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2‑Imidazole as a Substitute for the Electrophilic Group Giv..:

Henri T. Pätsi (11449332) ; Tommi P. Kilpeläinen (11449335) ; Samuli Auno (7340486)...
https://figshare.com/articles/journal_contribution/2_Imidazole_as_a_Substitute_for_the_Electrophilic_Group_Gives_Highly_Potent_Prolyl_Oligopeptidase_Inhibitors/16635651. , 2021

Link: https://doi.org/10.1021/acsmedchemlett.1c00399.s001

RT Journal
T1 <Title>2‑Imidazole as a Substitute for the Electrophilic Group Gives Highly Potent Prolyl Oligopeptidase Inhibitors</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16635651&Exemplar=1&LAN=DE
				
A1 Henri T. Pätsi (11449332)
A1 Tommi P. Kilpeläinen (11449335)
A1 Samuli Auno (7340486)
A1 Pyry M. J. Dillemuth (11449338)
A1 Khaled Arja (11449341)
A1 Maija K. Lahtela-Kakkonen (7865081)
A1 Timo T. Myöhänen (7865087)
A1 Erik A. A. Wallén (7865090)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Pharmacology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 typical electrophilic group
K1 protein – protein
K1 e
K1 dimerization
K1 highly potent inhibitors
K1 2 ‑ imidazole
K1 potent modulator
K1 basic imidazole
K1 synuclein dimerization
K1 proteolytic activity
K1 prolyl oligopeptidase
K1 opposite side
K1 molecular docking
K1 modulating effect
K1 membered nitrogen
K1 membered heteroaromatic
K1 linker length
K1 derived functions
K1 containing heteroaromatics
K1 binding mode
K1 autophagy )
JF https://figshare.com/articles/journal_contribution/2_Imidazole_as_a_Substitute_for_the_Electrophilic_Group_Gives_Highly_Potent_Prolyl_Oligopeptidase_Inhibitors/16635651
LK http://dx.doi.org/https://doi.org/10.1021/acsmedchemlett.1c00399.s001
DO https://doi.org/10.1021/acsmedchemlett.1c00399.s001
SF ELIB - SuUB Bremen

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