- 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
- 11-Methoxy-11-oxoundecanoic acid
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- 3-(4-Cyanophenyl)propanoic acid
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2-[3-(Methoxycarbonyl)bicyclo[1.1.1]pentan-1-yl]acetic acid
0 ImagesCat. No.: HY-W063710CAS No.: 1113001-63-0 -
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tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate hydrochloride
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tert-Butyl cis-4-(hydroxymethyl)cyclohexylcarbamate
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tert-Butyl 2-formyl-6-azaspiro[3.4]octane-6-carboxylate
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tert-Butyl 4-(methylamino)butanoate hydrochloride
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tert-Butyl (4-aminobutyl)(methyl)carbamate
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- 3-(Piperazin-1-yl)propanoic acid
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13-Bromotridecan-1-ol
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Monomethyl adipate
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2-(Aminooxy)ethanamine dihydrochloride
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3,3'-Thiodipropanoic acid
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Undecane-1,11-diol
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9-Decyn-1-ol
0 ImagesCat. No.: HY-130985CAS No.: 17643-36-69-Decyn-1-ol is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs. 9-Decyn-1-ol can be used to conjugate GDC-0068 with Lenalidomide to generate INY-03-041. INY-03-041 is a potent, highly selective and PROTAC-based pan-Akt degrader. INY-03-041 inhibits Akt1, Akt2 and Akt3 with IC50s of 2.0 nM, 6.8 nM and 3.5 nM, respectively. 9-Decyn-1-ol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. -
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Fmoc-NH-PEG9-CH2CH2COOH
0 ImagesFmoc-NH-PEG9-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG9-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. -
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Amino-PEG16-acid
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- DBCO-mPEG (MW 2kDa)
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Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane
0 ImagesAzido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG4-Amido-tri-(t-butoxycarbonylethoxymethyl)-methane is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. -
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- Fmoc-NH-PEG11-CH2CH2COOH
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