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2000
Volume 4, Issue 7
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

Human plasma protein binding (PPB) is an important pharmacokinetic property in drug design. Hologram quantitative structure-activity relationships (HQSAR) were conducted on a series of structurally diverse molecules with known PPB. The best statistical model (q2 = 0.72, r2 = 0.91) was used to predict the PPB of 62 test set compounds, and the predicted values were in good agreement with the experimental results.

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/content/journals/lddd/10.2174/157018007781788480
2007-10-01
2025-05-29
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/content/journals/lddd/10.2174/157018007781788480
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  • Article Type:
    Research Article
Keyword(s): ADME; Drug design; Pharmacokinetics; Plasma protein binding; QSAR
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