HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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快速发货 顺丰冷链运输,1-2 天到达
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技术支持
免费溶解

| 产品名称 | ERK ↓ ↑ | ERK1 ↓ ↑ | ERK2 ↓ ↑ | ERK5 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| DEL-22379 |
+
ERK, IC50: 0.5 μM |
+
ERK, IC50: 0.5 μM |
98% | ||||||||||||||||
| Pluripotin |
++
ERK1, Kd: 98 nM |
RasGAP | 98+% | ||||||||||||||||
| FR 180204 |
+
ERK1, Ki: 0.31 μM |
++
ERK2, Ki: 0.14 μM |
98% | ||||||||||||||||
| Ravoxertinib |
+++
ERK1, IC50: 1.1 nM |
++++
ERK2, IC50: 0.3 nM |
99%+ | ||||||||||||||||
| SCH772984 |
+++
ERK1, IC50: 4 nM |
++++
ERK2, IC50: 1 nM |
99%+ | ||||||||||||||||
| Temuterkib |
+++
ERK1, IC50: 5 nM |
+++
ERK2, IC50: 5 nM |
99%+ | ||||||||||||||||
| VX-11e |
+++
ERK2, Ki: <2 nM |
99%+ | |||||||||||||||||
| Ulixertinib |
++++
ERK2, IC50: <0.3 nM |
99%+ | |||||||||||||||||
| XMD17-109 |
++
ERK5, IC50: 162 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。 | |||||||||||||||||||
| 描述 | AS-8351 is a histone demethylase inhibitor used to induce the reprogramming of fibroblasts into functional cardiomyocytes. Combination of AS8351 with CHIR99021, A83-01, BIX01294, SC1, Y27632 and OAC2 could efficiently induce cardiac reprogramming. |
| 作用机制 | AS8351 affects epigenetic modifications by competing with α-ketoglutarate for chelating iron/Fe(II) required by JmjC-KDMs.[1] |
| Concentration | Treated Time | Description | References | |
| GrH2 rat hepatoma cells | 1 mM | 20 min | AG126 inhibits molybdate-stimulated nuclear export of GR | J Cell Biol. 1997 May 5;137(3):523-38 |
| RAW 264.7 macrophages | 20 μM | 30 min | Inhibited LTA-induced iNOS expression and NO release | Immunology. 2005 Jul;115(3):366-74 |
| PG tissue culture | 100 μM | 6 h | AG126 completely suppressed the LPS-induced decrease in AQP5 mRNA. | Am J Pathol. 2010 Aug;177(2):724-34 |
| J774.2 macrophages | 10 μM | 24 h | To investigate the effect of AG126 on LTA-induced NO synthesis, results showed that AG126 significantly inhibited NO synthesis. | Br J Pharmacol. 1996 Mar;117(6):1163-70 |
| Dose | Rat[2] (i.p.): 1 mg/kg - 10 mg/kg; Mice[3] (s.c.): 15 mg/kg |
| Administration | i.p., s.c. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.65mL 0.93mL 0.46mL |
23.24mL 4.65mL 2.32mL |
46.47mL 9.29mL 4.65mL |
|
| CAS号 | 118409-62-4 |
| 分子式 | C10H5N3O3 |
| 分子量 | 215.17 |
| SMILES Code | N#C/C(C#N)=C/C1=CC=C([N+]([O-])=O)C(O)=C1 |
| MDL No. | MFCD00236448 |
| 别名 | TYRPHOSTINAG126; Tyrphostin AG126 |
| 运输 | 蓝冰 |
| InChI Key | DUQADSPERJRQBW-UHFFFAOYSA-N |
| Pubchem ID | 2046 |
| 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, store in freezer, under -20°C |
| 溶解方案 |
DMSO: 105 mg/mL(488 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 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
|
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