100124-40-1Relevant articles and documents
Application of sulfonamide compounds in reinforcement of plant stress resistance and pesticide containing sulfonamide-class compound
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Paragraph 0139; 0140, (2018/03/13)
The invention relates to the field of pesticides, and discloses an application of sulfonamide compounds in reinforcement of plant stress resistance and a pesticide containing the sulfamide compounds. The sulfamide compounds have structures shown in a formula (1); and the active ingredient of the pesticide for reinforcing the plant stress resistance provided in the invention is at least one sulfonamide compound shown in the formula (1), and the active ingredient content is 0.1-100wt% calculated by the total weight of the pesticide. The sulfonamide compounds provided in the invention can remarkably reinforce plant tolerance to common abiotic stresses (coldness, drought, high temperature, osmotic pressure and the like) in environments.
Electron-withdrawing substituted benzenesulfonamides against the predominant community-associated methicillin-resistant Staphylococcus aureus strain USA300
Phetsang, Wanida,Chaturongakul, Soraya,Jiarpinitnun, Chutima
, p. 461 - 471 (2013/07/26)
A small focused chemical library constituted of sulfonamides was synthesized. These compounds were designed to lack the p-aminobenzene moiety typically found in sulfonamide antibiotics. Antimicrobial activities of these synthetic compounds were investigated against global predominant methicillin-resistant Staphylococcus aureus (MRSA) strain USA300 (SF8300) and control strains of Staphylococcus aureus (S. aureus) ATCC 25923 and ATCC 29213 using disk diffusion and microdilution assays. Based on susceptibility results, potent S. aureus and MRSA USA300 growth inhibitors such as N-[3,5- bis(trifluoromethyl)phenyl]-4-bromobenzenesulfonamide with minimum inhibitory concentration (MIC) as low as 5.6 μg/cm3 along with other effective sulfonamides were discovered. Structure-activity correlations revealed that these desamino-benzenesulfonamides required electron-withdrawing substituents to be effective inhibitors of bacterial pathogen growth. In addition, their ability to inhibit growth of S. aureus strains was retained even when bacterial folate synthetic intermediate, p-aminobenzoic acid (PABA), was supplemented, whereas PABA supplementation completely diminished the antibacterial activity of the known sulfa drug tested, sulfamethoxazole. The sulfa-resistant MRSA strain COL also showed great susceptibility to these desamino-benzenesulfonamides. These results imply a unique mechanism of growth inhibition by these potent desamino-benzenesulfonamides, different from the well-known folate pathway target of sulfonamide antibiotics.
Effect of para substitution on dissociation of N-phenylbenzenesulfonamides
Mansfeld, Martin,Parik, Patrik,Ludwig, Miroslav
, p. 1479 - 1490 (2007/10/03)
The reaction of substituted anilines and benzenesulfonyl chlorides has been used to prepare 49 substituted N-phenylbenzenesulfonamides of general formula 4-X-C6H4SO2NHC6H4-Y- 4′. Their purity was checked by elemental analysis. The substituents X and Y include H, CH3, CH3O, Cl, Br, CN, and NO2. The dissociation constants of all compounds were determined by potentiometric titration in methanol, acetonitrile, N,N-dimethylformamide, and pyridine. The obtained dissociation constants, pKHA, were correlated with various sets of substituent constants. It was found that the effects of substituents X and Y on the dissociation are best described by using the Hammett equation with σp constants and the Yukawa-Tsuno equation with σp- and σp constants, respectively. This result confirms the direct conjugation of Y substituent with the reaction centre. The explained variability using the additive model was above 96% in all the solvents used. The data also provided information about the transmission effect of the SO2 group. The average dissociation constants were further processed by the latent variables methods, principal components and conjugated deviations analyses.
