E-2012

CAS No. 870843-42-8

E-2012 ( E2012 )

Catalog No. M16327 CAS No. 870843-42-8

A potent, second-generation γ-secretase modulator that decreases Aβ(1-39), Aβ(1-40) and A(1-42), and increases Aβ(1-37).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 43 Get Quote
5MG 72 Get Quote
10MG 110 Get Quote
25MG 178 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    E-2012
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, second-generation γ-secretase modulator that decreases Aβ(1-39), Aβ(1-40) and A(1-42), and increases Aβ(1-37).
  • Description
    A potent, second-generation γ-secretase modulator that decreases Aβ(1-39), Aβ(1-40) and A(1-42), and increases Aβ(1-37).Alzheimer's Disease Discontinued
  • Synonyms
    E2012
  • Pathway
    Wnt/Notch/Hedgehog
  • Target
    γ-secretase
  • Recptor
    γ-secretase
  • Research Area
    Neurological Disease
  • Indication
    Alzheimer Disease

Chemical Information

  • CAS Number
    870843-42-8
  • Formula Weight
    419.49
  • Molecular Formula
    C25H26FN3O2
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C1N([C@H](C2=CC=C(F)C=C2)C)CCC/C1=C\C3=CC=C(N4C=C(C)N=C4)C(OC)=C3
  • Chemical Name
    2-Piperidinone, 1-[(1S)-1-(4-fluorophenyl)ethyl]-3-[[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]methylene]-, (3E)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Portelius E, et al. J Alzheimers Dis. 2010;21(3):1005-12.
2. Borgegard T, et al. J Biol Chem. 2012 Apr 6;287(15):11810-9.
3. Borghys H, et al. J Alzheimers Dis. 2012;28(4):809-22.
molnova catalog
related products
  • BMS-433796

    A potent, orally active γ-secretase inhibitor with cell IC50 of 0.3 nM.

  • BMS-299897

    A potent γ-secretase inhibitor that preferentially inhibits cleavage of the APP CTF cleavage with IC50 of 7.1 nM.

  • BMS-708163

    A potent, selective and orally bioavailable inhibitor of γ-secretase with Aβ40 IC50 of 3.0 nM.