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TitleStructure Based Drug Design: Development of Potent and Selective Factor IXa (FIXa) Inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 53, Page 1473-1482, Year 2010
Publish dateJan 9, 2010 (structure data deposition date)
AuthorsWang, S. / Beck, R. / Burd, A. / Blench, T. / Marlin, F. / Ayele, T. / Buxton, S. / Dagostin, C. / Malic, M. / Joshi, R. ...Wang, S. / Beck, R. / Burd, A. / Blench, T. / Marlin, F. / Ayele, T. / Buxton, S. / Dagostin, C. / Malic, M. / Joshi, R. / Barry, J. / Sajad, M. / Cheung, C. / Shaikh, S. / Chahwala, S. / Chander, C. / Baumgartner, C. / Holthoff, H.P. / Murray, E. / Blackney, M. / Giddings, A.
External linksJ. Med. Chem. / PubMed:20121197
MethodsX-ray diffraction
Resolution2.62 Å
Structure data

PDB-3lc5:
Selective Benzothiophine Inhibitors of Factor IXa
Method: X-RAY DIFFRACTION / Resolution: 2.62 Å

Chemicals

ChemComp-CA:
Unknown entry

ChemComp-IZX:
1-{4-[(R)-phenyl(3-phenyl-1,2,4-oxadiazol-5-yl)methoxy]-1-benzothiophen-2-yl}methanediamine

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHydrolase/Hydrolase Inhibitor / Protein-Inhibitor complex / Peptidase S1 / Blood coagulation / Calcium / Cleavage on pair of basic residues / Disease mutation / Disulfide bond / EGF-like domain / Gamma-carboxyglutamic acid / Glycoprotein / Hemophilia / Hydrolase / Hydroxylation / Pharmaceutical / Phosphoprotein / Polymorphism / Protease / Secreted / Serine protease / Sulfation / Zymogen / Hydrolase-Hydrolase Inhibitor complex

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