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TitleSynthesis and activity of N-acyl azacyclic urea HIV-1 protease inhibitors with high potency against multiple drug resistant viral strains
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 15, Page 5499-5503, Year 2005
Publish dateJun 28, 2005 (structure data deposition date)
AuthorsZhao, C. / Sham, H.L. / Sun, M. / Stoll, V.S. / Stewart, K.D. / Lin, S. / Mo, H. / Vasavanonda, S. / Saldivar, A. / Park, C. ...Zhao, C. / Sham, H.L. / Sun, M. / Stoll, V.S. / Stewart, K.D. / Lin, S. / Mo, H. / Vasavanonda, S. / Saldivar, A. / Park, C. / McDonald, E.J. / Marsh, K.C. / Klein, L.L. / Kempf, D.J. / Norbeck, D.W.
External linksBioorg. Med. Chem. Lett. / PubMed:16203141
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-2a4f:
Synthesis and Activity of N-Axyl Azacyclic Urea HIV-1 Protease Inhibitors with High Potency Against Multiple Drug Resistant Viral Strains.
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-AAU:
(5R,6R)-5-BENZYL-6-HYDROXY-2,4-BIS(4-HYDROXY-3-METHOXYBENZYL)-1-[3-(4-HYDROXYPHENYL)PROPANOYL]-1,2,4-TRIAZEPAN-3-ONE

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus 1
KeywordsHYDROLASE / HIV protease / aza-cyclic urea

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