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SHP2 PROTAC R1-5C

Chemical Structure : SHP2 PROTAC R1-5C

CAS No.:

SHP2 PROTAC R1-5C

Catalog No.: PC-38182Not For Human Use, Lab Use Only.

SHP2 PROTAC R1-5C is a potent and highly selective SHP2 PROTAC created by conjugating RMC-4550 with pomalidomide using a PEG linker, with a low nanomolar DC50.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

SHP2 PROTAC R1-5C is a potent and highly selective SHP2 PROTAC created by conjugating RMC-4550 with pomalidomide using a PEG linker, with a low nanomolar DC50.
SHP2 PROTAC R1-5C is highly selective for SHP2, induces degradation of SHP2 in leukemic cells at submicromolar concentrations.
SHP2 PROTAC R1-5C inhibits MAPK signaling, and suppresses cancer cell growth.
SHP2 PROTACs serve as an alternative strategy for targeting ERK-dependent cancers and are useful tools alongside allosteric inhibitors for dissecting the mechanisms by which SHP2 exerts its oncogenic activity.

Physicochemical Properties

M.Wt 1119.057
Formula C52H69Cl2N7O16
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-(23-(4-(5-((3S,4S)-4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-6-(hydroxymethyl)-3-methylpyrazin-2-yl)-2,3-dichlorophenoxy)-3,6,9,12,15,18,21-heptaoxatricosyl)-2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)acetamide

References

1. Vidyasiri Vemulapalli, et al. Biochemistry. 2021 Aug 31;60(34):2593-2609.

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