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TitleRational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitors.
Journal, issue, pagesScience, Vol. 263, Page 380-384, Year 1994
Publish dateFeb 14, 1994 (structure data deposition date)
AuthorsLam, P.Y. / Jadhav, P.K. / Eyermann, C.J. / Hodge, C.N. / Ru, Y. / Bacheler, L.T. / Meek, J.L. / Otto, M.J. / Rayner, M.M. / Wong, Y.N. ...Lam, P.Y. / Jadhav, P.K. / Eyermann, C.J. / Hodge, C.N. / Ru, Y. / Bacheler, L.T. / Meek, J.L. / Otto, M.J. / Rayner, M.M. / Wong, Y.N. / Chang, C.-H. / Weber, P. / Jackson, D.A. / Sharpe, T.R. / Erickson-Viitanen, S.
External linksPubMed:8278812
MethodsX-ray diffraction
Resolution1.8 Å
Structure data

PDB-1hvr:
RATIONAL DESIGN OF POTENT, BIOAVAILABLE, NONPEPTIDE CYCLIC UREAS AS HIV PROTEASE INHIBITORS
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-XK2:
[4R-(4ALPHA,5ALPHA,6BETA,7BETA)]-HEXAHYDRO-5,6-DIHYDROXY-1,3-BIS[2-NAPHTHYL-METHYL]-4,7-BIS(PHENYLMETHYL)-2H-1,3-DIAZEPIN-2-ONE

Source
  • human immunodeficiency virus 1
KeywordsHYDROLASE/HYDROLASE INHIBITOR / HYDROLASE / ACID PROTEINASE / HYDROLASE-HYDROLASE INHIBITOR complex

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