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Statistical Molecular Design, Parallel Synthesis, and Biological Evaluation of a Library of Thrombin Inhibitors
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2001 (English)In: Journal of Medicinal Chemistry, Vol. 44, no 21, 3424-39 p.Article in journal (Refereed) Published
Abstract [en]

A library of thrombin inhibitors has been designed using statistical molecular design. An aromatic scaffold was used, with three varied positions corresponding to three pockets at the active site of thrombin (the S-, P-, and D-pockets). The selection was performed in the building block space, and previously acquired data were included in the design procedure. The design resulted in six, four, and six building blocks for the first (S), second (P), and third (D) pockets, respectively. A second round of selection applied to the combined selected building blocks resulted in a subset of 18 compounds. The selected library was synthesized in parallel and biologically evaluated. The compounds were analyzed with respect to their inhibition (pIC50) of thrombin; membrane permeability, estimated by migration behavior in micellar media (CE log k') and pKa; and specificity with respect to inhibition (Ki) of trypsin. Multivariate QSAR studies of the responses yielded valuable results and information that could only be found using statistical molecular design in combination with multivariate analysis.

Place, publisher, year, edition, pages
2001. Vol. 44, no 21, 3424-39 p.
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URN: urn:nbn:se:umu:diva-9137DOI: 10.1021/jm010833fOAI: oai:DiVA.org:umu-9137DiVA: diva2:148808
Available from: 2008-03-04 Created: 2008-03-04 Last updated: 2013-02-28Bibliographically approved

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Linusson, AnnaWold, Svante
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CiteExportLink to record
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