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1416990-08-3

1416990-08-3 Structure

1416990-08-3 Structure
IdentificationBack Directory
[Name]

3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione
[CAS]

1416990-08-3
[Synonyms]

Lenalidomide-OH
3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione
3-(5-hydroxy-1-oxo-2,3-dihydro-1H-isoindol-2-yl)piperidine-2,6-dione
3-(1,3-Dihydro-5-hydroxy-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedione
2,6-Piperidinedione, 3-(1,3-dihydro-5-hydroxy-1-oxo-2H-isoindol-2-yl)-
[Molecular Formula]

C13H12N2O4
[MDL Number]

MFCD31794971
[MOL File]

1416990-08-3.mol
[Molecular Weight]

260.25
Chemical PropertiesBack Directory
[Boiling point ]

631.5±55.0 °C(Predicted)
[density ]

1.498±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

8.32±0.20(Predicted)
[color ]

Off-white to gray
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Lenalidomide-OH is an analog of cereblon (CRBN) ligand Lenalidomide for E3 ubiquitin ligase, and is used in the recruitment of CRBN protein. Lenalidomide-OH can be connected to the ligand for protein by a linker to form PROTACs, such as the PROTAC BTK degrader SJF620 (HY-133137)[1].
[IC 50]

Cereblon
[References]

[1] Jaime-Figueroa S, et al. Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic properties. 2020 Feb 1;30(3):126877. DOI:10.1016/j.bmcl.2019.126877
Spectrum DetailBack Directory
[Spectrum Detail]

3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione(1416990-08-3)1HNMR
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