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New promises for manipulation of kynurenine pathway in cancer and neurological diseases
Taylor & Francis Verlag | 2009| -
Computationally driven drug discovery meeting-3 – Verona (Italy): 4 – 6th of March 2014
Taylor & Francis Verlag | 2014| -
Unbinding Pathways of VEGFR2 Inhibitors Revealed by Steered Molecular Dynamics
American Chemical Society | 2014| -
Binding mode of 6ECDCA, a potent bile acid agonist of the farnesoid X receptor (FXR)
Online Contents | 2003| -
Homology model of the closed, functionally active, form of the amino terminal domain of mGluR1
Online Contents | 2001| -
DERIVATIVES OF NICOTINIC ACID N-OXIDE, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF ENZYME 3-HYDROXYANTHRANILATE-3, 4-DIOXYGENASE
Free accessEuropean Patent Office | 2016| -
Derivatives of nicotinic acid N-oxide, their preparation and their use as inhibitors of enzyme 3-hydroxyanthranilate-3, 4-dioxygenase
Free accessEuropean Patent Office | 2016| -
Farnesoid X Receptor: From Structure to Potential Clinical Applications
American Chemical Society | 2005| -
LiGen: A High Performance Workflow for Chemistry Driven de Novo Design
American Chemical Society | 2013|
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