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描述 | Palvanil, a Capsaicin analogue, exhibits potent TRPV1 receptor desensitization, resulting in anti-nociceptive and anti-inflammatory effects [1][2]. |
体内研究 | Subcutaneous administration of Palvanil (1 or 10 mg/kg; single dose) demonstrates a hypothermic effect [2]. Palvanil (Intraperitoneal injection, 100 μL, 15 nM per mouse; single dose) reduces Capsaicin-induced bronchoconstriction [2]. Palvanil (Intravenous administration, 0.5, 0.75, and 1 mg/kg; single dose) exhibits antinociceptive effects on Formalin-induced nocifensive behavior [2]. Palvanil (Intravenous administration, 0.5, 0.75, and 1 mg/kg; single dose) inhibits Carrageenan-induced inflammation [2]. Palvanil (Intravenous administration, 0.5 and 1 mg/kg; once daily; 7 days) reduces mechanical allodynia and thermal hyperalgesia in spared nerve injury (SNI) mice [2]. |
体外研究 | Palvanil (0.1-1000 nM; 0-300 min) induces intracellular calcium increase in HEK-293 cells [1]. Palvanil (1-10 nM; 5 min) significantly desensitizes TRPV1 to the effect of Capsaicin [1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.55mL 0.51mL 0.26mL |
12.77mL 2.55mL 1.28mL |
25.54mL 5.11mL 2.55mL |
CAS号 | 69693-13-6 |
分子式 | C24H41NO3 |
分子量 | 391.587 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,Store in freezer, under -20°C |
溶解度 | |
动物实验配方 |