N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide

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N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide manufacturers

  • p18SMI-21
  • p18SMI-21 pictures
  • $1520.00
  • 2026-05-11
  • CAS:20535-76-6
  • Purity:
  • Supply Ability: 10g
N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide Basic information
Product Name:N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide
Synonyms:Acetamide, N-[4-[[(2-hydroxyethyl)amino]sulfonyl]phenyl]-;p18SMI-21;p18SMI21,p-18SMI-21;N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide
CAS:20535-76-6
MF:C10H14N2O4S
MW:258.29
EINECS:
Product Categories:
Mol File:20535-76-6.mol
N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide Structure
N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide Chemical Properties
Melting point 126 °C
density 1.380±0.06 g/cm3(Predicted)
pka10.72±0.50(Predicted)
CAS DataBase Reference20535-76-6
Safety Information
MSDS Information
N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide Usage And Synthesis
Usesp18SMI-21 is a novel INK4C inhibitor that specifically blocks the biological activity of p18 protein. p18SMI-21 exerts its anti-gastric acid effect through direct contact, and the intensity of this effect varies with the dose. p18SMI-21 can significantly reduce the proteolytic activity of pepsin under certain conditions. The inhibitory effect of p18SMI-21 is best achieved in direct contact with the substrate. If it contacts the substrate first, the inhibitory effect will be lost[1].
References[1] [Biochemical studies on camomile components/III. In vitro studies about the antipeptic activity of (--)-alpha-bisabolol (author's transl)] PMID:21
N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide Preparation Products And Raw materials
Tag:N-(4-[[(2-Hydroxyethyl)amino]sulfonyl]phenyl)acetamide(20535-76-6) Related Product Information
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