s acetyl peg3 alcohol

S-acetyl-PEG3-alcohol, a PEG-based linker (PROTACs), connects essential ligands to form PROTAC molecules, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

S-acetyl-PEG2-Boc (S-Acetyl-PEG2-T-Butyl Ester) is a PEG-based PROTAC linker. S-acetyl-PEG2-Boc can be used in the synthesis of PROTACs.

(S,R,S)-AHPC-PEG3-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 5) is an E3 ligase ligand-linker conjugate that integrates the (S,R,S)-AHPC-based VHL ligand with a 3-unit PEG linker.

DBCO-S-S-PEG3-biotin is a cleavable reagent for the introduction of a biotin moiety to azide-containing biomolecules using copper-free Click Chemistry. The disulfide bond in this linker can be cleaved with reducing agents such as DTT, BME, and TCEP to remove the biotin label. PEG linkers can also be used in the synthesis of PROTACs.

S-acetyl-PEG6-alcohol is a PEG Linker, which is used to synthesize compounds and increases solubility in aqueous media.

m-PEG3-S-PEG1-C2-Boc is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

(S)-TCO-PEG3-amine is a PEG-based linker for PROTACs, joining two essential ligands to facilitate selective protein degradation via the ubiquitin-proteasome system within cells.

m-PEG3-S-PEG4-propargyl is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation using the ubiquitin-proteasome system within cells.

m-PEG3-CH2-alcohol is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

S-acetyl-PEG3-Boc 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.

t-Boc-Aminooxy-PEG3-alcohol is a polyethylene glycol (PEG)-based linker compound commonly used for the synthesis of proteolysis targeting chimeras (PROTACs) [1].

m-PEG3-S-PEG3-Boc is a polyethylene glycol (PEG) and alkyl ether-based linker used in the synthesis of PROteolysis TArgeting Chimeras (PROTACs) [1].

(S,R,R)-VH032-CO-C3-CONH-C2-PEG3-OH is a conjugate of the E3 ligase ligand and linker for PROTACNCOA4 degrader-1 (E3LigaseLigand-Linker Conjugates), utilized in the synthesis of PROTACs.

S-acetyl-PEG4-amine, a PEG-based linker for PROTACs, joins two essential ligands, crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Functionalized von-Hippel-Lindau (VHL) protein ligand for PROTAC research and development; incorporates an E3 ligase ligand plus a PEG linker ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. This product has been recently renamed. The previous name for this product was VH 032 - linker 4 PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license.

S-acetyl-PEG4-NHBoc is a PEG-based linker for PROTACs, joining two essential ligands to form PROTAC molecules, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

(S, R, S)-AHPC-PEG3-N3 (VHL Ligand-Linker Conjugates 8) is a synthesized E3 ligase ligand-linker conjugate. (S, R, S)-AHPC-PEG3-N3 incorporates the (S, R, S)-AHPC based VHL ligand and 3-unit PEG linker used in PROTAC technology.

S-acetyl-PEG6-Boc is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands, which is crucial for forming PROTAC molecules and enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

S-Acetyl-PEG8-OH, a PEG-based linker for PROTACs, facilitates the formation of PROTAC molecules by joining two essential ligands, enabling selective protein degradation through the ubiquitin-proteasome system within cells.

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].

(S,R,S)-AHPC-PEG3-NH2 is a synthetic conjugate composed of the (S,R,S)-AHPC VHL ligand and a 3-unit PEG linker, utilized in PROTAC technology as an E3 ligase ligand-linker.

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.

Azido-PEG3-S-PEG4-t-butyl ester, a PEG-based PROTAC linker, is used in PROTAC synthesis [1].

N-(Boc-PEG3)-N-bis(PEG2-alcohol) is a polyethylene glycol (PEG) based linker commonly used in the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

(VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH), also known as (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH, is a conjugate compound comprising a ligand-linker that targets E3 ligase and features a VHL ligand on one end. It is employed in PROTAC technology applications.

Mal-PEG3-alcohol is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

S-acetyl-PEG4-propargyl is a PEG-based PROTAC linker used for synthesizing PROTACs [1].

TCO-PEG3-alcohol is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Azido-PEG3-alcohol 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.

(S,R,S)-AHPC-C6-PEG3-C4-Cl is a small molecule HaloPROTAC incorporating the (S,R,S)-AHPC based VHL ligand and a 3-unit PEG linker, capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].

m-PEG3-S-Acetyl is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Biotin-PEG3-(CH2)3-NH2 TFA salt 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.

DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor used as a toxin payload in antibody-drug conjugates, is conjugated via a DBCO-(PEG)3-vc-PAB linker.

S-acetyl-PEG12-alcohol is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Biotin-PEG3-alcohol, a PEG-based linker for PROTACs, connects two essential ligands to form PROTAC molecules. This linker facilitates selective protein degradation by exploiting the ubiquitin-proteasome system within cells.

S-Acetyl-PEG3-C2-acid is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Azido-PEG3-S-PEG4-propargyl is a polyethylene glycol (PEG)-based linker containing azide and propargyl groups, designed specifically for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

S-acetyl-PEG20-alcohol is a PEG-based linker for PROTACs, joining two essential ligands and facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Tetrazine-Ph-NHCO-PEG3-alcohol is a polyethylene glycol (PEG) derived linker designed for synthesizing proteolysis targeting chimeras (PROTACs)[1].

S-acetyl-PEG4-Boc, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

(S,R,S)-AHPC-C2-PEG3-BCN (Compound 16b) serves as a VHL ligand and is applicable in the synthesis of PROTACs [1].'

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 is a synthetic E3 ligase ligand-linker conjugate composed of a VHL ligand and a linker, utilized in PROTAC BRD4 Degrader-5 and PROTAC BRD4 Degrader-5-CO-PEG3-N3.

S-acetyl-PEG5-alcohol is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

S-acetyl-PEG16-alcohol, a PEG-based linker for PROTACs, connects two essential ligands necessary for PROTAC molecule formation, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

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].

S-acetyl-PEG3-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

(S,R,S)-AHPC-(C3-PEG)2-C6-Cl is a small molecule HaloPROTAC incorporating the (S,R,S)-AHPC-based VHL ligand and a 2-unit PEG linker, capable of inducing degradation of GFP-HaloTag7 in cell-based assays [1].

Azido-PEG3-S-PEG3-azide is a polyethylene glycol (PEG)-derived linker engineered for the synthesis of proteolysis targeting chimeras (PROTACs)[1].