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Results for "
ho-peg-ch2cooh
" in TargetMol Product Catalog- Inhibitors & Agonists9
- PROTAC Products9
HO-PEG-CH2COOH (MW 3400)
T18002
HO-PEG-CH2COOH (MW 3400) is a PEGylated PROTAC linker with a molecular weight of 3400, serving as a PEG-based building block for PROTAC synthesis[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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HO-PEG10-CH2COOH
T180072250056-53-0
HO-PEG10-CH2COOH is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands and crucial for forming PROTAC molecules [that enable selective protein degradation via the ubiquitin-proteasome system within cells].
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HO-PEG12-CH2COOH
T18008
HO-PEG12-CH2COOH is a PEG-based linker for PROTACs [Proteolysis Targeting Chimeras] that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
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HO-PEG24-CH2COOH
T18013
HO-PEG24-CH2COOH 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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HO-PEG6-CH2COOH
T18016120394-66-3
HO-PEG6-CH2COOH is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
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HO-PEG8-CH2COOH
T18017780006-30-6
HO-PEG8-CH2COOH, a PEG-based linker for PROTACs, unites two essential ligands critical for forming PROTAC molecules. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
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HO-PEG7-CH2COOH
HO-PEG7-CH2COOH
T397732250056-27-8
HO-PEG7-CH2COOH, a PEG-based linker for PROTACs, connects two essential ligands necessary for PROTAC molecule formation, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
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HO-PEG5-CH2COOH
HO-PEG5-CH2COOH
T4059952026-48-9
HO-PEG5-CH2COOH is a PEG-based linker for PROTACs, joining two essential ligands critical for PROTAC molecule formation, enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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