Chemistry:Camonsertib

From HandWiki

Camonsertib is an investigational new drug that is being evaluated for the treatment of cancer. It is a selective oral small molecule inhibitor of ATR (Ataxia telangiectasia and Rad3 related), developed by Repare Therapeutics. This drug targets tumors with specific genetic alterations that create vulnerabilities in DNA damage response (DDR) pathways, particularly those with ATM or BRCA1/BRCA2 mutations.[1] It is currently in Phase 2 clinical trials both as a monotherapy and in combination with other agents, including PARP inhibitors, gemcitabine, and lunresertib.[2]

References

  1. "Discovery of the Potent and Selective ATR Inhibitor Camonsertib (RP-3500)". Journal of Medicinal Chemistry 67 (4): 2349–2368. February 2024. doi:10.1021/acs.jmedchem.3c01917. PMID 38299539. 
  2. "Pyrazolopyridine-based kinase inhibitors for anti-cancer targeted therapy". RSC Medicinal Chemistry 15 (5): 1452–1470. May 2024. doi:10.1039/d4md00003j. PMID 38784451.