Cinosulfuron is a sulfonylurea herbicide, widely used to control broadleaf weeds in various crops, including cereals, cotton, and soybeans. It acts by inhibiting acetolactate synthase (ALS), an essential enzyme in the biosynthesis of branched-chain amino acids, vital for plant growth. The synthesis of cinosulfuron involves multiple steps, including the reaction of a sulfonyl chloride with a substituted aniline derivative. It is a potent inhibitor of ALS, even at low concentrations, making it effective in controlling weeds. Cinosulfuron is studied for its potential to control resistant weeds and optimize its application for improved efficacy and minimal environmental impact. Its widespread use and effectiveness in controlling broadleaf weeds have made it a vital component of modern agricultural practices, contributing to increased crop yields and reduced weed pressure.'
ID Source | ID |
---|---|
PubMed CID | 92420 |
CHEBI ID | 81982 |
SCHEMBL ID | 54807 |
MeSH ID | M0443767 |
Synonym |
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AC-18027 |
cinosulfuron [iso] |
cga 142464 |
benzenesulfonamide, n-(((4,6-dimethoxy-1,3,5-triazin-2-yl)amino)carbonyl)-2-(2-methoxyethoxy)- |
cinosulfuron |
1-(4,6-dimethoxy-1,3,5-triazin-2-yl)-3-(2-(2-methoxyethoxy)phenylsulfonyl)urea (iupac) |
94593-91-6 |
1-(4,6-dimethoxy-1,3,5-triazin-2-yl)-3-[2-(2-methoxyethoxy)phenyl]sulfonylurea |
C18818 |
unii-53hyl452sb |
53hyl452sb , |
FT-0602948 |
AKOS015900059 |
SCHEMBL54807 |
1-(4,6-dimethoxy-1,3,5-triazin-2-yl)-3-(2-(2-methoxyethoxy)phenylsulfonyl)urea |
n-(((4,6-dimethoxy-1,3,5-triazin-2-yl)amino)carbonyl)-2-(2-methoxyethoxy)benzenesulfonamide |
cga-142464 |
CHEBI:81982 |
DTXSID5058220 |
cinosulfuron, pestanal(r), analytical standard |
n-(4,6-dimethoxy-1,3,5-triazin-2-ylcarbamoyl)-2-(2-methoxyethoxy)benzenesulfonamide |
Q2972826 |
n-[[(4,6-dimethoxy-1,3,5-triazin-2-yl)amino]carbonyl]-2-(2-methoxyethoxy)benzenesulfonamide |
A916426 |
Cinosulfuron is a sulfonylurea herbicide largely used in the extensive cultures of flooded rice in North Italy.
Excerpt | Reference | Relevance |
---|---|---|
"Cinosulfuron is a sulfonylurea herbicide largely used in the extensive cultures of flooded rice in North Italy. " | ( Cinosulfuron: chemical and biological degradability, adsorption and dissipation in flooded paddy field sediment. Baiocchi, C; Gennari, M; Nègre, M, 2005) | 3.21 |
Class | Description |
---|---|
aromatic ether | Any ether in which the oxygen is attached to at least one aryl substituent. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (80.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (21.80) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |