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2375283-62-6

2375283-62-6 Structure

2375283-62-6 Structure
IdentificationBack Directory
[Name]

Propanoic acid, 3-[2-[2-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-5-yl]amino]ethoxy]ethoxy]ethoxy]-
[CAS]

2375283-62-6
[Synonyms]

3-(2-(2-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)amino)ethoxy)ethoxy)ethoxy)propanoic acid
Propanoic acid, 3-[2-[2-[2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-5-yl]amino]ethoxy]ethoxy]ethoxy]-
[Molecular Formula]

C22H27N3O9
[MOL File]

2375283-62-6.mol
[Molecular Weight]

477.46
Chemical PropertiesBack Directory
[Boiling point ]

757.8±60.0 °C(Predicted)
[density ]

1.417±0.06 g/cm3(Predicted)
[solubility ]

DMSO : 125 mg/mL (261.80 mM; Need ultrasonic)
[form ]

Solid
[pka]

4.28±0.10(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Biological Activity]

Thalidomide-NH-PEG3-COOH is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1]. 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[2].
[References]

[1]. Sato T, et al. Cereblon-Based Small-Molecule Compounds to Control Neural Stem Cell Proliferation in Regenerative Medicine. Front Cell Dev Biol. 2021;9:629326. Published 2021 Mar 11. [2]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1002.
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