Chemical Structure : LY344864
CAS No.: 186544-26-3
货号: PC-49006Not For Human Use, Lab Use Only.
LY344864 is a potent, selective agonist of 5-HT1F receptor with Ki value of 6 nM, with little to no affinity for other serotonergic and non-serotonergic neuronal binding sites.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥980 | In stock | |
25 mg | ¥1780 | In stock | |
50 mg | ¥2980 | In stock | |
100 mg | Get quote |
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LY344864 is a potent, selective agonist of 5-HT1F receptor with Ki value of 6 nM, with little to no affinity for other serotonergic and non-serotonergic neuronal binding sites.
LY344864 inhibited forskolin-induced cyclic AMP accumulation in cells stably transfected with human 5-HT1F receptors with EC50 of 3 nM.
Oral and intravenous LY344864 administration potently inhibited dural protein extravasation caused by electrical stimulation of the trigeminal ganglion in rats.
LY 344864 decreased the number of capsaicin-induced c-fos-like immunoreactive cells within trigeminal nucleus caudalis (ID50=0.6 mg/kg).
分子量 | 351.425 | |
分子式 | C21H22FN3O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
N-[(3R)-3-(Dimethylamino)-2,3,4,9-tetrahydro-1H-carbazol-6-yl]-4-fluorobenzamide |
1. Phebus LA, et al. Life Sci. 1997;61(21):2117-26.
2. Mitsikostas DD, et al. Eur J Pharmacol. 1999 Mar 26;369(3):271-7.
3. Cohen ML, et al. J Pharmacol Exp Ther. 1999 Sep;290(3):935-9.
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