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Merck
CN

SML3521

Sigma-Aldrich

m-Trifluoromethyl-diphenyl diselenide

≥98% (HPLC)

别名:

1,2-Bis(3-(trifluoromethyl)phenyl)diselane, Bis(3-trifluoromethylphenyl) diselenide, Di(3-trifluoromethylphenyl) diselenide, TFDD, [(m-CF3-PhSe)2; Bis[3-(trifluoromethyl)phenyl] diselenide

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About This Item

经验公式(希尔记法):
C14H8F6Se2
CAS号:
分子量:
448.12
UNSPSC代码:
51111800
UNSPSC代码:
12352200
NACRES:
NA.25

质量水平

方案

≥98% (HPLC)

表单

oil

颜色

colorless to yellow

储存温度

-10 to -25°C

SMILES字符串

FC(F)(C1=CC([Se][Se]C2=CC=CC(C(F)(F)F)=C2)=CC=C1)F

InChI key

DGOYKERNPXVRDM-UHFFFAOYSA-N

生化/生理作用

Brain blood barrier penetrant organoselenium compound that exhibits antinociceptive and antidepressant effects
m-Trifluoromethyl-diphenyl diselenide (TFDD) is a brain blood barrier penetrant organoselenium compound that exhibits antinociceptive and antidepressant effects in animal models without development of tolerance or withdrawal sighs. m-Trifluoromethyl-diphenyl diselenide acts as opioid system modulator, which attenuates morphine withdrawal signs in mice. It exhibits antioxidant and anti-inflammatory properties which might contribute to neuro protective effects.

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Contribution of Opioid and Nitrergic Systems to m-Trifluoromethyl diphenyl Diselenide Attenuates Morphine-Induced Tolerance in Mice
ACS Chemical Neuroscience, 13(7), 910-919 (2022)
Carolina C Martins et al.
Progress in neuro-psychopharmacology & biological psychiatry, 98, 109803-109803 (2019-11-07)
The opioid withdrawal syndrome is defined as a complex phenomenon involving multiple cellular adaptations, which leads to the emergence of aversive physical and affective signs. The m-trifluoromethyl-diphenyl diselenide (m-CF3-PhSe)2 elicits an antidepressant-like effect by modulating the opioid system in different
Cleisson Schossler Garcia et al.
Molecular neurobiology, 58(10), 5078-5089 (2021-07-11)
Chronic pain and depression often coexist sharing common pathological mechanisms, and available analgesics and antidepressants have demonstrated limited clinical efficacy. Evidence has demonstrated that neuronal oxidative stress, apoptosis, and also glucocorticoid receptor dysregulation facilitate the occurrence and development of both

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