The length and composition of the linker play critical roles in the physicochemical properties and bioactivity of PROTACs. While linker design has historically received limited attention, the PROTAC field is evolving rapidly and undergoing an important shift from synthetically tractable alkyl and polyethylene glycol to more sophisticated functional linkers. Equally important, linker-mediated binding cooperativity also represents a potential source of affinity for the POI for PROTACs based on weak affinity warheads. However, the current consensus is that the linker composition, and particularly its length and attachment point to the anchor/warhead, must be optimized for each ligand pair.
产品编号 | 产品名称 | |
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T17786 | DBCO-PEG2-amine | DBCO-PEG2-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T14627 | Bis-PEG1-NHS ester | Bis-PEG1-NHS ester is a non-cleavable 1-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. |
T15122 | Diethyl 7-bromoheptylphosphonate | Diethyl 7-bromoheptylphosphonate is an alkyl chain-based PROTAC linker, commonly employed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. |
T15909 | m-PEG6-Br | m-PEG6-Br is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T18085 | m-PEG-azide (MW 5000) | m-PEG-azide (MW 5000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T15540 | Hydroxy-PEG9-Boc | Hydroxy-PEG9-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T18265 | Mal-PEG-mal (MW 5000) | Mal-PEG-mal (MW 5000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T14608 | Biotin-PEG6-Mal | Biotin-PEG6-Mal is a biotinylated PROTAC linker derived from a polyethylene glycol (PEG) scaffold. It serves as an essential component for the synthesis of PROTACs, which are targeted protein degraders[1]. |
T18187 | m-PEG3-Sulfone-PEG3-Boc | m-PEG3-Sulfone-PEG3-Boc is a polyethylene glycol (PEG)-derived proteolysis-targeting chimera (PROTAC) linker employed for the synthesis of PROTACs[1]. |
T17765 | DBCO-NHCO-PEG2-CH2COOH | DBCO-NHCO-PEG2-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T18095 | m-PEG-mal (MW 30000) | m-PEG-mal (MW 30000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T17488 | Azido-PEG15-t-butyl ester | Azido-PEG15-t-butyl ester is a polyethylene glycol (PEG) derived linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. |
T18254 | Mal-NH-PEG12-CH2CH2COOPFP ester | Mal-NH-PEG12-CH2CH2COOPFP ester is a polyethylene glycol (PEG) based linker molecule, designed specifically for the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. |
T14887 | Cbz-NH-PEG2-C2-acid | Cbz-NH-PEG2-C2-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T14653 | Bis-propargyl-PEG1 | Bis-propargyl-PEG1 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
T18705 | SPDMB | SPDMB is a glutathione-cleavable ADC linker used for antibody-drug conjugates (ADCs). |
T14437 | Azido-PEG4-4-nitrophenyl carbonate | Azido-PEG4-4-nitrophenyl carbonate, a PEG-derived PROTAC linker, enables the synthesis of PROTACs[1]. |
T18706 | SPDMV-sulfo | SPDMV-sulfo, a glutathione-cleavable ADC linker, facilitates the release of drugs from antibody-drug conjugates (ADCs). |
T17584 | Biotin-PEG4-Dde-TAMRA-PEG3-Azide | Biotin-PEG4-Dde-TAMRA-PEG3-Azide is a seven-unit polyethylene glycol (PEG) linker that is cleavable and employed in the synthetic production of antibody-drug conjugates (ADCs)[1]. |
T18564 | Propargyl-O-C1-amido-PEG4-C2-NHS ester | Propargyl-O-C1-amido-PEG4-C2-NHS ester is a non-cleavable 4-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. |