- Signaling Pathways
- PROTAC
- PROTAC Linkers
PROTAC Linkers
PROTACs (Proteolysis Targeting Chimeric Molecules) are heterobifunctional protein degraders and promising targeted therapeutics candidates for cancer. The PROTAC linker connects two functional motifs of a PROTAC, a target protein binder and an E3 ligase recruiter.
The linker plays an important role in a PROTAC. The features of the linker (type, length, attachment position) can affect the formation of ligase:PROTAC:target ternary complex, resulting in influencing the efficient ubiquitination of the target protein and its ultimate degradation. The optimal lengths of the PROTAC linkers are reported varying from 12-carbon to over 20-carbon, and the commonly used linkers in the development of PROTACs are PEGs, Alkyl-Chain and Alkyl/ether.
PROTAC Linkers Isoform Specific Products
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PROTAC Linkers Related Products (4102)
Related Products (4102)
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PROTAC Linkers Isoform Comparison
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Octa-1,7-diyne
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tert-Butyl 20-bromoicosanoate
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1-Boc-4-(4-Carboxybenzyl)piperazine
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6-tert-Butyl 2-methyl 6-azaspiro[3.4]octane-2,6-dicarboxylate
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N1,N4-Dimethylbutane-1,4-diamine
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tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate
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Thalidomide-O-PEG4-acid
0 ImagesCat. No.: HY-W800655CAS No.: 2446382-02-9Thalidomide-O-PEG4-Acid is a PROTAC linker that can react with Amine containing moiety in the presence of Activator EDC or HATU. -
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(S,E)-TCO2-PEG3-acid
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Methyl 2-[3-(aminomethyl)cyclobutyl]acetate hydrochloride
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2-(2-((Tert-butyldimethylsilyl)oxy)ethoxy)acetic acid
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- m-PEG49-NHS ester
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Methyl 10-hydroxydecanoate
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Benzyl 5-hydroxypentanoate
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Hex-3-enedinitrile
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4-(Azetidin-3-yl)piperazin-2-one hydrochloride
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- H2N-PEG6-Hydrazide
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4-Bromobutyl acetate
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- HO-PEG24-CH2CH2COOH
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5-Aminopentanoic acid hydrochloride
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endo-BCN-PEG3-NHS ester
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