1. Metabolic Enzyme/Protease
  2. NEDD8-activating Enzyme
  3. 2112731-49-2

2112731-49-2

N-(Biotin-PEG4)-N-bis(PEG4-acid) hydrochloride Chemical Structure

2112731-49-2

Chemical Structure

  • N-(Biotin-PEG4)-N-bis(PEG4-acid) hydrochloride
  • CAS No: 2112731-49-2
    Formula: C42H79ClN4O18S
    Molecular Weight: 995.61
  • IUPAC Name: 16-(16-oxo-20-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-3,6,9,12-tetraoxa-15-azaicosyl)-4,7,10,13,19,22,25,28-octaoxa-16-azahentriacontanedioic acid hydrochloride
  • InChIKey: UPHBIHBKUOLKFH-MRTVQABZSA-N
  • SMILES: OC(CCOCCOCCOCCOCCN(CCOCCOCCOCCOCCC(O)=O)CCOCCOCCOCCOCCNC(CCCC[C@H]1[C@]2([H])[C@](NC(N2)=O)([H])CS1)=O)=O.Cl

Biological Activity: N-(Biotin-PEG4)-N-bis(PEG4-acid) hydrochloride is a branched biotinylation reagent for labeling. The carboxylic acid groups can react with primary amines in the presence of EDC and HATU to form stable amide bonds.

Cat. No. Product Name Purity Description
HY-130598 N-(Azido-PEG3)-N-Boc-PEG4-acid N-(Azido-PEG3)-N-Boc-PEG4-acid is a PEG-based PROTAC linker with a terminal azide group and is used in the synthesis of PROTACs N-(Azido-PEG3)-N-Boc-PEG4-acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.