3-((±)2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) more potently antagonizes the high-affinity Mg2+ binding site on the receptor ion channel complex than the l-glutamate recognition site
- 1 April 1991
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 124 (2) , 229-231
- https://doi.org/10.1016/0304-3940(91)90100-8
Abstract
No abstract availableKeywords
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