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Title4-Substituted Trinems as Broad Spectrum beta-Lactamase Inhibitors: Structure-Based Design, Synthesis, and Biological Activity
Journal, issue, pagesJ. Med. Chem., Vol. 50, Page 4113-4121, Year 2007
Publish dateJun 13, 2007 (structure data deposition date)
AuthorsPlantan, I. / Selic, L. / Mesar, T. / Anderluh, P.S. / Oblak, M. / Prezelj, A. / Hesse, L. / Andrejasic, M. / Vilar, M. / Turk, D. ...Plantan, I. / Selic, L. / Mesar, T. / Anderluh, P.S. / Oblak, M. / Prezelj, A. / Hesse, L. / Andrejasic, M. / Vilar, M. / Turk, D. / Kocijan, A. / Prevec, T. / Vilfan, G. / Kocjan, D. / Copar, A. / Urleb, U. / Solmajer, T.
External linksJ. Med. Chem. / PubMed:17665896
MethodsX-ray diffraction
Resolution2.05 - 2.2 Å
Structure data

PDB-2q9m:
4-Substituted Trinems as Broad Spectrum-Lactamase Inhibitors: Structure-based Design, Synthesis and Biological Activity
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

PDB-2q9n:
4-Substituted Trinems as Broad Spectrum-Lactamase Inhibitors: Structure-based Design, Synthesis and Biological Activity
Method: X-RAY DIFFRACTION / Resolution: 2.2 Å

Chemicals

ChemComp-LK7:
(1R,4S,7AS)-1-(1-FORMYLPROP-1-EN-1-YL)-4-METHOXY-2,4,5,6,7,7A-HEXAHYDRO-1H-ISOINDOLE-3-CARBOXYLIC ACID

ChemComp-HOH:
WATER

ChemComp-LK5:
(1S,4R,7AR)-4-BUTOXY-1-[(1R)-1-FORMYLPROPYL]-2,4,5,6,7,7A-HEXAHYDRO-1H-ISOINDOLE-3-CARBOXYLIC ACID

Source
  • enterobacter cloacae (bacteria)
KeywordsHYDROLASE / beta-lactamase inhibitor / tricyclic carbapenem

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