1. Metabolic Enzyme/Protease Anti-infection
  2. HIV Integrase HIV
  3. Salicylanilide

Salicylanilide  (Synonyms: 水杨酰苯胺; 2-Hydroxybenzanilide)

目录号: HY-B1408 纯度: 99.20%
COA 产品使用指南

Salicylanilide 表现出广泛的生物学特性,包括通过抑制靶向 HIV-1 整合酶 (HIV-1 integrase) 或逆转录酶来抑制 HIV 病毒 (HIV virus) 的抗病毒效力。

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Salicylanilide Chemical Structure

Salicylanilide Chemical Structure

CAS No. : 87-17-2

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2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     可免费申领三个不同产品的试用装。

3.  试用装只面向终端客户

规格 价格 是否有货 数量
Free Sample (0.1 - 0.2 mg)   Apply now  
10 mM * 1 mL in DMSO ¥192
In-stock
5 g ¥175
In-stock
10 g ¥245
In-stock
25 g ¥525
In-stock
50 g   询价  

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Customer Review

查看 HIV 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Salicylanilide demonstrates a wide range of biological activities including antiviral potency which can inhibit HIV virus by targeting HIV-1 integrase or reverse transcriptase.

IC50 & Target

HIV-1

 

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
HEK293 CC50
> 100 μM
Compound: 16
Cytotoxicity against HEK293 cells assessed as reduction in cell viability after 48 hrs by Alamar Blue reporter assay
Cytotoxicity against HEK293 cells assessed as reduction in cell viability after 48 hrs by Alamar Blue reporter assay
[PMID: 30392371]
HepG2 IC50
89.8 μM
Compound: SAL-5
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 24 hrs by MTS assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 24 hrs by MTS assay
[PMID: 24953953]
体外研究
(In Vitro)

Some Salicylanilides and salicylamides could inhibit HIV virus by targeting of HIV-1 integrase or reverse transcriptase. Hepatitis C virus is another virus, which can be potentially afflicted by Salicylanilides on the level of two enzymes-NS3 protease and NS5B RNA polymerase[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

213.23

Formula

C13H11NO2

CAS 号
性状

固体

颜色

Light brown to brown

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
溶解性数据
细胞实验: 

DMSO 中的溶解度 : 170 mg/mL (797.26 mM; 超声加热助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 4.6898 mL 23.4489 mL 46.8977 mL
5 mM 0.9380 mL 4.6898 mL 9.3795 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 4.6898 mL 23.4489 mL 46.8977 mL 117.2443 mL
5 mM 0.9380 mL 4.6898 mL 9.3795 mL 23.4489 mL
10 mM 0.4690 mL 2.3449 mL 4.6898 mL 11.7244 mL
15 mM 0.3127 mL 1.5633 mL 3.1265 mL 7.8163 mL
20 mM 0.2345 mL 1.1724 mL 2.3449 mL 5.8622 mL
25 mM 0.1876 mL 0.9380 mL 1.8759 mL 4.6898 mL
30 mM 0.1563 mL 0.7816 mL 1.5633 mL 3.9081 mL
40 mM 0.1172 mL 0.5862 mL 1.1724 mL 2.9311 mL
50 mM 0.0938 mL 0.4690 mL 0.9380 mL 2.3449 mL
60 mM 0.0782 mL 0.3908 mL 0.7816 mL 1.9541 mL
80 mM 0.0586 mL 0.2931 mL 0.5862 mL 1.4656 mL
100 mM 0.0469 mL 0.2345 mL 0.4690 mL 1.1724 mL
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.

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产品名称:
Salicylanilide
目录号:
HY-B1408
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