nh2 peg3 hydrochloride

NH2-PEG3 hydrochloride is a PEG-based linker for PROTACs, crucial for joining two essential ligands to form PROTAC molecules. This compound facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

(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.

Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate, combines a Thalidomide-based cereblon ligand with a two-unit PEG linker for use in PROTAC technology[1].

Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate, incorporates a cereblon ligand derived from Thalidomide and a 3-unit PEG linker. This compound is specifically designed for use in PROTAC technology, which utilizes small molecules to induce protein degradation [1].

JQ-1 carboxylic acid-PEG3-C2-NH2 (hydrochloride) is an E3 ligase ligand-linker conjugate that is useful for synthesizing PRPTAC.

Thalidomide-PEG3-NH2 hydrochloride is a Thalidomide-based cereblon ligand that recruits CRBN proteins. This compound can be connected to a target protein ligand via a linker to form a PROTAC molecule, such as THAL-SNS-032.

Thalidomide-NH-amido-PEG3-C2-NH2 hydrochloride is a synthetic conjugate of an E3 ligase ligand-linker, comprising a Thalidomide-based cereblon ligand and one linker, and is utilized for synthesizing PROTAC.

Fmoc-NH-CH2-PEG3-C2-NH2 (hydrochloride) is a PROTAC linker designed for the synthesis of PROTAC molecules.

Pomalidomide-amino-PEG3-NH2 hydrochloride is an E3 ligase ligand-linker conjugate containing a pomalidomide-based cereblon ligand and a linker, which can be used to synthesize PROTACs.

Pomalidomide-PEG3-C2-NH2 hydrochloride, also known as Cereblon Ligand-Linker Conjugate 5, is a chemically synthesized E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Pomalidomide and a linker commonly employed in PROTAC technology.

Thalidomide-5-NH-PEG3-NH2 hydrochloride is a cereblon ligand based on Thalidomide that targets CRBN proteins. It utilizes a linker to attach to a target protein ligand, facilitating the formation of a PROTAC molecule, such as THAL-SNS-032.

Me-Tet-PEG3-NH2 hydrochloride is an ADC linker containing three PEG units. This compound, with its tetrazine group, specifically undergoes an inverse electron demand Diels-Alder reaction (iEDDA) with compounds bearing a TCO group.