ChemicalBook--->CAS DataBase List--->1010100-22-7

1010100-22-7

1010100-22-7 Structure

1010100-22-7 Structure
IdentificationBack Directory
[Name]

ODZXEQVQLJKSQH-UHFFFAOYSA-N
[CAS]

1010100-22-7
[Synonyms]

ODZXEQVQLJKSQH-UHFFFAOYSA-N
Thalidomide-5-CH2-NH2 (hydrochloride)
5-(aminomethyl)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride
5-(aminomethyl)-2-(2,6-dioxopiperidin-3-yl)-2,3-dihydro-1H-isoindole-1,3-dione hydrochloride
1H-Isoindole-1,3(2H)-dione, 5-(aminomethyl)-2-(2,6-dioxo-3-piperidinyl)-, hydrochloride (1:1)
[Molecular Formula]

C14H14ClN3O4
[MDL Number]

MFCD32666042
[MOL File]

1010100-22-7.mol
[Molecular Weight]

323.73
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

Solid
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Thalidomide-5-CH2-NH2 (hydrochloride) is the Thalidomide-based cereblon ligand used in the recruitment of CRBN protein. Thalidomide-5-CH2-NH2 (hydrochloride) can be connected to the ligand for protein by a linker to form PROTACs[1].
[IC 50]

Cereblon
[References]

[1] Makbul C, Nassal M, B?ttcher B. Slowly folding surface extension in the prototypic avian hepatitis B virus capsid governs stability. Elife. 2020;9:e57277. Published 2020 Aug 14. DOI:10.7554/eLife.57277
[2] Sato T, Ito T, Handa H. 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. DOI:10.3389/fcell.2021.629326
Spectrum DetailBack Directory
[Spectrum Detail]

ODZXEQVQLJKSQH-UHFFFAOYSA-N(1010100-22-7)1HNMR
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