4.6 Review

Topological Polar Surface Area: A Useful Descriptor in 2D-QSAR

Journal

CURRENT MEDICINAL CHEMISTRY
Volume 16, Issue 1, Pages 21-41

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/092986709787002817

Keywords

Antitumor agents; structure-activity relationships; 2D-QSAR; GSK-3; topological polar surface area (TPSA); antimalarial agents; ClogP; CMR

Funding

  1. University of Mississippi
  2. Office of Research and Sponsored Programs
  3. National Center for Zoonotic, Vector-borne, and Enteric Diseases (CK) of the Centers for Disease Control and Prevention [U01/CI000211]
  4. National Science Foundation [EPS-0556308]
  5. National Institutes of Health's National Center for Research Resources [P20 RR021929]
  6. NIH National Center for Research Resources [C06 RR-14503-01]
  7. NATIONAL CENTER FOR INFECTIOUS DISEASES (NCID) [U01CI000211] Funding Source: NIH RePORTER
  8. NATIONAL CENTER FOR RESEARCH RESOURCES [C06RR014503, P20RR021929] Funding Source: NIH RePORTER

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Topological polar surface area (TPSA), which makes use of functional group contributions based on a large database of structures, is a convenient measure of the polar surface area that avoids the need to calculate ligand 3D structure or to decide which is the relevant biological conformation or conformations. We demonstrate the utility of TPSA in 2D-QSAR for 14 sets of diverse pharmacological activity data. Even though a large pool of reports showing the importance of the classic 2D descriptors such as calculated logP (ClogP) and calculated molar refractivity (CMR) exists in the 2D-QSAR literature, this is the first report to demonstrate the value of TPSA as a relevant descriptor applicable to a large, structurally and pharmacologically diverse set of classes of compounds. We also address the limitations of applicability of this descriptor for 2D-QSAR analysis. We observed a negative correlation of TPSA with activity data for anticancer alkaloids, MT1 and MT2 agonists, MAO-B and tumor necrosis factor-inhibitors and a positive correlation with inhibitory activity data for telomerase, PDE-5, GSK-3, DNA-PK, aromatase, malaria, trypanosomatids and CB2 agonists.

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