propargyl peg1 ss alcohol

Propargyl-PEG1-SS-alcohol is a cleavable, 1-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

N-(Amino-PEG1)-N-bis(PEG2-propargyl) HCl salt is a PEG derivative with an amino group and two propargyl groups, which may be useful in developing antibody-drug conjugates [PEG Linkers].

1-Isothiocyanato-PEG4-alcohol, a polyethylene glycol (PEG)-derived linker compound, is suitable for incorporation into Proteolysis Targeting Chimeras (PROTACs).

Propargyl-PEG1-SS-PEG1-acid is a cleavable two-unit polyethylene glycol (PEG) linker frequently utilized in the synthesis of antibody-drug conjugates (ADCs) [1].

THP-SS-alcohol is a cleavable linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

THP-PEG1-alcohol is a useful organic compound for research related to life sciences. The catalog number is T67267 and the CAS number is 2162-31-4.

Propargyl-PEG10-alcohol, a PEG-based linker for PROTACs, connects two essential ligands critical for forming PROTAC molecules, enabling selective protein degradation through the ubiquitin-proteasome system within cells.

N-(PEG1-OH)-N-Boc-PEG2-propargyl is a polyethylene glycol (PEG)-based linker employed in the synthesis of proteolysis targeting chimeras (PROTACs).

Propargyl-PEG5-1-o-b-cyanoethyl-nn-diisopropylphosphoramidite is a polyethylene glycol (PEG)-based linker molecule designed for synthesizing proteolysis-targeting chimeras (PROTACs).

Propargyl-PEG3-1-o-b-cyanoethyl-NN-diisopropylphosphoramidite is a polyethylene glycol-based PROTAC linker used in the synthesis of PROTACs.

Bis-propargyl-PEG1, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Propargyl-PEG1-NH2, a PEG-based PROTAC linker, can be utilized in the synthesis of PROTACs[1].

Propargyl-PEG7-alcohol is a PEG-based PROTAC linker utilized in the synthesis of PROTACs [1].

Hydroxy-PEG3-SS-PEG3-alcohol, a 6-unit polyethylene glycol (PEG) linker that can be cleaved, is commonly used in the synthesis of antibody-drug conjugates (ADCs) [1].

Propargyl-PEG3-alcohol is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands to form PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Propargyl-PEG1-SS-PEG1-PFP ester is a cleavable linker containing a 1-unit polyethylene glycol (PEG) backbone, designed for the synthesis of antibody-drug conjugates (ADCs)[1].

N-(Boc-PEG1)-N-bis(PEG2-propargyl) is a polyethylene glycol (PEG)-derived linker used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Propargyl-PEG1-NHS ester is a non-cleavable 1-unit PEG linker used in antibody-drug conjugation (ADC) to link antibodies with drugs.

Propargyl-PEG14-alcohol is a PEG derivative containing a hydroxyl group and a propargyl group. PEG Linkers are useful in the development of antibody drug conjugates. The hydroxyl group enables further derivatization or replacement with other reactive func

THP-SS-PEG1-Tos is a cleavable 1-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

N-(Propargyl-PEG4-carbonyl)-N-bis(PEG1-methyl ester) is a polyethylene glycol (PEG)-based linker used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Azide-PEG-alcohol, a polyethylene glycol (PEG)-based PROTAC linker with a molecular weight of 2000, functions as a versatile option for the synthesis of PROTACs[1].

Propargyl-PEG1-SS-PEG1-C2-Boc is a cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

THP-SS-PEG1-Boc, a cleavable ADC linker with a one-unit PEG, is commonly used in the synthesis of antibody-drug conjugates (ADCs)[1].

Boc-aminooxy-PEG1-propargyl is a polyethylene glycol (PEG)-based linker commonly used in synthesizing proteolysis targeting chimeras (PROTACs) [1].

Propargyl-PEG1-THP is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules and enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthetic conjugate that combines a Thalidomide-based cereblon ligand and a linker, commonly utilized in PROTAC technology. This compound serves as a connector between the target protein and the E3 ligase, facilitating targeted protein degradation.

Propargyl-PEG4-alcohol is a PEG-based linker for PROTACs that joins two essential ligands, crucial for the formation of PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

N-(Biotin)-N-bis(PEG1-alcohol) is a PEG-based PROTAC linker used in PROTAC synthesis[1].

Propargyl-PEG1-acid, a PEG-based PROTAC linker, enables the synthesis of BTK-CRBN PROTACs, specifically Ibrutinib-based PROTAC 4 and PROTAC 5. At a concentration of 10 μM, PROTAC 5 facilitates the degradation of BTK and induces the degradation of CSK, LYN, and LAT2[1].

Propargyl-PEG6-alcohol is a PEG-based PROTAC linker used in the synthesis of PROTACs[1].

Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthesized E3 ligase ligand-linker, incorporating a cereblon ligand based on Thalidomide and a 3-unit PEG linker, specifically designed for PROTAC technology applications.

Aminooxy-PEG1-propargyl is a PEG-based linker for PROTACs, facilitating the combination of two essential ligands crucial for PROTAC molecule formation. This linker enables selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Propargyl-PEG1-acrylate is a polyethylene glycol (PEG) derived linker employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Propargyl-PEG1-Boc is an alkyl ether-based linker utilized in the synthesis of PROTACs [1].

Propargyl-PEG1-SS-PEG1-propargyl refers to a cleavable di-functional polyethylene glycol (PEG) linker composed of two units. This specific linker is employed in the synthesis of antibody-drug conjugates (ADCs), where it plays a critical role in linking the antibody to the drug. [1]