CAS 161314-17-6
:Acetamide,N-hydroxy-2-[[(4-methoxyphenyl)sulfonyl](2-methylpropyl)amino]-
Description:
Acetamide, N-hydroxy-2-[[(4-methoxyphenyl)sulfonyl](2-methylpropyl)amino]- is a chemical compound characterized by its complex structure, which includes an acetamide functional group, a hydroxyl group, and a sulfonamide moiety. The presence of a methoxyphenyl group contributes to its aromatic characteristics, while the 2-methylpropyl chain enhances its hydrophobic properties. This compound is typically classified as an organic sulfonamide, which may exhibit biological activity, potentially serving as a pharmaceutical agent or a research chemical. Its molecular structure suggests it may participate in hydrogen bonding due to the hydroxyl group, influencing its solubility and reactivity. The sulfonamide group is known for its role in medicinal chemistry, often associated with antibacterial properties. Overall, the compound's unique combination of functional groups may confer specific chemical reactivity and biological interactions, making it of interest in various fields, including medicinal chemistry and drug development. However, detailed studies would be necessary to fully elucidate its properties and potential applications.
Formula:C13H20N2O5S
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Found 5 products.
N-Hydroxy-2-((N-isobutyl-4-methoxyphenyl)sulfonamido)acetamide
CAS:N-Hydroxy-2-((N-isobutyl-4-methoxyphenyl)sulfonamido)acetamidePurity:99%Molecular weight:316.38g/molMMP-3 Inhibitor II
CAS:<p>MMP-3 Inhibitor II is a compound that inhibits the activity of MMP-3, an enzyme that breaks down extracellular matrix and plays a role in the development of bowel disease. The inhibition of this enzyme has been shown to stop the progression of bowel diseases. This compound has also been studied for its ability to inhibit the growth of bacteria and fungi. MMP-3 Inhibitor II has been found to have anti-inflammatory properties and may be used with other drugs for treatment of inflammatory bowel disease.<br>MMP-3 Inhibitor II is not active against human serum, but it does inhibit the growth of other types of cells, such as cancer cells. It binds to MMPs by competitive inhibition, preventing the formation of an enzyme-inhibitor complex with enzymes involved in the breakdown of extracellular matrixes.<br>The binding site on MMPs is located near the active site where proteolytic cleavage occurs and this binding suppresses prote</p>Formula:C13H20N2O5SPurity:Min. 95%Molecular weight:316.37 g/molNNGH
CAS:NNGH is a matrix metalloproteinase 3 (MMP-3) inhibitor with anticancer activity that counteracts the inhibitory effects of E2 and DHT on RANKL membrane-binding.Formula:C13H20N2O5SPurity:98.41%Color and Shape:SolidMolecular weight:316.37





