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Vadocaine

Vadocaine

产品编号 T35009   CAS 72005-58-4
别名: Vadocaina, Vadocainum

Vadocaine (Vadocaina) 是一种新型的镇咳化合物,可用于局部麻醉,可用于研究中枢神经系统和心血管系统。

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Vadocaine Chemical Structure
Vadocaine, CAS 72005-58-4
规格 价格/CNY 货期 数量
1 mg ¥ 995 现货
5 mg ¥ 2,520 现货
10 mg ¥ 3,710 现货
25 mg ¥ 5,980 现货
50 mg ¥ 8,270 现货
100 mg ¥ 10,900 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: Vadocaine (T35009)
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生物活性
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存储 & 溶解度
参考文献
产品描述 Vadocaine (Vadocaina) is a novel analgesic compound for local anaesthesia and can be used to study the central nervous system and cardiovascular system.
体内活性 In guinea pigs, vadocaine reduced by about 70% the cough episodes induced by sulphur dioxide or ammonia. The effective dose was 2.5 mg/kg p.o., and codeine phosphate was less effective. In cats, vadocaine (3 mg/kg i.v.) inhibited by about 80% for 10 min the cough reflex initiated by mechanical irritation of the trachea. When vadocaine was given via the vertebral artery, it was about 10 times more active than by the intravenous route. Codeine was 3 times as active as vadocaine by both routes. This result indicates an important central component in the antitussive action of vadocaine. In another cat model, 5 mg/kg of vadocaine was somewhat weaker than 1 mg/kg of codeine in inhibiting the cough caused by electrical stimulation of the laryngeal nerve (Domenjoz's method). In dogs, both oral and intravenous doses of 6 mg/kg of vadocaine and 2 mg/kg of codeine were approximately equiactive, inhibiting by 60-80% the cough induced by electrical stimulation of the trachea. Concentrations of vadocaine in serum were around 1 microgram/ml during oral administration. By both routes, the antitussive activity (inhibition of cough by 50% or more) lasted at least 2 h. Vadocaine caused local anaesthesia in the guinea pig wheal preparation at concentrations of 0.25% and 0.5%, and on the guinea pig cornea at 0.5%. The duration of anaesthesia was longer than that of lidocaine. Vadocaine did not affect the guinea pig tracheal strip preparation.[1]
别名 Vadocaina, Vadocainum
分子量 304.43
分子式 C18H28N2O2
CAS No. 72005-58-4

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 60 mg/mL (197.09 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.2848 mL 16.4241 mL 32.8483 mL 82.1207 mL
5 mM 0.657 mL 3.2848 mL 6.5697 mL 16.4241 mL
10 mM 0.3285 mL 1.6424 mL 3.2848 mL 8.2121 mL
20 mM 0.1642 mL 0.8212 mL 1.6424 mL 4.106 mL
50 mM 0.0657 mL 0.3285 mL 0.657 mL 1.6424 mL
100 mM 0.0328 mL 0.1642 mL 0.3285 mL 0.8212 mL

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TargetMol Library Books参考文献

1. Männistö PT, et al. Antitussive action of the new anilide derivative vadocaine hydrochloride compared with codeine phosphate in four animal models. Arzneimittelforschung. 1988 Apr;38(4A):598-604. 2. Paakkari I, et al. Cardiovascular and ventilator effects of vadocaine hydrochloride in urethane-anaesthetized rats and guinea-pigs. Arzneimittelforschung. 1988 Apr;38(4A):617-9.2. 3. Karttunen P, et al. Studies on the nonspecific central nervous system effects of the novel antitussive compound vadocaine hydrochloride. Arzneimittelforschung. 1988 Apr;38(4A):605-8. 4. Silvasti M, et al. The single dose and steady-state pharmacokinetics of a vadocaine tablet in healthy human volunteers. Int J Clin Pharmacol Ther Toxicol. 1989 Nov;27(11):558-63.

相关化合物库

该产品包含在如下化合物库中:
经典已知活性库 已知活性化合物库

TargetMol Calculator剂量换算

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母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

Vadocaine 72005-58-4 Others Vadocaina Vadocainum Inhibitor inhibitor inhibit

 

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