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Merck
모든 사진(1)

주요 문서

T3577

Sigma-Aldrich

Tolperisone hydrochloride

≥98% (HPLC), solid

동의어(들):

Menopatol, 2-Methyl-1-(4-methylphenyl)-3-(1-piperidyl)propan-1-one hydrochloride

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About This Item

실험식(Hill 표기법):
C16H23NO · HCl
CAS Number:
Molecular Weight:
281.82
EC Number:
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.77

Quality Level

분석

≥98% (HPLC)

형태

solid

저장 조건

desiccated

색상

white

solubility

H2O: >20 mg/mL

저장 온도

room temp

SMILES string

Cl.CC(CN1CCCCC1)C(=O)c2ccc(C)cc2

InChI

1S/C16H23NO.ClH/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17;/h6-9,14H,3-5,10-12H2,1-2H3;1H

InChI key

ZBUVYROEHQQAKL-UHFFFAOYSA-N

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생화학적/생리학적 작용

Tolperisone is derived from piperidine and possesses membrane stabilizing action. It helps in reducing the effect of spasticities associated with the nervous and muscular system. It exhibits muscle relaxant action through attenuating voltage-gated sodium channels in the brain stem.
Tolperisone regulates ionic currents in myelinates axons and subsequently decreases excitability and mediates its antispastic functions3.
Tolperisone is an ion channel blocker and centrally acting muscle relaxant.

제조 메모

Tolperisone hydrochloride dissolves in water at a concentration that is greater than 20 mg/ml.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Tolperisone: a typical representative of a class of centrally acting muscle relaxants with less sedative side effects
Quasthoff S, et al.
CNS Neuroscience & Therapeutics, 14(2), 107-119 (2008)
HPLC determination of tolperisone in human plasma
Bae JW, et al.
Archives of Pharmacal Research, 29(4), 339-342 (2006)
D Hinck et al.
General physiology and biophysics, 20(4), 413-429 (2002-05-07)
The actions of tolperisone on single intact Ranvier nodes of the toad Xenopus were investigated by means of the Hodgkin-Huxley formalism. Adding tolperisone to the bathing medium (100 micromol/l) caused the following fully reversible effects: 1. The sodium permeability P'Na
Doris Hofer et al.
European journal of pharmacology, 538(1-3), 5-14 (2006-05-03)
The specific, acute interaction of tolperisone, an agent used as a muscle relaxant and for the treatment of chronic pain conditions, with the Na(v1.2), Na(v1.3), Na(v1.4), Na(v1.5), Na(v1.6), Na(v1.7), and Na(v1.8) isoforms of voltage dependent sodium channels was investigated and
Pál Kocsis et al.
The Journal of pharmacology and experimental therapeutics, 315(3), 1237-1246 (2005-08-30)
The spinal reflex depressant mechanism of tolperisone and some of its structural analogs with central muscle relaxant action was investigated. Tolperisone (50-400 microM), eperisone, lanperisone, inaperisone, and silperisone (25-200 microM) dose dependently depressed the ventral root potential of isolated hemisected

문서

Voltage-gated sodium channels are present in most excitable cell membranes and play an important role in generating action potentials.

Chromatograms

application for HPLC

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