1243329-97-6

Lenalidomide hydrochloride Chemical Structure
1243329-97-6

Chemical Structure

Lenalidomide hydrochloride

Synonym(s): CC-5013 hydrochloride

  • CAS No.: 1243329-97-6
  • Formula:C13H14ClN3O3
  • Molecular Weight:295.72

IUPAC Name: 3-(4-amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione hydrochloride

InChIKey: RYWZLJSDFZVVTD-UHFFFAOYSA-N

SMILES: O=C1C2=CC=CC(N)=C2CN1C(C(N3)=O)CCC3=O.[H]Cl

Biological Activity: Lenalidomide hydrochloride (CC-5013 hydrochloride) is an orally active immunomodulatory agent that binds CRBN as a molecular glue to alter substrate specificity, inducing ubiquitination and proteasome-dependent degradation of IKZF1, IKZF3 and CK1α. Lenalidomide hydrochloride induces apoptosis by degrading IKZF1/3, and activates p53 by degrading CK1α. Lenalidomide hydrochloride promotes IL-2 release and effector functions of CD8+ T/NK cells, while inhibiting TNF-α secretion and M1-type pyroptosis. Lenalidomide hydrochloride can be used in research related to hematological malignancies, acute liver failure and acute kidney injury[1][2][3][4][5].

Cat. No. Product Name Purity Description Pricing
HY-A0003A
Lenalidomide hydrochloride Lenalidomide hydrochloride (CC-5013 hydrochloride) is an orally active immunomodulatory agent that binds CRBN as a molecular glue to alter substrate specificity, inducing ubiquitination and proteasome-dependent degradation of IKZF1, IKZF3 and CK1α. Lenalidomide hydrochloride induces apoptosis by degrading IKZF1/3, and activates p53 by degrading CK1α. Lenalidomide hydrochloride promotes IL-2 release and effector functions of CD8+ T/NK cells, while inhibiting TNF-α secretion and M1-type pyroptosis. Lenalidomide hydrochloride can be used in research related to hematological malignancies, acute liver failure and acute kidney injury.
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