(S,R,S)-AHPC-C6-PEG3-butyl-N3

CAT:
804-HY-151791
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  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
(S,R,S)-AHPC-C6-PEG3-butyl-N3 - image 1

(S,R,S)-AHPC-C6-PEG3-butyl-N3

  • CAS Number:

    2300155-90-0
  • UNSPSC Description:

    (S,R,S)-AHPC-C6-PEG3-butyl-N3 is a click chemistry reagent containing an azide group. (S,R,S)-AHPC-C6-PEG3-butyl-N3 serves as crosslinker-E3 ligase ligand conjugate, Click reactive protein degrader building block for PROTAC research, Template for synthesis of targeted protein degrader, VH032 conjugate[1]. (S,R,S)-AHPC-C6-PEG3-butyl-N3 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.
  • Target Antigen:

    ADC Linker; E3 Ligase Ligand-Linker Conjugates
  • Type:

    Reference compound
  • Related Pathways:

    Antibody-drug Conjugate/ADC Related;PROTAC
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Others
  • Assay Protocol:

    https://www.medchemexpress.com/s-r-s-ahpc-c6-peg3-butyl-n3.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    [N-]=[N+]=NCCCCCCOCCOCCOCCCCCC(N[C@@H](C(C)(C)C)C(N1[C@@H](C[C@H](C1)O)C(NCC2=CC=C(C3=C(C)N=CS3)C=C2)=O)=O)=O
  • Molecular Weight:

    757.98
  • References & Citations:

    [1]Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789.
  • Shipping Conditions:

    Room temperature
  • Clinical Information:

    No Development Reported