149648-49-7

Basic information

• Product Name: methyl N-benzyloxysuberoylamide
• Synonyms: methyl N-benzyloxysuberoylamide
• CAS NO: 149648-49-7
• Molecular Weight: 293.363
• Mol File: 149648-49-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl N-benzyloxysuberoylamide(CAS DataBase Reference)
• NIST Chemistry Reference: methyl N-benzyloxysuberoylamide(149648-49-7)
• EPA Substance Registry System: methyl N-benzyloxysuberoylamide(149648-49-7)

Safety Data

• Hazardous Substances Data: 149648-49-7(Hazardous Substances Data)

Upstream product

• 41624-92-4 methyl 8-chloro-8-oxooctanoate 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 3946-32-5 suberic acid monomethyl ester 

Downstream Products

• 251304-82-2 N-benzyloxy-N'-[1(S)-methoxycarbonyl-2-phenylethyl]suberoylbisamide 
• 449729-01-5 (S)-octanedioic acid benzyloxy-amide (2-naphthalen-1-yl-1-phenethylcarbamoyl-ethyl)amide 
• 449728-89-6 (S)-octanedioic acid benzyloxy-amide [2-phenyl-1-(3-phenyl-propylcarbamoyl)ethyl]amide 
• 449728-87-4 (S)-octanedioic acid benzyloxy-amide (1-phenethylcarbamoyl-2-phenyl-ethyl)amide 
• 449728-88-5 (R)-octanedioic acid benzyloxy-amide (1-phenethylcarbamoyl-2-phenyl-ethyl)amide 
• 449728-95-4 (S)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-biphenyl-4-yl-propionic acid methyl ester 
• 449728-85-2 (S)-octanedioic acid benzyloxyamide (2-phenyl-1-phenylcarbamoyl-ethyl)amide 
• 449728-98-7 (S)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-naphthalen-2-yl-propionic acid methyl ester 
• 449728-97-6 (S)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-naphthalen-1-yl-propionic acid methyl ester 
• 449728-92-1 (R)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-phenylpropionic acid 
• 449728-84-1 (S)-octanedioic acid benzyloxy-amide (1-carbamoyl-2-phenyl-ethyl)amide 
• 449728-91-0 (R)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-phenylpropionic acid methyl ester 
• 449728-96-5 (S)-2-(7-benzyloxycarbamoyl-heptanoylamino)-3-methyl-butyric acid methyl ester 

Relevant articles and documents

Inhibitors of histone deacetylase suppress the growth of MCF-7 breast cancer cells

Inhibitors of histone deacetylase are attracting increasing interest due to their influence on transcription, differentiation, and apoptosis. We have investigated two synthetic inhibitors 3 and 4 of histone deacetylase and the natural product inhibitor tr

HISTONE DEACETYLASE INHIBITORS

In recognition of the need to develop novel therapeutic agents, the present invention provides novel histone deacetylase inhibitors. These compounds include an ester bond making them sensitive to deactivation by esterases. Therefore, these compounds are p