CAS 139298-40-1: N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide

Description: N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide, with CAS number 139298-40-1, is a synthetic organic compound that belongs to the class of sulfonamides. This compound features a complex structure characterized by multiple functional groups, including a sulfonamide moiety, an ether group, and an alkenyl side chain. It is known for its potential biological activity, particularly in medicinal chemistry, where it may exhibit properties such as anti-inflammatory or antimicrobial effects. The presence of the 4-chlorophenyl group suggests that it may interact with biological targets through hydrophobic interactions. Additionally, the hydroxyl and methoxy groups can influence its solubility and reactivity. The compound's intricate structure may also contribute to its pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion. Overall, this substance represents a significant interest in drug development and research due to its unique chemical characteristics and potential therapeutic applications.

Formula: C₂₆H₂₉ClN₂O₄S

InChI: InChI=1S/C26H29ClN2O4S/c1-28(17-5-6-21-9-11-23(27)12-10-21)20-22-7-3-4-8-26(22)29(18-19-30)34(31,32)25-15-13-24(33-2)14-16-25/h3-16,30H,17-20H2,1-2H3

InChI key: InChIKey=LLLQTDSSHZREGW-UHFFFAOYSA-N

SMILES: O=S(=O)(C1=CC=C(OC)C=C1)N(C=2C=CC=CC2CN(C)CC=CC3=CC=C(Cl)C=C3)CCO

Synonyms:

• 2-[N-(2-Hydroxyethyl)-N-(4-Methoxybenzenesulfonyl)]Amino-N-(4-Chlorocinnamyl)-N-Methylbenzylamine
• Benzenesulfonamide, N-[2-[[[3-(4-chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxy-
• Benzenesulfonamide, N-[2-[[[3-(4-chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxy-
• Kn-93, Water-Soluble
• Methoxybenzene-Sulfonamide
• N-[2-({[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl](methyl)amino}methyl)phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
• N-[2-N-4-Chlorocinnamyl-N-Methylaminomethylphenyl]-N-[2-Hydroxyethyl]-4-Methoxybenzenesulfonamide
• N-[2-[[[3-(4'-Chlorophenyl)-2-Propenyl]Methylamino]Methyl]Phenyl]-N-(2-Hydroxyethyl)-4'-Methoxy-Benzenesulfonamide Phosphate
• N-[2-[[[3-(4-Chlorophenyl)-2-Propenyl]Methylamino]Methyl]Phenyl]-N-(2-Hydroxyethyl)-4-Methoxybenzenesulphonamide
• N-[2-[[[3-(4-Chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
• N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
• KN 93

KN-93

CAS: 139298-40-1

• Formula: C₂₆H₂₉ClN₂O₄S
• Purity: >98.0%(HPLC)
• Color and Shape: White to Light yellow powder to crystal
• Molecular weight: 501.04

Benzenesulfonamide, N-[2-[[[3-(4-chlorophenyl)-2-propen-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxy-

CAS: 139298-40-1

• Formula: C₂₆H₂₉ClN₂O₄S
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 501.0375

KN-93

CAS: 139298-40-1

• Purity: ≥98%
• Molecular weight: 501.04g/mol

KN-93

CAS: 139298-40-1

KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), competitively blocking CaM binding to …

• Formula: C₂₆H₂₉ClN₂O₄S
• Purity: 99.78% - 99.86%
• Color and Shape: White Solid
• Molecular weight: 501.04

KN-93

CAS: 139298-40-1

• Formula: C₂₆H₂₉ClN₂O₄S·H₃PO₄
• Purity: ≥ 98.0%
• Color and Shape: White to off-white solid
• Molecular weight: 599.03

KN 93

CAS: 139298-40-1

Inhibitor of calcium/calmodulin-dependent protein kinase 2

• Formula: C₂₆H₂₉ClN₂O₄S
• Purity: Min. 95%
• Molecular weight: 501.04 g/mol