(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical)
(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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(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical)(1864003-26-8)Related Product Information
- FMoc-D-4-Aph(tBu-CbM)-OH
- Fmoc-3-(2-Naphthyl)-D-alanine
- Fmoc-N-Me-Tyr(tBu)-OH
- FMOC-D-CIT-OH
- FMOC-D-alanine
- FMOC-D-4-Chlorophe
- FMOC-LYS(BOC)(ISOPROPYL)-OH
- Fmoc-Lys(nicotinoyl)-OH
- (R)-N-Acetyl-2-naphthylalanine
- Fmoc-D-Asn(Trt)-OH
- 4-[(AMinocarbonyl)aMino]-N-[(9H-fluoren-9-ylMethoxy)carbonyl]-D-phenylalanine
- Fmoc-D-homoArg(Et)2-OH·HCl
- Fmoc-Lys(Pal-Glu-OtBu)-OH
- (R)-N-Fmoc-(3-Pyridyl)alanine
- N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-4-[[[(4S)-hexahydro-2,6-dioxo-4-pyriMidinyl]carbonyl]aMino]-L-phenylalanine