Franco Manfré

X-ray analysis of D-xylose isomerase at 1.9 A: native enzyme in complex with substrate and with a mechanism-designed inactivator.

H. L. Carrell, Jenny P. Glusker, Virginia Burger et al. · Proceedings of the National Academy of Sciences · 1989 · 192 citations · Full text

Life Sciences, Biochemistry, Chemistry +17

Syntheses of proline analogs as potential mechanism-based inhibitors of proline dehydrogenase: 4-methylene-L-, (E)- and (Z)-4-(fluoromethylene)-L-, cis- and trans-5-ethynyl-(.+-.)-, and cis- and trans-5-vinyl-L-proline

Franco Manfré, Jean Marc Kern, Jean Francois Biellmann · The Journal of Organic Chemistry · 1992 · 59 citations

Life Sciences, Chemistry, Pharmacology +9

Enantiospecific synthesis and absolute configuration of (+)-RP 66803 a new non-peptide CCK antagonist

Franco Manfré, Jean Pierre Pulicani · Tetrahedron Asymmetry · 1994 · 42 citations

Pharmacy, Medicinal Chemistry, Pharmacology +12

Indeno[1,2-<i>b</i>]pyrazin-2,3-diones: A New Class of Antagonists at the Glycine Site of the NMDA Receptor with Potent in Vivo Activity

Patrick Jimonet, Yves Ribeill, Georg Andrees Böhme et al. · Journal of Medicinal Chemistry · 2000 · 23 citations

Medicine, Medicinal Chemistry, Pharmacology +16

Bioisosteres of 9-Carboxymethyl-4-oxo-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent In Vivo AMPA antagonists with longer durations of action

Patrick Jimonet, Georg Andrees Böhme, J Bouquerel et al. · Bioorganic & Medicinal Chemistry Letters · 2001 · 11 citations

Pharmacy, Medicinal Chemistry, Pharmacology +11