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Chemmedchem|March 3, 2011
Design, synthesis, and pharmacological characterization of novel spirocyclic quinuclidinyl-Δ2-isoxazoline derivatives as potent and selective agonists of α7 nicotinic acetylcholine receptorsClelia Dallanoce, Pietro Magrone, Carlo Matera, et al.
Chemmedchem|March 4, 2011
From β-amino-γ-sultone to unusual bicyclic pyridine and pyrazine heterocyclic systems: synthesis and cytostatic and antiviral activitiesSonia de Castro, Olga Familiar, Graciela Andrei, et al.
Chemmedchem|October 20, 2010
Modeling and biological investigations of an unusual behavior of novel synthesized acridine-based polyamine ligands in the binding of double helix and G-quadruplex DNACarla Bazzicalupi, Matteo Chioccioli, Claudia Sissi, et al.
Chemmedchem|October 12, 2010
Synthesis, in vitro and in vivo release kinetics, and anti-HIV activity of a sustained-release prodrug (mPEG-AZT) of 3'-azido-3'-deoxythymidine (AZT, Zidovudine)Wenjun Li, Yu Chang, Peng Zhan, et al.
Chemmedchem|March 25, 2011
Development of intravascular contrast agents for MRI using gadolinium chelatesKrisada Kittigowittana, Chang-Tong Yang, Wai Ching Cheah, et al.
Chemmedchem|May 17, 2011
The approach of conformational chimeras to model the role of proline-containing helices on GPCR mobility: the fertile case of Cys-LTR1Ilaria Bettinelli, Davide Graziani, Cristina Marconi, et al.
Chemmedchem|August 18, 2010
Probing the peptidylglycine alpha-hydroxylating monooxygenase active site with novel 4-phenyl-3-butenoic acid based inhibitorsEmma Langella, Sébastien Pierre, Wadih Ghattas, et al.
Chemmedchem|May 25, 2011
Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templatesPaul M Wood, L W Lawrence Woo, Mark P Thomas, et al.
Chemmedchem|October 7, 2009
Virtual screening against p50 NF-kappaB transcription factor for the identification of inhibitors of the NF-kappaB-DNA interaction and expression of NF-kappaB upregulated genesLaura Piccagli, Enrica Fabbri, Monica Borgatti, et al.
Chemmedchem|December 9, 2010
Discovery of 4-benzylamino-substituted α-carbolines as a novel class of receptor tyrosine kinase inhibitorsMartin Krug, Kanin Wichapong, German Erlenkamp, et al.
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