Results for Lipids & Polymers ( 10244 )
N-(amine-PEG23)-N-bis(PEG3-azide) is a PEG reagent containing a terminal amine and two azide groups. The hydrophilic PEG spacer increases solubility in aqueous media. The azide groups can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde), etc. Reagent grade, for research use only.
(S, R, S)-AHPC-PEG6-Azide is a click chemistry PROTAC linker that incorporates an E3 ligase ligand with a PEG6 arm to empower PROTAC research & discovery. The hydrophilic PEG spacer increases the solubility of a compound in aqueous media. Azide enables click chemistry with alkyne, DBCO, or BCN molecule. Reagent grade, for research use only.
(S, R, S)-AHPC-PEG2-Azide is a click chemistry PROTAC linker that incorporates an E3 ligase ligand with a PEG2 arm to empower PROTAC research & discovery. The hydrophilic PEG spacer increases the solubility of a compound in aqueous media. Azide enables click chemistry with alkyne, DBCO, or BCN molecule. Reagent grade, for research use only.
N-(t-butyl ester-PEG6)-N-bis(PEG6-amine) is a PEG reagent that can easily react with activated NHS esters or carboxylic acid in the presence of EDC or HATU. The t-butyl group can be deprotected under acidic conditions. The hydrophilic PEG spacers increase the compounds water solubility in aqueous media. Reagent grade, for research use only.
Mal-PEG4-NH-Boc is a PEG linker containing a maleimide group and a Boc protected amine group. The hydrophilic PEG spacer increases solubility in aqueous media. The protected amine can be deprotected under acidic conditions. The maleimide group will react with a thiol group to form a covalent bond. Reagent grade, for research use only.
- Ref: BP-29556Sizes: 100 MG, 50 MG, 500 MG, 250 MG
t-Boc-N-amido-Tri-(azide-PEG23-ethoxymethyl)-methane is a branched PEG linker with a terminal Boc-protected amino group and three terminal azides. The azide groups enables PEGylation via Click Chemistry. The Boc group can be deprotected under mild acidic conditions to form the free amine. Reagent grade, for research use only.