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Results for "

ald-ph-peg2-nh-boc

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    212
    TargetMol | Activity
  • Peptide Products
    7
    TargetMol | inventory
  • Dye Reagents
    1
    TargetMol | natural
  • PROTAC Products
    184
    TargetMol | composition
Ald-Ph-PEG2-NH-Boc
T141661807503-90-7
Ald-Ph-PEG2-NH-Boc is a PEG-based linker for PROTACs, joining 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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NH-bis(C1-Boc)
T1847985916-13-8
NH-bis(C1-Boc) is an uncleavable linker used for antibody-drug conjugates (ADC).
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NH2-C2-NH-Boc
PROTAC Linker 22
T1861657260-73-8
NH2-C2-NH-Boc (PROTAC Linker 22), an alkyl chain-based PROTAC linker, can be used in the synthesis of PROTACs.
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NH2-C4-NH-Boc
T1848568076-36-8
NH2-C4-NH-Boc (compound 15) is a PROTAC linker of the Alkyl ether class, suitable for synthesizing various PROTAC molecules.
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NH2-C5-NH-Boc
PROTAC Linker 23
T1861751644-96-3
NH2-C5-NH-Boc (PROTAC Linker 23) is an alkyl chain-based PROTAC linker used in the synthesis of PROTACs.
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Boc-NH-PEG1-OH
T1765926690-80-2
Boc-NH-PEG1-OH is a PEG-based PROTAC linker utilized in the synthesis of PROTACs.
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Boc-NH-PEG4-CH2COOH
T14746876345-13-0
Boc-NH-PEG4-CH2COOH is a cleavable ADC linker utilized in the development of antibody-drug conjugates (ADC)[1].
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NH2-C6-NH-Boc
T1848751857-17-1
NH2-C6-NH-Boc is a PROTAC linker used in the synthesis of the Mcl-1 inhibitor [based on PROTAC].
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Boc-NH-PEG7-Tos
t-Boc-N-Amido-PEG7-Tos
T176821292268-14-4
Boc-NH-PEG7-Tos (t-Boc-N-Amido-PEG7-Tos) is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
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Boc-NH-PEG11-OH
T176661556847-53-0
Boc-NH-PEG11-OH, a PEG-based PROTAC linker, is utilized in PROTAC synthesis.
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Ald-Ph-NHS ester
T1737260444-78-2
Ald-Ph-NHS ester is a non-cleavable linker utilized in antibody-drug conjugation (ADC).
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Boc-NH-PEG3
PROTAC Linker 10
T7701139115-92-7
Boc-NH-PEG3 (PROTAC Linker 10) is a PEG derivative featuring a hydroxyl group and a Boc-protected amino group, used as a PROTAC linker.
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Boc-NH-C12-NH2
T17652109792-60-1
Boc-NH-C12-NH2 is an alkyl ether-based PROTAC linker suitable for use in PROTAC synthesis.
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    Boc-NH-O-C1-NHS ester
    T1765580366-85-4
    Boc-NH-O-C1-NHS ester, an alkyl ether-based PROTAC linker, is utilized in PROTAC synthesis.
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      Boc-NH-PEG8-CH2CH2NH2
      T176841052207-59-6
      Boc-NH-PEG8-CH2CH2NH2 is a PEG-based PROTAC linker utilized in PROTAC synthesis.
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        Boc-NH-PEG7-NH2
        T14756206265-98-7
        Boc-NH-PEG7-NH2 is a PEG-based PROTAC linker.
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        Boc-NH-PEG12-NH2
        NHBoc-PEG12-amine
        T176681642551-09-4
        Boc-NH-PEG12-NH2 (NHBoc-PEG12-amine) is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
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        Boc-NH-PEG3-NHS ester
        T176772250216-93-2
        Boc-NH-PEG3-NHS ester is a PEG-based linker utilized in the synthesis of PROTACs.
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          Boc-NH-PEG4-CH2CH2NH2
          T17679811442-84-9
          Boc-NH-PEG4-CH2CH2NH2 is a cleavable 5-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1].
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          Boc-NH-PEG12-CH2CH2COOH
          T176671415981-79-1
          Boc-NH-PEG12-CH2CH2COOH is a PEG-based PROTAC linker utilized in PROTAC synthesis.
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          Boc-NH-PEG11-NH2
          T176651233234-77-9
          Boc-NH-PEG11-NH2 is a PEG-based PROTAC linker utilized in PROTAC synthesis.
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          Boc-NH-C4-acid
          T1765327219-07-4
          Boc-NH-C4-acid is a PROTAC linker of the Alkyl ether class, utilized in the synthesis of PROTAC1 for the degradation of EED, EZH2, and SUZ12 in [PRC2].
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          Boc-NH-C6-Br
          T17654142356-33-0
          Boc-NH-C6-Br is a cleavable linker used in antibody-drug conjugates (ADC).
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          Boc-NH-PEG3-CH2COOH
          T14741462100-06-7
          Boc-NH-PEG3-CH2COOH, a PEG-based PROTAC linker, can be utilized in PROTAC synthesis [1].
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          Boc-NH-PEG6-CH2COOH
          T17681391684-36-9
          Boc-NH-PEG6-CH2COOH is a PEG-based PROTAC linker employed in PROTAC synthesis.
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          Hydroxy-PEG4-(CH2)2-Boc
          T15529518044-32-1
          Hydroxy-PEG4-(CH2)2-Boc is an uncleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs) and can also be employed in the synthesis of PROTAC.
