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Results for "

br peg3 ethyl acetate

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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Br-PEG3-ethyl acetate
T40389308085-31-6
Br-PEG3-ethyl acetate is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands crucial for PROTAC molecule formation. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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S-acetyl-PEG3-phosphonic acid ethyl ester
T186582173125-29-4
S-acetyl-PEG3-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
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Hydroxy-PEG3-ethyl acetate
T38575118988-04-8
Hydroxy-PEG3-ethyl acetate is a polyethylene glycol (PEG)-based linker compound used in PROTAC synthesis.
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N-Ethyl-N-methylpropionamide-PEG1-Br
T391601695856-63-3
N-Ethyl-N-methylpropionamide-PEG1-Br, a PEG-derived PROTAC linker, is suitable for the synthesis of PROTACs.
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t-Butyl acetate-PEG3-CH2COOH
T389241442466-57-0
t-Butyl acetate-PEG3-CH2COOH is a polyethylene glycol-derived PROteolysis TArgeting Chimera (PROTAC) linker designed for incorporation into the synthesis of PROTAC molecules.
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Ethyl azetidine-3-carboxylate hydrochloride
T65152405090-31-5
Ethyl azetidine-3-carboxylate hydrochloride [Catalog No. T65152, CAS No. 405090-31-5] is a valuable organic compound for life sciences research.
    7-10 days
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    Br-PEG3-OH
    T1477057641-67-5
    Br-PEG3-OH 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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    7-10 days
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    Thiol-PEG3-phosphonic acid ethyl ester
    T188381360716-43-3
    Thiol-PEG3-phosphonic acid ethyl ester, a PEG-based linker, serves as a valuable component in the synthesis of PROTACs[1].
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    Amino-ethyl-SS-PEG3-NHBoc
    T142212144777-87-5
    Amino-ethyl-SS-PEG3-NHBoc is a cleavable 3-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1].
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    Br-PEG3-CH2COOH
    T147691346502-15-5
    Br-PEG3-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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    Biotin-PEG3-(CH2)3-NH2 TFA salt
    T145921374658-86-2
    Biotin-PEG3-(CH2)3-NH2 TFA salt 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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    DBCO-(PEG)3-VC-PAB-MMAE
    T17817
    DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor used as a toxin payload in antibody-drug conjugates, is conjugated via a DBCO-(PEG)3-vc-PAB linker.
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    Br-PEG3-C2-Boc
    T14768782475-37-0
    Br-PEG3-C2-Boc is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands crucial for PROTAC molecule formation, and enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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    7-10 days
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    PEG2-ethyl acetate
    T39034154773-33-8
    PEG2-ethyl acetate, a PEG-based linker for PROTACs, facilitates the formation of PROTAC molecules by joining two essential ligands and enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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    Ethyl acetate-PEG1
    T395052093-20-1
    Ethyl acetate-PEG1 is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system [within cells].
    • $36
    5 days
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    Azido-PEG3-phosphonic acid ethyl ester
    T144331337527-24-8
    Azido-PEG3-phosphonic acid ethyl ester, a PEG-based PROTAC linker, enables the synthesis of PROTACs[1].
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    PEG3-bis-(ethyl phosphonate)
    T16454160625-24-1
    PEG3-bis-(ethyl phosphonate), a polyethylene glycol (PEG)-based PROTAC linker, exhibits great potential in PROTAC synthesis[1].
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