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    Results for Lipids & Polymers ( 10111 )

      • Ref: T39483
        Sizes: 10 mg

        Hydroxy-PEG5-acid (Legacy Tebubio ref. 282T39483). Hydroxy-PEG5-acid is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

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      • Ref: T39505
        Sizes: 25 mg, 10 mg

        Ethyl acetate-PEG1 (Legacy Tebubio ref. 282T39505). Ethyl acetate-PEG1 is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system [within cells].

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      • Ref: T39532
        Sizes: 5 mg, 25 mg, 50 mg, 10 mg

        Bis-PEG4-t-butyl ester (Legacy Tebubio ref. 282T39532). Bis-PEG4-t-butyl ester, a PEG-based linker for PROTACs, facilitates the formation of PROTAC molecules by connecting two essential ligands, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

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      • Ref: T39619
        Sizes: 25 mg, 10 mg

        FmocNH-PEG4-t-butyl ester (Legacy Tebubio ref. 282T39619). FmocNH-PEG4-t-butyl ester is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the selective degradation of proteins through the ubiquitin-proteasome system within cells.

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      • Ref: T39689
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg

        Benzyl-PEG12-alcohol (Legacy Tebubio ref. 282T39689). Benzyl-PEG12-alcohol is a PEG-based linker for PROTACs, connecting two essential ligands to form PROTAC molecules. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

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      • Ref: T39806
        Sizes: 5 mg, 25 mg, 100 mg, 50 mg, 500 mg, 10 mg, 2 mg

        Pomalidomide 4'-PEG3-azide (Legacy Tebubio ref. 282T39806). Pomalidomide 4'-PEG3-azide is a chemically synthesized E3 ligase ligand-linker conjugate that incorporates the cereblon ligand derived from Pomalidomide, along with a linker. This compound is utilized in the synthesis of iRucaparib-TP3 (Compound 3), an effective PARP1 degrader developed through the PROTAC strategy and derived from Rucaparib.

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      • Ref: T39867
        Sizes: 25 mg, 100 mg, 50 mg

        Pomalidomide-amino-PEG4-NH2 hydrochloride (Legacy Tebubio ref. 282T39867). Pomalidomide-amino-PEG4-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate, incorporates the cereblon ligand derived from Pomalidomide, along with a linker commonly employed in PROTAC technology.

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      • Pomalidomide-PEG6-NH2 hydrochloride (Legacy Tebubio ref. 282T39875). Pomalidomide-PEG6-NH2 hydrochloride is a compound resulting from the synthesis of an E3 ligase ligand-linker conjugate, combining the cereblon ligand derived from Pomalidomide with a 6-unit PEG linker, specifically designed for application in PROTAC technology.

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      • Ref: T39895
        Sizes: 25 mg, 50 mg

        Thalidomide-Piperazine-PEG3-NH2 (Legacy Tebubio ref. 282T39895). Thalidomide-Piperazine-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that combines a Thalidomide-based cereblon ligand with a linker commonly used in [PROTAC] technology, functioning as an E3 ligase recruiter.

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