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H-ILE-ILE-GLY-LEU-MET-OH

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H-ILE-ILE-GLY-LEU-MET-OH Basic information

Product Name:
H-ILE-ILE-GLY-LEU-MET-OH
Synonyms:
  • β-Amyloid 31-35(TFA)
  • Isoleucinyl-isoleucinyl-glycinyl-leucinyl-methionine
  • AMyloid b-Protein (31-35)
  • AMYLOID BETA-PROTEIN (31-35)
  • AMYLOID-BETA PROTEIN (31-35), HUMAN, MOUSE, RAT
  • BETA-AMYLOID (31-35)
  • IIGLM
  • ILE-ILE-GLY-LEU-MET
CAS:
149385-65-9
MF:
C25H47N5O6S
MW:
545.74
Product Categories:
  • peptide
Mol File:
149385-65-9.mol
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H-ILE-ILE-GLY-LEU-MET-OH Chemical Properties

Boiling point:
866.4±65.0 °C(Predicted)
Density 
1.137±0.06 g/cm3(Predicted)
storage temp. 
−20°C
solubility 
Soluble in DMSO
pka
3.24±0.10(Predicted)
form 
Solid
color 
White to off-white
Sequence
H-Ile-Ile-Gly-Leu-Met-OH
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H-ILE-ILE-GLY-LEU-MET-OH Usage And Synthesis

Uses

β-Amyloid (31-35) is the shortest sequence of native Amyloid-β peptide that retains neurotoxic activity.

References

[1] Milton NG, et al. The amyloid-beta peptide binds to cyclin B1 and increases human cyclin-dependent kinase-1 activity. Neurosci Lett. 2002 Apr 5;322(2):131-3. DOI:10.1016/s0304-3940(02)00081-2
[2] Misiti F, et al. Fragment 31-35 of beta-amyloid peptide induces neurodegeneration in rat cerebellar granule cells via bax gene expression and caspase-3 activation. A crucial role for the redox state of methionine-35 residue. Neurochem Int. 2006 Oct;49(5):525-32. DOI:10.1016/j.neuint.2006.03.014
[3] M Jesús Pérez de Vega, et al. Synthesis and biological properties of beta-turned Abeta(31-35) constrained analogues. Bioorg Med Chem Lett. 2008 Mar 15;18(6):2078-82. DOI:10.1016/j.bmcl.2008.01.092

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