2. Neuronal Signaling
  3. Cholinesterase (ChE)
  4. Kuwanon U

Kuwanon U 是一种有效的胆碱酯酶 cholinesterase 抑制剂，对乙酰胆碱酯酶 (acetylcholinesterase) 和丁酰胆碱酯酶 (butyrylcholinesterase) 的 IC50 值分别为 19.69、10.11 µM，Ki 值分别为 6.48、9.59 µM。Kuwanon U 具有研究阿尔茨海默病 (AD) 的潜力。

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Kuwanon U Chemical Structure

Kuwanon U Chemical Structure

CAS No. : 123702-95-4

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规格 价格 是否有货 数量
1 mg ￥4520
1 - 2 周
5 mg   询价  
10 mg   询价  

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Kuwanon U 相关抗体

Top Publications Citing Use of Products

查看 Cholinesterase (ChE) 亚型特异性产品:

查看所有亚型
AChE BChE

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Kuwanon U is a potent cholinesterase inhibitor with IC50s of 19.69, 10.11 µM and Kis of 6.48, 9.59 µM for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), respectively. Kuwanon U has the potential for the research of Alzheimer’s disease (AD)[1].

IC50 & Target[1]

AChE

19.69 μM (IC50)

AChE

6.48 μM (IC50)

BChE

10.11 μM (Ki)

BChE

9.59 μM (Ki)

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
BJ EC50
> 10 μM
Compound: 14
Cytotoxicity against human BJ cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human BJ cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
CCRF-CEM EC50
> 10 μM
Compound: 14
Cytotoxicity against human CEM cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human CEM cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
HeLa EC50
> 10 μM
Compound: 14
Cytotoxicity against human HeLa cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human HeLa cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
MCF7 EC50
> 10 μM
Compound: 14
Cytotoxicity against human MCF7 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human MCF7 cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
RPMI-8226 EC50
> 10 μM
Compound: 14
Cytotoxicity against human RPMI8226 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human RPMI8226 cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
SR IC50
35.62 μM
Compound: Kuwanon U
Inhibition of SERCA1 in NewZealand rabbit skeletal muscle SR vesicles using ATP as substrate incubated for 2 mins followed by Ca2+ addition by NADH coupled enzyme assay
Inhibition of SERCA1 in NewZealand rabbit skeletal muscle SR vesicles using ATP as substrate incubated for 2 mins followed by Ca2+ addition by NADH coupled enzyme assay
[PMID: 32435418]
THP-1 EC50
> 10 μM
Compound: 14
Cytotoxicity against human THP1 cells after 72 hrs by erythosin B staining method
Cytotoxicity against human THP1 cells after 72 hrs by erythosin B staining method
[PMID: 20192247]
U-266 EC50
> 10 μM
Compound: 14
Cytotoxicity against human U266 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human U266 cells assessed as viable cells after 72 hrs by calcein AM assay
[PMID: 20192247]
分子量

438.51

Formula

C26H30O6
CAS 号
结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

Kuwanon U 相关分类

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  • 稀释计算器

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Kuwanon U123702-95-4Cholinesterase (ChE)Alzheimer’s diseaseInhibitorinhibitorinhibit

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目录号：
HY-N12581
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