m-peg-oh

m-PEG-OH (MW 2000) is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands to form PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.

m-PEG-OH (MW5000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

m-PEG-OH (MW 1000) serves as a macromolecular initiator, facilitating the synthesis of amphiphilic block copolymers. These copolymers are utilized to create nanoscale micelles for delivering active drugs. When hydrophobic anti-cancer agent Paclitaxel is encapsulated within these micelles, it demonstrates enhanced activity against cancer cells compared to free Paclitaxel. Additionally, it predominantly accumulates in tumor tissues, with only limited distribution in healthy organs.

m-PEG-OH (MW 10000) serves as a macromolecular initiator in the synthesis of amphiphilic block copolymers, which can be used to create nanoscale micelles for delivering active drugs. These micelles encapsulate the hydrophobic anticancer agent Paclitaxel and exhibit greater efficacy in killing cancer cells compared to free Paclitaxel. Moreover, they preferentially accumulate in tumor tissues while having limited distribution in healthy organs.

m-PEG-OH (MW 550) (mPEG-Hydroxy (MW 550)) is a derivative of polyethylene glycol (PEG) that can be employed in drug delivery applications.

m-PEG-OH (MW 750) (mPEG-Hydroxy (MW 750)) is a derivative of polyethylene glycol (PEG) that can be utilized for drug delivery applications.

m-PEG-OH (MW 350) [mPEG-Hydroxy (MW 350)] is a derivative of polyethylene glycol (PEG) that can be utilized for drug delivery.

m-PEG-OH (MW 20000) can serve as a macromolecular initiator and participate in the synthesis of amphiphilic block copolymers. These copolymers can be used to prepare nanoscale micelles for delivering active drugs. The micelles encapsulate the hydrophobic anticancer agent Paclitaxel , enhancing its ability to kill cancer cells compared to free Paclitaxel. Additionally, the micelles preferentially accumulate in tumor tissues while showing limited distribution in healthy organs.

4-Arm-PEG-OH (MW 10000) is a PEG derivative featuring a four-arm structure with hydroxyl (OH) functional groups. It can react through its hydroxyl groups with functional groups on biomolecules such as proteins, peptides, and antibodies, and is applicable in drug delivery.

4-Arm-PEG-OH (MW 5000) is a PEG derivative characterized by a four-arm structure and hydroxyl (OH) functional groups. It can react through the hydroxyl groups with functional groups on biomolecules such as proteins, peptides, and antibodies, making it suitable for drug delivery applications.

4-Arm-PEG-OH (MW 2000) is a PEG derivative featuring a four-arm structure and hydroxyl (OH) functional groups. This compound can react with functional groups on biomolecules (such as proteins, polypeptides, antibodies, etc.) via the hydroxyl groups and is applicable in drug delivery systems.

4-Arm-PEG-OH (MW 20000) is a PEG derivative with a four-arm structure and hydroxyl (OH) functional groups. It can react through these hydroxyl groups with functional groups on biomolecules, such as proteins, polypeptides, and antibodies, and is applicable in drug delivery.

m-PEG12-OH (Dodecaethylene Glycol Monomethyl Ether) is a PEG-based PROTAC linker. m-PEG12-OH can be used in the synthesis of PROTACs. m-PEG12-OH is also a non-cleavable 12 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

m-PEG3-OH 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.

m-PEG7-CH2-OH 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.

Bis(m-PEG4)-N-OH is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

m-PEG11-OH is a PEG-based linker for PROTACs, facilitating the joining of two essential ligands crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG3-S-PEG2-OH is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands necessary for forming PROTAC molecules, thereby enabling selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

m-PEG36-OH is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

m-PEG48-OH is a PEG-based linker for PROTACs that joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Mal-PEG4-Glu(OH)-NH-m-PEG24 is a polyethylene glycol-based (PEG-based) linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

NH2-PEG4-Glu(OH)-NH-m-PEG24 is a PEG-based PROTAC linker suitable for PROTAC synthesis [1].

m-PEG21-OH is a PROTAC linker that belongs to the PEG category, utilized in the synthesis of PROTAC molecules.