Methocarbamol D5
(Synonyms: 美索巴莫 D5) 目录号 : GC61046An internal standard for the quantification of methocarbamol
Cas No.:1189699-70-4
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Methocarbamol-d5 is intended for use as an internal standard for the quantification of methocarbamol by GC- or LC-MS. Methocarbamol is an orally bioavailable skeletal muscle relaxant.1 In vivo, methocarbamol inhibits the ability of mice to remain on a vertical ladder for 1 minute (ED50 = 15 mg/kg) and decreases forelimb grip strength by 35.9% when administered at a dose of 500 mg/kg.1,2 It abolishes femoral nerve-stimulated polysynaptic reflex contractions of the cat tibialis anterior muscle and prolongs the mean refractory period of directly or indirectly stimulated skeletal muscle when administered at a dose of 200 mg/kg.3 Methocarbamol also selectively inhibits human carbonic anhydrase (CA) isoform I over CAII (IC50s = 70 and ~80,000 μM, respectively).4 Formulations containing methocarbamol have been used to treat skeletal muscle spasms.
1.Cymbalist, M.A., and Shapero, M.A comparative study of the effect of some centrally acting skeletal muscle relaxants in miceJ. Pharm. Pharmacol.26(2)109-112(1974) 2.Nevins, M.E., Nash, S.A., and Beardsley, P.M.Quantitative grip strength assessment as a means of evaluating muscle relaxation in micePsychopharmacology (Berl)110(1-2)92-86(1993) 3.Crankshaw, D.P., and Raper, C.Some studies on peripheral actions of mephenesin, methocarbamol and diazepamBr. J. Pharmacol.34(3)579-590(1968) 4.Parr, J.S., and Khalifah, R.G.Inhibition of carbonic anhydrases I and II by N-unsubstituted carbamate estersJ. Biol. Chem.267(35)25044-25050(1992)
Cas No. | 1189699-70-4 | SDF | |
别名 | 美索巴莫 D5 | ||
Canonical SMILES | OC(C([2H])([2H])OC1=CC=CC=C1OC)([2H])C([2H])([2H])OC(N)=O | ||
分子式 | C11H10D5NO5 | 分子量 | 246.27 |
溶解度 | DMF: soluble,DMSO: soluble,Methanol: soluble | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 4.0606 mL | 20.3029 mL | 40.6058 mL |
5 mM | 0.8121 mL | 4.0606 mL | 8.1212 mL |
10 mM | 0.4061 mL | 2.0303 mL | 4.0606 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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