692778-52-2

Basic information

• Product Name: N-Cbz-belactosin A
• Synonyms: N-Cbz-belactosin A
• CAS NO: 692778-52-2
• Molecular Weight: 503.552
• Mol File: 692778-52-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-Cbz-belactosin A(CAS DataBase Reference)
• NIST Chemistry Reference: N-Cbz-belactosin A(692778-52-2)
• EPA Substance Registry System: N-Cbz-belactosin A(692778-52-2)

Safety Data

• Hazardous Substances Data: 692778-52-2(Hazardous Substances Data)

Upstream product

• 1013331-16-2 (1R,2S)-1-[(2S)-(N-Cbz-L-alanylamino)-3-butenyl]-2-{[(2R,3S)-3-((2S)-2-methylpropyl)-4-oxooxetan-2-yl]carbonylamino}cyclopopane 
• 73-32-5 L-isoleucine 
• 28977-69-7 (S)-3-methylpentanoic acid chloride 
• 1730-92-3 (3S)-methylvaleric acid 
• 692778-40-8 (3S,4R)-3-((S)-sec-butyl)-4-oxooxetane-2-carboxylic acid 
• 228267-64-9 (4R,3'S)-3-(3'-methyl-1'-oxopentyl)-4-benzyl-2-oxazolidinone 
• 692778-49-7 (3R,4S)-3-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-4-methyl-hexanoic acid tert-butyl ester 
• 692778-50-0 2-sec-butyl-succinic acid 4-tert-butyl ester 
• 692778-51-1 3-sec-butyl-4-oxo-oxetane-2-carboxylic acid tert-butyl ester 

Relevant articles and documents

Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: Development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy

The development of potent proteasome inhibitors based on the stereochemical diversity-oriented strategy using a conformationally rigid cyclopropane structure was investigated. Thus, a series of stereo- and regioisomeric analogs of belactosin A (2), a cycl

Total synthesis of (+)-belactosin A.

A concise first total synthesis of the antitumour antibiotic belactosin A is reported, involving coupling of beta-lactone carboxylic acid 3 with N-Ala-aminocyclopropyl alanine 11.