905591-33-5

Basic information

• Product Name: tert-butyl (2E)-3-(2-{[4-(3,4-diethoxyphenyl)-4-oxobutanoyl]amino}-4-phenylquinoline-7-yl)acrylate
• Synonyms: tert-butyl (2E)-3-(2-{[4-(3,4-diethoxyphenyl)-4-oxobutanoyl]amino}-4-phenylquinoline-7-yl)acrylate
• CAS NO: 905591-33-5
• Molecular Weight: 594.708
• Mol File: 905591-33-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl (2E)-3-(2-{[4-(3,4-diethoxyphenyl)-4-oxobutanoyl]amino}-4-phenylquinoline-7-yl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2E)-3-(2-{[4-(3,4-diethoxyphenyl)-4-oxobutanoyl]amino}-4-phenylquinoline-7-yl)acrylate(905591-33-5)
• EPA Substance Registry System: tert-butyl (2E)-3-(2-{[4-(3,4-diethoxyphenyl)-4-oxobutanoyl]amino}-4-phenylquinoline-7-yl)acrylate(905591-33-5)

Safety Data

• Hazardous Substances Data: 905591-33-5(Hazardous Substances Data)

Upstream product

• 905590-60-5 N-(5-benzyl-4-phenyl-1,3-thiazol-2-yl)-4-phenyl-4-oxobutanamide 
• 905591-32-4 N-(7-bromo-4-phenylquinolin-2-yl)-4-(3,4-diethoxyphenyl)-4-oxobutanamdie 
• 14036-55-6 t-butyl vinylacetate 

Relevant articles and documents

AMIDE COMPOUND

The present invention relate to a compound represented by the formula (I) or (II) wherein ring A is an optionally substituted ring (the ring should not be pyrrolidine, piperidine and piperazine), ring B is an optionally substituted aromatic ring, ring D is an optionally substituted ring, R1 and R2 are each independently a hydrogen atom or a substituent, R3 is a hydrogen atom or a C1-6 alkyl group, or R3 is bonded to ring A to form a non-aromatic ring, ring Aa is an optionally substituted aromatic hydrocarbon, Y is CH or N, Ra1 is an optionally substituted hydrocarbon group, and Ra2 and Ra3 are each independently a hydrogen atom or a substituent, or a salt thereof. The present invention provides a compound having a DGAT inhibitory activity, which is useful for the treatment or amelioration of diseases or pathologies caused by high expression or high activation of DGAT.