CHEBI:82047 - triflusulfuron-methyl

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ChEBI Name triflusulfuron-methyl
ChEBI ID CHEBI:82047
Definition A methyl ester resulting from the formal condensation of the carboxy group of triflusulfuron with methanol. A proherbicide for triflusulfuron.
Stars This entity has been manually annotated by the ChEBI Team.
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Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): EC 2.2.1.6 (acetolactate synthase) inhibitor
An EC 2.2.1.* (transketolase/transaldolase) inhibitor that interferes with the action of acetolactate synthase (EC 2.2.1.6).
Application(s): proherbicide
A compound that, on administration, must undergo chemical conversion by biochemical (enzymatic), chemical (possibly following an enzymatic step), or physical (e.g. photochemical) activation processes before becoming the pharmacologically active herbicide for which it is a proherbicide.
agrochemical
An agrochemical is a substance that is used in agriculture or horticulture.
Related Structures
triflusulfuron-methyl is a Structural Derivative of
triflusulfuron
Mass : 478.405
Formula : C16H17F3N6O6S
142847
methanol
Mass : 32.04186
Formula : CH4O
17790
urea
Mass : 60.05534
Formula : CH4N2O
16199
sulfonic acid
Mass : 82.08008
Formula : H2O3S
29214
oxoacid
Definition : A compound which contains oxygen, at least one other element, and at least one hydrogen bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
ammonia
Mass : 17.03056
Formula : H3N
16134
benzoic acids
Definition : Any aromatic carboxylic acid that consists of benzene in which at least a single hydrogen has been substituted by a carboxy group.
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Relationship Types
is a
has part
is conjugate base of
is conjugate acid of
is tautomer of
is enantiomer of
has functional parent
has parent hydride
is substituent group from
has role
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