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Merck

F132

Sigma-Aldrich

氟西汀 盐酸盐

≥98% (TLC), solid, selective serotonin reuptake inhibitor 

别名:

氟西汀 HCl, (±)-N-甲基-γ-[4-(三氟甲基)苯氧基]苯丙胺 盐酸盐, LY-110,140 盐酸盐, Prozac®

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About This Item

经验公式(希尔记法):
C17H18F3NO · HCl
CAS号:
分子量:
345.79
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

product name

氟西汀 盐酸盐, solid

形狀

solid

顏色

white

溶解度

H2O: 4 mg/mL
DMSO: >5 mg/mL

起源

Eli Lilly

SMILES 字串

CNCCC(C1=CC=CC=C1)OC2=CC=C(C(F)(F)F)C=C2.[H]Cl

InChI

1S/C17H18F3NO.ClH/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20;/h2-10,16,21H,11-12H2,1H3;1H

InChI 密鑰

GIYXAJPCNFJEHY-UHFFFAOYSA-N

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一般說明

盐酸氟西汀是一种精神类药物,是最早的抗抑郁药物之一,是选择性血清素再摄取抑制剂。它是百忧解有效成分之一。®

應用

盐酸氟西汀可以用于研究它对于小鼠放射药物 123I-标记2-((2-((二甲基氨基)甲基)苯基)硫基)-5-碘苯基胺([123I]ADAM)和SERT(血清素载体)结合的作用。它还可用于光照不足动物的长期治疗。

生化/生理作用

盐酸氟西汀是选择性血清素再摄取抑制剂,可用作抗抑郁药物。该药物作用于突触前末梢,它能够避免血清素再摄取,导致突触细胞外液体中血清素积累。
选择性羟色胺再摄取抑制剂;抗抑郁剂。

特點和優勢

该化合物是ADME Tox和胞凋亡研究的特色产品。发现更多的ADME Tox细胞凋亡特色产品。想要了解有关生物活性小分子在其他研究领域应用的更多信息,请访问 sigma.com/discover-bsm
该化合物是由 Eli Lilly研发。想要浏览其他由制药公司开发的化合物以及已批准物/候选药物清单, 请单击此处
该化合物被记录在受体分类和信号传导手册生物胺转运蛋白氯化物通道网页上。想要浏览手册的其他页面, 请单击此处

法律資訊

经 Eli Lilly and Company 授权销售。
Prozac is a registered trademark of Eli Lilly and Co.

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - STOT RE 2 - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 38(7), 1163-1175 (2013-02-02)
Light is a powerful modulator of higher-order cognitive processes such as mood but it remains unclear which neural circuits mediate the impact of light on affective behavior. We found that light deprivation produces a depressive-like behavioral state that is reversed

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