Mal-PEG1-Val-Cit-PAB-PNP
Mal-PEG1-Val-Cit-PAB-PNP Basic information
- Product Name:
- Mal-PEG1-Val-Cit-PAB-PNP
- Synonyms:
-
- Mal-PEG1-Val-Cit-PAB-PNP
- Mal-PEG1-Val-Cit-PAB-PNP ISO 9001:2015 REACH
- L-Ornithinamide, N-[3-[2-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)ethoxy]-1-oxopropyl]-L-valyl-N5-(aminocarbonyl)-N-[4-[[[(4-nitrophenoxy)carbonyl]oxy]methyl]phenyl]-
- CAS:
- 2249935-92-8
- MF:
- C34H41N7O12
- MW:
- 739.73
- Mol File:
- 2249935-92-8.mol
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Mal-PEG1-Val-Cit-PAB-PNP Chemical Properties
- Boiling point:
- 1039.5±65.0 °C(Predicted)
- Density
- 1.366±0.06 g/cm3(Predicted)
- solubility
- Soluble in DMSO, DMF
- pka
- 13.24±0.70(Predicted)
- form
- Solid
- color
- White to off-white
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Mal-PEG1-Val-Cit-PAB-PNP Usage And Synthesis
Description
Mal-PEG1-Val-Cit-PAB-PNP is a cleavable peptide linker. The Val-Cit was designed to be cleaved by Cathepsin B. Maleimide (Mal) group is reactive toward thiol groups at pH 6.5 to 7.5. PNP is a good leaving group.
Uses
Mal-PEG1-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
IC 50
Protease Cleavable Linker; Cleavable Linker
References
[1] Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337. DOI:10.1038/nrd.2016.268
Mal-PEG1-Val-Cit-PAB-PNPSupplier
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