benzyl

5-ALA benzyl ester hydrochloride (Benzyl-ALA hydrochloride) is a protoporphyrin precursor used as a photodetection agent. It induces protoporphyrin IX (PPIX) accumulation in colon carcinoma cell lines.

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.

Benzyl-α-GalNAc (O-glycosylation-IN-1) is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.

Benzyl-PEG1-Tos, a PEG-based linker for PROTACs, joins two essential ligands necessary for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Benzyl-PEG2-amine is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Benzyl-PEG2-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs.

Benzyl-PEG2-CH2-Boc is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands necessary for PROTAC molecule formation. This linker promotes selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Benzyl-PEG2-Tos 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.

Benzyl-PEG3-CH2-Boc 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.

Benzyl-PEG4-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for PROTAC molecule formation, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Benzyl-PEG5-amine is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Benzyl-PEG5-azide, a PEG-based linker for PROTACs, joins two essential ligands crucial for the formation of PROTAC molecules, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Benzyl-PEG5-Ms 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.

N-Benzyl-N-bis-PEG2 is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands necessary for PROTAC molecule formation, and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

N-Benzyl-N-bis-PEG4 is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

Amino-PEG4-benzyl ester, a PEG- and Alkyl/ether-based PROTAC linker, serves as a valuable component for the synthesis of PROTACs[1].

Benzyl-N-bis(PEG3-Boc) is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands necessary for PROTAC formation, thereby enabling selective protein degradation via the ubiquitin-proteasome system within cells.

HO-PEG1-benzyl ester is a PEG-based linker for PROTACs, joining two essential ligands and enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

HO-PEG4-benzyl ester 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.

N-Benzyl-N-bis(PEG3-acid) is a polyethylene glycol (PEG)-based PROTAC linker that facilitates the synthesis of PROTACs[1].

Benzyl 2-naphthyl ether causes the activation of the aryl hydrocarbon receptor.

Valsartan benzyl ester is a intermediate of Valsartan.

Acetamide, 2,2-dichloro-N-(2-hydroxyethyl)-N-(o-(methylsulfonyl)benzyl)- is a bioactive chemical.

Acetamide, 2,2-dichloro-N-(2-hydroxyethyl)-N-(p-(methylsulfonyl)benzyl)-, acetate (ester) is a bioactive chemical.