ChemicalBook--->CAS DataBase List--->2055047-18-0

2055047-18-0

2055047-18-0 Structure

2055047-18-0 Structure
IdentificationBack Directory
[Name]

Azido-PEG3-Val-Cit-PAB-PNP
[CAS]

2055047-18-0
[Synonyms]

Azido-PEG3-Val-Cit-PAB-PNP
[Molecular Formula]

C34H47N9O12
[MDL Number]

MFCD30527416
[MOL File]

2055047-18-0.mol
[Molecular Weight]

773.8
Chemical PropertiesBack Directory
[solubility ]

Soluble in DMSO, DMF
[form ]

Solid
[color ]

White to light yellow
[InChIKey]

HLBCDJANEWKOSX-XIKWSGLJNA-N
[SMILES]

[C@@H](CCCNC(=O)N)(NC(=O)[C@H](C(C)C)NC(=O)CCOCCOCCOCCN=[N+]=[N-])C(=O)NC1C=CC(COC(=O)OC2C=CC(N(=O)=O)=CC=2)=CC=1 |&1:0,11,r|
Hazard InformationBack Directory
[Description]

Azido-PEG3-Val-Cit-PAB-PNP is a cleavable peptide ADC linker. The Val-Cit will specifically be cleaved by Cathepsin B. PNP groupg is a good leaving group when treating with aminebearing payload. Azido group will react with DBCO, BCN or other Alkyne group through click chemistry, PEG spacer increases aqueous solubility.
[Uses]

Azido-PEG3-Val-Cit-PAB-PNP is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. Azido-PEG3-Val-Cit-PAB-PNP is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[2]. Azido-PEG3-Val-Cit-PAB-PNP 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]

PEGs; Protease Cleavable Linker; 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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