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Principaux documents

Y101

Supelco

YS-035 hydrochloride

analytical standard, for drug analysis

Synonyme(s) :

N-(-2-[3,4-Dimethoxyphenyl]ethyl)-3,4-dimethoxy-N-methylbenzeneethanamine

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About This Item

Formule empirique (notation de Hill) :
C21H29NO4 · HCl
Numéro CAS:
Poids moléculaire :
395.92
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard, for drug analysis

Niveau de qualité

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

Chaîne SMILES 

Cl[H].COc1ccc(CCN(C)CCc2ccc(OC)c(OC)c2)cc1OC

InChI

1S/C21H29NO4.ClH/c1-22(12-10-16-6-8-18(23-2)20(14-16)25-4)13-11-17-7-9-19(24-3)21(15-17)26-5;/h6-9,14-15H,10-13H2,1-5H3;1H

Clé InChI

GYBONEHHSUABAO-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

S L Mironov et al.
The European journal of neuroscience, 12(2), 520-526 (2000-03-11)
A hyperpolarization-activated current, Ih, is often implied in pacemaker-like depolarizations during rhythmic oscillatory activity. We describe Ih in the isolated respiratory centre of immature mice (P6-P11). Ih was recorded in 15% (22/146) of all inspiratory neurons examined. The mean half-maximal
R Deana et al.
The Biochemical journal, 218(3), 899-905 (1984-03-15)
Compound YS 035 [NN-bis-(3,4-dimethoxyphenethyl)-N-methylamine] is a new synthetic compound capable of inhibiting Ca2+ uptake by different cells. The inhibition of Ca2+ uptake by muscle cells isolated from chicken embryo is dose-dependent in the compound YS 035 concentration range 10-30 microM.
Carbamazepine and L-type calcium channel inhibitors: a binding assay study.
E T Ngan et al.
Biological psychiatry, 39(11), 979-981 (1996-06-01)
T Kammer et al.
Arzneimittel-Forschung, 43(3), 302-308 (1993-03-01)
In isolated guinea-pig papillary muscle ([K+]o: 4.7 mmol/l, stimulation rate: 1 Hz) the verapamil derivative NN-bis-(3,4-dimethoxyphenethyl)-N-methylamine)-HCl (YS035; 0.3-100 mumol/l) increased the action potential duration measured at 90% repolarization level (APD90) up to 132% of control and enhanced the force of
F Berger et al.
Naunyn-Schmiedeberg's archives of pharmacology, 344(6), 653-661 (1991-12-01)
The electrophysiologic mode of action and potency of the verapamil derivative YS 035 (N,N-bis-(3,4-dimethoxyphenethyl)-N-methyl amine) were investigated in sheep cardiac Purkinje fibres. Action potential duration measured at a repolarization level of -60 mV (APD-60) and membrane currents recorded with the

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