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CAS: 40045-50-9
分子式: C5H3N5O2S3
分子量: 261.29
中文名称: 
2-氨基-5-[(5-硝基-2-噻唑基)硫代]-1,3,4-噻二唑
英文名称: 
2-amino-5-[(5-nitro-2-thiazolyl)thio]-1,3,4-thiadiazole
su 3327
推荐供应商
货号品牌产品名称规格包装、参考价格详情
A869156MACKLIN2-氨基-5-[(5-硝基-2-噻唑基)硫代]-1,3,4-噻二唑96%269元/10mg;   509元/50mg;   1206元/250mg;   3211元/1g;   展开
储存:-20°C
状态:浅黄色到琥珀色到深绿色粉末到晶体
A2940TCI2-Amino-5-[(5-nitro-2-thiazolyl)thio]-1,3,4-thiadiazole>96.0%(HPLC)995元/20MG;   展开

基本信息

纯度/分析方法>96.0%(HPLC)
分子式/分子量C5H3N5O2S3 = 261.29
外观与形状(20℃)固体
储存温度<0℃
应避免的情况加热
包装和容器 20MG-带有塑料内管的玻璃瓶 (查看图片)
Reaxys-RN1139980
PubChem物质ID354333624
MDL编号MFCD01927019

技术规格

AppearanceLight yellow to Amber to Dark green powder to crystal
Purity(HPLC)min. 96.0 area%

物性(参考值)

熔点160 ℃(dec.)

安全信息

图形或危害标志
信号词警告
危险性说明H315 : 造成皮肤刺激。
H319 : 造成严重眼刺激。
防范说明P264 : 作业后彻底清洗皮肤。
P280 : 戴防护手套/戴防护眼罩/戴防护面具。
P302 + P352 : 如皮肤沾染:用水充分清洗。
P337 + P313 : 如仍觉眼刺激:求医/就诊。
P305 + P351 + P338 : 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。
P362+P364 : 脱掉沾污的衣服,清洗后方可重新使用。
P332 + P313 : 如发生皮肤刺激:求医/就诊。
420144Sigma-AldrichJNK Inhibitor XIII-CAS 40045-50-9-CalbiochemThe JNK Inhibitor XIII, also referenced under CAS 40045-50-9, controls the biological activity of JNK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation appli1954.93元/10 MG;   展开

产品说明

一般描述

A cell-permeable non-peptidyl thiazolyl-thiadiazole alternative to pepJIP1 (TI-JIP1153-163) and TAT-pepJIP1 (Cat. Nos. 420133 & 420134, respectively) as a JIP-docking site-targeting (IC50 = 239 nM against pepJIP1 binding to JNK1) and substrate-competitive JNK inhibitor (IC50 = 700 nM against ATF2 phosphorylation by JNK1), while exhibiting little activity (IC50 >50 µM) toward p38α, Akt, furin, or lethal factor. Shown to inhibit the phosphorylation of overexpressed GFP-c-Jun in HeLa cultures upon TNF-α stimulation (IC50 = 6.23 µM) in vitro and restore insulin sensitivity in a murine of type-2 diabetes model (25 mg/kg, i.p.) in vivo. Biostability analysis with rat liver microsome preparations results in a compound half-life of 27 min at 37.5°C.
A cell-permeable non-peptidyl thiazolyl-thiadiazole alternative to pepJIP1 (TI-JIP1153-163) and TAT-pepJIP1 (Cat. Nos. 420133 & 420134, respectively) as a JIP-docking site-targeting (IC50 = 239 nM against pepJIP1 binding to JNK1) and substrate-competitive JNK inhibitor (IC50 = 700 nM against ATF2 phosphorylation by JNK1), while exhibiting little activity (IC50 >50 µM) toward p38α, Akt, furin, or lethal factor. Shown to inhibit the phosphorylation of overexpressed GFP-c-Jun in HeLa cultures upon TNF-α stimulation (IC50 = 6.23 µM) in vitro and restore insulin sensitivity in a murine of type-2 diabetes model (25 mg/kg, i.p.) in vivo. Biostability analysis with rat liver microsome preparations results in a compound half-life of 27 min at 37.5°C.

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

其他说明

De, S.K., et al. 2009. J. Med. Chem.52, 1943.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C5H3N5O2S3
分子量261.30

产品性质

质量水平100
测定≥95% (HPLC)
形式solid
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
protect from light
颜色pale yellow
溶解性ethanol: 4 mg/mL
DMSO: 50 mg/mL
运输wet ice
储存温度−20℃

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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