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TitleStructure-based drug design of pyrrolidine-1, 2-dicarboxamides as a novel series of orally bioavailable factor Xa inhibitors
Journal, issue, pagesChem. Biol. Drug Des., Vol. 69, Page 444-450, Year 2007
Publish dateMay 3, 2007 (structure data deposition date)
AuthorsVan Huis, C.A. / Bigge, C.F. / Casimiro-Garcia, A. / Cody, W.L. / Dudley, D.A. / Filipski, K.J. / Heemstra, R.J. / Kohrt, J.T. / Narasimhan, L.S. / Schaum, R.P. ...Van Huis, C.A. / Bigge, C.F. / Casimiro-Garcia, A. / Cody, W.L. / Dudley, D.A. / Filipski, K.J. / Heemstra, R.J. / Kohrt, J.T. / Narasimhan, L.S. / Schaum, R.P. / Zhang, E. / Bryant, J.W. / Haarer, S. / Janiczek, N. / Leadley, R.J. / McClanahan, T. / Thomas Peterson, J. / Welch, K.M. / Edmunds, J.J.
External linksChem. Biol. Drug Des. / PubMed:17581239
MethodsX-ray diffraction
Resolution1.5 Å
Structure data

PDB-2pr3:
Factor XA inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

Chemicals

ChemComp-CA:
Unknown entry

ChemComp-237:
(2R,4R)-N~1~-(4-CHLOROPHENYL)-N~2~-[3-FLUORO-2'-(METHYLSULFONYL)BIPHENYL-4-YL]-4-METHOXYPYRROLIDINE-1,2-DICARBOXAMIDE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsBLOOD CLOTTING / FXA COAGULATION FACTOR INHIBITOR

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