Antileishmanial chalcones: statistical design, synthesis, and three-dimensional quantitative structure-activity relationship analysis

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  • S F Nielsen
  • S B Christensen
  • G Cruciani
  • A Kharazmi
  • T Liljefors
A large number of substituted chalcones have been synthesized and tested for antileishmanial and lymphocyte-suppressing activities. A subset of the chalcones was designed by using statistical methods. 3D-QSAR analyses using 67 (antileishmanial activity) and 63 (lymphocyte-suppressing activity) of the compounds for the training sets and 9 compounds as an external validation set were performed by using the GRID/GOLPE methodology. The Smart Region Definition procedure with subsequent region selection as implemented in GOLPE reduced the number of variables to approximately 1300 yielding 3D-QSAR models of high quality (lymphocyte-suppressing model, R2 = 0. 90, Q2 = 0.80; antileishmanial model, R2 = 0.73, Q2 = 0.63). The coefficient plots indicate that steric interactions between the chalcones and the target are of major importance for the potencies of the compounds. A comparison of the coefficient plots for the antileishmanial effect and the lymphocyte-suppressing activity discloses significant differences which should make it possible to design chalcones having a high antileishmanial activity without suppressing the proliferation of lymphocytes.
Original languageEnglish
JournalJournal of Medicinal Chemistry
Volume41
Issue number24
Pages (from-to)4819-32
Number of pages13
ISSN0022-2623
DOIs
Publication statusPublished - 1998

Bibliographical note

Keywords: Animals; Cell Division; Chalcone; Humans; Inhibitory Concentration 50; Leishmania donovani; Lymphocytes; Models, Molecular; Molecular Conformation; Reproducibility of Results; Structure-Activity Relationship; Trypanocidal Agents

ID: 18054495