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          Boc-NH-PEG8-CH2CH2COOH
          T176831334169-93-5
          Boc-NH-PEG8-CH2CH2COOH is a PEG-based PROTAC linker utilized in PROTAC synthesis.
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          Thalidomide-NH-C4-NH-Boc
          T188072093388-52-2
          Thalidomide-NH-C4-NH-Boc is a synthesized conjugate used in PROTAC technology, combining a Thalidomide-based cereblon ligand with a linker.
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          Thalidomide-NH-(CH2)2-NH2 TFA
          T806461957235-67-4
          Thalidomide-NH-(CH2)2-NH2 TFA, an alkyl-modified derivative of Thalidomide, functions as a Cereblon ligand to recruit CRBN proteins and serves as a crucial intermediate in the synthesis of CRBN-based PROTAC molecules targeting the SHP2 protein.
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          Tetrazine-Ph-NHCO-PEG6-NH-Boc
          T18798
          Tetrazine-Ph-NHCO-PEG6-NH-Boc is a PEG-based PROTAC linker used for PROTAC synthesis [1].
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          DBCO-C2-PEG4-NH-Boc
          T17745
          DBCO-C2-PEG4-NH-Boc is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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          Ald-Ph-PEG2-Boc
          T173742100306-65-6
          Ald-Ph-PEG2-Boc is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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          (S,R,S)-AHPC-(C3-​PEG)​2-​C6-​Cl
          VHL Ligand-Linker Conjugates 11,E3 ligase Ligand-Linker Conjugates 11
          T179121835705-61-7
          (S,R,S)-AHPC-(C3-PEG)2-C6-Cl is a small molecule HaloPROTAC incorporating the (S,R,S)-AHPC-based VHL ligand and a 2-unit PEG linker, capable of inducing degradation of GFP-HaloTag7 in cell-based assays [1].
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          N-Mal-N-bis(PEG2-NH-Boc)
          T162302128735-26-0
          N-Mal-N-bis(PEG2-NH-Boc) is a polyethylene glycol (PEG) derived linker designed for synthesizing proteolysis targeting chimeras (PROTACs)[1].
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          Boc-NH-PEG6-azide
          T147511292268-15-5
          Boc-NH-PEG6-azide, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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          NH-bis(C2-PEG2-NH-Boc)
          T162962182601-69-8
          NH-bis(C2-PEG2-NH-Boc) is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system in cells.
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            Ald-Ph-amido-PEG4-propargyl
            Ald-benzyl-amide-PEG4-propargyl
            T173711969299-27-1
            Ald-Ph-amido-PEG4-propargyl is a non-cleavable, 4-unit polyethylene glycol (PEG) antibody-drug conjugate (ADC) linker used in ADC synthesis[1].
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            Boc-NH-PEG5-propargyl
            T147492062663-67-4
            Boc-NH-PEG5-propargyl is a PEG-based linker for PROTACs, facilitating the binding of two essential ligands necessary for PROTAC formation. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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            Pomalidomide-amido-C4-amido-C6-NH-Boc
            Cereblon Ligand-Linker Conjugates 21,E3 Ligase Ligand-Linker Conjugates 54
            T17907
            Pomalidomide-amido-C4-amido-C6-NH-Boc, a synthesized conjugate, is a ligand-linker that incorporates the cereblon ligand based on Pomalidomide and a PROTAC technology linker.
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            Boc-NH-C6-amido-C4-acid
            PROTAC Linker 32
            T1862510436-21-2
            Boc-NH-C6-amido-C4-acid (PROTAC Linker 32) is an alkyl ether-based linker widely used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
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            Boc-NH-PEG36-CH2CH2COOH
            T17678
            Boc-NH-PEG36-CH2CH2COOH is a polyethylene glycol (PEG)-based PROTAC linker used in the synthesis of PROTACs[1].
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            Boc-NH-PEG15-azide
            T17670
            Boc-NH-PEG15-azide, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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            NH-bis(PEG4-C2-NH-Boc)
            T163072182601-75-6
            NH-bis(PEG4-C2-NH-Boc) is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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              Biotin-PEG5-NH-Boc
              T14605189209-28-7
              Biotin-PEG5-NH-Boc is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands required for PROTAC molecule formation and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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              N-(Boc-PEG4)-NH-PEG4-NH-Boc
              T162162112737-17-2
              N-(Boc-PEG4)-NH-PEG4-NH-Boc is a polyethylene glycol (PEG)-based PROteolysis TArgeting Chimera (PROTAC) linker designed for PROTAC synthesis [1].
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              NH2-PEG4-Lys(Boc)-NH-(m-PEG24)
              T18491
              NH2-PEG4-Lys(Boc)-NH-(m-PEG24) is a 28-unit polyethylene glycol (PEG) linker with a cleavable bond, frequently used in the production of antibody-drug conjugates (ADCs)[1].
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              Boc-NH-PEG5-CH2CH2COOH
              T147481347750-78-0
              Boc-NH-PEG5-CH2CH2COOH is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands necessary for PROTAC molecule formation, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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              7-10 days
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              Ald-Ph-amido-PEG1-C2-Pfp ester
              T173802101206-67-9
              Ald-Ph-amido-PEG1-C2-Pfp ester is a non-cleavable 1-unit PEG linker used in antibody-drug conjugation (ADC) to link antibodies with drugs.
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