Azido-PEG3-Val-Cit-PAB-PNP

98%

  • Product Code: 121088
  CAS:    2055047-18-0
Molecular Weight: 773.79 g./mol Molecular Formula: C₃₄H₄₇N₉O₁₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This compound is primarily utilized in the development of antibody-drug conjugates (ADCs), where it serves as a linker to connect cytotoxic drugs to antibodies. The azide group enables click chemistry reactions, facilitating efficient and selective conjugation. The Val-Cit dipeptide sequence is cleavable by cathepsin B, an enzyme overexpressed in many cancer cells, allowing for targeted drug release. The PAB (para-aminobenzyl) spacer enhances the stability of the linker, while the PNP (p-nitrophenyl) group acts as a leaving group during the conjugation process. This design ensures precise delivery of therapeutic agents to cancer cells, minimizing off-target effects and improving treatment efficacy.
Product Specification:
Test Specification
Appearance Yellow Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days £832.31
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Azido-PEG3-Val-Cit-PAB-PNP
This compound is primarily utilized in the development of antibody-drug conjugates (ADCs), where it serves as a linker to connect cytotoxic drugs to antibodies. The azide group enables click chemistry reactions, facilitating efficient and selective conjugation. The Val-Cit dipeptide sequence is cleavable by cathepsin B, an enzyme overexpressed in many cancer cells, allowing for targeted drug release. The PAB (para-aminobenzyl) spacer enhances the stability of the linker, while the PNP (p-nitrophenyl) group acts as a leaving group during the conjugation process. This design ensures precise delivery of therapeutic agents to cancer cells, minimizing off-target effects and improving treatment efficacy.
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