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Iproniazid phosphate

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Chemical Structure| 305-33-9 同义名 : -
CAS号 : 305-33-9
货号 : A152838
分子式 : C9H16N3O5P
纯度 : 98%
分子量 : 277.214
MDL号 : MFCD00012831
存储条件:

粉末 Inert atmosphere,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 105 mg/mL(378.77 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 50 mg/mL(180.37 mM)

动物实验配方:
生物活性
描述 Iproniazid phosphate is a non-selective, irreversible monoamine oxidase (MAO) inhibitor of the hydrazine class. Iproniazid phosphate has antidepressive activity[3]. Isaxonine phosphate induce acute hepatitis which in most cases is reversible after withdrawal of the drug[4]. This amount of octopamine was not significantly increased by either the monoamine oxidase inhibitor iproniazid phosphate (0.1 mM) or the uptake inhibitor desipramine (10 mM) alone, but was by both together. Nominally calcium-free saline containing 20 mM Mg++ significantly decreased octopamine release[5]. Iproniazid phosphate (0.36mM) increased the concentrations of the same acids in osmotically ruptured synaptosomes[6].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.61mL

0.72mL

0.36mL

18.04mL

3.61mL

1.80mL

36.07mL

7.21mL

3.61mL

参考文献

[1]Ibrahim F, Belal F, et al. Spectrophotometric determination of some MAO inhibitors using 7,7,8,8-tetracyanoquinodimethane and iodine monochloride. J Pharm Biomed Anal. 1991;9(2):101-7.

[2]Nussbaun HE, Leff W, et al. The effects of iproniazid phosphate (marsilid) on hypertension. Angiology. 1957 Apr;8(2):198-200.

[3]Inhibition of mono amine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors

[4]Davy A, Ottignon Y, Vuitton D, Bachour A, Borel B, Carbillet JP, Boillot A, Gallinet E, Tabourot M, Verwaerde JC, et al. Hépatotoxicité du phosphate d'isaxonine: quatre observations d'hépatites subaiguës sévères [Hepatotoxicity of isaxonine phosphate: 4 cases of severe subacute hepatitis]. Gastroenterol Clin Biol. 1984 Oct;8(10):715-9. French

[5]Belanger JH, Orchard I. Release of octopamine by Leydig cells in the central nervous system of the leech Macrobdella decora, and its possible neurohormonal role. J Comp Physiol A. 1988 Feb;162(3):405-12

[6]Price CJ, Rowe CE. Stimulation of the production of unesterified fatty acids in nerve endings of guinea-pig brain in vitro by noradrenaline and 5-hydroxytryptamine. Biochem J. 1972 Feb;126(3):575-85