In Situ “Click” Assembly of Small Molecule Matrix Metalloprotease Inhibitors Containing Zinc-Chelating Groups
Author:
Affiliation:
1. Departments of Chemistry and Biological Sciences, NUS MedChem Program of the Office of Life Sciences, National University of Singapore, Singapore 117543
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol802286g
Reference17 articles.
1. Validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy
2. Design and Therapeutic Application of Matrix Metalloproteinase Inhibitors
3. The Design of Inhibitors for Medicinally Relevant Metalloproteins
4. New Beginnings for Matrix Metalloproteinase Inhibitors: Identification of High-Affinity Zinc-Binding Groups
5. Evaluation and Binding-Mode Prediction of Thiopyrone-Based Inhibitors of Anthrax Lethal Factor
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