785043-78-9

Basic information

• Product Name: (R)-2-Amino-3-[(R)-2-amino-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester
• Synonyms: (R)-2-Amino-3-[(R)-2-amino-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester
• CAS NO: 785043-78-9
• Molecular Weight: 688.822
• Mol File: 785043-78-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-Amino-3-[(R)-2-amino-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-Amino-3-[(R)-2-amino-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester(785043-78-9)
• EPA Substance Registry System: (R)-2-Amino-3-[(R)-2-amino-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester(785043-78-9)

Safety Data

• Hazardous Substances Data: 785043-78-9(Hazardous Substances Data)

Upstream product

• 10389-65-8 di-t-butoxycarbonyl-L-cystine 
• 192999-56-7 4-(hydroxymethyl)phenyl 2-phenylacetate 

Downstream Products

• 330970-71-3 (R)-2-((2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoylamino)-3-[(R)-2-((2S,3S)-2-tert-butoxycarbonylamino-3-methyl-pentanoylamino)-2-(4-phenylacetoxy-benzyloxycarbonyl)-ethyldisulfanyl]-propionic acid 4-phenylacetoxy-benzyl ester 
• 330970-76-8 (R)-2-[(2S,3S)-2-((2S,3R)-2-tert-Butoxycarbonylamino-3-hydroxy-butyrylamino)-3-methyl-pentanoylamino]-3-hexadecanoylsulfanyl-propionic acid 4-phenylacetoxy-benzyl ester 
• 330970-73-5 (R)-2-((2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoylamino)-3-hexadecanoylsulfanyl-propionic acid 4-phenylacetoxy-benzyl ester 

Relevant articles and documents

Synthesis and membrane-binding properties of a characteristic lipopeptide from the membrane-anchoring domain of influenza virus A hemagglutinin

On the trail of the influenza virus! Fluorescent-labeled lipopeptides, such as the characteristic S-palmitoylated partial structure from influenza virus hemagglutinin A (see picture), can be synthesized efficiently by employing a new enzymatic protecting-group technique in the key steps. Their binding to model membranes was determined in a kinetic assay, so leading to a first approximation of the membrane-anchoring ability of the corresponding lipopeptide motif in the parent protein.