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    Results for Activators & Inhibitors ( 79993 )

      • S-(1-Hydroxy-2-methylpropan-2-yl) methanesulfonothioate, an ADC linker, is a glutathione cleavable compound used for the attachment of monoclonal antibodies (mAb) in antibody-drug conjugates (ADCs). It specifically refers to the Alkyl-Chain composition of the linker portion of these molecules [1].

        Product detail
      • Ref: T18660
        Sizes: 1 mg

        (S,R,S)-AHPC-amido-C5-acid is a chemical compound that contains a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker. It can be utilized in the design of XY028-133[1].

        Product detail
      • Ref: T18668
        Sizes: 1 mg, 2 mg

        (S,R,S)-AHPC-Me-C10-Br is a chemically synthesized conjugate that functions as a ligand-linker for E3 ligases. This compound incorporates a VHL E3 ligase linker and MS432, derived from the MEK1/2 inhibitor PD0325901[1].

        Product detail
      • Ref: T18671
        Sizes: 1 mg

        (S,R,S)-AHPC-Me-C7 ester is a E3 ligase ligand-linker conjugate used to synthesise BCL-XL PROTAC degraders[1].

        Product detail
      • Ref: T18683
        Sizes: 1 mg

        SMPT, a non-cleavable ADC linker, is utilized in the production of antibody-drug conjugates (ADCs)[1].

        Product detail
      • Ref: T18699
        Sizes: 1 mg

        SNPB is a cleavable linker that is used for making antibody-drug conjugate (ADC).

        Product detail
      • Ref: T18707
        Sizes: 1 mg, 5 mg, 2 mg

        SPDMV is a glutathione-cleavable linker utilized in antibody-drug conjugates (ADCs)[1].

        Product detail
      • Ref: T18751
        Sizes: 1 mg, 2 mg

        TCO-OH is a alkyl chain-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

        Product detail
      • Ref: T18809
        Sizes: 1 mg, 5 mg, 2 mg

        Thalidomide-NH-C6-NH2 TFA is a synthetic conjugate compound that combines a cereblon ligand based on Thalidomide with a linker used in PROTAC technology, functioning as an E3 ligase ligand-linker conjugate[1].

        Product detail