alcohol

Aminooxy-PEG4-alcohol is both a non-cleavable 4-unit PEG ADC linker and a PEG-based PROTAC linker.

Azide-PEG12-alcohol, a PEG-based PROTAC linker, is utilized in PROTAC synthesis.

4-(Trifluoromethoxy)benzyl alcohol, with CAS No. 1736-74-9, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 4-(Trifluoromethoxy)benzyl alcohol provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Mebeverine alcohol [Mebeverine metabolite]: Mebeverine alcohol is a primary metabolite of the antispasmodic agent Mebeverine.

Mebeverine metabolite O-desmethyl Mebeverine alcohol is a potent α1 repector inhibitor, causing relaxation of the gastrointestinal tract. Mebeverine metabolite O-desmethyl Mebeverine alcohol is a metabolite of Mebeverine.

1,1,1-Trifluoroethyl-PEG4-alcohol is a polyethylene glycol (PEG) derivative typically used as a linker in the synthesis of protein degrader molecules, known as PROTACs [1].

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

(2-Pyridyldithio)-PEG4-alcohol, a PEG-based PROTAC linker, is used for the synthesis of PROTACs[1].

Amino-PEG4-alcohol is a PEG-based PROTAC linker used for synthesizing PROTACs[1] and a non-cleavable 4-unit PEG ADC linker for synthesizing antibody-drug conjugates (ADCs)[2].

Amino-PEG6-OH is a non-cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Aminooxy-PEG2-alcohol is a non-cleavable PEG linker comprising two units, used in the synthesis of antibody-drug conjugates (ADCs) [1] and as a PEG-based PROTAC linker for the synthesis of PROTACs [2].

Azide-PEG8-alcohol is a PEG-based linker used for PROTACs, facilitating the connection of two essential ligands and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Azido-PEG2-alcohol, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, thereby 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.

Azido-PEG4-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.

Azido-PEG5-alcohol, a non-cleavable 5 unit polyethylene glycol (PEG) ADC linker, finds application in the synthesis of antibody-drug conjugates (ADCs)[1]. Additionally, it serves as a PEG-based PROTAC linker for the synthesis of PROTACs[2].

Azido-PEG6-alcohol is a polyethylene glycol (PEG)-based PROTAC linker utilized in PROTAC synthesis[1]. It also functions as a non-cleavable PEG linker consisting of six units, specifically employed in the synthesis of antibody-drug conjugates (ADCs)[2].

Azido-PEG7-alcohol 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 (brackets).

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.

Biotin-PEG6-alcohol is a PEG-based PROTAC linker containing a biotin label. This compound serves as a key component in the synthesis of PROTACs, facilitating the conjugation of target-recruiting moiety and E3 ligase-recruiting moiety [1].

Biotin-PEG8-alcohol is a PEG-based linker for PROTACs, joining two essential ligands and facilitating selective protein degradation through the ubiquitin-proteasome system within cells.

Bromo-PEG2-alcohol, 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.

Bromo-PEG5-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.

Bromo-PEG6-alcohol is a PEG-based linker for PROTACs (Proteolysis Targeting Chimeras) that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.