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ho-peg-ch2cooh

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  • 抑制剂&激动剂
    25
    TargetMol | Inhibitors_Agonists
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    TargetMol | Recombinant_Protein
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  • PROTAC
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    TargetMol | PROTAC
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    TargetMol | Reagent_Kits
HO-PEG-CH2COOH (MW 3400)
T18002
HO-PEG-CH2COOH (MW 3400) is a PEGylated PROTAC linker with a molecular weight of 3400. It serves as a PEG-based building block for the synthesis of PROTACs[1].
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HO-PEG-CH2COOH (MW 5000)
T18003
HO-PEG-CH2COOH (MW 5000), a polyethylene glycol (PEG)-based PROTAC linker, serves as a valuable component in the synthesis of PROTACs[1].
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(S,R,S)-AHPC-(C3-​PEG)​2-​C6-​ClVHL 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].
  • ¥ 387
5日内发货
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Pomalidomide-C2-amido-(C1-O-C5-O-C1)2-COOHE3 ligase Ligand-Linker Conjugates 49,Cereblon Ligand-Linker Conjugates 14
T179032351103-63-2
Pomalidomide-C2-amido-(C1-O-C5-O-C1)2-COOH is a chemically synthesized compound, designed as an E3 ligase ligand-linker conjugate, integrating the cereblon ligand derived from Pomalidomide and a linker employed in PROTAC technology. This compound serves to facilitate targeted protein degradation through the modulation of E3 ligase activity, enabling the selective elimination of specific proteins of interest.
  • ¥ 525
5日内发货
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HO-PEG-mal (MW 5000)
T18005
HO-PEG-mal (MW 5000) is a PEG-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.
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HO-PEG-amine (MW 10000)
T17998
HO-PEG-amine (MW 10000) is a polyethylene glycol (PEG) derivative utilized as a PROTAC linker for the synthesis of PROTACs[1].
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HO-PEG-amine (MW 5000)
T18001
HO-PEG-amine (MW 5000) is a PEG-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.
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HO-PEG-amine (MW 1000)
T17997
HO-PEG-amine (MW 1000) is a PEG-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.
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HO-PEG-amine (MW 2000)
T17999
HO-PEG-amine (MW 2000) is a PEG-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.
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Thalidomide-O-amido-PEG1-(C1-​PEG)2-C2-NH2E3 Ligase Ligand-Linker Conjugates 23 TFA,Cereblon Ligand-Linker Conjugates 12 TFA
T17917
Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthesized conjugate compound known as an E3 ligase ligand-linker. It incorporates a cereblon ligand based on Thalidomide and a 3-unit PEG linker. This compound is specifically designed for use in PROTAC technology applications.
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HO-PEG-amine (MW 3400)
T18000
HO-PEG-amine (MW 3400) is a PEG-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.
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HO-PEG-mal (MW 3400)
T18004
HO-PEG-mal (MW 3400) is a PEG-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.
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Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2,Cereblon Ligand-Linker Conjugates 12,E3LigaseLigand-LinkerConjugates23
T400942435572-48-6
Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthetic conjugate compound that combines a Thalidomide-based cereblon ligand and a linker, which is commonly utilized in PROTAC technology. This compound acts as a connector between the target protein and the E3 ligase, facilitating targeted protein degradation.
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DSPE-PEG-2-Aminoethyl-alpha-mannopyranoside (MW 2000)
T17847
DSPE-PEG-2-Aminoethyl-alpha-mannopyranoside (MW 2000) is a polyethylene glycol (PEG) derived linker. This specific linker is utilized in the synthesis of PROTACs, or proteolysis targeting chimeras [1].
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HO-PEG6-CH2COOH
T18016120394-66-3
HO-PEG6-CH2COOH is a PEG-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.
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HO-PEG8-CH2COOH
T18017780006-30-6
HO-PEG8-CH2COOH is a PEG-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.
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HO-PEG10-CH2COOH
T180072250056-53-0
HO-PEG10-CH2COOH is a PEG-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.
  • ¥ 142
5日内发货
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HO-PEG5-CH2COOHHO-PEG5-CH2COOH
T4059952026-48-9
HO-PEG5-CH2COOH is a PEG-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.
  • ¥ 1254
5日内发货
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HO-PEG7-CH2COOHHO-PEG7-CH2COOH
T397732250056-27-8
HO-PEG7-CH2COOH is a PEG-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.
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HO-PEG24-CH2COOH
T18013
HO-PEG24-CH2COOH is a PEG-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.
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HO-PEG12-CH2COOH
T18008
HO-PEG12-CH2COOH is a PEG-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.
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