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Die Pharmazie|February 1, 1991
(-)-N,N'-but-2-ene-1,4-diylbimorphinansH Schmidhammer, C F Smith, E Dalkner, et al.Journal of Medicinal Chemistry|April 1, 1990
Synthesis and biological evaluation of 14-alkoxymorphinans. 3. Extensive study on cyprodime-related compoundsH Schmidhammer, C F Smith, D Erlach, et al.Archiv Der Pharmazie|April 1, 1991
Synthesis and biological evaluation of 14-alkoxymorphinans, V: 6-Deoxyocyprodime, an opioid antagonist with decreased mu receptor selectivity in comparison to cyprodimeH Schmidhammer, H K Jennewein, C F SmithJournal of Medicinal Chemistry|February 1, 1989
Synthesis and biological evaluation of 14-alkoxymorphinans. 2. (-)-N-(cyclopropylmethyl)-4,14-dimethoxymorphinan-6-one, a selective mu opioid receptor antagonistH Schmidhammer, W P Burkard, L Eggstein-Aeppli, et al.Journal of Pharmaceutical Sciences|July 18, 2001
Polymorphism of racemic felodipine and the unusual series of solid solutions in the binary system of its enantiomersJ M Rollinger, A BurgerCurrent Medicinal Chemistry|March 30, 2012
Recent advances in the development of 14-alkoxy substituted morphinans as potent and safer opioid analgesicsM Spetea, H SchmidhammerJournal of Pharmaceutical Sciences|June 1, 1997
Binary system of (R)- and (S)-nitrendipine--polymorphism and structureA Burger, J M Rollinger, P BrüggellerPlanta Medica|June 20, 2006
Integrated in silico tools for exploiting the natural products' bioactivityJ M Rollinger, T Langer, H StuppnerAnesthesia and Analgesia|May 29, 2000
14-methoxymetopon, a potent opioid, induces no respiratory depression, less sedation, and less bradycardia than sufentanil in the dogE Freye, H Schmidhammer, L LataschCurrent Medicinal Chemistry|June 22, 2006
Strategies for efficient lead structure discovery from natural productsJ M Rollinger, T Langer, H StuppnerPageof 16