PeptideDB

CH7233163

CH7233163

CAS No.:

CH7233163 is a non-covalent ATP competitive inhibitor of EGFR-Del19/T790M/C797S. CH7233163 can overcome Osimertinib resi
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This product is for research use only, not for human use. We do not sell to patients.

CH7233163 is a non-covalent ATP competitive inhibitor of EGFR-Del19/T790M/C797S. CH7233163 can overcome Osimertinib resistance EGFR-Del19/T790M/C797S mutation. CH7233163 blocks EGFR phosphorylation in Del19/T790M/C797S_NIH3T3 cells. CH7233163 has anti-tumor activity.

Physicochemical Properties


Related CAS # NA for CH 7233163; CH-7233163
Appearance Off-white to light yellow solid powder
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


References

[1]. CH7233163 Overcomes Osimertinib-Resistant EGFR-Del19/T790M/C797S Mutation. Mol Cancer Ther. 2020 Nov;19(11):2288-2297.


Solubility Data


Solubility (In Vitro) May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
Solubility (In Vivo) Solubility in Formulation 1: ≥ 2.5 mg/mL (3.73 mM) (saturation unknown) in 10% DMSO + 40% PEG300 +5% Tween-80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 + to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

 (Please use freshly prepared in vivo formulations for optimal results.)