| Name | acetolactate synthase |
|---|---|
| Synonyms | Acetolactate synthase; OR10B1P |
| Name | chlorimuron |
|---|---|
| CAS | 2-[[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoic acid |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 11374163 | Burgos NR, Kuk YI, Talbert RE: Amaranthus palmeri resistance and differential tolerance of Amaranthus palmeri and Amaranthus hybridus to ALS-inhibitor herbicides. Pest Manag Sci. 2001 May;57(5):449-57. Suspected imazaquin-resistant accessions of Amaranthus palmeri were studied to determine the magnitude of resistance and cross-resistance to acetolactate synthase (ALS)-inhibiting herbicides and compare differential tolerance of A palmeri and Amaranthus hybridus to ALS inhibitors. The most imazaquin-resistant accession, accession 7, also showed 74, 39 and 117 times higher resistance than the susceptible biotype to chlorimuron, diclosulam and pyrithiobac, respectively. |
1(0,0,0,1) | Details |
| 15920784 | Zawoznik MS, Tomaro ML: Effect of chlorimuron-ethyl on Bradyrhizobium japonicum and its symbiosis with soybean. Pest Manag Sci. 2005 Oct;61(10):1003-8. Possible side-effects of the acetolactate synthase (ALS)-inhibiting herbicide chlorimuron-ethyl on Bradyrhizobium japonicum (Kirchner & Jordan) in pure culture and on inoculated soybean plants growing under controlled conditions were investigated. |
81(1,1,1,1) | Details |
| 12723887 | Miller RP, Martinson KB, Sothern RB, Durgan BR, Gunsolus JL: Circadian response of annual weeds in a natural setting to high and low application rates of four herbicides with different modes of actions. Chronobiol Int. 2003 Mar;20(2):299-324. Four herbicides (GLYT), an amino acid synthesis inhibitor; glufosinate (GLUF), a glutamine synthetase inhibitor; fomesafen (FOME), a protoporphyrinogen oxidase inhibitor, and chlorimuron ethyl (CLIM), an acetolactate synthase inhibitor] were used to examine the influence of time of day of application on the control of a variety of annual broadleaf weeds in field studies conducted in Minnesota (five studies on GLYT and GLUF, three studies on FOME and CLIM). |
31(0,1,1,1) | Details |
| 12127485 | Chung KR, Shilts T, Li W, Timmer LW: Engineering a genetic transformation system for Colletotrichum acutatum, the causal fungus of lime anthracnose and postbloom fruit drop of citrus. FEMS Microbiol Lett. 2002 Jul 16;213(1):33-9. A genetic transformation system was developed for C. acutatum to confer resistance to sulfonylurea (chlorimuron ethyl) by expressing an acetolactate synthase gene (sur) cassette from Magnaporthe grisea. |
6(0,0,1,1) | Details |
| 12231935 | Schmitzer PR, Eilers RJ, Cseke C: Lack of Cross-Resistance of Imazaquin-Resistant strumarium Acetolactate Synthase to Flumetsulam and Chlorimuron. Plant Physiol. 1993 Sep;103(1):281-283. |
7(0,0,1,2) | Details |
| 18029803 | McNaughton J, Roberts M, Smith B, Rice D, Hinds M, Schmidt J, Locke M, Brink K, Bryant A, Rood T, Layton R, Lamb I, Delaney B: Comparison of broiler performance when fed diets containing event DP-356O43-5 (Optimum GAT), nontransgenic near-isoline control, or commercial reference soybean meal, hulls, and oil. Poult Sci. 2007 Dec;86(12):2569-81. The expression products of these genes are the acetyltransferase 4601 and acetolactate synthase proteins, respectively. Diets were prepared using processed fractions (meal, hulls, and oil) from untreated 356043 soybean plants or from soybean plants treated with a mixture of chlorimuron, and thifensulfuron (356043 + Gly/SU). |
2(0,0,0,2) | Details |
| 12496246 | Pang SS, Guddat LW, Duggleby RG: Molecular basis of sulfonylurea herbicide inhibition of acetohydroxyacid synthase. J Biol Chem. 2003 Feb 28;278(9):7639-44. Epub 2002 Dec 20. Acetohydroxyacid synthase (AHAS) (acetolactate synthase, EC ) catalyzes the first step in branched-chain amino acid biosynthesis and is the target for sulfonylurea and imidazolinone herbicides. Here we report the 2.8 A resolution crystal structure of yeast AHAS in complex with a sulfonylurea herbicide, chlorimuron ethyl. |
1(0,0,0,1) | Details |