6,6-Dicarboxy-3,4-methano-L-proline (L-DCMP, 7) has been prepared by the rhodium(II)acetate dimer catalyzed decomposition of dimethyl diazomalonate in the presence of a 3,4-didehydroproline derivative. When evaluated against NMDA- and kainate-induced toxicity in cultured cortical neurons, L-DCMP (7) exhibited good neuroprotective activity.

Synthesis of 6,6-dicarboxy-3,4-methano-L-proline, a new constrained glutamate analog endowed with neuroprotective properties / M., Marinozzi; B., Natalini; G., Costantino; R., Pellicciari; Bruno, Valeria Maria Gloria; Nicoletti, Ferdinando. - In: IL FARMACO. - ISSN 0014-827X. - STAMPA. - 51:2(1996), pp. 121-124.

Synthesis of 6,6-dicarboxy-3,4-methano-L-proline, a new constrained glutamate analog endowed with neuroprotective properties

BRUNO, Valeria Maria Gloria;NICOLETTI, Ferdinando
1996

Abstract

6,6-Dicarboxy-3,4-methano-L-proline (L-DCMP, 7) has been prepared by the rhodium(II)acetate dimer catalyzed decomposition of dimethyl diazomalonate in the presence of a 3,4-didehydroproline derivative. When evaluated against NMDA- and kainate-induced toxicity in cultured cortical neurons, L-DCMP (7) exhibited good neuroprotective activity.
1996
animals; cells cultured; cerebral cortex drug effects; female; mice; neuroprotective agents chemical synthesis/pharmacology; pregnancy; proline analogs /&/ derivatives/chemical synthesis/pharmacology; receptors glutamate drug effects
01 Pubblicazione su rivista::01a Articolo in rivista
Synthesis of 6,6-dicarboxy-3,4-methano-L-proline, a new constrained glutamate analog endowed with neuroprotective properties / M., Marinozzi; B., Natalini; G., Costantino; R., Pellicciari; Bruno, Valeria Maria Gloria; Nicoletti, Ferdinando. - In: IL FARMACO. - ISSN 0014-827X. - STAMPA. - 51:2(1996), pp. 121-124.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/461027
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