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bdp fl peg4 tco

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  • Inhibitors & Agonists
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BDP FL-PEG4-TCO
T145182183473-16-5
BDP FL-PEG4-TCO is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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(E)-TCO-PEG4-NHS ester
(E)-TCO-PEG4-NHS ester
T390921621096-79-4
(E)-TCO-PEG4-NHS ester is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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TCO-PEG4-biotin
T170162183440-30-2
TCO-PEG4-biotin is a PROTAC linker belonging to the PEG class.TCO-PEG4-biotin can be used to synthesise a range of PROTAC molecules.
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TCO-PEG-TCO (MW 5000)
T18752
TCO-PEG-TCO (MW 5000) is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules, and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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TCO-PEG4-amine
T187722243569-24-4
TCO-PEG4-amine is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the selective protein degradation by leveraging the ubiquitin-proteasome system within cells. [PROTACs]
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BDP FL-PEG5-azide
T145192093197-91-0
BDP FL-PEG5-azide is a PEG-based linker for PROTACs, joining two essential ligands to facilitate selective protein degradation via the ubiquitin-proteasome system within cells.
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BDP FL-PEG5-propargyl
T145202093197-93-2
BDP FL-PEG5-propargyl, a PEG-based linker for PROTACs, connects two essential ligands necessary for forming PROTAC molecules. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
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(S)-TCO-PEG4-acid
T17015L
(S)-TCO-PEG4-acid is a PEG-based linker for PROTACs, joining two essential ligands critical for PROTAC molecule formation, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
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TCO-PEG4-acid
T170151802913-21-8
TCO-PEG4-acid is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands crucial for forming PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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TCO-PEG4-TCO
T187742243569-23-3
TCO-PEG4-TCO is a PEG-based linker used in PROTACs that connects two ligands critical for PROTAC molecule formation, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
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BDP FL-PEG4-amine
T145172183473-14-3
BDP FL-PEG4-amine is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
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Azido-PEG4-4-nitrophenyl carbonate
T144371422540-98-4
Azido-PEG4-4-nitrophenyl carbonate, a PEG-derived PROTAC linker, enables the synthesis of PROTACs[1].
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DBCO-PEG4-SS-TCO
T17799
DBCO-PEG4-SS-TCO is a cleavable 4-unit polyethylene glycol (PEG) linker crucial for the synthesis of antibody-drug conjugates (ADCs)[1], facilitating the connection of the drug payload to the antibody and enabling targeted drug delivery.
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BDP FL DBCO
T145162093197-94-3
BDP FL DBCO, a cleavable linker crucial in ADC synthesis, connects cytotoxic drugs to antibodies for targeted delivery to cells or proteins. Its cleavable nature ensures controlled drug release, optimizing ADC effectiveness.
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TCO-PEG4-DBCO
T187731801863-88-6
TCO-PEG4-DBCO is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
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N-(m-PEG4)-N'-(4-Hydroxycyclohexyl-1-amido-PEG4)-Cy5
n-m-peg4-n-4-hydroxycyclohexyl-1-amido-peg4-cy5
T184202107273-72-1
N-(m-PEG4)-N'-(4-Hydroxycyclohexyl-1-amido-PEG4)-Cy5 is a polyethylene glycol (PEG)-based linker compound primarily used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
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TCO-PEG4-NHS ester
T170171613439-69-2
TCO-PEG4-NHS ester is a PROTAC linker bridge in the PEG class, used for synthesizing various PROTAC molecules. As a cleavable and synthetic ADC, it is also utilized in the synthesis of antibody-drug conjugates (ADCs).
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7-10 days
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