Synthesis, Molecular Modeling Studies, and Preliminary Pharmacological Characterization of All Possible 2-(2‘-Sulfonocyclopropyl)glycine Stereoisomers as Conformationally Constrained L-Homocysteic Acid Analogs

Author:

Pellicciari Roberto1,Marinozzi Maura1,Macchiarulo Antonio1,Fulco Maria Carmela1,Gafarova Julia1,Serpi Michaela1,Giorgi Gianluca1,Nielsen Søren1,Thomsen Christian1

Affiliation:

1. Dipartimento di Chimica e Tecnologia del Farmaco, Università di Perugia, Via del Liceo, 1- 06123 Perugia, Italy, Dipartimento di Chimica, Università di Siena, Via A. Moro, 53100 Siena, Italy, and H. Lundbeck A/S, 9 Ottilavej, DK-2500 Valby, Copenhagen, Denmark

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference74 articles.

1. Pellicciari, R.; Curini, M.; Natalini, B.; Ceccherelli, P.Abstract of the IXInternational Symposium on Medicinal Chemistry, Berlin, Germany, 1986; p 118.

2. Pellicciari, R.; Natalini, B.; Monahan, J. B.; Lanthorn, T. H.; Pilipauskas, D.; Snyder, J. P.6th Camerino-Noordwijkerout Symposium on RecentAdvances in Receptor Chemistry, Camerino, Italy, 1987; pp 73−74.

3. Pellicciari, R.; Natalini, B.; Marinozzi, M., et al. InFrontiers inExcitatory Amino Acid Research; Cavalheiro, E. A., Lehman, J., Turski. L., Eds.; Alan R. Liss, Inc.  New York, 1988; p 67.

4. Potent NMDA-like actions and potentiation of glutamate responses by conformational variants of a glutamate analogue in the rat spinal cord

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