Synthesis, biological, and biophysical studies of DAG-indololactones designed as selective activators of RasGRP.
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Protein kinase C in cancer: The top five unanswered questions.Exploring the influence of indololactone structure on selectivity for binding to the C1 domains of PKCα, PKCε, and RasGRP.Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C.Characterization of AJH-836, a DAG-lactone with selectivity for novel PKC isozymes.
P2860
Synthesis, biological, and biophysical studies of DAG-indololactones designed as selective activators of RasGRP.
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Synthesis, biological, and bio ...... elective activators of RasGRP.
@ast
Synthesis, biological, and bio ...... elective activators of RasGRP.
@en
type
label
Synthesis, biological, and bio ...... elective activators of RasGRP.
@ast
Synthesis, biological, and bio ...... elective activators of RasGRP.
@en
prefLabel
Synthesis, biological, and bio ...... elective activators of RasGRP.
@ast
Synthesis, biological, and bio ...... elective activators of RasGRP.
@en
P2093
P2860
P1476
Synthesis, biological, and bio ...... selective activators of RasGRP
@en
P2093
Colin S Hill
James A Kelley
Jessica S Kelsey
Lia C Garcia
Lucia Gandolfi Donadío
Maria J Comin
Marina Santos
Nancy E Lewin
P2860
P304
P356
10.1016/J.BMC.2014.04.024
P407
P577
2014-04-20T00:00:00Z