Nomifensine maleate

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Chemical Structure| 32795-47-4 同义名 : (±)-Nomifensine maleat
CAS号 : 32795-47-4
货号 : A428762
分子式 : C20H22N2O4
纯度 : 98%
分子量 : 354.4
MDL号 : MFCD00069320
存储条件:

Pure form Sealed in dry, room temperature

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 Nomifensine Maleate (Nomifensine) is an isoquinoline antidepressant that inhibits the reuptake of dopamine at central synapses. It also inhibits norepinephrine reuptake but is only a weak inhibitor of 5-hydroxytryptamine[3]. Nomifensine is a safe and effective antidepressant with a fairly unique pharmacological profile[4]. Short-term use of nomifensine was relatively free from side effects and was remarkably effective in the treatment of ADD(attention deficit disorder)-RT(residual type)[5]. Nomifensine and some of its structural analogues produce behavioral effects indicative of indirect dopaminergic agonist properties, such as hyperlocomotion. Both PTIQ (nomifensine analogue 4-phenyl-1,2,3,4-tetrahydroisoquinoline) and nomifensine significantly augmented METH-induced stereotypical behavior and locomotion in mice[6]. Nomifensine elevates the tone of rapid dopamine signals in the brain[7].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.82mL

0.56mL

0.28mL

14.11mL

2.82mL

1.41mL

28.22mL

5.64mL

2.82mL

参考文献

[1]Shu Z, Taylor IM, et al. Region- and domain-dependent action of nomifensine. Eur J Neurosci. 2014 Jul;40(2):2320-8.

[2]Kinney JL. Nomifensine maleate: a new second-generation antidepressant. Clin Pharm. 1985 Nov-Dec;4(6):625-36.

[3]Fields ED. Nomifensine maleate (Merital, Hoechst-Roussel). Drug Intell Clin Pharm. 1982 Jul-Aug;16(7-8):547-52

[4]Kinney JL. Nomifensine maleate: a new second-generation antidepressant. Clin Pharm. 1985 Nov-Dec;4(6):625-36

[5]Shekim WO, Masterson A, Cantwell DP, Hanna GL, McCracken JT. Nomifensine maleate in adult attention deficit disorder. J Nerv Ment Dis. 1989 May;177(5):296-9

[6]Kitanaka J, Kitanaka N, Hall FS, Uhl GR, Asano H, Chatani R, Hayata S, Yokoyama H, Tanaka KI, Nishiyama N, Takemura M. Pretreatment with nomifensine or nomifensine analogue 4-phenyl-1,2,3,4-tetrahydroisoquinoline augments methamphetamine-induced stereotypical behavior in mice. Brain Res. 2012 Feb 23;1439:15-26

[7]Robinson DL, Wightman RM. Nomifensine amplifies subsecond dopamine signals in the ventral striatum of freely-moving rats. J Neurochem. 2004 Aug;90(4):894-903