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Chemmedchem|July 14, 2007
Synthesis, Cruzain docking, and in vitro studies of aryl-4-oxothiazolylhydrazones against Trypanosoma cruziAna Cristina Lima Leite, Diogo Rodrigo de M Moreira, Marcos V de O Cardoso, et al.Chemmedchem|July 14, 2007
AT1 receptor ligands: virtual-screening-based design with TOPP descriptors, synthesis, and biological evaluation of pyrrolidine derivativesClaudia Lamanna, Alessia Catalano, Alessia Carocci, et al.Chemmedchem|July 27, 2007
Structure-activity relationships for a family of benzothiophene selective estrogen receptor modulators including raloxifene and arzoxifeneCassia R Overk, Kuan-Wei Peng, Rezene T Asghodom, et al.Chemmedchem|May 12, 2007
Modeling promiscuity based on in vitro safety pharmacology profiling dataKamal Azzaoui, Jacques Hamon, Bernard Faller, et al.Chemmedchem|May 17, 2007
Apparent asymmetry in fingerprint similarity searching is a direct consequence of differences in bit densities and molecular sizeYuan Wang, Hanna Eckert, Jürgen BajorathChemmedchem|May 18, 2007
1,2-Mannobioside mimic: synthesis, DC-SIGN interaction by NMR and docking, and antiviral activityJosé J Reina, Sara Sattin, Donatella Invernizzi, et al.Chemmedchem|May 29, 2007
Malaria chemotherapeutics part I: History of antimalarial drug development, currently used therapeutics, and drugs in clinical developmentMartin SchlitzerChemmedchem|May 29, 2007
Paclitaxel and docetaxel resistance: molecular mechanisms and development of new generation taxanesElena Galletti, Matteo Magnani, Michela L Renzulli, et al.Chemmedchem|May 29, 2007
Synthesis and evaluation of 3-phenylpyrazolo[3,4-d]pyrimidine-peptide conjugates as Src kinase inhibitorsAnil Kumar, Yuehao Wang, Xiaofeng Lin, et al.Chemmedchem|June 2, 2007
Highly potent and selective substrate analogue factor Xa inhibitors containing D-homophenylalanine analogues as P3 residue: part 2Anne Stürzebecher, Daniel Dönnecke, Andrea Schweinitz, et al.Pageof 469