Mechanism and pattern of resistance to some ACCase inhibitors in winter wild oat (Avena sterilis subsp. ludoviciana (Durieu) Gillet & Magne) biotypes collected within canola fields was written by Hassanpour-bourkheili, Saeid;Gherekhloo, Javid;Kamkar, Behnam;Ramezanpour, S. Sanaz. And the article was included in Crop Protection in 2021.Quality Control of 1H-Benzo[d][1,2,3]triazol-1-amine This article mentions the following:
Due to the reports regarding unsuccessful control of Avena sterilis subsp. ludoviciana (Durieu) Gillet & Magne by haloxyfop-R-Me in canola fields, the following study was conducted to investigate the resistance of this weed to haloxyfop-R-Me. These biotypes were then subjected to various rates of clodinafop propargyl, sethoxydim, pinoxaden and mesosulfuron Me + iodosulfuron-Me herbicides and their and cross-resistance to clodinafop propargyl and sethoxydim was confirmed. However, no resistance was observed to pinoxaden and mesosulfuron-Me + iodosulfuron-Me herbicides. Indirect study of metabolism by P 450 using 1- aminobenzotriazole and piperonyl butoxide showed that this enzyme had no contribution to occurrence of resistance in the studied biotypes. Allele-specific PCR results indicated that Ile-2041-Asn mutation is responsible for resistance of A. sterilis subsp. ludoviciana biotypes, which was confirmed by sequencing of the samples. Since pinoxaden neg. affects canola, the growers face a serious limitation in their choice for chem. management and thus, implementation of integrated weed management such as introduction of row crops such as faba bean in crop rotation and increasing the diversity of herbicide mode of action by cultivation of crops such as sugar beet in crop rotation may prove helpful. This was the first case of A. sterilis subsp. ludoviciana resistance to ACCase inhibitors in canola fields. In the experiment, the researchers used many compounds, for example, 1H-Benzo[d][1,2,3]triazol-1-amine (cas: 1614-12-6Quality Control of 1H-Benzo[d][1,2,3]triazol-1-amine).
1H-Benzo[d][1,2,3]triazol-1-amine (cas: 1614-12-6) belongs to triazole derivatives. Triazoles are important five-member nitrogen heterocycles involved in a wide range of industrial applications such as agrochemicals, corrosion inhibitors, dyes, optical brighteners, as well as biologically active agents. Due to the structural characteristics, both 1,2,3- and 1,2,4-triazoles are able to accommodate a broad range of substituents (electrophiles and nucleophiles) around the core structures and pave the way for the construction of diverse novel bioactive molecules.Quality Control of 1H-Benzo[d][1,2,3]triazol-1-amine
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics