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Merck
CN

SML0408

Sigma-Aldrich

羧酰氨基三唑

≥98% (HPLC)

别名:

5-氨基-1-(3,5-二氯-4-(4-氯苯甲酰基)苄基甲基)-1H-1,2,3-三氮唑-4-羧酰胺, CAI, L-651582

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About This Item

经验公式(希尔记法):
C17H12Cl3N5O2
CAS号:
分子量:
424.67
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 10 mg/mL (clear solution)

储存温度

2-8°C

SMILES字符串

NC(=O)c1nnn(Cc2cc(Cl)c(c(Cl)c2)C(=O)c3ccc(Cl)cc3)c1N

InChI

1S/C17H12Cl3N5O2/c18-10-3-1-9(2-4-10)15(26)13-11(19)5-8(6-12(13)20)7-25-16(21)14(17(22)27)23-24-25/h1-6H,7,21H2,(H2,22,27)

InChI key

WNRZHQBJSXRYJK-UHFFFAOYSA-N

生化/生理作用

羧胺三唑(CAI)是一种没有细胞毒性的抗癌药物。它具有抗炎特性,并减少促炎细胞因子的释放。CAI可以在体外体内阻止多种人类癌细胞和内皮细胞的增殖和侵袭行为。它可用于治疗多种急性和慢性炎症模型,如佐剂性关节炎和炎症性肠病(IBD)。CAI在体外阻断肿瘤细胞增殖并刺激细胞凋亡。
羧酰氨基三唑是一种钙通道阻滞剂/钙通量抑制剂;阻断 CRAC 通道功能。
羧酰氨基三唑(L-651582)是一种口服活性钙通道阻滞剂。羧酰氨基三唑阻断细胞内和线粒体钙的进入和通量,从而抑制细胞增殖、激活钙释放激活的钙通道(CRAC)功能并维持线粒体膜电位。

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral

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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J Y Hu et al.
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Equilibrium condensation of solar gas is often invoked to explain the abundance of refractory elements in planets and meteorites. This is partly motivated, by the observation that the depletions in both the least and most refractory rare earth elements (REEs)
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Molecular cancer research : MCR, 6(4), 535-545 (2008-04-12)
Growth factor-induced intracellular calcium signals in endothelial cells regulate cytosolic and nuclear events involved in the angiogenic process. Among the intracellular messengers released after proangiogenic stimulation, arachidonic acid (AA) plays a key role and its effects are strictly related to
Jens Henrik Norum et al.
The FEBS journal, 272(9), 2304-2316 (2005-04-28)
We have previously reported the Ras-dependent activation of the mitogen-activated protein kinases p44 and p42, also termed extracellular signal-regulated kinases (ERK)1 and 2 (ERK1/2), mediated through Gs-coupled serotonin receptors transiently expressed in human embryonic kidney (HEK) 293 cells. Whereas Gi-
Fabienne Largey et al.
Neurology(R) neuroimmunology & neuroinflammation, 6(6) (2019-09-27)
To investigate the effects of natalizumab (NAT) treatment on intrathecally produced antiviral antibodies in MS. We performed a longitudinal, observational study analyzing both serum and CSF samples collected before and during NAT treatment for antibodies against measles, rubella, mumps, influenza
Lei Guo et al.
European journal of pharmacology, 746, 14-21 (2014-12-03)
Carboxyamidotriazole (CAI) is a non-cytotoxic anti-tumor drug, which also shows considerable anti-inflammatory effects in a variety of animal models of inflammation. The exact target and mechanism of CAI were not clearly understood yet. In the present study, we demonstrate that

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