- Description
-
Details
Nα-Fmoc-Nε-Boc-D-lysine - Additional Information
-
Additional Information
Catalog Number 42010 CAS 92122-45-7 M.W. 468.54 Formula C26H32N2O6 IUPAC Name 2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid Synonym Nα-Fmoc-Nε-Boc-D-lysine Also Known As - 2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
- 6-(tert-butoxycarbonylamino)-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
- 6-[(tert-butoxy-oxomethyl)amino]-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]hexanoic acid
- 71989-26-9
- N6-(tert-Butoxycarbonyl)-N2-((9H-fluoren-9-ylmethoxy)carbonyl)-L-lysine
- L-Lysine, N(6)-[(1,1-dimethylethoxy)carbonyl]-N(2)-[(9H-fluoren-9-ylmethoxy)carbonyl]-
- NSC334302
- EINECS 276-256-4
- N-.alpha.-Fmoc-N-.epsilon.-t-boc-L-lysine
InChIKey UMRUUWFGLGNQLI-UHFFFAOYSA-N InChI InChI=1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30) SMILES CC(C)(C)OC(=O)NCCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13 - Cited Uses
-
Details
1. Kenyon NJ et al, "Self-Assembling Nanoparticles Containing Dexamethasone as a Novel Therapy in Allergic Airways Inflammation", PLoS ONE, 8(10) pp.e77730 ().2. Xiao K et al, "The effect of surface charge on in vivo biodistribution of PEG-oligocholic acid based micellar nanoparticles", Biomaterials, 32(13) pp.3435-3446 (2011 May).3. Balhorn R et al, "Hexa-arginine enhanced uptake and residualization of selective high affinity ligands by Raji lymphoma cells", Molecular Cancer, 8() pp.25 (). - Reviews
-
Peptides & Peptide Synthesis Products