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Safety, pharmacodynamics, and exposure-response modeling results from a first-in-human phase 1 study of nedosiran (PHYOX1) in primary hyperoxaluria
381 Nonetheless, AT-101 and its derivative FX-11, galloflavin, and N-hydroxyindole-based compounds are promising cell-active LDHA inhibitors, which pharmaceutic effect hasnt been applied in clinical practice
BAVEREL, G., FORISSIER, M., & PELLET, M
Iron chelators were identified as inhibitors of cell death induction after RSL3 treatment [99]
Downregulation of calcium-dependent NMDA receptor desensitization by sodium-calcium exchangers: a role of membrane cholesterol
10.3389/fphar.2024.1378335 4 BooY
