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These combine monothiophosphate-backbone-substituted aptamers for enhanced stability and protein binding with chemically modified uridine (referred to as X) that allows drug-like compounds or additional functionalities to be attached to the aptamers

1 Discovery of DP as a potent inhibitor of HSCs activation

Characterization of thermo-responsive hydrogel and its skin adhesion and liposomal delivery potential CMC1-4 was synthesized via the chloroacetic acid oxidation of CS (Figure S12A)

NNMT-DNMT1 axis is essential for maintaining cancer cell sensitivity to oxidative phosphorylation inhibition

J Biol Chem 84:269320 Kazuhiko T, Yoshiyuki Y (2014) Method for production of glutathione or gamma-glutamylcysteine