𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Structure-activity relations for the neurotoxicity of kainic acid derivatives and glutamate analogues

✍ Scribed by SCHWARCZ, R; SCHOLZ, D; COYLE, J


Book ID
121978283
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
914 KB
Volume
17
Category
Article
ISSN
0028-3908

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


The activation of glutamate receptors by
✍ David R. Hampson; Jerrie Lynn Manalo πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 56 KB

The neurotoxins kainic acid and domoic acid are potent agonists at the kainate and aamino-5-methyl-3-hydroxyisoxazolone-4-propionate (AMPA) subclasses of ionotropic glutamate receptors. Although it is well established that AMPA receptors mediate fast excitatory synaptic transmission at most excitato

The synthesis of 4,5-methano congeners o
✍ Stephen Hanessian; Sacha Ninkovic; Ulrich Reinhold πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 French βš– 236 KB

The synthesis of diastereomeric 4.5-methano-L-proline 3-acetic acids is described starting from D-serine. The key reactions include a free-radical carbocyclization and an acid-catalyzed destannylative cyclopropanatian of an iminium ion intermediate.

Immunosuppressive structure-activity rel
✍ Douglas G. Batt; Robert A. Copeland; Randine L. Dowling; Tracy L. Gardner; Eliza πŸ“‚ Article πŸ“… 1995 πŸ› Elsevier Science 🌐 English βš– 321 KB

The immunosuppressive structure-activity relationships of substituted cinchoninic acid derivatives related to Brequinar were explored. Activities as inhibitors of dibydroorotate dehydrogenase and the mixed lymphocyte reaction were related to benzo-ring substitution, replacement of the benzo-ring by