Design, synthesis, and conformational analysis of a novel series of HIV protease inhibitors
A combination of structure-based design and both solution, and solid-phase synthesis were utilized to derive a potent (nM) series of HIV-1 protease inhibitors bearing a structurally novel backbone. Detailed structural analysis of several inhibitors prepared in this series has suggested that rigidifi...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 1998-12, Vol.8 (24), p.3631-3636 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A combination of structure-based design and both solution, and solid-phase synthesis were utilized to derive a potent (nM) series of HIV-1 protease inhibitors bearing a structurally novel backbone. Detailed structural analysis of several inhibitors prepared in this series has suggested that rigidification of the P
1/P
2 region of this class of molecules may result in compounds with improved potency.
A combination of structure-based design and both solution, and solid-phase synthesis were utilized to derive a potent (nM) series of HIV-1 protease inhibitors bearing a structurally novel backbone. Detailed structural analysis of several inhibitors prepared in this series has suggested that rigidification of the P
1/P
2 region of this class of molecules may result in compounds with improved potency. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/S0960-894X(98)00669-6 |