- 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 (4114)
Related Products (4114)
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PROTAC Linkers Isoform Comparison
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H2N-PEG4-Hydrazide
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14-((tert-Butoxycarbonyl)amino)tetradecanoic acid
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4,4'-(Hexane-1,6-diylbis(oxy))dibenzonitrile
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Bn-PEG8-OBn
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tert-Butyl 2-(piperidin-4-yl)acetate hydrochloride
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OH-PEG3-Cl
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1-Bromo-4-(4-bromobutyl)benzene
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3-Cyanocyclobutane-1-carboxylic acid
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Ethyl hex-5-ynoate
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- 8-Iodooctan-1-amine
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tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoyl)piperazine-1-carboxylate
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HO-PEG8-CH2COOH
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2-Propargyl-(trans)-4-cyclohexanediamine
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3-Hydroxy-2,2,4,4-tetramethylcyclobutan-1-one oxime
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