Amanote Research
Register
Sign In
Enzymatically Activated Glyco-Prodrugs of Doxorubicin Synthesized by a Catalysis-Free DielsAlder Reaction
doi 10.1021/acs.bioconjchem.8b00314.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Catalysis of the Aza-DielsAlder Reaction by Hydrogen and Halogen Bonds
Thermal Upgrade of Enzymatically Synthesized Aliphatic and Aromatic Oligoesters
Materials
Materials Science
Condensed Matter Physics
Pentapeptide Nanoreactor as a Platform for Halogenations, DielsAlder Reaction, and MoritaBaylisHillman Reaction
Evolutionary Selection of Enzymatically Synthesized Semiconductors From Biomimetic Mineralization Vesicles
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Prostate Activated Prodrugs and Imaging Agents
Isohexide and Sorbitol-Derived, Enzymatically Synthesized Renewable Polyesters With EnhancedTg
Biomacromolecules
Bioengineering
Materials Chemistry
Biomaterials
Plastics
Polymers
Design, Synthesis, and Preliminary Evaluation of Doxazolidine Carbamates as Prodrugs Activated by Carboxylesterases
Anticancer Prodrugs of Butyric Acid and Formaldehyde Protect Against Doxorubicin-Induced Cardiotoxicity
British Journal of Cancer
Cancer Research
Oncology
Catalysis by Heteropolyacid. I. Polymerization Reaction of Benzyl Alcohols
Bulletin of the Chemical Society of Japan
Chemistry
