Azido-PEG4-Val-Cit-PAB-OH
Azido-PEG4-Val-Cit-PAB-OH Basic information
- Product Name:
- Azido-PEG4-Val-Cit-PAB-OH
- Synonyms:
-
- Azido-PEG4-Val-Cit-PAB-OH
- N3-PEG4-Val-Cit-PAB
- 1-azido-N-((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)-3,6,9,12-tetraoxapentadecan-15-amide
- CAS:
- 2055024-64-9
- MF:
- C29H48N8O9
- MW:
- 652.75
- Product Categories:
-
- ADC LINKER
- Mol File:
- 2055024-64-9.mol
Azido-PEG4-Val-Cit-PAB-OH Chemical Properties
- form
- Solid
- color
- White to off-white
Azido-PEG4-Val-Cit-PAB-OH Usage And Synthesis
Description
Azido-PEG4-Val-Cit-PAB-OH is a cleavable peptide linker. The Val-Cit will specifically be cleaved by Cathepsin B. Azido group enable click chemistry with DBCO, BCN or other Alkyne group. PEG spacer increases aqueous solubility.
Uses
Azido-PEG4-Val-Cit-PAB-OH is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. Azido-PEG4-Val-Cit-PAB-OH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[2]. Azido-PEG4-Val-Cit-PAB-OH 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.
IC 50
Protease Cleavable Linker; PEGs; Cleavable Linker
References
[1] Dan N, et al. Antibody-Drug Conjugates for Cancer Therapy: Chemistry to Clinical Implications. Pharmaceuticals (Basel). 2018 Apr 9;11(2). pii: E32. DOI:10.3390/ph11020032
[2] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562. DOI:10.1016/j.ebiom.2018.09.005
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