In Situ Click Chemistry: Enzyme‐Generated Inhibitors of Carbonic Anhydrase II
- 15 December 2004
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (1), 116-120
- https://doi.org/10.1002/anie.200461580
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- In Situ Click Chemistry: Enzyme Inhibitors Made to Their Own SpecificationsJournal of the American Chemical Society, 2004
- DNA-Templated Dimerization of Hairpin PolyamidesJournal of the American Chemical Society, 2003
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie International Edition, 2002
- Target-Accelerated Combinatorial Synthesis and Discovery of Highly Potent Antibiotics Effective Against Vancomycin-Resistant BacteriaAngewandte Chemie, 2000
- Target-Accelerated Combinatorial Synthesis and Discovery of Highly Potent Antibiotics Effective Against Vancomycin-Resistant BacteriaPublished by Wiley ,2000
- Enantioselective Synthesis of AL-4414A, a Topically Active Carbonic Anhydrase InhibitorThe Journal of Organic Chemistry, 1997
- Benzenesulfonamide-peptide conjugates as probes for secondary binding sites near the active site of carbonic anhydraseBioorganic & Medicinal Chemistry Letters, 1996
- Lack of Effect of the Length of Oligoglycine- and Oligo(ethylene glycol)-Derived para-Substituents on the Affinity of Benzenesulfonamides for Carbonic Anhydrase II in SolutionJournal of the American Chemical Society, 1994
- Self-Assembling CytotoxinsScience, 1986
- Hypoglycaemic agents: variants of tolbutamideJournal of Pharmacy and Pharmacology, 1964