Evaluation of synthetic acridones and 4-quinolinones as potent inhibitors of cathepsins L and V-Reference-Cited by-同舟云学术

Evaluation of synthetic acridones and 4-quinolinones as potent inhibitors of cathepsins L and V

Published:2012-08 Issue: Volume:54 Page:10-21
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Marques Emerson F.,Bueno Mauro A.,Duarte Patrícia D.,Silva Larissa R.S.P.,Martinelli Ariani M.,dos Santos Caio Y.,Severino Richele P.,Brömme Dieter,Vieira Paulo C.,Corrêa Arlene G.

Funder

State of São Paulo Research Foundation

National Council for Scientific and Technological Development

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference73 articles.

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4. Combination therapy for visceral leishmaniasis

5. Synthesis of mono- and di-substituted 2,4,5-trifluorobenzoic acid synthons, key precursors for biologically active 6-fluoroquinolones

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