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mal-peg5-mal

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  • Inhibitors & Agonists
    9
    TargetMol | Inhibitors_Agonists
  • PROTAC Products
    8
    TargetMol | PROTAC
Mal-PEG5-mal
T18296113387-03-4
Mal-PEG5-mal is a PEG-based linker for PROTACs, joining two essential ligands crucial for PROTAC molecule formation and enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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Mal-PEG5-Boc
Mal-PEG5-T-Butyl Ester, Mal-PEG5-COOtBu
T182952250216-91-0
Mal-PEG5-Boc (Mal-PEG5-COOtBu) is a PEG-based PROTAC linker. Mal-PEG5-Boc can be used in the synthesis of PROTACs.
  • $29
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Mal-PEG5-acid
T159961286755-26-7
Mal-PEG5-acid is a PEG-based linker for PROTACs, joining two essential ligands essential for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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    Mal-PEG5-NHS ester
    T159971807537-42-3
    Mal-PEG5-NHS ester, an alkyl ether and PEG-based PROTAC linker, is utilized for the synthesis of PROTACs.
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    Mal-PEG5-PFP ester
    T159981807512-46-4
    Mal-PEG5-PFP ester is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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    Bis-Mal-PEG5
    T17605
    Bis-Mal-PEG5 is a PEG-based linker for PROTACs, joining two essential ligands necessary for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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    Mal-amido-PEG5-C2-​NHS ester
    T182431315355-92-0
    Mal-amido-PEG10-C2-NHS ester is a noncleavable ADC linker with a maleimide group and an NHS ester, used as a labeling agent for primary amines (-NH2) in proteins, amine-modified oligonucleotides, and other amine-containing molecules [1][2].
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    7-10 days
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    Mal-PEG5-C2-NH2 hydrochloride
    Mal-PEG5-C2-NH2 hydrochloride
    T401182454216-21-6
    Mal-PEG5-C2-NH2 hydrochloride is a polyethylene glycol (PEG)-based linker used in the synthesis of proteolysis targeting chimeras (PROTACs).
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