HO-PEG24-OH

CAS No. 2243942-52-9

HO-PEG24-OH ( —— )

Catalog No. M26965 CAS No. 2243942-52-9

HO-PEG24-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 30 Get Quote
25MG 48 Get Quote
50MG 68 Get Quote
100MG 113 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    HO-PEG24-OH
  • Note
    Research use only, not for human use.
  • Brief Description
    HO-PEG24-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
  • Description
    HO-PEG24-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.(In Vitro):PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Leishmania tropica; SK?channels
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2243942-52-9
  • Formula Weight
    1075.3
  • Molecular Formula
    C48H98O25
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Bhuniya D, et al. Aminothiazoles: Hit to lead development to identify antileishmanial agents. Eur J Med Chem. 2015 Sep 18;102:582-93.
molnova catalog
related products
  • TPI-1

    TPI-1 is a SHP-1 inhibitor.

  • 11-Oxomogroside IVa

    The fruits of Siraitia grosvenorii Swingle.

  • Gap19 acetate(150793...

    Gap19 is a peptide that corresponds to a sequence on the cytoplasmic loop (CL) of Cx43.Hemichannel inhibition is due to the binding of Gap19 to the C-terminus (CT) thereby preventing intramolecular CT-CL interactions.?The peptide inhibited Cx43 hemichannel unitary currents in both HeLa cells exogenously expressing Cx43 and acutely isolated pig ventricular cardiomyocytes.?