TAT-NR2B9C is a synthetic peptide fusion of the nine C-terminal residues of the NR2B subunit of the N-methyl-D-aspartate (NMDA) receptor and the cell membrane protein transduction domain of the HIV-1 tat protein. It is a postsynaptic density protein-95 (PSD95) inhibitor with neuroprotective properties. It is under development for the treatment of acute stroke and acute cerebral ischemia.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/31213815
Curator's Comment: Low brain penetrability.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Discovery and development of NA-1 for the treatment of acute ischemic stroke. | 2018-05 |
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| Neuroprotective efficacy of poly-arginine R18 and NA-1 (TAT-NR2B9c) peptides following transient middle cerebral artery occlusion in the rat. | 2017-01 |
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| PDZ protein interactions underlying NMDA receptor-mediated excitotoxicity and neuroprotection by PSD-95 inhibitors. | 2007-09-12 |
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FDA ORPHAN DRUG |
377812
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FDA ORPHAN DRUG |
412713
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C170212
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100000174143
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D45TI2TWMA
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GH-179
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500992-11-0
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DB12595
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44568939
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ACTIVE MOIETY
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