205812-42-6

Basic information

• Product Name: (S)-4-[(S)-3-Benzyloxycarbonyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester
• Synonyms: (S)-4-[(S)-3-Benzyloxycarbonyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester
• CAS NO: 205812-42-6
• Molecular Weight: 607.701
• Mol File: 205812-42-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-4-[(S)-3-Benzyloxycarbonyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-[(S)-3-Benzyloxycarbonyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester(205812-42-6)
• EPA Substance Registry System: (S)-4-[(S)-3-Benzyloxycarbonyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester(205812-42-6)

Safety Data

• Hazardous Substances Data: 205812-42-6(Hazardous Substances Data)

Upstream product

• 24277-39-2 N-tert-butoxycarbonyl glutamic acid tert-butyl ester 
• 89092-94-4 (S)-4-Amino-4-(ethoxycarbonylmethyl-carbamoyl)-butyric acid benzyl ester 
• 13574-13-5 Boc-Glu(OBzl)-OH 
• 72917-81-8 N-α-tert-butoxycarbonyl-γ-benzyl ester L-glutamylglycine ethyl ester 

Downstream Products

• 205812-45-9 (S)-4-[(S)-3-(Benzyloxy-methyl-carbamoyl)-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester 
• 205812-44-8 (S)-4-[(S)-3-Benzyloxycarbamoyl-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-2-tert-butoxycarbonylamino-butyric acid tert-butyl ester 
• 205812-43-7 (S)-2-tert-Butoxycarbonylamino-4-[(S)-3-carboxy-1-(ethoxycarbonylmethyl-carbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester 

Relevant articles and documents

Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I

Hydroxamate-containing tripeptide analogs resembling a reactive intermediate in glyoxalase I catalysis were prepared by solution methods and were found to be competitive inhibitors of the enzyme from Saccharomyces cerevisiae. Electronic properties of the hydroxamate functionality as well as those of the expected intermediates in the enzyme-catalyzed reaction were compared.