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Chemmedchem|October 10, 2013
Sigma-2 receptor agonists as possible antitumor agents in resistant tumors: hints for collateral sensitivityMauro Niso, Carmen Abate, Marialessandra Contino, et al.
Chemmedchem|October 10, 2013
Amythiamicin D and related thiopeptides as inhibitors of the bacterial elongation factor EF-Tu: modification of the amino acid at carbon atom C2 of ring C dramatically influences activityStefan Gross, Fabian Nguyen, Matthias Bierschenk, et al.
Chemmedchem|October 12, 2013
Target hopping as a useful tool for the identification of novel EphA2 protein-protein antagonistsMassimiliano Tognolini, Matteo Incerti, Daniele Pala, et al.
Chemmedchem|April 25, 2012
Structure-activity relationships and mechanism of action of Eph-ephrin antagonists: interaction of cholanic acid with the EphA2 receptorMassimiliano Tognolini, Matteo Incerti, Iftiin Hassan-Mohamed, et al.
Chemmedchem|August 27, 2016
Development of Dipeptidic hGPR54 AgonistsChristelle Doebelin, Isabelle Bertin, Séverine Schneider, et al.
Chemmedchem|August 24, 2016
Flavonoids and Naphthoflavonoids: Wider Roles in the Modulation of Cytochrome P450 Family 1 EnzymesJinyun Dong, Qijing Zhang, Qing Cui, et al.
Chemmedchem|August 24, 2016
Identification and Optimization of the First Highly Selective GLUT1 Inhibitor BAY-876Holger Siebeneicher, Arwed Cleve, Hartmut Rehwinkel, et al.
Chemmedchem|March 18, 2010
Chiral aryloxyalkylamines: Selective 5-HT(1B/1D) activation and analgesic activityAlessia Carocci, Giovanni Lentini, Alessia Catalano, et al.
Chemmedchem|March 17, 2010
Triazolyl azabicyclo[3.1.0]hexanes: A class of potent and selective dopamine D(3) receptor antagonistsGiorgio Bonanomi, Simone Braggio, Anna Maria Capelli, et al.
Chemmedchem|December 30, 2009
Identification, SAR studies, and X-ray co-crystallographic analysis of a novel furanopyrimidine aurora kinase A inhibitorMohane Selvaraj Coumar, Ming-Tsung Tsai, Chang-Ying Chu, et al.
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