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Elsevier电子期刊(3)
在“
Elsevier电子期刊
”中,
命中:
3
条,耗时:0.0429836 秒
在所有数据库中总计命中:
3
条
1.
Discovery of a novel class of highly potent inhibitors of the p53-MDM2 interaction by structure-ba
se
d design starting from a conformational argument
作者:
Pascal Furet
;
pascal.furet@novartis.com" class="auth_mail" title="E-mail the corresponding author
;
Keiichi Masuya
;
Joerg Kallen
;
Thé
;
rè
;
se
Stachyra
-
Valat
;
Stephan Ruetz
;
Vito Guagnano
;
Philipp Holzer
;
Robert Mah
;
Stefan Stutz
;
Andrea Vaupel
;
Patrick Chè
;
ne
;
Sé
;
bastien Jeay
;
Achim Schlapbach
关键词:
p53&ndash
;
MDM2 inhibitors
;
Protein&ndash
;
protein interaction inhibitors
;
Anticancer agents
;
Structure-ba
se
d design
刊名:Bioorganic & Medicinal Chemistry Letters
出版年:2016
2.
Tetra-substituted imidazoles as a new class of inhibitors of the p53-MDM2 interaction
作者:
Andrea Vaupel
;
andrea.vaupel@novartis.com" class="auth_mail
;
Guido Bold
;
Alain De Pover
;
Thé
;
rè
;
se
Stachyra
-
Valat
;
Joanna Hergovich-Lisztwan
;
Joerg Kallen
;
Keiichi Masuya
;
Pascal Furet
;
pascal.furet@novartis.com" class="auth_mail
关键词:
Protein&ndash
;
protein interaction inhibitors
;
Structure-ba
se
d design
;
p53
;
MDM2
刊名:Bioorganic and Medicinal Chemistry Letters
出版年:1 May, 2014
3.
The central valine concept provides an entry in a new class of non peptide inhibitors of the p53-MDM2 interaction
作者:
Pascal Furet
;
pascal.furet@novartis.com
;
Patrick Chè
;
ne
;
Alain De Pover
;
Thé
;
rè
;
se
Stachyra
Valat
;
Joanna Hergovich Lisztwan
;
Joerg Kallen
;
Keiichi Masuya
关键词:
p53&ndash
;
MDM2 inhibitors
;
Protein&ndash
;
protein interaction inhibitors
;
Anticancer agents
;
Structure-ba
se
d design
刊名:Bioorganic and Medicinal Chemistry Letters
出版年:2012
1
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