470473-93-9

Basic information

• Product Name: 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid
• Synonyms: 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid
• CAS NO: 470473-93-9
• Molecular Weight: 558.761
• Mol File: 470473-93-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid(470473-93-9)
• EPA Substance Registry System: 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid(470473-93-9)

Safety Data

• Hazardous Substances Data: 470473-93-9(Hazardous Substances Data)

Upstream product

• 470473-91-7 8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoic acid 
• 470473-90-6 8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoic acid methyl ester 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 77420-98-5 methyl 8-aminooctanoate hydrochloride 
• 17994-94-4 methyl 7-aminoheptanoate hydrochloride 
• 470473-92-8 7-(8-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-octanoylamino)-heptanoic acid methyl ester 

Relevant articles and documents

Cyclic PNA hexamer-based compound: Modelling, synthesis and inhibition of the HIV-1 RNA dimerization process

A cyclic molecule constituted by (i) a hexameric PNA moiety complementary to six among the nine residues of the dimerization initiation site loop of HIV-1 and (ii) a spacer tethering the N- to the C-extremities of the PNA, has been elaborated to inhibit the dimerization process of HIV-1 genome. This compound has been synthesized following a liquid-phase procedure (fully protected backbone approach). Preliminary agarose gel electrophoresis analyses have shown that the cyclic PNA conjugate is able to inhibit the HIV-1 dimerization.