Basic information Safety Supplier Related

Pomalidomide-C6-NH2?hydrochloride

Basic information Safety Supplier Related

Pomalidomide-C6-NH2?hydrochloride Basic information

Product Name:
Pomalidomide-C6-NH2?hydrochloride
Synonyms:
  • Pomalidomide-C6-NH2?hydrochloride
  • 4-((6-aminohexyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
  • Thalidomide-NH-C6-NH2 HCl
  • Thalidomide-NH-C6-NH2 hydrochloride
  • E3 Ligase Ligand-Linker Conjugates,inhibit,Thalidomide-NH-C-6-NH2 hydrochloride,ThalidomideNHC6NH2 hydrochloride,Thalidomide NH C6 NH2 hydrochloride,Inhibitor
  • 4-((6-Aminohexyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride, Crosslinker?E3 ligase ligand conjugate, Pomalidomide conjugate, Protein degrader building block for PROTAC? research, Template for synthesis of targeted protein degrader
  • Poma-C6-NH2·HCl
  • Pomalidomide 4'-alkylC6-amine
CAS:
2375194-37-7
MF:
C19H25ClN4O4
MW:
408.88
Mol File:
2375194-37-7.mol
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Pomalidomide-C6-NH2?hydrochloride Chemical Properties

storage temp. 
2-8°C
solubility 
DMSO: Soluble
Methanol: Soluble
form 
Solid
color 
Light yellow to yellow
InChI
1S/C19H24N4O4.ClH/c20-10-3-1-2-4-11-21-13-7-5-6-12-16(13)19(27)23(18(12)26)14-8-9-15(24)22-17(14)25;/h5-7,14,21H,1-4,8-11,20H2,(H,22,24,25);1H
InChIKey
PBGMRXNTLPSDNR-UHFFFAOYSA-N
SMILES
O=C(C(CC1)N(C2=O)C(C3=C2C=CC=C3NCCCCCCN)=O)NC1=O.Cl
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Safety Information

WGK Germany 
WGK 3
Storage Class
6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications
Repr. 1B
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Pomalidomide-C6-NH2?hydrochloride Usage And Synthesis

Uses

Thalidomide-NH-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1].

reaction suitability

reactivity: carboxyl reactive
reagent type: ligand-linker conjugate

IC 50

Cereblon

References

[1] Sato T, et al. 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
[2] Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-985. DOI:10.7554/eLife.57277
[3] ZHIQIANG SUN . Discovery of pomalidomide-based PROTACs for selective degradation of histone deacetylase 8[J]. European Journal of Medicinal Chemistry, 2022, 239: Article 114544. DOI: 10.1016/j.ejmech.2022.114544

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