Orthogonal non-natural amino acids add aldehyde, azide, or hydroxylamine groups to proteins for selective, stable covalent linkage formation.
Structural changes to dolaproine-dolaisoleuine peptides improve metabolic stability while preserving microtubule-disrupting anticancer activity.
A dual-linker protein-drug conjugate balances plasma stability with hydrolase-cleavable release while controlling payload ratio to limit aggregation.
Targeting SARS-CoV-2 nsp5 protease with a pyrazolopyrimidine urea compound helps suppress viral replication and reduce COVID-19 severity.
Combining tasquinimod with proteasome inhibitors, immunomodulatory imides, and antibodies helps counter myeloma relapse and resistance.
An aromatic-cationic peptide raises TAZ1 expression to stabilize cardiolipin remodeling and reduce Barth syndrome severity.
Reverse dropwise solvent crystallization replaces silica gel chromatography to purify MMAE with higher yield, purity, and scale-up efficiency.
Targeting adipose FATP2 with PKCα-derived peptides reduces liver steatosis, triglycerides, and fibrosis when existing NAFLD treatments fall short.