- 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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2-Boc-2-Azaspiro[3.3]heptane-6-methanesulfonate
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4-(((tert-Butoxycarbonyl)amino)methyl)cyclohexane-1-carboxylic acid
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Benzyl 4-hydroxybutanoate
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4-Piperidineacetic acid hydrochloride
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16-Bromohexadecanoic acid
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rel-(1r,4r)-4-Aminocyclohexane-1-carbonitrile hydrochloride
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Tert-butyl-dimethyl-pent-4-ynoxy-silane
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PEG2-MeN-Boc
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tert-Butyl 5-iodopentanoate
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1-Bromo-5-chloropentane
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tert-Butyl (2-(2-bromoethoxy)ethyl)(methyl)carbamate
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Boc-PEG2-I
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2-(2-(1,3-Dioxolan-2-yl)ethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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tert-Butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate
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6-(Benzyloxycarbonylamino)caproic acid
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