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ChemicalBook--->CAS DataBase List--->1323403-33-3

1323403-33-3

1323403-33-3 Structure

1323403-33-3 Structure
IdentificationBack Directory
[Name]

CC220
[CAS]

1323403-33-3
[Synonyms]

CC220
CS-2470
Iberdomide
Iberdomide(CC220)
CC-220 Iberdomide
CC220; CC 220; CC-220
(S)-3-[4-(4-morpholin-4-yl-methyl-benzyloxy)-1-oxo-1,3-dihydro-isoindol-2-yl]-piperidine-2,6-dione
2,6-Piperidinedione, 3-[1,3-dihydro-4-[[4-(4-morpholinylmethyl)phenyl]methoxy]-1-oxo-2H-isoindol-2-yl]-, (3S)-
[Molecular Formula]

C25H27N3O5
[MDL Number]

MFCD31382133
[MOL File]

1323403-33-3.mol
[Molecular Weight]

449.5
Chemical PropertiesBack Directory
[Boiling point ]

717.8±60.0 °C(Predicted)
[density ]

1.332±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:125.0(Max Conc. mg/mL);278.09(Max Conc. mM)
[form ]

A crystalline solid
[pka]

10.70±0.40(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Iberdomide (CC-220) is an orally active and potent cereblon (CRBN) E3 ligase modulator (CELMoD) with an IC50 of ~150?nM for cereblon-binding affinity. Iberdomide, a derivative of Thalidomide (HY-14658), has antitumor and immunostimulatory activities[1][2].
[in vivo]

Iberdomide (CC-220; 10 mg/kg; oral gavage) after 6 or 24 hours causes higher hCRBN expression in hC343 splenocytes correlated to deeper IKZF1/3 downregulation in WT (C57BL/6), hC123, or-343, (representing two different transgenic founder lines expressing hCRBN) and mCrbn-/- mice[2].

[IC 50]

Cereblon
[storage]

Store at -20°C
[References]

[1] Chad C Bjorklund, et al. Iberdomide (CC-220) is a potent cereblon E3 ligase modulator with antitumor and immunostimulatory activities in lenalidomide- and pomalidomide-resistant multiple myeloma cells with dysregulated CRBN. Leukemia. 2020 Apr;34(4):1197-1201. DOI:10.1038/s41375-019-0620-8
[2] Erin W Meermeier, et al. Tumor burden limits bispecific antibody efficacy through T cell exhaustion averted by concurrent cytotoxic therapy. Blood Cancer Discov. 2021 Jul;2(4):354-369. DOI:10.1158/2643-3230.BCD-21-0038
Spectrum DetailBack Directory
[Spectrum Detail]

CC220(1323403-33-3)1HNMR
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