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AT-130 {[allProObj[0].p_purity_real_show]}

货号:A1487543

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+
AT-130 化学结构 CAS号:211364-06-6
AT-130 化学结构
CAS号:211364-06-6
AT-130 3D分子结构
CAS号:211364-06-6
AT-130 化学结构 CAS号:211364-06-6
AT-130 3D分子结构 CAS号:211364-06-6
规格 价格 会员价 库存 数量
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AT-130 纯度/质量文件 产品仅供科研

货号:A1487543 标准纯度: {[allProObj[0].p_purity_real_show]}
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Trifluridine 98%
Robinetin 99%+
Carboplatin 99%
Cidofovir 99%
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Cytarabine ++++

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Acelarin ++++

DNA synthesis, EC50: 0.2 nM

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Oxaliplatin 98%
YK-4-279 99%+
ML216 +

BLMfull-length, IC50: 2.98 μM

BLM636-1298, IC50: 0.97 μM

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RK-33 98%
Brr2-IN-3 99%+
Phen-DC3 Trifluoromethanesulfonate 95%
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YB-1, IC50: 1.73 μM

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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。

AT-130 生物活性

描述 AT-130, a phenylpropenamide derivative, acts as a potent non-nucleoside inhibitor of HBV replication, effectively inhibiting viral DNA synthesis with an EC50 of 0.13 μM and showing activity against both wild-type and mutant HBVs in hepatoma cells[1][2][3]. It inhibits wild-type HBV with an IC50 of 2.4 μM, rtL180M HBV with an IC50 of 9.8 μM, and rtM204I HBV with an IC50 of 35.6 μM. When applied to HepG2 cells transduced with HBV baculovirus at concentrations ranging from 0.1 to 100 μM for 7 days, AT-130 induces a dose-dependent suppression of wild-type HBV replication. Specifically, 2.5 μM of AT-130 cuts encapsidated HBV DNA by 50% (IC50), and 18.5 μM reduces it by 90% (IC90). AT-130 is non-toxic to HepG2 or Huh-7 cells even at concentrations as high as 250 μM[1]. Moreover, AT-130, at varying concentrations from 0.005 to 50 μM, does not directly inhibit the endogenous DNA polymerase reaction of HBV in Huh 7 or HepG2 cells, indicating that its inhibition of HBV DNA replication in hepatoma cells does not affect viral DNA polymerase activity or core protein translation. Additionally, AT-130 at 2.5 and 18.5 μM does not alter total HBV RNA production but does decrease encapsidated RNA levels. It does not impact the production of core protein or nucleocapsids, nor does it affect the activity of the protein expression vector[3].

AT-130 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.05mL

0.41mL

0.20mL

10.24mL

2.05mL

1.02mL

20.48mL

4.10mL

2.05mL

AT-130 技术信息

CAS号211364-06-6
分子式C22H22BrN3O5
分子量 488.33
SMILES Code O=C(N/C(C(N1CCCCC1)=O)=C(Br)\C2=CC=CC=C2OC)C3=CC=C([N+]([O-])=O)C=C3
MDL No. MFCD30533282
别名
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案 请根据您的动物给药指南选择适当的溶解方案。
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
方案一
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