Powder: -20°C for 3 years | In solvent: -80°C for 1 year
N3-PEG3-CH2CH2COOH, a PEG-based PROTAC linker, is utilized in the synthesis of BI-3663, BI-4216, and BI-0319. Additionally, Azido-PEG3-acid, a non-cleavable 3-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs).
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Description | N3-PEG3-CH2CH2COOH, a PEG-based PROTAC linker, is utilized in the synthesis of BI-3663, BI-4216, and BI-0319. Additionally, Azido-PEG3-acid, a non-cleavable 3-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs). |
In vitro | PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. |
Molecular Weight | 247.2484 |
Formula | C9H17N3O5 |
CAS No. | 1056024-94-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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N3-PEG3-CH2CH2COOH 1056024-94-2 Others N3PEG3CH2CH2COOH N-3-PEG3-CH2CH2COOH N3 PEG3 CH2CH2COOH inhibitor inhibit