Pure Diastereomers of a Tranylcypromine-Based LSD1 Inhibitor: Enzyme Selectivity and In-Cell Studies.
about
Medicinal chemistry insights in the discovery of novel LSD1 inhibitors.TCPs: privileged scaffolds for identifying potent LSD1 inhibitors for cancer therapy.Histone Lysine Demethylase Inhibitors.Structural insight into inhibitors of flavin adenine dinucleotide-dependent lysine demethylases.Towards the development of activity-based probes for detection of lysine-specific demethylase-1 activity.
P2860
Pure Diastereomers of a Tranylcypromine-Based LSD1 Inhibitor: Enzyme Selectivity and In-Cell Studies.
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին 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
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@ast
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@en
type
label
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@ast
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@en
prefLabel
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@ast
Pure Diastereomers of a Tranyl ...... lectivity and In-Cell Studies.
@en
P2093
P2860
P50
P356
P1476
Pure Diastereomers of a Tranyl ...... electivity and In-Cell Studies
@en
P2093
Biagina Marrocco
Bruna Saponara
Ciro Mercurio
Donatella Labella
Giovanni Ruoppolo
Giuseppe Ciossani
Mario Varasi
Oronza A Botrugno
Paola Dessanti
Saverio Minucci
P2860
P304
P356
10.1021/ML500424Z
P577
2014-12-08T00:00:00Z