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主要文件

R116

Sigma-Aldrich

利鲁唑

≥98% (HPLC), solid, glutamate release inhibitor

别名:

2-氨基-6-(三氟甲氧基)苯并噻唑

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100 μL
¥4,239.58

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100 μL
¥4,239.58

About This Item

经验公式(希尔记法):
C8H5F3N2OS
CAS号:
分子量:
234.20
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

¥4,239.58


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新价格,新优惠!

获取大包装报价

产品名称

利鲁唑, solid

表单

solid

质量水平

创始人

Sanofi Aventis

SMILES字符串

Nc1nc2ccc(OC(F)(F)F)cc2s1

InChI

1S/C8H5F3N2OS/c9-8(10,11)14-4-1-2-5-6(3-4)15-7(12)13-5/h1-3H,(H2,12,13)

InChI key

FTALBRSUTCGOEG-UHFFFAOYSA-N

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此商品
557324B9934G9420
利鲁唑 solid

R116

利鲁唑

Riluzole A cell-permeable benzothiazole compound that potently inhibits glutamate release and blocks Na+ channels.

557324

Riluzole

BTA-1 ≥98% (HPLC), solid

B9934

BTA-1

GNF-2 ≥98% (HPLC), solid

G9420

GNF-2

form

solid

form

solid

form

solid

form

solid

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

originator

Sanofi Aventis

originator

-

originator

-

originator

-

Gene Information

human ... SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)
rat ... Scnn1g(24768)

Gene Information

-

Gene Information

human ... APP(351)

Gene Information

-

生化/生理作用

谷氨酸释放抑制剂;抗惊厥

特点和优势

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该化合物是由赛诺菲安万特开发的。想要浏览其他由制药公司开发的化合物以及已批准药物/候选药物清单, 请单击此处

象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 2 Oral

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

  • 技术规格说明书

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    Ryan S Phillips et al.
    eLife, 11 (2022-07-08)
    Previously our computational modeling studies (Phillips et al., 2019) proposed that neuronal persistent sodium current (INaP) and calcium-activated non-selective cation current (ICAN) are key biophysical factors that, respectively, generate inspiratory rhythm and burst pattern in the mammalian preBötzinger complex (preBötC)
    B C Cheah et al.
    Current medicinal chemistry, 17(18), 1942-1199 (2010-04-10)
    Amyotrophic lateral sclerosis (ALS) is a universally fatal neurodegenerative disease of the human motor system. Aetiological mechanisms implicated in the development of ALS have been linked to the glutamatergic neurotransmitter system, with destruction of motor neurons triggered through excessive activation
    Mark C Bellingham
    CNS neuroscience & therapeutics, 17(1), 4-31 (2010-03-20)
    Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disease of adults which preferentially attacks the neuromotor system. Riluzole has been used as the only approved treatment for amyotrophic lateral sclerosis since 1995, but its mechanism(s) of action in
    Gwen Schwartz et al.
    Progress in brain research, 137, 177-190 (2002-11-21)
    Traumatic spinal cord injury is a consequence of a primary mechanical insult and a sequence of progressive secondary pathophysiological events that confound efforts to mitigate neurological deficits. Pharmacotherapy aimed at reducing the secondary injury is limited by a narrow therapeutic
    Steve Vucic et al.
    Brain : a journal of neurology, 136(Pt 5), 1361-1370 (2013-04-26)
    Riluzole, a benzothiazole derivative, has been shown to be effective in prolonging survival in amyotrophic lateral sclerosis. The mechanisms by which riluzole exerts neuroprotective effects in amyotrophic lateral sclerosis remains to be fully elucidated, although inhibition of glutamatergic transmission and

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