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54739-18-3

中文名稱 氟伏沙明
英文名稱 Fluvoxamine
CAS 54739-18-3
分子式 C15H21F3N2O2
MDL 編號(hào) MFCD00865345
分子量 318.33
MOL 文件 54739-18-3.mol
更新日期 2026/05/26 15:27:11
54739-18-3 結(jié)構(gòu)式 54739-18-3 結(jié)構(gòu)式

基本信息

中文別名
(E)-5-甲氧基-4-三氟甲基苯戊酮氧-2-氨乙酰基肟
氟伏沙明
氟提肟氨
英文別名
2-[[5-methoxy-1-[4-(trifluoromethyl)phenyl]-pentylidene]amino]oxyethanamine
FLUVOXAMINE
(E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanoneo-(2-aminoethyl)oxime
(1E)-5-Methoxy-1-[4-(trifluoromethyl)phenyl]pentanal O-(2-aminoethyl)oxime
(E)-ω-Methoxy-4'-(trifluoromethyl)valerophenone O-(2-aminoethyl)oxime
δ-Methoxy-4'-(trifluoromethyl)valerophenone (E)-O-(2-aminoethyl)oxime
所屬類別
原料藥:抗抑郁、躁狂藥

物理化學(xué)性質(zhì)

熔點(diǎn)120-122.5°C
沸點(diǎn)370.6±52.0 °C(Predicted)
密度1.16±0.1 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,2-8°C
溶解度可溶于氯仿(少量)、DMSO(少量)、甲醇(少量)
酸度系數(shù)(pKa)pKa 8.7 (Uncertain)
形態(tài)Oil
顏色無(wú)色
InChIInChI=1S/C15H21F3N2O2/c1-21-10-3-2-4-14(20-22-11-9-19)12-5-7-13(8-6-12)15(16,17)18/h5-8H,2-4,9-11,19H2,1H3/b20-14+
InChIKeyCJOFXWAVKWHTFT-XSFVSMFZSA-N
SMILESC(=N/OCCN)(\C1=CC=C(C(F)(F)F)C=C1)/CCCCOC
CAS 數(shù)據(jù)庫(kù)54739-18-3(CAS DataBase Reference)
NIST化學(xué)物質(zhì)信息Fluvoxamine(54739-18-3)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)環(huán)境危害 (GHS09)有毒 (GHS06)
GHS07,GHS09,GHS06
警示詞危險(xiǎn)
危險(xiǎn)性描述H302-H335-H331-H410-H319
REACH 注冊(cè)登記Active
氟伏沙明價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2025/12/22HY-B0103氟伏沙明
Fluvoxamine
54739-18-35 mg240元
2025/12/22HY-B0103氟伏沙明
Fluvoxamine
54739-18-310 mM * 1 mLin DMSO264元
2025/12/22HY-B0103氟伏沙明
Fluvoxamine
54739-18-310mg360元

常見(jiàn)問(wèn)題列表

生物活性
Fluvoxamine (DU-23000) 是5-羥色胺再吸收抑制劑,有抗抑郁活性。
靶點(diǎn)

SSRIs.

體內(nèi)研究

Fluvoxamine (DU-23000) 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 was available in isolation [ED50: 4.0 (2.7-5.9) and 5.1 (4.3-6.0)]. Effects on food were similar under each condition in which food was available. The results demonstrate that the potency of fluvoxamine in reducing ethanol-maintained behavior depends on whether ethanol is available in isolation or in the context of concurrently scheduled food reinforcement.

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