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Structure paper

TitleDesign and Synthesis of Orally Active Pyrrolidin-2-One-Based Factor Xa Inhibitors
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 16, Page 3784-, Year 2006
Publish dateApr 3, 2006 (structure data deposition date)
AuthorsWatson, N.S. / Brown, D. / Campbell, M. / Chan, C. / Chaudry, L. / Convery, M.A. / Fenwick, R. / Hamblin, J.N. / Haslam, C. / Kelly, H.A. ...Watson, N.S. / Brown, D. / Campbell, M. / Chan, C. / Chaudry, L. / Convery, M.A. / Fenwick, R. / Hamblin, J.N. / Haslam, C. / Kelly, H.A. / King, N.P. / Kurtis, C.L. / Leach, A.R. / Manchee, G.R. / Mason, A.M. / Mitchell, C. / Patel, C. / Patel, V.K. / Senger, S. / Shah, G.P. / Weston, H.E. / Whitworth, C. / Young, R.J.
External linksBioorg. Med. Chem. Lett. / PubMed:16697194
MethodsX-ray diffraction
Resolution2.1 Å
Structure data

PDB-2cji:
Crystal structure of a Human Factor Xa inhibitor complex
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-CA:
Unknown entry

ChemComp-GSK:
6-CHLORO-N-{(3S)-1-[(1S)-1-METHYL-2-(4-MORPHOLINYL)-2-OXO ETHYL]-2-OXO-3-PYRROLIDINYL}-2-NAPHTHALENESULFONAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / BLOOD COAGULATION / GAMMA-CARBOXYGLUTAMIC ACID / HYDROXYLATION / EGF-LIKE DOMAIN / SERINE PROTEASE / CALCIUM / ZYMOGEN / PROTEASE / GLYCOPROTEIN / POLYMORPHISM

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