NMDA:使

Arif Jamal Siddiqui1, Riadh Badraoui1, Sadaf Jahan2

  • 1Department of Biology, College of Science, University of Hail, Hail, Saudi Arabia.

PubMed
概括

研究人员发现了新的小分子,它们作为N-甲基-D-酸盐受体 (NMDARs) 的强大对手. 这些化合物通过选择性抑制含有GluN2B的受体来治疗大脑疾病有前途,提供了新的治疗策略.

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