Amy L Gentry

Most-cited papers

1. 4-Substituted cyclohexyl sulfones as potent, orally active γ-secretase inhibitors

   I. Churcher, D. Beher, J. Best, J. L. Castro +16 more

   200670 citations Open access

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2. 1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists: modifications of the arylpropylpiperidine side chains.

   C. L. Lynch, C. A. Willoughby, J. Hale, Edward J Holson +26 more

   2003Bioorganic & Medicinal Chemistry Letters38 citations Open access

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3. 1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 4: synthesis of N-1 acidic functionality affording analogues with enhanced antiviral activity against HIV.

   C. L. Lynch, J. Hale, R. Budhu, Amy L Gentry +19 more

   2002Bioorganic & Medicinal Chemistry Letters33 citations Open access

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4. CCR5 antagonists: bicyclic isoxazolidines as conformationally constrained N-1-substituted pyrrolidines.

   C. L. Lynch, Amy L Gentry, J. Hale, S. Mills +18 more

   2002Bioorganic & Medicinal Chemistry Letters30 citations Open access

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5. Design and synthesis of conformationally constrained 3-(N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors.

   Lin Yan, J. Hale, C. L. Lynch, R. Budhu +12 more

   2004Bioorganic & Medicinal Chemistry Letters27 citations Open access

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6. CCR5 antagonists: 3-(pyrrolidin-1-yl)propionic acid analogues with potent anti-HIV activity.

   C. L. Lynch, J. Hale, R. Budhu, Amy L Gentry +22 more

   2003Organic Letters12 citations

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7. 4-substituted cyclohexyl sulfones as potent, orally active gamma-secretase inhibitors.

   I. Churcher, D. Beher, J. Best, J. L. Castro +16 more

   2006Bioorganic & Medicinal Chemistry Letters11 citations

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