Fupentixol Dihydrochloride
CAS No. 2413-38-9
Fupentixol Dihydrochloride ( Flupenthixol dihydrochloride | Flupentixol dihydrochloride | (E/Z)-Flupentixol Dihydrochloride )
产品货号. M19923 CAS No. 2413-38-9
氟哌噻吨用于治疗精神分裂症以及抗焦虑症和抑郁症。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥392 | 有现货 |
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| 10MG | ¥549 | 有现货 |
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| 25MG | ¥892 | 有现货 |
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| 50MG | ¥1293 | 有现货 |
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| 100MG | ¥1557 | 有现货 |
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| 500MG | ¥3843 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥439 | 有现货 |
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生物学信息
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产品名称Fupentixol Dihydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述氟哌噻吨用于治疗精神分裂症以及抗焦虑症和抑郁症。
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产品描述Flupentixol is used in therapy of schizophrenia as well as in anxiolytic and depressive disorders.(In Vitro):Flupentixol (2.5-40 μM; 72 h) treatment inhibits the viability of lung cancer cells in a dose-dependent manner.Flupentixol (2.5-40 μM; 24 h) induces apoptosis in lung cancer cells.Flupentixol (2.5-15 μM; 24 h) inhibits p-AKT and Bcl-2 expression levels.(In Vivo):Flupentixol (intragastric injection; 40 mg/kg; once daily; 21 d) suppresses A549 xenografted tumor growth in nude mice.
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体外实验Flupentixol (2.5-40 μM; 72 h) treatment inhibits the viability of lung cancer cells in a dose-dependent manner.Flupentixol (2.5-40 μM; 24 h) induces apoptosis in lung cancer cells.Flupentixol (2.5-15 μM; 24 h) inhibits p-AKT and Bcl-2 expression levels. Cell Viability AssayCell Line:A549, H661, SK-SEM-1, and NCAL-H520 cells Concentration:2.5, 5, 10, 20, or 40 μM Incubation Time:72 hours Result:Showed the IC50s of 5.708 μM and 6.374 μM for A549 and H661 cells, respectively.Apoptosis Analysis Cell Line:A549 and H661 cells Concentration:5, 10, 20 and 40 μM Incubation Time:24 hours Result:Increased the percentage of cells in early apoptosis compared with the negative control in both A549 and H661 (p<0.05).Induced the cleavage of PARP and caspase-3 in a dose-dependent manner.Western Blot Analysis Cell Line:A549 and H661 cells Concentration:2.5, 5, 10, and 15 μM Incubation Time:24 hours Result:Decreased AKT phosphorylation levels in a dose-dependent manner, decreased the expression levels of Bcl-2.
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体内实验Flupentixol (intragastric injection; 40 mg/kg; once daily; 21 d) suppresses A549 xenografted tumor growth in nude mice. Animal Model:BALB/C nude mice injected with A549 cellsDosage:40 mg/kg Administration: Intragastric injection; 40 mg/kg; once daily; 21 days Result:Reduced tumor volumes compared to the vehicle control (p<0.05), reduced tumor weights by 64.1% (p<0.05).
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同义词Flupenthixol dihydrochloride | Flupentixol dihydrochloride | (E/Z)-Flupentixol Dihydrochloride
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体D1 D2
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研究领域Neurological Disease
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适应症schizophrenia
化学信息
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CAS Number2413-38-9
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分子量507.43
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分子式C23H27Cl2F3N2OS
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纯度>98% (HPLC)
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溶解度DMSO: 95 mg/mL;Water: 95 mg/mL;Ethanol: 25 mg/mL
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SMILESCl.Cl.OCCN1CCN(CC\C=C2\c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Yonar D et al. Effect of cis-(Z)-flupentixol on DPPC membranes in the presence and absence of cholesterol. Chem Phys Lipids. 2016 Jun;198:61-71.
产品手册
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