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Merck
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主要文件

SML0968

Sigma-Aldrich

Y11

≥98% (HPLC)

别名:

1-(2-Hydroxyethyl)-3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane bromide, NSC206142

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About This Item

经验公式(希尔记法):
C8H17N4O · Br
分子量:
265.15
UNSPSC代码:
12352200
NACRES:
NA.77

方案

≥98% (HPLC)

表单

powder

储存条件

desiccated

颜色

white to beige

溶解性

H2O: 25 mg/mL, clear

储存温度

−20°C

生化/生理作用

Y11 inhibits the activity of focal adhesion kinase (FAK) by binding to the amino-terminal domain of FAK and blocking autophosphorylation of tyrosine residue Y397. Y11 inhibits the viability of SW620 and BT474 cancer cell lines and significantly reduces tumor volume in mouse xenografts.
Y11 inhibits the activity of focal adhesion kinase (FAK).
Y11 has high cytotoxic effects with IC50 values ranging from 3.87 to 4.66 mM, against non-small cell lung carcinoma (NSCLC) A549 cells.[1] It plays a major role in the protein structures across the kunitz protein domain of viperids and elapids.[2]

特点和优势

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

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警示用语:

Warning

危险声明

预防措施声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Synthesis of novel tetrandrine derivatives and their inhibition against NSCLC A549 cells
Yang, et al.
Journal of Asian natural products research, 1-11 (2018)
Comparative analyses of putative toxin gene homologs from an Old World viper, Daboia russelii
Krishnan, et al.
PeerJ, 5, e4104-e4104 (2017)

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Discover Bioactive Small Molecules for Kinase Phosphatase Biology

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