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    Results for PEG ( 6576 )

      • Ref: BP-42138
        Sizes: 100 MG, 50 MG, 250 MG

        (4R,5S)-Nutlin carboxylic acid is a Nutlin 3-derived ligand that targets MDM2. It can be linked to a protein ligand via a connector to create PROTACs.

        Product detail
      • Ref: BP-42139
        Sizes: 1 MG, 5 MG

        CC-3060 is a cereblon modulator that facilitates the degradation of ZBTB16. It selectively targets ZBTB16 by engaging specific structural degrons across its zinc finger domains.

        Product detail
      • 3-(1-Oxo-6-piperazin-1-yl-isoindolin-2-yl)piperidine-2,6-dione

        Product detail
      • Ref: BP-42141
        Sizes: 25 MG, 100 MG, 50 MG, 250 MG

        Cis VH032 amine dihydrochloride is a VHL ligand useful for regulating hypoxia signaling pathways and investigating conditions like chronic anemia or ischemia.

        Product detail
      • Ref: BP-42142
        Sizes: 25 MG, 100 MG, 50 MG, 10 MG

        BWA-522 intermediate-1 is a key component in the synthesis of PROTAC BWA-522, acting as a ligand for cereblon E3 ubiquitin ligase. It plays a role in targeting specific proteins for degradation.

        Product detail
      • Ref: BP-42144
        Sizes: 1 MG, 5 MG

        SJ995973 is a potent PROTAC molecule designed to degrade bromodomain and extra-terminal (BET) proteins, targeting key structural domains for protein degradation.

        Product detail
      • Ref: BP-42145
        Sizes: 1 MG, 500 UG

        SNX7886 is a potent PROTAC designed to selectively degrade CDK8 and CDK19 proteins, effectively targeting these kinases in cellular systems.

        Product detail
      • Ref: BP-42146
        Sizes: 1 MG, 5 MG, 10 MG

        DB1113 is a bifunctional compound designed for targeted protein degradation of various kinases. It effectively mediates the degradation of multiple kinase targets, facilitating the study of processes related to dysregulated kinase activity.

        Product detail
      • Ref: BP-42147
        Sizes: 1 MG

        SJ1008030 TFA is a PROTAC specifically designed to target and degrade JAK2. This compound demonstrates selective inhibition of cell growth in MHH–CALL-4 cells, making it useful for studying mechanisms related to leukemia.

        Product detail