Fluvoxamine maleate (Synonyms: 马来酸氟伏沙明; DU-23000 maleate)
目录号: PL11262 纯度: ≥99%
CAS No. :61718-82-9
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中文名称
Fluvoxamine maleate
中文别名
马来酸氟伏沙明;(E)-5-甲氧基-1-(4-三氟甲苯基)-O-(2-胺乙肟基)-1-戊酮马来酸盐;Fluvoxamine Maleate 马来酸氟伏沙明;氟伏沙明系统适应性 EP标准品;马来酸氟伐沙明;马来酸氟伏沙明 EP标准品;马来酸氟伏沙明 USP标准品;马来酸氟伏沙明,AR;马来酸氟伏沙明标准品;马来酸氟伏沙明标准品(JP);马来酸氟伏沙明杂质标准;马来酸氟戊肟胺;(E)-5-甲氧基-1-[4-(三氟甲基)苯基]-O-(2-胺乙肟基)-1-戊酮马来酸盐;(E)-5-甲氧基-4-三氟甲基苯戊酮-O-(2-氨乙基)肟马来酸盐;伏氟沙明马来酸盐;马来酸氟;氟伏沙明马来酸盐
英文名称
Fluvoxamine maleate
英文别名
(E)-5-Methoxy-1-(4-(trifluoromethyl)phenyl)pentan-1-one O-(2-aminoethyl) oxime maleate;1-Pentanone, 5-methoxy-1-(4-(trifluoromethyl)phenyl)-, O-(2-aminoethyl)oxime, (Z)-2-butenedioate (1:1);5-Methoxy-4'-trifluoromethylvalerophenone (E)-O-2-aminoethyloxime monomaleate;(E)-Fluvoxamine Maleate;Fluvoxamine (maleate);Fluvoxamine maleate;(E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone 2-aminoethyloxime maleate;(E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]pentan-1-one O-2-aminoethyl oxime (Z)-but-2-enedoic acid salt;(E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]pentan-1-one O-2-aminoethyl oxime maleate;Dumirox;Faverin;faverin50;Fevarin;Floxyfral;Fluvoxamine Maleat;Luvox;Maveral;MK-264;(E)-5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone-O-(2-aminoethyl)oxime maleate;(E)-5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone O-(2-Aminoethyl)oxime Maleate;(Z)-But-2-enedioic acid;1,1,2,2-tetradeuterio-2-[(Z)-[5-methoxy-1-[4-(trifluoromethyl)phenyl]pentyli;(Z)-But-2-enedioic acid;1,1,2,2-tetradeuterio-2-[(Z)-[5-methoxy-1-[4-(trifluoromethyl)phenyl]pentylidene]amino]oxyethanamine;Fluvoxamine Maleate
Cas No.
61718-82-9
分子式
C19H25F3N2O6
分子量
438.43
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
Fluvoxamine maleate (DU-23000 maleate) 是5-羟色胺再吸收抑制剂,有抗抑郁活性。
生物活性
Fluvoxamine maleate (DU-23000 maleate) is an antidepressant which functions pharmacologically as a selective serotonin reuptake inhibitor.
性状
Solid
IC50 & Target[1][2]
SSRIs.
体内研究(In Vivo)
Fluvoxamine maleate (DU-23000 maleate) is effective in inhibiting 5-ht uptake by blood platelets and brain synaptosomes. The antagonism by fluvoxamine of the reserpine-induced lowering of the pentamethylenetetrazole convulsive threshold can be regarded as due to an effect upon 5-HT uptake. In contrast to the effects of desmethylimipramine and imipramine, no stimulatory effects are found in rats when rapidly acting reserpine-like compounds are given following a dose of fluvoxamine. Fluvoxamine (DU-23000) appears to improve combat-related PTSD symptoms but not depressive symptoms. The high attrition rate and lack of a placebo group limits the conclusions of our study. Controlled studies of fluvoxamine in the treatment of PTSD are warranted. Fluvoxamine (DU-23000) was less potent at decreasing ethanol self-administration when food was available concurrently versus when ethanol wa
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
ClinicalTrial
参考文献
[1]. Ginsburg, B.C., J.W. Pinkston, and R.J. Lamb, The potency of fluvoxamine to reduce ethanol self-administration decreases with concurrent availability of food. Behav Pharmacol, 2012. 23(2): p. 134-42.
[2]. Claassen, V., et al., Fluvoxamine, a specific 5-hydroxytryptamine uptake inhibitor. Br J Pharmacol, 1977. 60(4): p. 505-16.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (230.20 mM)H2O : 20 mg/mL (46.04 mM; Need ultrasonic)
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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