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Y101

Supelco

YS-035 hydrochloride

analytical standard, for drug analysis

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C21H29NO4 · HCl
Numero CAS:
33978-72-2
Peso molecolare:
395.92
Numero MDL:
MFCD00153884
Codice UNSPSC:
41116107
ID PubChem:
329831585
NACRES:
NA.24

Grado

analytical standard, for drug analysis

Livello qualitativo

100

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Formato

neat

Stringa SMILE

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
GYBONEHHSUABAO-UHFFFAOYSA-N

Applicazioni

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number

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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.
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
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
P C Levesque et al.
Toxicology and applied pharmacology, 94(1), 55-65 (1988-06-15)
Agents known to disrupt intraterminal Ca2+ buffering, N,N-dimethylamino-8-octyl-3,4,5-trimethoxybenzoate (TMB-8), 25 microM; caffeine, 7.5 mM; N,N-bis(3,4-dimethoxyphenethyl)-N-methylamine (YS035), 180 microM; ouabain, 200 microM; and dantrolene, 50 microM, were tested for the ability to alter effects of methyl mercury (MeHg) on spontaneous quantal
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