Peptides & Peptide Synthesis Products

Fmoc-Lys(ivDde)-OH

Fmoc-Lys(ivDde)-OH

$165.00
$165.00
Fmoc-Lys(ivDde)-OH, Catalog No: 41087
Nα-Fmoc-Nε-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine, CAS: 204777-78-6, MW: 574.71, Formula: C34H42N2O6
Catalog No: 41087
Nα-Fmoc-Nε-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine, CAS: 204777-78-6, MW: 574.71, Formula: C34H42N2O6
Description

Details

Nα-Fmoc-Nε-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine
Additional Information

Additional Information

Catalog Number 41087
CAS 204777-78-6
M.W. 574.71
Formula C34H42N2O6
IUPAC Name (2S)-6-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
Synonym Nα-Fmoc-Nε-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine
Also Known As
  • (2S)-6-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
  • (2S)-6-[[1-(4,4-dimethyl-2,6-dioxo-cyclohexylidene)-3-methyl-butyl]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
  • (2S)-6-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]hexanoic acid
  • (2S)-6-[[1-(2,6-diketo-4,4-dimethyl-cyclohexylidene)-3-methyl-butyl]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
  • 29207_FLUKA
  • Fmoc-Lys(Ddiv)-OH
  • Nalpha-Fmoc-Nepsilon-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine
InChIKey PYCBVLUBTMHNPW-MHZLTWQESA-N
InChI InChI=1S/C34H42N2O6/c1-21(2)17-28(31-29(37)18-34(3,4)19-30(31)38)35-16-10-9-15-27(32(39)40)36-33(41)42-20-26-24-13-7-5-11-22(24)23-12-6-8-14-25(23)26/h5-8,11-14,21,26-27,35H,9-10,15-20H2,1-4H3,(H,36,41)(H,39,40)/t27-/m0/s1
SMILES CC(C)CC(=C1C(=O)CC(CC1=O)(C)C)NCCCC[C@@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Cited Uses

Details

1. Melvin AT et al, "A Comparative Analysis of the Ubiquitination Kinetics of Multiple Degrons to Identify an Ideal Targeting Sequence for a Proteasome Reporter", PLoS ONE, 8(10) pp.e78082 ().
2. Pathuri G et al, "Synthesis and Evaluation of Novel Tc-99m Labeled Probestin Conjugates for Imaging APN/CD13 Expression In Vivo", Bioconjugate Chemistry, 23(1) pp.115-124 (2012 Jan 18).
3. Luo K et al, "Biodegradable Multiblock Poly[N-(2-hydroxypropyl)methacrylamide] via Reversible Addition-Fragmentation Chain Transfer Polymerization and Click Chemistry", Macromolecules, 44(8) pp.2481-2488 (2011 Apr 26).
4. Bicker KL et al, "Boronic acid functionalized peptidyl synthetic lectins: Combinatorial library design, peptide sequencing, and selective glycoprotein recognition", ACS combinatorial science, 13(3) pp.232-243 (2011 May 9).
5. Kimura RH et al, "A dual-labeled knottin peptide for PET and near-infrared fluorescence imaging of integrin expression in living subjects", Bioconjugate chemistry, 21(3) pp.436-444 (2010 Mar 17).
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