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一般描述
磺酰胺,一种与格氏试剂相容的极性非质子溶剂,可用作医学化学中的官能团。
应用
磺胺被用于合成以下物质:
- ArCH=NSO2NH2型席夫碱
- 1H,3H-2,1,3-苯并噻二嗪-4-酮-2,2-二氧化物(BTDD)
- 在一项PPARα激活的研究中,合成油酰乙醇胺类似物的磺酰胺类似物。
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Anomeric effects in sulfamides
The Journal of Physical Chemistry A, 120, 3677-3682 (2016)
Sulfamides and sulfonamides as polar aprotic solvents
The Journal of Organic Chemistry, 52, 479-483 (1987)
Bioorganic & medicinal chemistry letters, 19(3), 650-653 (2009-01-06)
The inhibition of a coral carbonic anhydrase (CA, EC 4.2.1.1) has been investigated with a series of inorganic anions such as halogenides, pseudohalogenides, bicarbonate, carbonate, nitrate, nitrite, hydrogen sulfide, bisulfite, perchlorate, sulfate. The full-length scleractinian coral Stylophora pistillata CA, STPCA
Bioorganic & medicinal chemistry letters, 15(9), 2353-2358 (2005-04-20)
A small library of N-hydroxysulfamides was synthesized by an original approach in order to investigate whether this zinc-binding function is efficient for the design of inhibitors targeting the cytosolic (hCA I and II) and transmembrane, tumor-associated (hCA IX and XII)
Journal of enzyme inhibition, 15(5), 443-453 (2000-10-13)
Sulfamide and sulfamic acid are the simplest compounds containing the SO2NH2 moiety, responsible for binding to the Zn(II) ion within carbonic anhydrase (CA, EC 4.2.1.1) active site, and thus acting as inhibitors of the many CA isozymes presently known. Here
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