Imipramine (hydrochloride)
CAS No. 113-52-0
Imipramine (hydrochloride) ( Imipramine HCl | G 22355 | Tofranil | Melipramine )
产品货号. M21122 CAS No. 113-52-0
丙咪嗪(盐酸盐)是第一代三环类抗抑郁药,主要作为血清素和去甲肾上腺素转运蛋白的抑制剂(Kds 分别为 1.4 和 37 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
100MG | ¥429 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Imipramine (hydrochloride)
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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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产品简述丙咪嗪(盐酸盐)是第一代三环类抗抑郁药,主要作为血清素和去甲肾上腺素转运蛋白的抑制剂(Kds 分别为 1.4 和 37 nM)。
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产品描述Imipramine (hydrochloride) is a first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM respectively).(In Vitro):Imipramine (0.5-300 μM, 3 days) inhibits HCT-116 cell viability. Imipramine (20 μM) inhibits cell migration (7 h) and invasion (48 h). Imipramine (50 μM, 0-240 min) inhibites the PI3K/Akt/mTOR signaling pathway in U-87MG glioma cells. Imipramine (60 μM, 24 h) stimulates U-87MG glioma cells autophagy. Imipramine (80 μM, 24 h) induces HL-60 cell apoptosis.(In Vivo):Imipramine (20 mg/kg, i.p. or 15 mg/kg, p.o.; daily for 24 days) attenuates neuroinflammatory signaling and reverses stress-induced social avoidance in mice.
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体外实验Imipramine (0.5-300 μM, 3 days) inhibits HCT-116 cell viability.?Imipramine (20 μM) inhibits cell migration (7 h) and invasion (48 h).?Imipramine (50 μM, 0-240 min) inhibites the PI3K/Akt/mTOR signaling pathway in U-87MG glioma cells.Imipramine (60 μM, 24 h) stimulates U-87MG glioma cells autophagy.Imipramine (80 μM, 24 h) induces HL-60 cell apoptosis. Cell Viability AssayCell Line:DLD-1, HCT-116, and SW-480 Concentration:0.5-300 μM Incubation Time:3 days Result:Inhibited cell viability and HCT-116 was more sensitive than DLD-1 and SW-480.Cell Migration Assay Cell Line:SW-480, DLD-1, and HCT-116 Concentration:20 μM Incubation Time:7?h Result:Produced a remarkable inhibition of migration in all assayed cell lines.Cell Invasion Assay Cell Line:HCT-116 Concentration:20 μM Incubation Time:48 h Result:Inhibited cell invasion through Matrigel.Western Blot Analysis Cell Line:U-87MG Concentration:50 μM Incubation Time:0, 15, 30, 60, 120 and 240 min Result:Markedly inhibited the phosphorylation of both Akt (Ser473) and mTOR (Ser2481) in a time-dependent manner. Also dephosphorylated p70 S6K, a downstream target of mTOR.Cell Autophagy Assay Cell Line:U-87MG Concentration:60 μM Incubation Time:24 h Result:Stimulated the induction of autophagy through the redistribution of LC3 in U-87MG glioma cells.Cell Autophagy Assay Cell Line:HL-60 Concentration:80 μMIncubation Time:24 hResult:Induced cell apoptosis.
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体内实验Imipramine (20 mg/kg, i.p. or 15 mg/kg, p.o.; daily for 24 days) attenuates neuroinflammatory signaling and reverses stress-induced social avoidance in mice. Animal Model:Male C57BL/6 mice (6–8 weeks old) subjected to RSD (repeated social defeat) and HCC (home cage control) Dosage:20 mg/kg or 15 mg/kg Administration:Intraperitoneal injection or oral administration, daily for 24 days Result:Reversed RSD-induced social avoidance behavior, significantly increasing the interaction time, significantly decreased stress-induced mRNA levels for IL-6 in brain microglia.
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同义词Imipramine HCl | G 22355 | Tofranil | Melipramine
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通路Others
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靶点Other Targets
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受体serotonin
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研究领域Neurological Disease
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适应症Depression
化学信息
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CAS Number113-52-0
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分子量316.87
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分子式C19H25ClN2
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纯度>98% (HPLC)
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溶解度H2O:100 mg/mL (315.59 mM);DMSO:100 mg/mL (315.59 mM)
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SMILESCN(C)CCCN1c2ccccc2CCc2ccccc21.Cl
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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.Glassman A H . The Clinical Pharmacology of Imipramine[J]. Archives of General Psychiatry 1973 28(5):649.
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