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peg-2-cl

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  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
  • PROTAC Products
    7
    TargetMol | PROTAC
(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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PEG2-Cl
PEG2-Cl
T4089478925-46-9
PEG2-Cl is a PEG-based linker for PROTACs that 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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(S,R,S)-AHPC-PEG2-C4-Cl
E3 ligase Ligand-Linker Conjugates 10, VHL Ligand-Linker Conjugates 7, VH032-PEG2-C4-Cl
T179101835705-57-1
(S,R,S)-AHPC-PEG2-C4-Cl is a small molecule HaloPROTAC, comprising the (S,R,S)-AHPC based VHL ligand and a 2-unit PEG linker, that induces the degradation of GFP-HaloTag7 in cell-based assays[1].
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VH032-PEG5-C6-Cl
HaloPROTAC 2
T179961799506-06-1
VH032-PEG5-C6-Cl (HaloPROTAC 2) is a small molecule that includes the VH032-based VHL ligand and a 5-unit PEG linker, capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
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Cl-PEG2-acid
Cl-PEG2-acid
T39163170304-76-4
Cl-PEG2-acid is a PEG-based linker for PROTACs, essential for joining two ligands critical to forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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7-10 days
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Thalidomide-5-PEG2-Cl
Thalidomide-5-PEG2-Cl
T397212230956-57-5
Thalidomide-5-PEG2-Cl, a Thalidomide-derived cereblon ligand, serves as the ligand for the recruitment of CRBN protein. It can be conjugated to the protein ligand via a linker to produce PROTACs.
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Azido-PEG2-C6-Cl
T402012568146-55-2
Azido-PEG2-C6-Cl is a PROTAC linker belonging to the PEG class and can be used to synthesize PROTAC molecules.
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