Comparison

SHP2-D26 European Partner

Item no. HY-145162-1mg
Manufacturer MedChem Express
CASRN 2458219-65-1
Amount 1 mg
Quantity options 100 mg 10 mg 1 ea 1 mg 25 mg 5 mg
Specific against other
Purity 95.03
Citations [1]Wang M, et al. Discovery of SHP2-D26 as a First, Potent, and Effective PROTAC Degrader of SHP2 Protein [published correction appears in J Med Chem. 2021 Jan 14;64(1):906-908]. J Med Chem. 2020;63(14):7510-7528.
Smiles ClC(C(SC1=NC=C(N2CCC(N)(CC2)C)N=C1N)=CC=C3)=C3NC(CCC(N(CC4)CCN4CCCCCCCCC(N[C@@H](C(C)(C)C)C(N5[C@@H](C[C@H](C5)O)C(N[C@H](C6=CC=C(C7=C(C)N=CS7)C=C6)C)=O)=O)=O)=O)=O
Available
Product Description
SHP2-D26 is a first, potent and effective SHP2 degrader. SHP2-D26 induces SHP2 degradation requires binding to VHL-1 and SHP2 proteins. SHP2-D26 is also neddylation- and proteasome-dependent[1].
StorageTemperature
-20°C, 3 years; 4°C, 2 years (Powder)
Shipping
Room Temperature
Manufacturers Applications
Cancer-programmed cell death
MolecularWeight
1115.89
Clinical Information
No Development Reported
Manufacturers Research Area
Cancer
Solubility
DMSO : 83.33 mg/mL (ultrasonic)
Target
Phosphatase; PROTACs; SHP2
Manufacturers Target
Phosphatase; PROTACs; SHP2
Manufacturers Pathway
Metabolic Enzyme/Protease; PROTAC; Protein Tyrosine Kinase/RTK
Manufacturers Product type
Reference compound

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 mg
Available: In stock
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