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Results for "

T1833

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    11
    TargetMol | All_Pathways
  • PROTAC Products
    10
    TargetMol | PROTAC
  • ADC/ADC Related
    6
    TargetMol | All_Pathways
NSI189
NSI-189, NSI 189
T18331270138-40-3
NSI189 (NSI-189) is a nootropic and neurogenic research chemical derived from nicotinamide and pyrazine.
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MC-Val-Cit-PAB-vinblastine
T183302055896-92-7
MC-Val-Cit-PAB-vinblastine is a potent antitumor drug-linker conjugate for Antibody-Drug Conjugates (ADC), featuring vinblastine (a microtubule protein inhibitor) connected through the MC-Val-Cit-PAB [ADC linker].
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MC-VC-PABC-DNA31
T183311639352-03-6
MC-VC-PABC-DNA31 is a drug-linker conjugate designed for Antibody-Drug Conjugates (ADC), exhibiting potent antitumor activity. It utilizes DNA31, a powerful inhibitor of RNA polymerase, connected via the MC-VC-PABC ADC linker.
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MC-VC-PABC-Aur0101
T183321438849-92-3
MC-VC-PABC-Aur0101 is a potent anticancer drug-linker conjugate for Antibody-Drug Conjugates (ADCs), incorporating Aur0101, an auristatin microtubule inhibitor, linked via the MC-VC-PABC linker to boost antitumor efficacy.
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mDPR(Boc)-Val-Cit-PAB
T183332281797-55-3
mDPR(Boc)-Val-Cit-PAB is a cleavable linker used in antibody-drug conjugates (ADCs), which are biopharmaceuticals combining the specificity of monoclonal antibodies with the potency of cytotoxic drugs for targeted cancer therapy [1].
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Methoxy-Tr-NH-PEG7
T183342353409-88-6
Methoxy-Tr-NH-PEG7 is a PEG-based linker for PROTACs, joining 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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Methylcyclopropene-PEG3-amine
T18335
Methylcyclopropene-PEG3-amine is a cleavable three-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
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Methylcyclopropene-PEG4-NHS
T18336
Methylcyclopropene-PEG4-NHS is a four-unit PEG ADC linker, which can be cleaved. It is utilized in the synthesis of antibody-drug conjugates (ADCs)[1].
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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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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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Methyltetrazine-PEG13-acid
T18339
Methyltetrazine-PEG13-acid is a PEGylated linker derived from PEG that serves as a valuable component in the production of PROTACs, a class of compounds known for their targeted protein degradation properties[1].
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