(–)-Ropivacaine-d7 (hydrochloride) - CAS:1217667-10-1

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(–)-Ropivacaine-d7 (hydrochloride) (Synonyms:盐酸罗哌卡因-d7)

目录号 : KCM10688 CAS No. : 1217667-10-1 纯度 : 98%

Data Sheet 产品使用指南

(–)-Ropivacaine-d is intended for use as an internal standard for the quantification of (–)-ropivacaine by GC- or LC-MS. (–)-Ropivacaine is a potent and reversible blocker of sodium channels in nerve fibers. In vivo, (–)-ropivacaine induces complete impairment of proprioception, motor function, and nociception in the hindleg of rats when 100 μL of an 8 mM solution is injected percutaneously into the sciatic nerve. (–)-Ropivacaine depresses myocardial contractile force in isolated rat hearts less potently than (±)-ropivacaine, as well as (–)- and (±)-bupivacaine . Formulations containing (–)-ropivacaine have been used as local anesthetics during surgery and childbirth.

规格	价格	是否有货	数量
500μg		In-stock
1mg		In-stock

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Bupivacaine-d9 hydrochloride In-stock
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Empagliflozin-d4 In-stock
Ertugliflozin-d5 In-stock

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生物活性

Ropivacaine-d7 hydrochloride is a deuterium labeled Ropivacaine (hydrochloride) . Ropivacaine hydrochloride is a potent sodium channel blocker and blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibrese. Ropivacaine is also an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM in COS-7 cell's membrane. Ropivacaine is widely used for neuropathic pain management in vivo.

分子式

C₁₇H₁₉D₇N₂O^.HCl

分子量

317.91

CAS号

1217667-10-1

中文名称

盐酸罗哌卡因-d7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	6 months
	-20°C	1 month

纯度： 98%

Data Sheet

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Other Forms of Rapamycin:

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