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methyltetrazine amido peg5 alkyne

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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Methyltetrazine-amido-PEG5-alkyne
T183372322322-23-4
Methyltetrazine-amido-PEG5-alkyne, a polyethylene glycol (PEG) derivative, is commonly employed as a linker in proteolysis targeting chimeras (PROTACs) synthesis [1].
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7-10 days
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Thalidomide-O-amido-PEG-C2-NH2 hydrochloride
T188182204226-02-6
Thalidomide-O-amido-PEG-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, incorporating a Thalidomide-based cereblon ligand and a linker. This compound is used in the synthesis of PROTACs.
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TargetMol | Inhibitor Sale
Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2
Thalidomide-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 that combines a Thalidomide-based cereblon ligand and a linker, commonly utilized in PROTAC technology. This compound serves as a connector between the target protein and the E3 ligase, facilitating targeted protein degradation.
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Methyltetrazine-PEG5-NHS ester
T160601802907-92-1
Methyltetrazine-PEG5-NHS ester, a PEG-linked PROTAC linker, enables the synthesis of PROTACs[1].
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Boc-N-Amido-PEG5-Ms
T176502128735-28-2
Boc-N-Amido-PEG5-Ms 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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Mal-amido-PEG5-C2-​NHS ester
T182431315355-92-0
Mal-amido-PEG10-C2-NHS ester is a noncleavable ADC linker with a maleimide group and an NHS ester, used as a labeling agent for primary amines (-NH2) in proteins, amine-modified oligonucleotides, and other amine-containing molecules [1][2].
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7-10 days
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Amino-PEG6-amido-bis-PEG5-N3
T17436
Amino-PEG6-amido-bis-PEG5-N3 is a cleavable 11-unit polyethylene glycol (PEG) linker utilized in the synthesis of antibody-drug conjugates (ADCs) [1].
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Thalidomide-O-amido-PEG-C2-NH2
Thalidomide-O-amido-PEG-C2-NH2
T394272022182-59-6
Thalidomide-O-amido-PEG-C2-NH2 is a synthesized conjugate formulation designed as an E3 ligase ligand-linker conjugate, incorporating a cereblon ligand based on Thalidomide and a linker component commonly used in PROTAC technology.
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7-10 days
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Methyltetrazine-PEG5-alkyne
T160591802907-97-6
Methyltetrazine-PEG5-alkyne, a PEG-based PROTAC linker, is utilized in synthesizing PROTACs[1].
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7-10 days
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Methyltetrazine-amido-PEG7-azide
T183382112731-46-9
Methyltetrazine-amido-PEG7-azide is a PEG-based PROTAC linker used for synthesizing PROTACs[1].
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Thalidomide-O-amido-PEG1-(C1-​PEG)2-C2-NH2
E3 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 E3 ligase ligand-linker, incorporating a cereblon ligand based on Thalidomide and a 3-unit PEG linker, specifically designed for PROTAC technology applications.
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Methyltetrazine-PEG5-methyltetrazine
T18353
Methyltetrazine-PEG5-methyltetrazine is a PEG-based PROTAC linker used in the synthesis of PROTACs [1].
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Methyltetrazine-PEG5-triethoxysilane
T183542353410-01-0
Methyltetrazine-PEG5-triethoxysilane is a polyethylene glycol (PEG)-based PROTAC linker suitable for PROTAC synthesis[1].
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7-10 days
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