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Trospium-d8 (chloride) Sale

(Synonyms: 曲司氯铵 d8 (氯化物)) 目录号 : GC48209

A neuropeptide with diverse biological activities

Trospium-d8 (chloride) Chemical Structure

规格 价格 库存 购买数量
500 μg
¥2,552.00
现货
1 mg
¥4,848.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

Trospium-d8 is intended for use as an internal standard for the quantification of trospium by GC- or LC-MS. Trospium is an antagonist of muscarinic (M) receptors (Kis = 0.50-2.3 nM for human M1-5 recombinant receptors, respectively).1 Formulations containing antimuscarinics, including trospium, are used to manage overactive bladder by relieving urgency, frequency, and incontinence.1,2,3

1.Hegde, S.S.Muscarinic receptors in the bladder: From basic research to therapeuticsBr. J. Pharmacol.147(2)S80-S87(2006) 2.Maggiore, U.L.R., Salvatore, S., Alessandri, F., et al.Pharmacokinetics and toxicity of antimuscarinic drugs for overactive bladder treatment in femalesExpert Opin.Drug Metab.Toxicol.8(11)1387-1408(2012) 3.Michel, M.C., and de la Rosette, J.J.M.C.H.Role of muscarinic receptor antagonists in urgency and nocturiaBJU Int.96(Suppl 1)37-42(2005)

Chemical Properties

Cas No. N/A SDF
别名 曲司氯铵 d8 (氯化物)
Canonical SMILES O=C(C(C1=CC=CC=C1)(O)C2=CC=CC=C2)OC3C[C@]([N+]45C([2H])([2H])C([2H])([2H])C([2H])([2H])C4([2H])[2H])([H])CC[C@@]5([H])C3.[Cl-]
分子式 C25H22D8NO3.Cl 分子量 436
溶解度 DMSO: soluble 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.2936 mL 11.4679 mL 22.9358 mL
5 mM 0.4587 mL 2.2936 mL 4.5872 mL
10 mM 0.2294 mL 1.1468 mL 2.2936 mL
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Research Update

Determination of the quaternary ammonium compound trospium in human plasma by LC-MS/MS: application to a pharmacokinetic study

J Chromatogr B Analyt Technol Biomed Life Sci 2010 Apr 15;878(13-14):981-6.PMID:20303326DOI:10.1016/j.jchromb.2010.02.028

A highly sensitive, specific and evaporation free SPE extraction, LC-MS/MS method has been developed for the estimation of trospium in human plasma using Trospium-d8 as an internal standard (IS). The analyte was separated using isocratic mobile phase on reverse phase column and analyzed by MS/MS in the multiple reaction monitoring mode using the respective [M(+)] cations, m/z 392-164 for trospium and m/z 400-172 for the IS. The total run time was 3.50 min and the elution of trospium and Trospium-d8 (IS) occurred at 2.8 min. The developed method was validated in human plasma with a lower limit of quantification of 0.05 ng/mL. A linear response function was established for the range of concentrations 0.05-10 ng/mL (r>0.998) for trospium in human plasma. The intra- and inter-day precision values for trospium met the acceptance as per FDA guidelines. Trospium was stable in the battery of stability studies viz., bench-top, auto-sampler, dry extracts and freeze/thaw cycles. The developed assay method was applied to an oral pharmacokinetic study in humans.