Potent selective thienoxazinone inhibitors of herpes proteases
- 8 July 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (13), 1733-1738
- https://doi.org/10.1016/s0960-894x(97)00300-4
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Inhibition of HSV-1 protease by benzoxazinonesBioorganic & Medicinal Chemistry Letters, 1996
- Novel, selective mechanism-based inhibitors of the herpes proteasesBioorganic & Medicinal Chemistry Letters, 1996
- Structure of the Human Cytomegalovirus Protease Catalytic Domain Reveals a Novel Serine Protease Fold and Catalytic TriadCell, 1996
- Unique fold and active site in cytomegalovirus proteaseNature, 1996
- A new serine-protease fold revealed by the crystal structure of human cytomegalovirus proteaseNature, 1996
- Three-dimensional structure of human cytomegalovirus proteaseNature, 1996
- Unambiguous assignment of the 13C NMR spectra of methylindolesMagnetic Resonance in Chemistry, 1988
- The preparation of 2-(heterocyclyl)thikno[3,2-b]pyridine derivativesTetrahedron, 1987
- A new synthesis of biotinTetrahedron Letters, 1981
- Über die Synthese von 5-Phenyl-1H-thieno[3,2-e]1,4-diazepin-2(3H)-onMonatshefte für Chemie / Chemical Monthly, 1973