The chemical substance known as 2-(1H-indol-3-yl)-N-{2-[(4-methoxyphenyl)amino]-1-(4-methylphenyl)-2-oxoethyl}-N-methylacetamide, with the CAS number 871700-29-7, is a synthetic compound characterized by its complex molecular structure, which includes an indole moiety and an acetamide functional group. This compound features multiple aromatic rings, contributing to its potential biological activity and interactions. The presence of methoxy and methyl substituents on the phenyl rings may influence its solubility, stability, and reactivity. Typically, compounds of this nature are investigated for their pharmacological properties, including potential anti-cancer or anti-inflammatory effects, due to the indole structure's known biological significance. The specific arrangement of functional groups suggests that it may engage in hydrogen bonding and π-π stacking interactions, which are critical for its biological activity. As with many synthetic organic compounds, understanding its characteristics requires consideration of its physical properties, such as melting point, solubility, and spectral data, which are essential for applications in medicinal chemistry and drug development.

2-(1H-indol-3-yl)-N-{2-[(4-methoxyphenyl)amino]-1-(4-methylphenyl)-2-oxoethyl}-N-methylacetamide

871700-29-7: The chemical substance known as 2-(1H-indol-3-yl)-N-{2-[(4-methoxyphenyl)amino]-1-(4-methylphenyl)-2-oxoethyl}-N-methylacetamide, with the CAS number 871700-29-7, is a synthetic compound characterized by its complex molecular structure, which includes an indole moiety and an acetamide functional group. This compound features multiple aromatic rings, contributing to its potential biological activity and interactions. The presence of methoxy and methyl substituents on the phenyl rings may influence its solubility, stability, and reactivity. Typically, compounds of this nature are investigated for their pharmacological properties, including potential anti-cancer or anti-inflammatory effects, due to the indole structure's known biological significance. The specific arrangement of functional groups suggests that it may engage in hydrogen bonding and π-π stacking interactions, which are critical for its biological activity. As with many synthetic organic compounds, understanding its characteristics requires consideration of its physical properties, such as melting point, solubility, and spectral data, which are essential for applications in medicinal chemistry and drug development.

CFTR activator 2

CFTR activator 2 (WAY-326769) is an activator of mutant CFTR (cystic fibrosis transmembrane conductance regulator), which increases ion transport activity and can be used for research into cystic fibrosis (CF).

CAS 871700-29-7

2-(1H-indol-3-yl)-N-{2-[(4-methoxyphenyl)amino]-1-(4-methylphenyl)-2-oxoethyl}-N-methylacetamide

CFTR activator 2

Ref: 54-BUP22430

CFTR activator 2

Ref: TM-T203322