Thiazolidine derivatives as potent and selective inhibitors of the PIM kinase family.
The PIM family of serine/threonine kinases have become an attractive target for anti-cancer drug development, particularly for certain hematological malignancies. Here, we describe the discovery of a series of inhibitors of the PIM kinase family using a high throughput screening strategy. Through a...
المؤلفون الرئيسيون: | Bataille, C, Brennan, M, Byrne, S, Davies, S, Durbin, M, Fedorov, O, Huber, K, Jones, A, Knapp, S, Liu, G, Nadali, A, Quevedo, C, Russell, A, Walker, R, Westwood, R, Wynne, G |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Elsevier
2017
|
مواد مشابهة
-
New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights.
حسب: López-Ramos, M, وآخرون
منشور في: (2010) -
New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights.
حسب: López-Ramos, M, وآخرون
منشور في: (2010) -
Pim-selective inhibitor DHPCC-9 reveals Pim kinases as potent stimulators of cancer cell migration and invasion
حسب: Prudhomme Michelle, وآخرون
منشور في: (2010-10-01) -
New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights (September, pg 3175, 2010)
حسب: Lopez-Ramos, M, وآخرون
منشور في: (2011) -
Structure and substrate specificity of the Pim-1 kinase
حسب: Bullock, A, وآخرون
منشور في: (2005)