(Q)SAR Studies to Design New Human Choline Kinase Inhibitors as Antiproliferative Drugs

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Abstract:

Most of the signal transduction pathways are mediated by protein kinases regulating every aspect of cell function. Mutations which deregulate their expression or their function or both result in cancers. Therefore, protein kinase inhibitors have become the focus of development of new therapies for cancer. A comprehensive review of Choline kinase (ChoK) was published by us in 2003. Since then, molecular information of ChoK inhibitors has been accumulated. In this review, we intend to summarize the new lines of evidence that will include the design of the most active antiproliferative agents so far described against ChoK. Studies have been aimed at the establishment of structure-activity relationships and the structural parameters that define ChoK inhibitory and antiproliferative activities of a set of twenty-five acyclic biscationic pyridophane and forty acyclic biscationic quinolinephane compounds. The corresponding QSAR equation was obtained for the whole set of bisquinolinium compounds for the antiproliferative activity, taking into consideration the electronic parameter σR of R4, the molar refractivity (MR) of R8, and the lipophilic parameters clog P and πlinker. The most potent antiproliferative agent shows an IC50 = 0.45 μM, predicted by the QSAR equation, whilst its experimental value is IC50 = 0.20 μM. Finally, toxicity assays were performed for the most promising compounds because of their interesting antiproliferative activities [IC50 HT-29 = 0.70, 0.80, 1.50 and 1.90 μM] and low toxicity [LD50 = 16.7, 12.5, > 25 and > 20 μg/kg of mouse]. These biological activities justify further analysis for antitumoral assays under in vivo conditions.

Keywords: Ab initio calculations; Antitumor drugs; Bicyclophanes; Bispyridinium compounds; Bisquinolinium compounds; Choline Kinase; Cyclophanes; QSAR

Document Type: Research Article

DOI: http://dx.doi.org/10.2174/092986706776872961

Affiliations: Departamento de Quimica Farmaceutica y Organica, Facultad de Farmacia, c/ Campus de Cartuja, s/n, 18071 Granada, Spain.

Publication date: May 1, 2006

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  • Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of the current topics in medicinal chemistry. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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