(–)-Ropivacaine-d7 (hydrochloride) (Synonyms:盐酸罗哌卡因-d7)
目录号 : KCM10688 CAS No. : 1217667-10-1 纯度 : 98%
(–)-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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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
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