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Merck

M3778

Sigma-Aldrich

N-Methyl-N-propargyl-3-(2,4-dichlorophenoxy)propylamine hydrochloride

≥97% (GC)

Sinónimos:

Clorgyline

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50 MG
MXP 2,504.00
100 MG
MXP 4,257.00
500 MG
MXP 14,524.00

MXP 2,504.00


Fecha estimada de envío01 de junio de 2025


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50 MG
MXP 2,504.00
100 MG
MXP 4,257.00
500 MG
MXP 14,524.00

About This Item

Fórmula empírica (notación de Hill):
C13H15Cl2NO · HCl
Número de CAS:
Peso molecular:
308.63
Número CE:
Número MDL:
Código UNSPSC:
12352116
ID de la sustancia en PubChem:
NACRES:
NA.77

MXP 2,504.00


Fecha estimada de envío01 de junio de 2025


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Ensayo

≥97% (GC)

Formulario

powder

solubilidad

DMSO: 10 mg/mL, clear, colorless to faintly yellow

temp. de almacenamiento

2-8°C

cadena SMILES

Cl.CN(CCCOc1ccc(Cl)cc1Cl)CC#C

InChI

1S/C13H15Cl2NO.ClH/c1-3-7-16(2)8-4-9-17-13-6-5-11(14)10-12(13)15;/h1,5-6,10H,4,7-9H2,2H3;1H

Clave InChI

BBAZDLONIUABKI-UHFFFAOYSA-N

Información sobre el gen

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Aplicación

N-Methyl-N-propargyl-3-(2,4-dichlorophenoxy)propylamine hydrochloride has been used as a monoamine oxidase A (MAO-A) inhibitor:
  • in MAO-A biochemical assay[1]
  • to study its effects on the transit of serotonin (5-HT) in the human placenta explants[2]
  • to study its effects on human prostate cancer cells[3]

Acciones bioquímicas o fisiológicas

MAO-A inhibitor.

Características y beneficios

This compound is featured on the Dopamine and Norepinephrine Metabolism page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictogramas

Skull and crossbones

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 3 Oral

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Visite la Librería de documentos

J C Shih et al.
Journal of neural transmission. Supplementum, 52, 1-8 (1998-06-13)
MAO-A and -B are defined by their substrate and inhibitor preferences. To determine which regions of the isoenzymes confer these preferences, we have constructed six chimeric MAO enzymes by reciprocally exchanging corresponding N-terminal, C-terminal, and internal segments of MAO-A and
Toshiaki Shinka et al.
Oncology letters, 2(2), 211-215 (2011-03-01)
Prostate cancer is one of the most common tumors in males and its incidence is steadily increasing worldwide. Serotonin or 5-hydroxytryptamine (5-HT) is a well-known neurotransmitter that mediates a wide variety of physiological effects. An increase in the number of
H Inoue et al.
The Journal of pharmacology and experimental therapeutics, 291(2), 856-864 (1999-10-19)
In an attempt to provide a better understanding of the scope and limitations of animal models used in some drug development programs and to further our understanding of potential metabolic bioactivation reactions, we have undertaken studies to profile the monoamine
Melissa D'Ascenzio et al.
Journal of enzyme inhibition and medicinal chemistry, 30(6), 908-919 (2015-03-26)
Several (thiazol-2-yl)hydrazone derivatives from 2-, 3- and 4-acetylpyridine were synthesized and tested against human monoamine oxidase (hMAO) A and B enzymes. Most of them had an inhibitory effect in the low micromolar/high nanomolar range, being derivatives of 4-acetylpyridine selective hMAO-B
Abhishek Jauhari et al.
The Journal of clinical investigation, 130(6), 3124-3136 (2020-03-18)
Chronic inflammation is a pathologic feature of neurodegeneration and aging; however, the mechanism regulating this process is not understood. Melatonin, an endogenous free radical scavenger synthesized by neuronal mitochondria, decreases with aging and neurodegeneration. We proposed that insufficient melatonin levels

Artículos

Serotonin is stored in cells and metabolized by MAO, influencing CNS, GI, and platelet functions.

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