Peptides & Peptide Synthesis Products

Fmoc-Pra-OH

Fmoc-Pra-OH

$115.00
$115.00
Fmoc-Pra-OH, Catalog No: 47252
Fmoc-L-propargylglycine, CAS: 198561-07-8, MW: 335.35, Formula: C20H17NO4
Catalog No: 47252
Fmoc-L-propargylglycine, CAS: 198561-07-8, MW: 335.35, Formula: C20H17NO4
Description

Details

Fmoc-L-propargylglycine
Additional Information

Additional Information

Catalog Number 47252
CAS 198561-07-8
M.W. 335.35
Formula C20H17NO4
IUPAC Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid
Synonym Fmoc-L-propargylglycine
Also Known As
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid
  • (2S)-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]pent-4-ynoic acid
  • 198561-07-8
  • FL378-1
  • (S)-2-(Fmoc-amino)-4-pentynoic acid
  • 00397_FLUKA
  • Fmoc-L-2-propargylglycine
  • Fmoc-propargyl-Gly-OH
  • Fmoc-L-Propargylglycine
InChIKey DJGMNCKHNMRKFM-SFHVURJKSA-N
InChI InChI=1S/C20H17NO4/c1-2-7-18(19(22)23)21-20(24)25-12-17-15-10-5-3-8-13(15)14-9-4-6-11-16(14)17/h1,3-6,8-11,17-18H,7,12H2,(H,21,24)(H,22,23)/t18-/m0/s1
SMILES C#CC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
Cited Uses

Details

1. Tarallo R et al, "Dendrimers functionalized with membrane-interacting peptides for viral inhibition", International Journal of Nanomedicine, 8() pp.521-534 (2013).
2. Kawamoto SA et al, "Design of Triazole-stapled BCL9 ?-Helical Peptides to Target the ?-Catenin/B-cell CLL/lymphoma 9 (BCL9) Protein-Protein Interaction", Journal of Medicinal Chemistry, 55(3) pp.1137-1146 (2012 Feb 9).
3. Fehr F et al, "Semi-Synthesis and Analysis of Chemically Modified Zif268 Zinc-Finger Domains", ChemistryOpen, 1(1) pp.26-32 (2012 Feb).
4. Dutot L et al, "Glycosylated cell-penetrating peptides and their conjugates to a proapoptotic peptide: preparation by click chemistry and cell viability studies", Journal of Chemical Biology, 3(2) pp.51-65 ().
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