2j4i: Difference between revisions

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{{STRUCTURE_2j4i|  PDB=2j4i  |  SCENE=  }}  
{{STRUCTURE_2j4i|  PDB=2j4i  |  SCENE=  }}  


'''CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX'''
===CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX===




==Overview==
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Structure-based drug design was exploited in the synthesis of 3-(6-chloronaphth-2-ylsulfonyl)aminopyrrolidin-2-one-based factor Xa (fXa) inhibitors, incorporating an alanylamide P4 group with acyclic tertiary amide termini. Optimized hydrophobic contacts of one amide substituent in P4 were complemented by hydrophobicity-modulating features in the second, producing potent fXa inhibitors including examples with excellent anticoagulant properties.
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{{ABSTRACT_PUBMED_16982190}}


==About this Structure==
==About this Structure==
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[[Category: Serine protease]]
[[Category: Serine protease]]
[[Category: Zymogen]]
[[Category: Zymogen]]
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