 |
PDBsum entry 2f9b
|
|
|
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
|
|
|
|
|
|
|
Hydrolase/blood clotting
|
PDB id
|
|
|
|
2f9b
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
Contents |
 |
|
|
|
|
|
|
|
|
|
94 a.a.
|
 |
|
|
|
|
|
|
|
254 a.a.
|
 |
|
|
|
|
|
|
|
149 a.a.
|
 |
|
|
|
|
|
|
|
|
|
|
|
References listed in PDB file
|
 |
|
Key reference
|
 |
|
Title
|
 |
Discovery of novel heterocyclic factor viia inhibitors.
|
 |
|
Authors
|
 |
R.Rai,
A.Kolesnikov,
P.A.Sprengeler,
S.Torkelson,
T.Ton,
B.A.Katz,
C.Yu,
J.Hendrix,
W.D.Shrader,
R.Stephens,
R.Cabuslay,
E.Sanford,
W.B.Young.
|
 |
|
Ref.
|
 |
Bioorg Med Chem Lett, 2006,
16,
2270-2273.
[DOI no: ]
|
 |
|
PubMed id
|
 |
|
 |
 |
|
Abstract
|
 |
|
Structure-activity relationships and binding mode of novel heterocyclic factor
VIIa inhibitors will be described. In these inhibitors, a highly basic
5-amidinoindole moiety has been successfully replaced with a less basic
5-aminopyrrolo[3,2-b]pyridine scaffold.
|
 |
|
|
|
|
 |