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Methocarbamol
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Methocarbamol图片
CAS NO:532-03-6
规格:≥98%
包装与价格:
包装价格(元)
500mg电议
1g电议
5g电议
10g电议
25g电议
50g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)241.24
FormulaC11H15NO5
CAS No.532-03-6
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 48 mg/mL (199.0 mM)
Water: < 1 mg/mL
Ethanol: 48 mg/mL (199.0 mM)
SMILESOC(COC1=CC=CC=C1OC)COC(N)=O
SynonymsAHR 85; Methocarbamol; Robaxin; Lumirelax; AHR-85; AHR85; Metocarbamolo
实验参考方法
In Vitro

In vitro activity: Methocarbamol is metabolized via dealkylation and hydroxylation followed by conjugation to form both glucuronides and sulfates.

In VivoMethocarbamol results in a median terminal half-life, mean transit time, mean absorption time, and apparent oral clearance of 2.89 hours, 2.67 hours, 0.410 hours, and 16.5 mL/min/kg in the horse. Methocarbamol is rapidly absorbed and extensively metabolized after oral administration to horses as indicated by a short absorption time and modest systemic bioavailability of 54.4% in the horse. Methocarbamol is a centrally acting muscle relaxant available in both IV and oral forms in cats. Methocarbamol (100 mg/kg) does not change the heart rate, cardiac output, mean pulmonary arterial blood pressure, systolic, diastolic and mean aortic blood pressure, respiratory rate and arterial blood gases, but mild to moderate depression is observed in five of eight horses administered i.v. Methocarbamol, and in all horses administered oral Methocarbamol. Plasma Methocarbamol concentration declines very rapidly during the initial or rapid disposition phase after i.v. administration; the terminal elimination half-life ranged from 59 minutes to 90 minutes in horse. Peak plasma Methocarbamol concentrations following oral administration occur within 15 to 45 minutes in horse.
Animal modelHorse
Formulation & Dosage16.5 mL/min/kg i
References

J Vet Pharmacol Ther. 2014 Feb;37(1):25-34; Equine Vet J Suppl. 1992 Feb;(11):41-4.