5',7-hexol | CHEBI_71224 | [A hydroxyflavan that is 3,4-dihydro-2H-chromene which is substituted at positions 3, 5, and 7 by hydroxy groups, and at position 2 by a 3,4,5-trihydroxyphenyl group.] |
| (+)-epigallocatechin | CHEBI_71227 | [A flavan-3,3',4',5,5',7-hexol that has (2S,3S)-configuration.] |