Asandeutertinib
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| Other names | Runnor-9591, TY 9591 |
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| Formula | C28H30D3N7O2 |
| Molar mass | 502.636 g·mol−1 |
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Asandeutertinib is an investigational new drug that is being evaluated for the treatment of cancer. It is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) with antineoplastic properties.[1][2] Developed by TYK Medicines, this small molecule drug is currently being investigated for the treatment of non-small cell lung cancer (NSCLC), particularly in patients with EGFR mutations.[1][3]
It is a deuterated derivative of osimertinib, in which three hydrogen atoms are replaced by deuterium.[4]
References
- 1 2 "Asandeutertinib". PatSnap.
- ↑ "Asandeutertinib". IUPHAR/BPS Guide to PHARMACOLOGY.
- ↑ Han B, Zhang W, Wu L, Chen B, Zhao Y, Liu J, et al. (October 2024). "P1. 12A. 07 A Phase 1 Study of TY-9591 in Advanced Non-Small Cell Lung Cancer (NSCLC) Patients with EGFR Positive Mutation". Journal of Thoracic Oncology. 19 (10): S195. doi:10.1016/j.jtho.2024.09.353.
- ↑ Park CJ, Li MS, Ou SI (June 2025). "Old Wine in New Bottles? Deuterium Switch (Replacing Hydrogen With Deuterium) Comes to Thoracic Oncology as Deuterated Lorlatinib (Deulorlatinib, TGRX-326) and Deuterated Osimertinib (Asandeutertinib, TY-9591) in ALK+ NSCLC and EGFR+ NSCLC, Respectively". Journal of Thoracic Oncology. 20 (6): 708–713. doi:10.1016/j.jtho.2025.03.034. PMID 40484487.
