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Merck

43530

Supelco

Reserpine Standard for LC-MS

analytical standard, for LC-MS

Sinónimos:

Reserpine, (3β, 16β, 17α, 18β, 20α)-11,17-Dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylic acid methyl ester

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About This Item

Fórmula empírica (notación de Hill):
C33H40N2O9
Número de CAS:
Peso molecular:
608.68
Beilstein:
102014
Número MDL:
Código UNSPSC:
41121800
ID de la sustancia en PubChem:
NACRES:
NB.21

grado

analytical standard

Nivel de calidad

caducidad

limited shelf life, expiry date on the label

concentración

5 mg/L in water: isopropyl alcohol (1:1)

técnicas

LC/MS: suitable

mp

~265 °C (dec.)

idoneidad

corresponds for mass spectrometry

temp. de almacenamiento

2-8°C

cadena SMILES

CO[C@H]1[C@@H](C[C@@H]2CN3CCc4c([nH]c5cc(OC)ccc45)[C@H]3C[C@@H]2[C@@H]1C(=O)OC)OC(=O)c6cc(OC)c(OC)c(OC)c6

InChI

1S/C33H40N2O9/c1-38-19-7-8-20-21-9-10-35-16-18-13-27(44-32(36)17-11-25(39-2)30(41-4)26(12-17)40-3)31(42-5)28(33(37)43-6)22(18)15-24(35)29(21)34-23(20)14-19/h7-8,11-12,14,18,22,24,27-28,31,34H,9-10,13,15-16H2,1-6H3/t18-,22+,24-,27-,28+,31+/m1/s1

Clave InChI

QEVHRUUCFGRFIF-MDEJGZGSSA-N

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Descripción general

Reserpine is a 36 carbon indole alkaloid mostly used as a tranquilizing agent in medicine. It is mostly used as drug for hypertension.

Aplicación

It was used as mass recalibration standard in coupling capillary electrophoresis with electrospray ionization time-of-flight mass spectrometry (CE-TOFMS) to overcome the problem of decreasing the sensitivity during the detection of metabolome differential display.

Acciones bioquímicas o fisiológicas

Inhibits vesicular uptake of catecholamines and serotonin.

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Pictogramas

FlameExclamation mark

Palabra de señalización

Danger

Frases de peligro

Consejos de prudencia

Clasificaciones de peligro

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Órganos de actuación

Central nervous system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

71.6 °F - closed cup

Punto de inflamabilidad (°C)

22.0 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Stimulation of reserpine biosynthesis in the callus of Rauvolfia tetraphylla L. by precursor feeding.
Anitha, S and BD Ranjitha Kumari
African Journal of Biotechnology, 5.8, 659-659 (2006)
Tomoyoshi Soga et al.
The Journal of biological chemistry, 281(24), 16768-16776 (2006-04-13)
Metabolomics is an emerging tool that can be used to gain insights into cellular and physiological responses. Here we present a metabolome differential display method based on capillary electrophoresis time-of-flight mass spectrometry to profile liver metabolites following acetaminophen-induced hepatotoxicity. We
Naomi S Rajapaksa et al.
Organic letters, 15(3), 706-709 (2013-01-22)
A catalytic, enantioselective synthesis of (+)-reserpine is reported. The route features a highly diastereoselective, chiral catalyst-controlled formal aza-Diels-Alder reaction between a 6-methoxytryptamine-derived dihydro-β-carboline and an enantioenriched α-substituted enone to form a key tetracyclic intermediate. This approach addresses the challenge of
Alexander C Sutton et al.
Journal of neurophysiology, 109(2), 363-374 (2012-10-19)
Deep brain stimulation (DBS) employing high-frequency stimulation (HFS) is commonly used in the globus pallidus interna (GPi) and the subthalamic nucleus (STN) for treating motor symptoms of patients with Parkinson's disease (PD). Although DBS improves motor function in most PD
Kari A Johnson et al.
Neuropharmacology, 66, 187-195 (2012-05-02)
Metabotropic glutamate receptors (mGlus) are 7 Transmembrane Spanning Receptors (7TMs) that are differentially expressed throughout the brain and modulate synaptic transmission at both excitatory and inhibitory synapses. Recently, mGlus have been implicated as therapeutic targets for many disorders of the

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