What is the catalog number for Iproniazid?

The catalog number for Iproniazid is HY-B0886A.

What sizes are available for Iproniazid?

Iproniazid is available in the following size(s): 100 mg, 10 mM - 1 mL.

How many pack sizes does Iproniazid come in?

Iproniazid is available in 2 different pack sizes.

Is Iproniazid in stock?

Iproniazid is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures Iproniazid?

Iproniazid is manufactured by QuantiMol.

What is the estimated delivery time for Iproniazid?

Estimated delivery time for Iproniazid is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for Iproniazid?

The safety data sheet for Iproniazid is available here: http://file.medchemexpress.com/batch_PDF/HY-B0886A/Iproniazid-SDS-MedChemExpress.pdf.

Iproniazid

Iproniazid is an orally active, irreversible, non-selective monoamine oxidase (MAO) inhibitor. Iproniazid inhibits MAO activity and enhances Rotenone -induced Apoptosis. Iproniazid modulates neurotransmitter levels, affects neuronal function, induces hepatic necrosis, and interferes with the endocrine system. Iproniazid can be used in the research of depression, Parkinson's disease, and hepatotoxicity[1][2][3][4][5][6][7].

Product Specifications

CAS Number

54-92-2

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Apoptosis; Monoamine Oxidase

Type

Reference compound

Related Pathways

Apoptosis; Neuronal Signaling

Applications

Neuroscience-Neuromodulation

Field of Research

Endocrinology; Metabolic Disease; Neurological Disease

Assay Protocol

https://www.medchemexpress.com/iproniazid.html

Concentration

10mM

Purity

99.91

Solubility

DMSO : 100 mg/mL (ultrasonic) |H2O : ≥ 100 mg/mL

Smiles

O=C(C1=CC=NC=C1)NNC(C)C

Molecular Formula

C9H13N3O

Molecular Weight

179.22

Precautions

H302, H315, H319, H335

References & Citations

[1]Fagervall I, et al. Inhibition of monoamine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors. Biochemical pharmacology 35 (8) : 1381–1387|[2]Watabe M, et al. Mitochondrial complex I inhibitor rotenone-elicited dopamine redistribution from vesicles to cytosol in human dopaminergic SH-SY5Y cells. J Pharmacol Exp Ther. 2007 Nov;323 (2) :499-507. |[3]Dodson AM, et al. Serotonin uptake and metabolism by cultured guinea pig airway smooth muscle cells. Pulm Pharmacol Ther. 2004;17 (1) :19-25. |[4]De Oliveira LF, et al. Effects of 5-hydroxytryptophan, iproniazid and p-chlorophenylalanine on lidocaine seizure threshold of mice. Eur J Pharmacol. 1974 Nov;29 (1) :5-9.|[5]Nelson SD, et al. Hepatotoxicity and metabolism of iproniazid and isopropylhydrazine. J Pharmacol Exp Ther. 1978 Sep;206 (3) :574-85.|[6]SETNIKAR I V O, et al. Retardation of sexual development in female rats due to iproniazid treatment. Endocrinology, 1960, 67 (4) : 511-520.|[7]Huang J T, et al. The effect of pretreatment with iproniazid on the behavioral activities of β-phenylethylamine in rats. Psychopharmacologia, 1974, 35 (1) : 77-81.