Iberdomide

Chemical compound From Wikipedia, the free encyclopedia

Iberdomide (CC-220) is an experimental thalidomide analog[1] that works as an cereblon E3 ligase modulator; it has a higher binding affinity than lenalidomide or pomalidomide. It is developed by Bristol Myers Squibb for various cancers[2][3][4][5][6][7][8] and was also tested in people with lupus.[9]

CAS Number
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Iberdomide
Identifiers
  • (3S)-3-[7-({4-[(morpholin-4-yl)methyl]phenyl}methoxy)-3-oxo-1H-isoindol-2-yl]piperidine-2,6-dione
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC25H27N3O5
Molar mass449.507 g·mol−1
3D model (JSmol)
  • O=C1CC[C@H](N2Cc3c(OCc4ccc(CN5CCOCC5)cc4)cccc3C2=O)C(=O)N1
  • InChI=1S/C25H27N3O5/c29-23-9-8-21(24(30)26-23)28-15-20-19(25(28)31)2-1-3-22(20)33-16-18-6-4-17(5-7-18)14-27-10-12-32-13-11-27/h1-7,21H,8-16H2,(H,26,29,30)/t21-/m0/s1
  • Key:IXZOHGPZAQLIBH-NRFANRHFSA-N
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Iberdomide has been tested in combination with Bi-specific T-cell engagers in the B-Cell Non-Hodgkin Lymphoma setting,[10] but has been dropped in favor of golcadomide (CC-99282).

References

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