| [1] | Yoshinari T., Nagashima T., Ishioka H., et al. (2025). Discovery of KRAS(G12D) selective degrader ASP3082. Commun. Chem. 8:254. DOI:10.1038/s42004-025-01662-4 |
| [2] | Khan N., Raza U., Ali Zaidi S.A., et al. (2025). Drugging the 'undruggable' KRAS: Breakthroughs, challenges, and opportunities in pancreatic cancer. Cancer Biol. Med. 22:762−788. DOI:10.20892/j.issn.2095-3941.2025.0122 |
| [3] | Miyamoto-Sato E., Imanishi S., Huang L., et al. (2023). A first-class degrader candidate targeting both KRAS G12D and G12V mediated by CANDDY technology independent of ubiquitination. Molecules 28:5600. DOI:10.3390/molecules28145600 |
| [4] | Nalawansha D.A., Mazis G., Husemoen G., et al. (2025). LYMTACs: Chimeric small molecules repurpose lysosomal membrane proteins for target protein relocalization and degradation. Nat. Commun. 16:7812. DOI:10.1038/s41467-025-63128-4 |
| [5] | Ghazi Vakili M., Gorgulla C., Snider J., et al. (2025). Quantum-computing-enhanced algorithm unveils potential KRAS inhibitors. Nat. Biotechnol. 43:1954−1959. DOI:10.1038/s41587-024-02526-3 |
| Du X. and Cao X. (2026). Breaking undruggable: The emergence of KRASG12D targeted therapy. The Innovation Medicine 4:100198. https://doi.org/10.59717/j.xinn-med.2026.100198 |
To request copyright permission to republish or share portions of our works, please visit Copyright Clearance Center's (CCC) Marketplace website at marketplace.copyright.com.
The strategy for breaking undruggable of KRASG12D.