[CAS NO. 71320-77-9]  Moclobemide (Ro 111163)

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PRODUCTS SPECIFICATIONS [71320-77-9]

Catalog
SLK-S3212
Brand
Selleck
CAS
71320-77-9

DESCRIPTION [71320-77-9]

Overview

MDLMFCD00865388
Molecular Weight268.74
Molecular FormulaC13H17ClN2O2
SMILESC(NCCN1CCOCC1)(=O)C2=CC=C(Cl)C=C2

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Description

Moclobemide is a inhibitor with of 6.1 μM.

Targets

MAO-A (5-HT) [1]
6.1 μM

In vitro

Moclobemide orally administered 2 hours before decapitation preferentially inhibits MAO-A and PEA in rat brain with ED50 of 7.6 μmol/kg and 78 μmol/kg, respectively. Moclobemide orally administered 2 hours before decapitation preferentially inhibits MAO-A and PEA in rat liver with ED50 of 8.4 μmol/kg and 6.6 μmol/kg, respectively. Moclobemide (0.1 mM), which inhibits brain MAO-A activity by over 80%, does not affect benzylamine oxidase (rat heart) and diamine oxidase (rat small intestine) activity in vitro. Moclobemide (10 mM-100 mM) includes in the culture medium during anoxia or with glutamate significantly increases in a concentration-dependent manner the amount of surviving neurons compared to controls in neuronal-astroglial cultures from rat cerebral cortex.

In vivo

Moclobemide (10 mg/kg p.o.) induces a significant decrease of all monoamine metabolites measured in rat brain. Moclobemide, given via the drinking water (4.5 mg/kg/day), produces significant decreases in adrenal weight of rats after 5 (-23%) and 7 weeks (-16%) of treatment. Moclobemide upregulates hippocampal mineralocorticoid receptor (MR) levels in rats by 65%, 76% and 19% at 2 weeks, 5 weeks and 7 weeks of treatment, and upregulates Glucocorticoid receptor (GR) levels in this limbic brain structure by 10% at 5 weeks. Moclobemide treatment (5 weeks, 4.5 mg/kg/day) significantly attenuates stress (30 min novel environment)-induced plasma ACTH (-35%) and corticosterone (-29%) levels. Moclobemide (2.5 mg/kg/day) decreases immobility and increases climbing behavior following treatment for 3 days, but increases in both swimming and climbing behaviors are measured following treatment for 14 days. Moclobemide (15 mg/kg/day) decreased immobility and increased swimming for 3 days, whereas treatment for 14 days significantly increases both active behavior (swimming and climbing). Moclobemide (100 mg/kg/day) combined with triethyltin blocks the development of brain edema and the increase in the cerebral chloride content induced by triethyltin in rats. Moclobemide (100 mg/kg/day) reduces the increase in the cerebral sodium content and attenuates the neurological deficit in rats.


Synonyms

Benzamide, 4-chloro-N-[2-(4-morpholinyl)ethyl]-
4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide
Ro 11-1163
Moclobemide
4-Chloro-N-(2-morpholin-4-ylethyl)benzamide
Aurorix
4-Chloro-N-(2-morpholinoethyl)benzamide
Moclaime
Ro 11-1163/000
Manerix
p-Chloro-N-(2-morpholinoethyl)-benzamide
Auromid