Arylsulphonyl hydroxamic acids: potent and selective matrix metalloproteinase inhibitors-Reference-Cited by-同舟云学术

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Arylsulphonyl hydroxamic acids: potent and selective matrix metalloproteinase inhibitors

Published:2001-06 Issue:11 Volume:11 Page:1465-1468
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Baxter Andrew D,Bhogal Ranjev,Bird John,Keily John F,Manallack David T,Montana John G,Owen David A,Pitt William R,Watson Robert J,Wills Ruth E

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. Clinical Potential of Matrix Metalloprotease Inhibitors in Cancer Therapy

2. Design and Therapeutic Application of Matrix Metalloproteinase Inhibitors

3. Design, Synthesis, and Biological Evaluation of Matrix Metalloproteinase Inhibitors Derived from a Modified Proline Scaffold

4. Baxter, A. D.; Bird, J.; Bannister, R.; Bhogal, R.; Manallack, D. T.; Watson R. J.; Owen, D. A.; Montana, J. G.; Henshilwood, J.; Jackson, R. C. In Cancer Drug Discovery and Development: Matrix Metalloproteinase Inhibitors in Cancer Therapy; Clandennin, N. J., Appelt K., Eds.; Humana: Totowa, NJ, 2000; Vol. 8, pp 193–221.

5. Bird, J. Gordon Research Conference: Matrix Metalloproteinases, New London, NH, 1999.

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