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2000
Volume 1, Issue 2
  • ISSN: 1573-4099
  • E-ISSN: 1875-6697

Abstract

A major problem in traditional quantitative structure-activity relationships (QSARs) analysis is to select suitable chemical descriptors from a large pool of variables. Decisions against or in favor of a particular descriptor depends entirely on the result of statistically based hypothesis testing. Uncertain results may be produced in presence of multicollinear descriptors and flagged observations (high-leverage points, outliers, influential data). To satisfy the assumptions for hypothesis testing, diagnostic statistics and subsequent design repair are employed. Here we show an example with nonnucleoside HIV-1 reverse transcriptase inhibitors.

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/content/journals/cad/10.2174/1573409053585654
2005-04-01
2025-10-12
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