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Harmalol hydrochloride (Harmidol hydrochloride) 是一种可从Peganum harmala L.的种子中提取出来的β-咔啉生物碱。Harmalol hydrochloride 是Harmaline 的主要代谢产物,在转录和翻译后水平上显著抑制二恶英介导的 CYP1A1 诱导。Harmalol hydrochloride 在去氧肾上腺素或KCl 预先收缩的分离大鼠胸主动脉制剂中显示出血管松弛活性。 Harmalol hydrochloride 具有抗氧化活性.
Harmalol hydrochloride (Harmidol hydrochloride) 是一种可从Peganum harmala L.的种子中提取出来的β-咔啉生物碱。Harmalol hydrochloride 是Harmaline 的主要代谢产物,在转录和翻译后水平上显著抑制二恶英介导的 CYP1A1 诱导。Harmalol hydrochloride 在去氧肾上腺素或KCl 预先收缩的分离大鼠胸主动脉制剂中显示出血管松弛活性。 Harmalol hydrochloride 具有抗氧化活性.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 329 | 现货 | |
5 mg | ¥ 788 | 现货 | |
10 mg | ¥ 1,230 | 现货 | |
25 mg | ¥ 2,490 | 现货 | |
50 mg | ¥ 3,730 | 现货 | |
100 mg | ¥ 5,390 | 现货 |
产品描述 | Harmalol hydrochloride (Harmidol hydrochloride) is a β-carboline alkaloid that can be extracted from the seeds of Peganum harmala L. Harmalol hydrochloride is the major metabolite of Harmaline and significantly inhibits dioxin-mediated induction of CYP1A1 at both transcriptional and post-translational levels. Harmalol hydrochloride showed vasorelaxant activity in isolated rat thoracic aortic preparations preconstricted with phenylephrine or KCl. Harmalol hydrochloride has antioxidant activity. |
靶点活性 | DYRK1A:0.63 μM, H4 human glioblastoma:23.7 μM(IC50s), MAO-A:0.66 μM |
体外活性 | Harmalol (0.5-12.5 μM) 通过减少2,3,7,8-四氯二苯并对二恶英 (TCDD) 在HepG2细胞中诱导的细胞色素P450 (CYP) 同型酶CYP1A1水平的增加,并阻止TCDD在豚鼠肝脏胞质提取物中诱导的芳香烃受体 (AhR) 的激活。[1] 另外,Harmalol (25 μM) 能减轻谷氨酸诱导的PC12细胞的细胞毒性、细胞色素c释放、caspase-3激活以及活性氧种(ROS)的生成。[2] |
别名 | 盐酸骆驼蓬酚, Harmidol hydrochloride |
分子量 | 236.7 |
分子式 | C12H13ClN2O |
CAS No. | 6028-07-5 |
Smiles | Cl.CC1=NCCc2c1[nH]c1cc(O)ccc21 |
密度 | no data available |
存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 90.0 mg/mL (380.2 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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