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Enantiomers of C(5)-chiral 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives: Analytical and semipreparative HPLC separation, chiroptical properties, absolute configuration, and inhibitory activity against monoamine oxidase.
Cirilli R, Ferretti R, Gallinella B, Turchetto L, Bolasco A, Secci D, Chimenti P, Pierini M, Fares V, Befani O, La Torre F. Cirilli R, et al. Among authors: secci d. Chirality. 2004 Nov;16(9):625-36. doi: 10.1002/chir.20085. Chirality. 2004. PMID: 15382204
Analytical and semipreparative high performance liquid chromatography enantioseparation of new substituted 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazoles on polysaccharide-based chiral stationary phases in normal-phase, polar organic and reversed-phase conditions.
Cirilli R, Simonelli A, Ferretti R, Bolasco A, Chimenti P, Secci D, Maccioni E, La Torre F. Cirilli R, et al. Among authors: secci d. J Chromatogr A. 2006 Jan 6;1101(1-2):198-203. doi: 10.1016/j.chroma.2005.10.003. Epub 2005 Oct 24. J Chromatogr A. 2006. PMID: 16246349
Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole derivatives.
Chimenti F, Maccioni E, Secci D, Bolasco A, Chimenti P, Granese A, Befani O, Turini P, Alcaro S, Ortuso F, Cirilli R, La Torre F, Cardia MC, Distinto S. Chimenti F, et al. Among authors: secci d. J Med Chem. 2005 Nov 17;48(23):7113-22. doi: 10.1021/jm040903t. J Med Chem. 2005. PMID: 16279769
116 results