Chemical Structure : UCM-A86
CAS No.: 1210899-51-6
货号: PC-26121Not For Human Use, Lab Use Only.
UCM-A86 is a selective positive allosteric modulator (PAM) of GluN1/GluN3 NMDA receptors with EC50 of 21 μM and 19 μM at GluN1/GluN3A and GluN1/GluN3B receptors, respectively, selective over GluN1/GluN2A-D receptors.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥980 | In stock | |
| 10 mg | ¥1480 | In stock | |
| 25 mg | ¥2580 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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UCM-A86 is a selective positive allosteric modulator (PAM) of GluN1/GluN3 NMDA receptors with EC50 of 21 μM and 19 μM at GluN1/GluN3A and GluN1/GluN3B receptors, respectively, selective over GluN1/GluN2A-D receptors.
UCM-A86 selectively potentiates GluN1/GluN3A and GluN1/GluN3B receptors by 436% and 174%, respectively, relative to activation by glycine, with no activity at GluN1/GluN2A-D receptors.
UCM-A86 selectively potentiates responses from native GluN1/GluN3A receptors expressed in somatostatin-expressing interneurons of the somatosensory cortex with no modulation of hippocampal AMPA receptor-mediated and GluN1/2 NMDA receptor-mediated excitatory postsynaptic currents.
UCM-A86 demonstrates specific modulation of GluN3-containing NMDA receptors without affecting GluN2-containing NMDA receptors or AMPA receptors.
| 分子量 | 338.35 | |
| 分子式 | C15H13F3N4S | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
6-((4-isopropylphenyl)thio)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine |
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1. Benton AJ, et al. Mol Pharmacol. 2026 Jan 23;108(3):100103.
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