Thalidomide-PEG5-NH2 hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: I042496
  • CAS Number: 2703775-06-6
  • Molecular Formula: C23H32ClN3O9
  • Molecular Weight: 529.97
  • Purity: ≥95%
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Thalidomide-PEG5-NH2 hydrochloride (Cat No.: I042496) is a thalidomide-based compound modified with a five-unit polyethylene glycol (PEG5) linker terminating in a primary amine group. This design enhances solubility, flexibility, and biocompatibility, making it ideal for constructing PROTACs and other targeted therapeutic conjugates. The PEG5 spacer allows optimal spatial orientation for binding to target proteins and E3 ligases, such as cereblon, facilitating selective protein degradation. The hydrochloride salt form improves stability and handling, supporting its use in drug discovery, chemical biology, and medicinal chemistry research.


CAS Number 2703775-06-6
Synonyms

5-[2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione;hydrochloride

Molecular Formula C23H32ClN3O9
Purity ≥95%
InChI InChI=1S/C23H31N3O9.ClH/c24-5-6-31-7-8-32-9-10-33-11-12-34-13-14-35-16-1-2-17-18(15-16)23(30)26(22(17)29)19-3-4-20(27)25-21(19)28;/h1-2,15,19H,3-14,24H2,(H,25,27,28);1H
InChIKey BNZDMYCPKJWMFA-UHFFFAOYSA-N
SMILES C1CC(=O)NC(=O)C1N2C(=O)C3=C(C2=O)C=C(C=C3)OCCOCCOCCOCCOCCN.Cl
Reference

[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.
[Content Brief]

[2]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1005.
[Content Brief]

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