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PDBsum entry 2vh6

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Hydrolase PDB id
2vh6
Contents
Protein chains
232 a.a.
54 a.a.
Ligands
GSV
Waters ×171

References listed in PDB file
Key reference
Title Structure and property based design of factor xa inhibitors: pyrrolidin-2-Ones with biaryl p4 motifs.
Authors R.J.Young, A.D.Borthwick, D.Brown, C.L.Burns-Kurtis, M.Campbell, C.Chan, M.Charbaut, C.W.Chung, M.A.Convery, H.A.Kelly, N.Paul king, S.Kleanthous, A.M.Mason, A.J.Pateman, A.N.Patikis, I.L.Pinto, D.R.Pollard, S.Senger, G.P.Shah, J.R.Toomey, N.S.Watson, H.E.Weston.
Ref. Bioorg Med Chem Lett, 2008, 18, 23-27.
PubMed id 18054228
Abstract
Structure and property based drug design was exploited in the synthesis of sulfonamidopyrrolidin-2-one-based factor Xa (fXa) inhibitors, incorporating biaryl P4 groups, producing highly potent inhibitors with encouraging oral pharmacokinetic profiles and significant but sub-optimal anticoagulant activities.
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