Exploring aigialomycin d and its analogues as protein kinase inhibitors for cancer targets.
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Isolation, semisynthesis, covalent docking and transforming growth factor beta-activated kinase 1 (TAK1)-inhibitory activities of (5Z)-7-oxozeaenol analoguesRational design of resorcylic acid lactone analogues as covalent MNK1/2 kinase inhibitors by tuning the reactivity of an enamide Michael acceptor.An efficient synthesis of an exo-enone analogue of LL-Z1640-2 and evaluation of its protein kinase inhibitory activities.
P2860
Exploring aigialomycin d and its analogues as protein kinase inhibitors for cancer targets.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@ast
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@en
type
label
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@ast
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@en
prefLabel
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@ast
Exploring aigialomycin d and i ...... inhibitors for cancer targets.
@en
P2093
P2860
P356
P1476
Exploring aigialomycin d and i ...... inhibitors for cancer targets
@en
P2093
P2860
P304
P356
10.1021/ML200067T
P577
2011-07-17T00:00:00Z