Chemical Structure : Traxoprodil
CAS No.: 134234-12-1
货号: PC-61514Not For Human Use, Lab Use Only.
Traxoprodil (CP101606) is a potent, selective N-methyl-D-aspartate (NMDA) antagonist with selectivity for the NR2B subunit, potently protects cultured hippocampal neurons from glutamate toxicity (IC50=10 nM).
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|---|---|---|---|
| 5 mg | ¥580 | In stock | |
| 10 mg | ¥880 | In stock | |
| 25 mg | ¥1480 | In stock | |
| 50 mg | ¥2480 | In stock | |
| 100 mg | Get quote |
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Traxoprodil (CP101606) is a potent, selective N-methyl-D-aspartate (NMDA) antagonist with selectivity for the NR2B subunit, potently protects cultured hippocampal neurons from glutamate toxicity (IC50=10 nM).
Traxoprodil (CP101606) dramatically reduces both the open dwell-time and frequency of channel opening of NR1/NR2B-containing receptors, but only modestly inhibits NR1/NR2A and NR1/NR2C channel activity.
Traxoprodil (CP101606) exhibits neuroprotective, analgesic, and anti-Parkinsonian effects in animal studies.
| 分子量 | 327.42 | |
| 分子式 | C20H25NO3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
(1S,2S)-1-(4-hydroxy-phenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol |
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1. Chenard BL, et al. J Med Chem. 1995 Aug 4;38(16):3138-45.
2. Taniguchi K, et al. Br J Pharmacol. 1997 Nov;122(5):809-12.
3. Brimecombe JC, et al. Proc Natl Acad Sci U S A. 1997 Sep 30;94(20):11019-24.
4. Guscott MR, et al. Eur J Pharmacol. 2003 Aug 29;476(3):193-9.
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