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ITEM#: 2946-092450
MFR#: 0924/50
(+)-MK 801 maleate, high affinity (Ki = 37.2 nM), selective NMDA antagonist, acts at ion channel site, prevents Ca2+ flux, anti-ischemic in animal models, increases motor activity in rats, inhibits proliferation and increases apoptosis in hippocampal
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
DL-AP5, potent NMDA antagonist, 50mg, Tocris Bioscience
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DL-AP5, potent NMDA antagonist, 50mg, Molecular Weight: 197.127, Percent Purity: >98%, CAS: 76326-31-3, Molecular Formula: C5H12NO5P, IUPAC Name: 2-amino-5-phosphonopentanoic acid, Tocris Bioscience | 2946-010550 | EA | |
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DNQX, Selective non-NMDA receptor antagonist, 50mg, Tocris Bioscience
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DNQX, 50mg, Tocris Bioscience. Selective non-NMDA receptor antagonist. Molecular Weight: 252.142, Percent Purity: >98%, CAS: 2379-57-9, Molecular Formula: C8H4N4O6, IUPAC Name: 6,7-dinitro-1,4-dihydroquinoxaline-2,3-dione | 2946-018950 | EA | |
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(+)-Bicuculline, GABAA antagonist, 50mg, Tocris Bioscience
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(+)-Bicuculline, classical GABAA antagonist, 50mg, Tocris Bioscience, Molecular Weight: 367.357, Percent Purity: >99%, CAS: 485-49-4, ChEBI: CHEBI:3092, Formula Weight: 367.36, InChI Key: IYGYMKDQCDOMRE-ZWKOTPCHSA-N | 2946-013050 | EA | |
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SR 95531 hydrobromide, GABAA antagonist, 50mg, Tocris Bioscience
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SR 95531 hydrobromide, 50mg, selective competitive GABAA antagonist, IC50 200 nM, Ki 150 nM, purity >98%, CAS 104104-50-9, molecular weight 368.231, Tocris Bioscience | 2946-126250 | EA | |
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L-745,870 trihydrochloride, D4 antagonist, 50mg, Tocris Bioscience
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L-745,870 trihydrochloride, highly potent and selective D4 dopamine receptor antagonist, Ki: 0.51 nM (D4), 2300 nM (D3), 960 nM (D2), 1000-fold selectivity over 5-HT2, D1, D5; 50mg, >99% purity, Molecular Weight: 436.202, CAS: 866021-03-6, InChI Key: | 2946-100250 | EA |