Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-(1H-pyrrol-3-yl)-2-oxazolidinones.
about
Triazole-dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration.A Rh(II)-catalyzed multicomponent reaction by trapping an α-amino enol intermediate in a traditional two-component reaction pathway.Pathophysiological implications of mitochondrial oxidative stress mediated by mitochondriotropic agents and polyamines: the role of tyrosine phosphorylation.A straightforward one-pot synthesis of bioactive N-aryl oxazolidin-2-ones via a highly efficient Fe3O4@SiO2-supported acetate-based butylimidazolium ionic liquid nanocatalyst under metal- and solvent-free conditions
P2860
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-(1H-pyrrol-3-yl)-2-oxazolidinones.
description
2011 nî lūn-bûn
@nan
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
2011年论文
@zh
2011年论文
@zh-cn
name
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-
@nl
Novel reversible monoamine oxi ...... pyrrol-3-yl)-2-oxazolidinones.
@en
type
label
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-
@nl
Novel reversible monoamine oxi ...... pyrrol-3-yl)-2-oxazolidinones.
@en
prefLabel
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-
@nl
Novel reversible monoamine oxi ...... pyrrol-3-yl)-2-oxazolidinones.
@en
P50
P356
P1476
Novel reversible monoamine oxi ...... pyrrol-3-yl)-2-oxazolidinones.
@en
P2093
Giampiero Tempera
Stefania Saccoccio
P304
P356
10.1021/JM201011X
P407
P577
2011-11-07T00:00:00Z