Structure-Based Design of Non-Nucleoside Reverse Transcriptase Inhibitors of Drug-Resistant Human Immunodeficiency Virus

@article{Mao1999StructureBasedDO,
  title={Structure-Based Design of Non-Nucleoside Reverse Transcriptase Inhibitors of Drug-Resistant Human Immunodeficiency Virus},
  author={C. Mao and E. Sudbeck and T. Venkatachalam and F. Uckun},
  journal={Antiviral Chemistry and Chemotherapy},
  year={1999},
  volume={10},
  pages={233 - 240}
}
  • C. Mao, E. Sudbeck, +1 author F. Uckun
  • Published 1999
  • Medicine, Biology
  • Antiviral Chemistry and Chemotherapy
  • A computer model of reverse transcriptase (RT) from human immunodeficiency virus type 1 (HIV-1) was used to design thiourea compounds that were predicted to inhibit RT. The RT model was used to approximate how changes in binding pocket shape, volume and chemical properties resulting from residue mutations would affect inhibitor binding. Our lead compound, N-[2-(2,5-dime-thoxyphenylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea (HI-236) was tested against clinically observed non-nucleoside inhibitor… CONTINUE READING
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