Basic information Safety Supplier Related

(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical)

Basic information Safety Supplier Related

(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical) Basic information

Product Name:
(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical)
Synonyms:
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical)
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl
  • (2S)-6-[(E)-N',N''-diethylcarbamimidamido]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid hydrochloride
  • Fmoc-L-Homo-Arg(Et)2-OH.HCl
  • Fmoc-L-hArg(Et)2-OH HCl
  • (S,E)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(2,3-diethylguanidino)hexanoic acid hydrochloride
  • (E)-N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N6-(N,N'-diethylcarbamimidoyl)-L-lysine hydrochloride
  • Fmoc-L-HomoArg(Et),-OH·HCl
CAS:
1864003-26-8
MF:
C26H35ClN4O4
MW:
503.04
Mol File:
1864003-26-8.mol
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(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical) Usage And Synthesis

Uses

Fmoc-L-Homoarg(Et)2-OH hydrochloride is a derivative of amino acid with protecting groups. Fmoc-L-Dap(Boc,Me)-OH can be used for synthesis of homoarginine containing peptide[1].

References

[1] Clemente C, et al., Biochemical characterization of a cyanobactin arginine-N-prenylase from the autumnalamide biosynthetic pathway. Chem Commun (Camb). 2022 Oct 27;58(86):12054-12057. DOI:10.1039/d2cc01799g

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