Benzenesulfonamide
(Synonyms:苯磺酰胺;苯磺酰胺基;苯磺醯胺;苯磺酰胺(BSA);Benzenesulfonamide 苯磺酰胺;苯磺酰胺,Benzenesulfonamide;邻对甲苯磺酰胺)
目录号 : KG10530
CAS No. : 98-10-2
纯度 : 98%
Benzenesulfonamide, the amide of benzenesulfonic acid, has been used to produce various derivatives, especially those used as intermediates in the synthesis of photochemicals, dyes, disinfectants, as well as pharmaceuticals.
In vitro: In a previous study, a series of N-aryl-β-alanine- and diazo-derivatives of benzenesulfonamide were designed, synthesized, and their binding affinities to carbonic anhydrases (CA) I, II, VI, VII, XII, and XIII was investigated by the use of isothermal titration calorimetry and fluorescent thermal shift assay. The results indicated that 4-substituted diazobenzenesulfonamides were found to be most potent CA binders among the synthesized derivatives. In addition, the majority of the N-aryl-β-alanine derivatives had better affinity for CA II while diazobenzenesulfonamides showed nanomolar affinities towards CA I isozyme. Moreover, the X-ray crystallographic data showed the binding modes of both derivative groups .
In vivo: In the rat CPE model, the most potnet benzenesulfonamide indole derivative at 10 mg/kg in the MC/TW formulation displayed oral efficacy. Moreover, this compound, when administered in another preferred, minimal formulation in the same in vivo model, demonstrated superior oral efficacy to the lead phenylmethane sulfonamide WAY-196025 orally administered in a lipid-based formulation. In addition, this benzenesulfonamide indole derivative was also orally efficacious at 1 mg/kg by attenuating both LAR and the associated AHR to aerosolized carbachol in naturally sensitized sheep, which had been challenged through the airways with A. suum antigen .
Clinical trial: Up to now, benzenesulfonamide is still in the preclinical development stage.
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分子式 |
C6H7NO2S
|
分子量 |
157.19
|
CAS号 |
98-10-2
|
中文名称 |
苯磺酰胺
|
储存方式 |
Store at -20°C
|