European Journal of Medicinal Chemistry 2011-02-01

Predicting hERG activities of compounds from their 3D structures: development and evaluation of a global descriptors based QSAR model.

Nandita Sinha, Srikanta Sen

文献索引：Eur. J. Med. Chem. 46 , 618-30, (2011)

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摘要

A QSAR based predictive model of hERG activity in terms of 'global descriptors' has been developed and evaluated. The QSAR was developed by training 77 compounds covering a wide range of activities and was validated based on an external 'test set' of 80 compounds using neural network method. Statistical parameters and examination of enrichment factor indicated the effectiveness of the present model. Randomization test demonstrated the robustness of the model and cross-validation test further validated the QSAR. Domain of applicability test indicated to the high degree of reliability of the predicted results. Satisfactory performance in classifying compounds into 'active' and 'inactive' groups was also obtained. The cases where the QSAR failed, the possible sources of errors have been discussed.Copyright © 2010 Elsevier Masson SAS. All rights reserved.

相关化合物

  • 氧氟沙星
  • 尼群地平
  • 4-氨基吡啶
  • 特非那定
  • 咖啡因
  • 甲氧苄氨嘧啶
  • 克霉唑
  • (+/-)-尼古丁
  • 卡马西平
  • 他莫昔芬

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