Phenylephrine-2,4,6-d3 (hydrochloride)

目录号: PL05349
Phenylephrine-2,4,6-d3 (hydrochloride) 是 Phenylephrine hydrochloride 的氘代物。(R)-(-)-Phenylephrine hydrochloride是一种选择性的α1-肾上腺素能受体激动剂,对α1D,α1B 和α1A 受体的pKis 分为5.86,4.87和4.70。
CAS No. :1276197-50-2
商品编号 规格 价格 会员价 是否有货 数量
PL05349-1mg 1mg ¥3857.00 请登录
PL05349-5mg 5mg ¥7875.00 请登录
PL05349-10mg 10mg ¥12697.00 请登录
PL05349-50mg 50mg 询价 询价
PL05349-100mg 100mg 询价 询价
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
*注意事项:下单时请联系销售核实产品价格及货期,避免后续产生不便,感谢支持!
中文名称
Phenylephrine-2,4,6-d3 (hydrochloride)
中文别名
盐酸苯肾上腺素-D3氘代内标;(R)-(-)-去氧-D3盐酸;(R)-(-)-盐酸脱羟肾上腺素-D3;盐酸苯肾上腺素-D3;[2H3] -R-( - ) - 去氧肾上腺素HCL
英文名称
Phenylephrine-2,4,6-d3 (hydrochloride)
英文别名
(R)-(-)-Phenylephrine-2,4,6-d3?HCl;(R)-(-)-Phenylephrine-d3 HCl;Phenylephrine Impurity 47((R)-Phenylephrine-d3 HCl);(R)-(-)-Phenylephrine D3 HydrochlorideQ: What is (R)-(-)-Phenylephrine D3 Hydrochloride Q: What is the CAS Number of (R)-(-)-Phenylephrine D3 Hydrochloride Q: What is the storage condition of (R)-(-)-Phenylephrine D3 Hydrochloride Q: What are the applications of (R)-(-)-Phenylephrine D3 Hydrochloride
Cas No.
1276197-50-2
分子式
C9H14ClNO2
分子量
206.68
包装储存
Please store the product under the recommended conditions in the Certificate of Analysis.
详情描述
Phenylephrine-2,4,6-d3 (hydrochloride) 是 Phenylephrine hydrochloride 的氘代物。(R)-(-)-Phenylephrine hydrochloride是一种选择性的α1-肾上腺素能受体激动剂,对α1D,α1B 和α1A 受体的pKis 分为5.86,4.87和4.70。
产品详情
Phenylephrine-2,4,6-d3 (hydrochloride) 是 Phenylephrine hydrochloride 的氘代物。(R)-(-)-Phenylephrine hydrochloride是一种选择性的α1-肾上腺素能受体激动剂,对α1D,α1B 和α1A 受体的pKis 分为5.86,4.87和4.70。
生物活性
Phenylephrine-2,4,6-d 3 (hydrochloride) is the deuterium labeled Phenylephrine hydrochloride. (R)-(-)-Phenylephrine hydrochloride is a selective α1-adrenoceptor agonist with pKis of 5.86, 4.87 and 4.70 for α1D, α1B and α1A receptors respectively.
体外研究(In Vitro)
Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
[2]. Ford AP, et al. Pharmacological pleiotropism of the human recombinant alpha1A-adrenoceptor: implications foralpha1-adrenoceptor classification. Br J Pharmacol. 1997 Jul;121(6):1127-35.
搜索质检报告(COA)
[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
[2]. Ford AP, et al. Pharmacological pleiotropism of the human recombinant alpha1A-adrenoceptor: implications foralpha1-adrenoceptor classification. Br J Pharmacol. 1997 Jul;121(6):1127-35.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2