货号:A310094
同义名:
Hexahydroadiphenine hydrochloride; Drofenine Hydrochloride
Drofenine HCl是一种强效竞争性胆碱酯酶抑制剂,Drofenine的Ki值为3 μM。
HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解

| 描述 | Drofenine hydrochloride is a potent competitive inhibitor of BChE, and the ki values of drofenine is calculated to be 3 μM. |
| Concentration | Treated Time | Description | References | |
| Primary microglia | 10 μmol/L | To evaluate the inhibitory effect of Drofenine on NLRP3 inflammasome activation in microglia. Results showed that Drofenine inhibited Aβ-induced NLRP3 inflammasome activation. | Acta Pharm Sin B. 2025 Jan;15(1):371-391 | |
| HaCaT cells | 50-1000 μmol/L | Evaluating the activation of TRPV3 by Drofenine in HaCaT cells, with an EC50 of 605 μmol/L, and more effective than 2-APB and carvacrol. | Pharmacol Res Perspect. 2014 Oct;2(5):e00062 | |
| CHO-Kv2.1 cells | 10 μmol/L | 12 hours | To evaluate the inhibitory effect of Drofenine on Kv2.1 channel and its impact on potassium efflux. Results showed that Drofenine inhibited Aβ-induced potassium efflux. | Acta Pharm Sin B. 2025 Jan;15(1):371-391 |
| CHO-Kv2.1 cell | 5, 10, 20 μM | 30 minutes | Dfe inhibited membrane potential in CHO-Kv2.1 cell with an IC50 of 9.53 μM. | iScience. 2020 Sep 28;23(10):101617 |
| Administration | Dosage | Frequency | Description | References | ||
| 5×FAD-AD mice | 5×FAD-AD mouse model | Intraperitoneal injection | 10 mg/kg/day | Once daily for 8 weeks | To evaluate the ameliorative effect of Drofenine on cognitive impairment in 5×FAD-AD mice. Results showed that Drofenine improved cognitive function in mice. | Acta Pharm Sin B. 2025 Jan;15(1):371-391 |
| Mice | Diabetic peripheral neuropathy (DPN) model | Intraperitoneal injection | 10, 20 mg/kg | Once daily for 4 weeks | Dfe ameliorated DPN-like pathology in diabetic mice by inhibiting Kv2.1 channel, including promoting neurite outgrowth, improving nerve conduction deficiency and hypoalgesia. | iScience. 2020 Sep 28;23(10):101617 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.83mL 0.57mL 0.28mL |
14.13mL 2.83mL 1.41mL |
28.25mL 5.65mL 2.83mL |
|
| CAS号 | 548-66-3 |
| 分子式 | C20H32ClNO2 |
| 分子量 | 353.93 |
| SMILES Code | O=C(OCCN(CC)CC)C(C1CCCCC1)C2=CC=CC=C2.[H]Cl |
| MDL No. | MFCD00034983 |
| 别名 | Hexahydroadiphenine hydrochloride; Drofenine Hydrochloride; Hexahydroadiphenine hydrochloride, IT-19, NSC 42559, Profenene hydrochloride, Trasentin H, Trasentine A, Trasentine-A; Cycloadiphenine hydrochloride, Cyclohexylphenylacetyldiethylaminoethanol hydrochloride, Cyclospasmol (tempelhof), Cyclovegantine, Drofenine HCl, Drofenine hydrochloride |
| 运输 | 蓝冰 |
| InChI Key | WIELVDXKOYPANK-UHFFFAOYSA-N |
| Pubchem ID | 92806 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 80 mg/mL(226.04 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 30 mg/mL(84.76 mM) 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
|
沪公网安备 31011702889066号
沪ICP备2024050318号-1