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| | (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 | | EINECS: | | | Product Categories: | | | Mol File: | 1864003-26-8.mol | ![(9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical) Structure](CAS/20180808/GIF/1864003-26-8.gif) |
| | (9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical) Chemical Properties |
| | (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 |
| | (9H-Fluoren-9-yl)MethOxy]Carbonyl HomoArg(Et)2-OH·HCl (symmetrical) Preparation Products And Raw materials |
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