OM99-2

CAT:
804-HY-P2713
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
OM99-2 - image 1

OM99-2

  • Description :

    OM99-2, an eight residue peptidomimetic, tight-binding inhibitor of human brain memapsin 2 with a Ki value of 9.58 nM[1]. OM99-2 is significantly advanced the development of BACE1 inhibitor[2]. OM99-2 has the potential for the research of the Alzheimer's disease[3].
  • UNSPSC :

    12352209
  • Target :

    Beta-secretase
  • Type :

    Peptides
  • Related Pathways :

    Neuronal Signaling
  • Applications :

    Neuroscience-Neurodegeneration
  • Field of Research :

    Neurological Disease
  • Assay Protocol :

    https://www.medchemexpress.com/om99-2.html
  • Solubility :

    10 mM in DMSO
  • Smiles :

    OC([C@H](CC1=CC=CC=C1)NC([C@H](CCC(O)=O)NC([C@H](C)NC([C@H](C)C[C@H](O)[C@H](CC(C)C)NC([C@H](CC(N)=O)NC([C@H](C(C)C)NC([C@@H](N)CCC(O)=O)=O)=O)=O)=O)=O)=O)=O
  • Molecular Formula :

    C41H64N8O14
  • Molecular Weight :

    892.99
  • References & Citations :

    [1]Ghosh AK, et al. Design of Potent Inhibitors for Human Brain Memapsin 2 (β-Secretase) . J Am Chem Soc. 2000;122 (14) :3522-3523.|[2]Zhao J, et al. Targeting Amyloidogenic Processing of APP in Alzheimer's Disease. Front Mol Neurosci. 2020;13:137. Published 2020 Aug 4.|[3]Dash C, et al. Aspartic peptidase inhibitors: implications in drug development. Crit Rev Biochem Mol Biol. 2003;38 (2) :89-119.|[4]Park H, et al. Determination of the active site protonation state of beta-secretase from molecular dynamics simulation and docking experiment: implications for structure-based inhibitor design. J Am Chem Soc. 2003;125 (52) :16416-16422.
  • Shipping Conditions :

    Room temperature
  • Scientific Category :

    Peptides
  • Clinical Information :

    No Development Reported
  • Isoform :

    BACE1
  • CAS Number :

    [314266-76-7]

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