1354899-39-0

Basic information

• Product Name: (R)-2-benzyl-3-(formyl-hydroxy-amino)-N-[(S)-1-methylcarbamoyl-2-phenyl-ethyl]-propionamide
• CAS NO: 1354899-39-0
• Molecular Weight: 383.447
• Mol File: 1354899-39-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-benzyl-3-(formyl-hydroxy-amino)-N-[(S)-1-methylcarbamoyl-2-phenyl-ethyl]-propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-benzyl-3-(formyl-hydroxy-amino)-N-[(S)-1-methylcarbamoyl-2-phenyl-ethyl]-propionamide(1354899-39-0)
• EPA Substance Registry System: (R)-2-benzyl-3-(formyl-hydroxy-amino)-N-[(S)-1-methylcarbamoyl-2-phenyl-ethyl]-propionamide(1354899-39-0)

Safety Data

• Hazardous Substances Data: 1354899-39-0(Hazardous Substances Data)

Upstream product

• 709673-94-9 (R)-2-benzyl-3-hydroxypropanoic acid methyl ester 
• 220805-30-1 (S)-4-Benzyl-3-((R)-2-benzyloxymethyl-3-phenyl-propionyl)-oxazolidin-2-one 
• 218285-61-1 (R)-N-Benzyloxy-2-hydroxymethyl-3-phenyl-propionamide 
• 218285-65-5 (3R)-N-benzyloxy-3-benzyl-2-azetidinone 
• 197902-88-8 (R)-2-(Benzyloxyamino-methyl)-3-phenyl-propionic acid 
• 123803-51-0 2R-benzyl-3-benzyloxypropanoic acid 
• 123802-80-2 (R)-2-hydroxymethyl-3-phenylpropionic acid 
• 64-18-6 formic acid 

Relevant articles and documents

Inhibition of invasion and capillary-like tube formation by retrohydroxamate-based MMP inhibitors

Matrix metalloproteinases (MMPs), a family of zinc-containing endopeptidases, participate in many normal processes such as embryonic development and wound repair, and in many pathological situations such as cancer, atherosclerosis, and arthritis. Peptidomimetic MMP inhibitors were designed and synthesized with Nformylhydroxylamine (retrohydroxamate) as a zinc-binding group and various side chains on the α, P1′, and P2′ positions. Using in vitro MMP assays with purified MMPs (MMP-1, MMP-2, MMP-3, MMP-9, and MMP-14) and fluorogenic peptide substrates, it was found that compounds 2d and 2g selectively inhibit gelatinases (MMP-2 and MMP-9) and interstitial collagenase (MMP-1). They also inhibited the chemo-invasion of fibrosarcoma HT-1080 cells and tube formation of human umbilical vascular endothelial cells in a dosedependent manner. Our results suggest that retrohydroxamate-based MMP inhibitors, especially compounds 2d and 2g, have the potential to be used as therapeutic drugs for cancer and other MMP-related diseases.