A conformationally restricted analogue of L-glutamate, the (2S,3R,4S) isomer of L-alpha-(carboxycyclopropyl)glycine, activates the NMDA-type receptor more markedly than NMDA in the isolated rat spinal cord. [electronic resource]
Producer: 19890616Description: 355-9 p. digitalISSN:- 0006-8993
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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