A facile enzymatic process for the preparation of (s)-Naproxen ester prodrug in organic solvents
- 30 June 1997
- journal article
- Published by Elsevier in Enzyme and Microbial Technology
- Vol. 20 (8) , 635-639
- https://doi.org/10.1016/s0141-0229(96)00222-0
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Pharmacokinetic results on naproxen prodrugs based on poly(ethyleneglycol)sJournal of Biomaterials Science, Polymer Edition, 1995
- Synthesis and Evaluation of Morpholinoalkyl Ester Prodrugs of Indomethacin and NaproxenPharmaceutical Research, 1993
- Ester and Amide Prodrugs of Ibuprofen and Naproxen: Synthesis, Anti-inflammatory Activity, and Gastrointestinal ToxicityJournal of Pharmaceutical Sciences, 1992
- Naproxen A Reappraisal of its Pharmacology, and Therapeutic Use in Rheumatic Diseases and Pain StatesDrugs, 1990
- Macromolecular prodrugs. XIV. Absorption characteristics of naproxen after oral administration of a dextran T-70-naproxen ester prodrug in pigsInternational Journal of Pharmaceutics, 1989
- Macromolecular Prodrugs. XVI. Colon-Targeted Delivery—Comparison of the Rate of Release of Naproxen from Dextran Ester Prodrugs in Homogenates of Various Segments of the Pig Gastrointestinal (GI) TractPharmaceutical Research, 1989
- Macromolecular Prodrugs. XV. Colon-Targeted Delivery—Bioavailability of Naproxen from Orally Administered Dextran–Naproxen Ester Prodrugs Varying in Molecular Size in the PigPharmaceutical Research, 1989
- Synthesis and Biological Evaluation of Ω-(N,N,N-Trialkylammonium)alkyl Esters and Thioesters of Carboxylic Acid Nonsteroidal Antiinflammatory AgentsPharmaceutical Research, 1989
- Glycolamide Esters as Biolabile Prodrugs of Carboxylic Acid Agents: Synthesis, Stability, Bioconversion, and Physicochemical PropertiesJournal of Pharmaceutical Sciences, 1988
- Glycolamide esters as a novel biolabile prodrug type for non-steroidal anti-inflammatory carboxylic acid drugsInternational Journal of Pharmaceutics, 1988