跳转至内容
Merck

A6060

Sigma-Aldrich

钙蛋白酶抑制剂 II

powder

别名:

N-乙酰基-L-亮氨酰基-L-亮氨酰基-L-蛋氨酸

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C19H35N3O4S
分子量:
401.56
Beilstein:
7693643
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

化驗

≥95% (HPLC)

形狀

powder

顏色

white

溶解度

ethanol: 20 mg/mL

儲存溫度

−20°C

SMILES 字串

[H]C(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(C)=O

InChI

1S/C19H35N3O4S/c1-12(2)9-16(20-14(5)24)19(26)22-17(10-13(3)4)18(25)21-15(11-23)7-8-27-6/h11-13,15-17H,7-10H2,1-6H3,(H,20,24)(H,21,25)(H,22,26)/t15-,16-,17-/m0/s1

InChI 密鑰

RJWLAIMXRBDUMH-ULQDDVLXSA-N

正在寻找类似产品? 访问 产品对比指南

應用

钙蛋白酶抑制剂 II 已用于蛋白质印迹。此外,它还用于研究Spy1A(一类细胞周期蛋白)在细胞周期中的降解机制。
钙蛋白酶抑制剂II是一种细胞透过性肽,可限制钙蛋白酶、组织蛋白酶 L 和组织蛋白酶 B 的活性。钙蛋白酶抑制剂 II 还可以防止甲基汞诱导的大鼠小脑神经元细胞死亡。

生化/生理作用

钙蛋白酶是在神经系统中表达的半胱氨酸蛋白酶。钙蛋白酶表现出钙依赖性酶活性。在小鼠模型中,抑制钙蛋白酶可防止血管紧张素II诱导的白细胞浸润,并减轻血管周围炎症。

其他說明

以前为 CAS# 136632-32-1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Spontaneous epileptiform discharges in a mouse model of Alzheimer's disease are suppressed by antiepileptic drugs that block sodium channels
Ziyatdinova S, et al.
Epilepsy Research (2011)
Keduo Qian et al.
Bioorganic & medicinal chemistry letters, 21(19), 5944-5947 (2011-08-23)
In this study, 22 new betulinic acid (BA) derivatives were synthesized and tested for their inhibition of the chymotrypsin-like activity of 20S proteasome. From the SAR study, we concluded that the C-3 and C-30 positions are the pharmacophores for increasing
Aneurysm: New Insights for the Healthcare Professional, 56-57 (2013)
Motoharu Sakaue et al.
Toxicology, 213(1-2), 97-106 (2005-06-29)
Methylmercury, an environmental neurotoxicant, induces the apoptotic death of cerebellar granule cells in vitro at a low concentration. To further understand the mechanism of cell death, we used a rat cerebellar granule cell culture system to investigate whether the calpain/cyclin-dependent
M W Luong et al.
Toxicology and industrial health, 25(3), 169-176 (2009-06-02)
The objective of this study was to examine the potential of arsenate to induce cardiomyocyte cell death and to explore the cellular mechanisms of arsenate toxicity. Isolated cardiomyocytes in culture from embryonic chick hearts were treated with a pentavalent arsenic

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门