- 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 (4098)
Related Products (4098)
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PROTAC Linkers Isoform Comparison
- Pent-4-yn-1-ol
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Bis-PEG9-NHS ester
0 ImagesBis-PEG9-NHS ester is a PEG/Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. Bis-PEG9-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). -
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- 2-(2-(6-chlorohexyloxy)ethoxy)ethanamine hydrochloride
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Decanedioic acid
0 ImagesSynonyms: Sebacic acidDecanedioic acid is a straight-chain dicarboxylic acid. Dodecanedioic acid overcomes metabolic inflexibility in type 2 diabetes. Decanedioic acid prevents and reverses metabolic-associated liver disease and obesity. Decanedioic acid is associated with carnitine-acylcarnitine translocase deficiency and medium chain acyl-CoA dehydrogenase deficiency. -
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TCO-NHS ester
0 ImagesCat. No.: HY-141165CAS No.: 1191901-33-3 -
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- tert-Butyl 3-bromopropanoate
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- Boc-NH-C4-Br
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N3-PEG3-CH2CH2COOH
0 ImagesN3-PEG3-CH2CH2COOH a PEG-based PROTAC linker can be used in the synthesis of BI-3663 (HY-111546), BI-4216 and BI-0319. Azido-PEG3-acid is also a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N3-PEG3-CH2CH2COOH 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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Azido-PEG1-amine
0 ImagesAzido-PEG1-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG1-amine 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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- Biotin-PEG3-NHS ester
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- tert-Butyl N-[4-(aminomethyl)phenyl]carbamate
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- 3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic acid
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- tert-Butyl 4-formylpiperidine-1-carboxylate
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Glycolic acid
0 ImagesCat. No.: HY-W015967CAS No.: 79-14-1Synonyms: Hydroxyethanoic acidGlycolic acid is an inhibitor of tyrosinase, suppressing melanin formation and lead to a lightening of skin colour. -
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Bis-PEG5-NHS ester
0 ImagesBis-PEG5-NHS ester is a PEG/Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. Bis-PEG5-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). -
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Suberic acid
0 ImagesSynonyms: Octanedioic acid -
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- 2,2-Oxybis(ethylamine)
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5-Hexynoic acid
0 ImagesCat. No.: HY-Y0925CAS No.: 53293-00-8Synonyms: Hex-5-ynoic acid5-Hexynoic acid (Hex-5-ynoic acid) is an alkynoic acid. 5-Hexynoic acid serves as a drug intermediate for the synthesis of 3-alkoxy-2-cyclohexenone. -
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α-Lipoic acid-NHS
0 ImagesSynonyms: DL-α-Lipoic acid-NHS -
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Azido-PEG6-acid
0 ImagesAzido-PEG6-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG6-acid 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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