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Aurothiomalate sodium/金硫丁二钠 {[allProObj[0].p_purity_real_show]}

货号:A429214 同义名: 金硫丁二酸钠;金硫苹果酸钠

Aurothiomalate sodium/金硫丁二钠 化学结构 CAS号:12244-57-4
Aurothiomalate sodium/金硫丁二钠 化学结构
CAS号:12244-57-4
Aurothiomalate sodium/金硫丁二钠 3D分子结构
CAS号:12244-57-4
Aurothiomalate sodium/金硫丁二钠 化学结构 CAS号:12244-57-4
Aurothiomalate sodium/金硫丁二钠 3D分子结构 CAS号:12244-57-4
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Aurothiomalate sodium/金硫丁二钠 纯度/质量文件 产品仅供科研

货号:A429214 标准纯度: {[allProObj[0].p_purity_real_show]}
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全球学术期刊中引用的产品

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产品名称 PKC PKCα PKCβ PKCγ PKCδ PKCε PKCζ PKCη PKCθ 其他靶点 纯度
Daphnetin +

PKC, IC50: 25.01 μM

PKA,EGFR 95%
Dequalinium Chloride 99%+
Quercetin Sirtuin,Src 97%
Myricetrin 96%
Go 6983 +++

PKCα, IC50: 7 nM

+++

PKCβ, IC50: 7 nM

+++

PKCγ, IC50: 6 nM

+++

PKCδ, IC50: 10 nM

++

PKCζ, IC50: 60 nM

99%+
Go6976 +++

PKC, IC50: 7.9 nM

++++

PKCα, IC50: 2.3 nM

+++

PKCβ1, IC50: 6.2 nM

FLT3 99%+
Bisindolylmaleimide I +++

PKCα, IC50: 20 nM

+++

PKCβ2, IC50: 16 nM

PKCβ1, IC50: 17 nM

+++

PKCγ, IC50: 20 nM

99%+
Lawsone methyl ether 99%
Sotrastaurin ++++

PKCα, Ki: 0.95 nM

++++

PKCβ1, Ki: 0.64 nM

++++

PKCδ, Ki: 2.1 nM

++++

PKCε, Ki: 3.2 nM

++++

PKCη, Ki: 1.8 nM

++++

PKCθ, Ki: 0.22 nM

99%+
Enzastaurin ++

PKCα, IC50: 39 nM

+++

PKCβ, IC50: 6 nM

+

PKCγ, IC50: 83 nM

+

PKCε, IC50: 110 nM

98%
Midostaurin ++

PKCα, IC50: 22 nM

++

PKCβ2, IC50: 31 nM

PKCβ1, IC50: 30 nM

++

PKCγ, IC50: 24 nM

+

PKCδ, IC50: 330 nM

+

PKCε, IC50: 1.25 μM

+

PKCη, IC50: 160 nM

99%
Ro 31-8220 mesylate ++++

PKCα, IC50: 5 nM

+++

PKCβ2, IC50: 14 nM

PKCβ1, IC50: 24 nM

++

PKCγ, IC50: 27 nM

++

PKCε, IC50: 24 nM

99%+
Staurosporine ++++

PKCα, IC50: 2 nM

++++

PKCγ, IC50: 5 nM

+++

PKCδ, IC50: 20 nM

++

PKCε, IC50: 73 nM

++++

PKCη, IC50: 4 nM

99%+
Ruboxistaurin HCl +

PKCα, IC50: 0.36 μM

++++

PKCβ2, IC50: 5.9 nM

PKCβ1, IC50: 4.7 nM

+

PKCγ, IC50: 0.3 μM

+

PKCδ, IC50: 0.25 μM

++

PKCη, IC50: 0.052 μM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 ALK1 ALK2 ALK3 ALK4 ALK6 Smad3 TGF-β TGFβRI/ALK5 TGFβRII 其他靶点 纯度
LDN193189 ++++

