CAS 1446350-60-2

1H-Imidazole-4-carboxylic acid, 4,5-dihydro-2-(4-methoxyphenyl)-4-phenyl-1-(phenylmethyl)-5-[4-[(phenylmethyl)amino]phenyl]-, ethyl ester, (4R,5R)-rel-

Description:

1H-Imidazole-4-carboxylic acid, 4,5-dihydro-2-(4-methoxyphenyl)-4-phenyl-1-(phenylmethyl)-5-[4-[(phenylmethyl)amino]phenyl]-, ethyl ester, (4R,5R)-rel- is a complex organic compound characterized by its imidazole ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms. This substance features multiple aromatic rings, including a methoxy-substituted phenyl group and a phenylmethyl group, contributing to its potential for various interactions in biological systems. The presence of the ethyl ester functional group suggests it may exhibit moderate lipophilicity, influencing its solubility and permeability. The stereochemistry indicated by the (4R,5R)- designation implies specific spatial arrangements of atoms, which can significantly affect the compound's biological activity and interactions. Overall, this compound's intricate structure may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. However, detailed studies would be necessary to elucidate its specific properties and potential applications.

Formula: C₃₉H₃₇N₃O₃

Synonyms:

• 1H-Imidazole-4-carboxylic acid, 4,5-dihydro-2-(4-methoxyphenyl)-4-phenyl-1-(phenylmethyl)-5-[4-[(phenylmethyl)amino]phenyl]-, ethyl ester, (4R,5R)-rel-

TCH-165

CAS: 1446350-60-2

Formula: C₃₉H₃₇N₃O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 595.7294

Ref: IN-DA01V2PW

TCH-165

CAS: 1446350-60-2

TCH-165

Formula: C₃₉H₃₇N₃O₃

Purity: ≥98%

Molecular weight: 595.73

Ref: 54-BUP12824

TCH-165

CAS: 1446350-60-2

TCH-165 boosts 20S proteasome levels, enhancing IDP breakdown.

Formula: C₃₉H₃₇N₃O₃

Purity: 98.2% - 99.97%

Color and Shape: White Solid

Molecular weight: 595.73

Ref: TM-T17011

TCH-165

CAS: 1446350-60-2

TCH-165 is a synthetic compound, which is derived from specialized chemical synthesis processes with precision-targeted interactions in biochemical systems. This compound operates primarily through its capacity to modulate specific signaling pathways, affecting cellular responses at the molecular level. It is engineered to interact selectively with key proteins, altering their activity and thereby influencing downstream biological effects.

Formula: C₃₉H₃₇N₃O₃

Purity: Min. 95%

Molecular weight: 595.7 g/mol

Ref: 3D-WHC35060