 |
PDBsum entry 4ewh
|
|
|
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
|
|
|
|
|
|
|
Transferase/transferase inhibitor
|
PDB id
|
|
|
|
4ewh
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
References listed in PDB file
|
 |
|
Key reference
|
 |
|
Title
|
 |
Synthesis and optimization of substituted furo[2,3-D]-Pyrimidin-4-Amines and 7h-Pyrrolo[2,3-D]pyrimidin-4-Amines as ack1 inhibitors.
|
 |
|
Authors
|
 |
X.Jiao,
D.J.Kopecky,
J.Liu,
J.Liu,
J.C.Jaen,
M.G.Cardozo,
R.Sharma,
N.Walker,
H.Wesche,
S.Li,
E.Farrelly,
S.H.Xiao,
Z.Wang,
F.Kayser.
|
 |
|
Ref.
|
 |
Bioorg Med Chem Lett, 2012,
22,
6212-6217.
|
 |
|
PubMed id
|
 |
|
 |
 |
|
Abstract
|
 |
|
Two classes of ACK1 inhibitors, 4,5,6-trisubstituted
furo[2,3-d]pyrimidin4-amines and 4,5,6-trisubstituted
7H-pyrrolo[2,3-d]pyrimidin-4-amines, were discovered and evaluated as ACK1
inhibitors. Further structural refinement led to the identification of potent
and selective dithiolane inhibitor 37.
|
 |
|
|
|
|
 |