Product Description: IACS-13909 is a selective, potent and orally active SHP2 allosteric inhibitor with an IC50 of 15.7 nM and a Kd of 32 nM. IACS-13909 is more selective for SHP2 than other phosphatases (including SHP1). IACS-13909 has antitumor activities and suppresses MAPK pathway signaling in receptor tyrosine kinases (RTK)-dependent cancers[1].
Applications: Cancer-Kinase/protease
Formula: C17H18Cl2N6
References: [1]Yuting Sun, et al. Allosteric SHP2 Inhibitor, IACS-13909, Overcomes EGFR-Dependent and EGFR-Independent Resistance Mechanisms toward Osimertinib. Cancer Res. 2020 Nov 1;80(21):4840-4853.
CAS Number: 2160546-07-4
Molecular Weight: 377.27
Compound Purity: 99.97
Research Area: Cancer
Solubility: DMSO : 10 mg/mL (ultrasonic)
Target: Phosphatase;SHP2