Rationally Engineered, Chemically Stable Tunicamycin Analogues Decouple DPAGT1 Inhibition from Non-Selective Toxicity
Katsuhiko Mitachi, Antonio Sánchez‐Ruiz, David Mingle, Iván Cheng‐Sánchez, Jacob M. Kirsh, Francisco Sarabia, William Clemons, Michio Kurosu
This paper develops chemically stable tunicamycin analogues that inhibit DPAGT1 selectively with reduced toxicity and improved pharmacokinetics.
bioRxiv · Jul 29, 2026 · PreprintBiochemistry