Fragment-based design, docking, synthesis, biological evaluation and structure–activity relationships of 2-benzo/benzisothiazolimino-5-aryliden-4-thiazolidinones as cycloxygenase/lipoxygenase inhibitors-Reference-Cited by-同舟云学术

Fragment-based design, docking, synthesis, biological evaluation and structure–activity relationships of 2-benzo/benzisothiazolimino-5-aryliden-4-thiazolidinones as cycloxygenase/lipoxygenase inhibitors

Published:2012-01 Issue: Volume:47 Page:111-124
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Eleftheriou Phaedra,Geronikaki Athina,Hadjipavlou-Litina Dimitra,Vicini Paola,Filz Olga,Filimonov Dmitry,Poroikov Vladimir,Chaudhaery Shailendra S.,Roy Kuldeep K.,Saxena Anil K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

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