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吡那地尔

    
10mM in DMSO

Pinacidil monohydrate

源叶(MedMol)
S56515 一键复制产品信息
85371-64-8
C13H19N5 · H2O
263.34
(±)-N-Cyano-N′-4-pyridinyl-N″-(1,2,2-trimethylpropyl)guanidine monohydrate;(±)-N-Cyano-N′-4-pyridinyl-N″-(1,2,2-trimethylpropyl)guanidine monohydrate
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S56515-1ml促销
10mM in DMSO

¥309.00 ¥240.00

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产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Pinacidil is a K+ channel opener. Pinacidil is demonstrated to induce relaxation of serotonin-produced contractions in porcine and human arterial rings. This action is suppressed by the ATP-dependent K+ (KATP) channel blockers Glibenclamide and Tetrapentylammonium salts, suggesting that relaxations induced by Pinacidil are mediated by opening of KATP channels.;Pinacidil is a K+ channel opener. Pinacidil is demonstrated to induce relaxation of serotonin-produced contractions in porcine and human arterial rings. This action is suppressed by the ATP-dependent K+ (KATP) channel blockers Glibenclamide and Tetrapentylammonium salts, suggesting that relaxations induced by Pinacidil are mediated by opening of KATP channels.A K+ channel activator; antihypertensive
体内研究: Pinacidil (3-30 μg,静脉注射,单次给药) monohydrate 在非糖尿病小鼠 (ED50 = 16.1)和糖尿病小鼠 (ED50 = 22.3) 中呈剂量依赖性地增加甩尾反应潜伏期。
Pinacidil (10-100 μg,i.t.,单次给药) monohydrate 在糖尿病小鼠中产生剂量依赖性显著的抗伤害作用,而 100 μg 剂量在非糖尿病小鼠中没有产生显著的抗伤害作用 (ED50 = 18.5),而糖尿病小鼠的 ED50 为 95.6。
Pinacidil (30 μg,静脉注射,单次给药) monohydrate 不受 β-Funaltrexamine (20 和 40 mg/kg,皮下注射) 预处理对糖尿病小鼠的抗伤害作用的影响。
Pinacidil (30 μg,i.t.,单次给药) monohydrate 会剂量依赖性地降低 β-Funaltrexamine (20 和 40 mg/kg,s.c.) 的抗伤害作用,且该作用可被 7-Benzylidenenaltrexon (0.3 mg/kg)、Naltriben (0.3 mg/kg) 或 nor-Binaltorphimine (20 mg/kg,s.c.) 预处理所拮抗。
参考文献: 1. Hamilton TC, et al., Cromakalim, nicorandil and pinacidil: novel drugs which open potassium channels in smooth muscle. Gen Pharmacol. 1989;20(1):1-9.
2. Jung-Ae Kim, et al., Activation of Na+, K+, Cl−-Cotransport Mediates Intracellular Ca2+ Increase and Apoptosis Induced by Pinacidil in HepG2 Human Hepatoblastoma Cells, Biochemical and Biophysical Research Communications, Volume 281, Issue 2, 2001, Pages 511-519, ISSN 0006-291X,3. Weston, A.H., et al., In Vitro Studies on the Mode of Action of Pinacidil. Drugs 36 (Suppl 7), 10–28 (1988). 4. Ko Zushida, et al ., Effect of diabetes on pinacidil-induced antinociception in mice, European Journal of Pharmacology, Volume 453, Issues 2–3, 2002, Pages 209-215, ISSN 0014-2999.
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.797 ml 18.987 ml 37.974 ml
5 mM 0.759 ml 3.797 ml 7.595 ml
10 mM 0.38 ml 1.899 ml 3.797 ml
50 mM 0.076 ml 0.38 ml 0.759 ml
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参考文献

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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