ALK1, IC50: 0.8 nM

++++

ALK2, IC50: 0.8 nM

+++

ALK3, IC50: 5.3 nM

+++

ALK6, IC50: 16.7 nM

99%+
LDN-212854 ++++

ALK1, IC50: 2.4 nM

++++

ALK2, IC50: 1.3 nM

+

ALK3, IC50: 85.8 nM

+

ALK4, IC50: 2133 nM

+

ALK5, IC50: 9276 nM

99%+
ML347 ++

ALK1, IC50: 46 nM

++

ALK2, IC50: 32 nM

98%
K02288 ++++

ALK1, IC50: 1.8 nM

++++

ALK2, IC50: 1.1 nM

++

ALK3, IC50: 34.4 nM

+++

ALK6, IC50: 6.4 nM

99%+
LDN-193189 2HCl ++++

ALK1, IC50: 0.8 nM

++++

ALK2, IC50: 0.8 nM

+++

ALK3, IC50: 5.3 nM

+++

ALK6, IC50: 16.7 nM

99%
LDN-214117 ++

ALK2, IC50: 24 nM

98%
DMH-1 +

ALK2, IC50: 107.9 nM

99%+
SB-505124 +

ALK4, IC50: 129 nM

++

ALK5, IC50: 47 nM

99%+
Vactosertib +++

ALK4, IC50: 13 nM

+++

ALK5, IC50: 11 nM

99%+
Alantolactone 98%
SIS3 97%
Pirfenidone 98%
Hesperetin 97%
RepSox ++++

TGFβR1(ALK5), IC50: 4 nM

98%
GW788388 +++

ALK5, IC50: 18 nM

98%
LY364947 ++

TGFβRI, IC50: 59 nM

+

TGFβRII, IC50: 0.4 μM

98%
SD-208 ++

TGF-βRI (ALK5), IC50: 48 nM

99%
SB-525334 +++

TGFβR1(ALK5), IC50: 14.3 nM

99%+
LY2109761 ++

TβRI, Ki: 38 nM

+

TβRII, Ki: 300 nM

99%+
Galunisertib ++

TβRI, IC50: 56 nM

98%
SB 431542 +

ALK5, IC50: 94 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Aurothiomalate sodium/金硫丁二钠 生物活性

描述 Aurothiomalate sodium is a potent and selective inhibitor of oncogenic PKCι signalling. Aurothiomalate sodium inhibits tumour cell proliferation but not apoptosis. Aurothiomalate sodium is a potent inhibitor of TrxR. Aurothiomalate sodium is an antirheumatic drug with strong antitumour activity[1][2][3].At concentrations of 0.001, 0.01, 0.1, 1, 10, 100, and 1000 uM, Aurothiomalate sodium induced inhibition of anchorage-independent growth in a dose-dependent manner in subject cell lines with IC50 of 300 nM-107 µM. Aurothiomalate sodium can induce inhibition of anchorage-independent growth in a dose-dependent manner with an IC50 of 300 nM-107 µM, including the A549, H1437, H2170, H460, H510, H187, H1703, and A427 lung cancer cell lines. Lung adenocarcinoma (LAC) and small cell lung cancer (SCLC) cells were more sensitive to Aurothiomalate sodium, while lung adenocarcinoma (LAC) was less sensitive to Aurothiomalate sodium. Aurothiomalate sodium blocked PKCι-Par6- by binding PKCι Rac1-Pak-Mek 1,2-Erk 1,2 signalling pathway activation and inhibits the growth of non-small lung cancer (NSCLC)[1].Aurothiomalate sodium inhibits TNFα-induced NF-kB activation and the expression of NF-kB-targeted pro-inflammatory genes (e.g., E-selectin and COX-2) at a concentration of 25 uM for 6 hours[3].

Aurothiomalate sodium/金硫丁二钠 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.70mL

0.54mL

0.27mL

13.51mL

2.70mL

1.35mL

27.02mL

5.40mL

2.70mL

Aurothiomalate sodium/金硫丁二钠 技术信息

CAS号12244-57-4
分子式C4H6AuNaO4S
分子量 370.11
SMILES Code [Na].[Au].O=C(O)CC(S)C(=O)O
MDL No. MFCD00064304
别名 金硫丁二酸钠;金硫苹果酸钠
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place, inert atmosphere, room temperature

溶解方案 配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
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