108146
苯磺酰胺
≥98%
别名:
Phenylsulfonamide
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关于此项目
线性分子式:
C6H5SO2NH2
化学文摘社编号:
分子量:
157.19
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39093209
UNSPSC Code:
12352100
EC Number:
202-637-1
MDL number:
Beilstein/REAXYS Number:
1100566
Assay:
≥98%
Form:
solid
Application
苯磺酰胺被用于开发同时测定环境水中苯并三唑、苯并噻唑和苯磺酰胺污染物的分析方法 。
Biochem/physiol Actions
苯磺酰胺是人碳酸酐酶 B 的抑制剂 。苯磺酰胺衍生物对治疗癌症等增殖性疾病有效 。用于合成染料、光化学物和消毒剂 。
Preparation Note
苯磺酰胺溶于甲醇，浓度为 25 mg/mL，形成澄清、无色溶液。
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Asha Chandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 92, 84-90 (2012-03-27)
The FT-IR and FT-Raman spectra of (E)-N-carbamimidoyl-4-((4-methoxybenzylidene)amino)benzenesulfonamide were recorded and analyzed. Geometry and harmonic vibrational wavenumbers were calculated theoretically using Gaussian 03 set of quantum chemistry codes. Calculations were performed at the Hartree-Fock (HF) and density functional theory (DFT) levels
Astrid Goubet et al.
Bioorganic & medicinal chemistry letters, 23(3), 761-763 (2012-12-26)
C5-Ethynylbenzenesulfonamide-modified nucleotide (EBNA) was investigated as substrate of various DNA polymerases. The experiments revealed that KOD, Phusion and Klenow DNA polymerases successfully accepted EBNA-T nucleotide as a substrate and yielded the fully extended DNA. KOD DNA polymerase was found to
Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases.
Edita Čapkauskaitė et al.
European journal of medicinal chemistry, 51, 259-270 (2012-03-24)
A series of [(2-pyrimidinylthio)acetyl]benzenesulfonamides were designed and synthesized. Their binding affinities as inhibitors of several recombinant human carbonic anhydrase (CA) isozymes were determined by isothermal titration calorimetry (ITC) and thermal shift assay (TSA). A group of compounds containing a chlorine
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 108146-100G | 04061838679284 |
| 108146-500G | 04061838679291 |
| 108146-5G | 04061838679307 |