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  5. 2-Desoxy-4-epi-pulchellin

2-Desoxy-4-epi-pulchellin 

目录号: HY-N1725 纯度: 99.76%
COA 产品使用指南

2-Desoxy-4-epi-pulchellin (compound 13) 是从 Polygonum hydropiper 的二氯甲烷可溶部分中分离得到的化合物。

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2-Desoxy-4-epi-pulchellin Chemical Structure

2-Desoxy-4-epi-pulchellin Chemical Structure

CAS No. : 122872-03-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

2-Desoxy-4-epi-pulchellin (compound 13) is a compound isolated from dichloromethane-soluble portion of Polygonum hydropiper[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
A549 IC50
6.2 μM
Compound: 4
Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay
Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
DU-145 IC50
3.1 μM
Compound: 4
Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay
Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
HCT-116 IC50
4.43 μM
Compound: 1; PCL
Cytotoxicity against human HCT116 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 30711391]
HeLa IC50
6 μM
Compound: 4
Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay
Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay
[PMID: 26316467]
HL-60 IC50
2.4 μM
Compound: 4
Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay
Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
HT-29 IC50
3.37 μM
Compound: 1; PCL
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 30711391]
K562 IC50
17 μM
Compound: 4
Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay
Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
MCF7 IC50
11 μM
Compound: 4
Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay
Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
MCF7 IC50
9.8 μg/mL
Compound: 9, pseudoguaianolide
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
[PMID: 21109433]
MDCK IC50
29.3 μM
Compound: 4
Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
[PMID: 26316467]
MDCK IC50
47.3 μM
Compound: 4
Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
[PMID: 26316467]
MOLT-4 IC50
5.5 μM
Compound: 4
Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay
Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
NCI-H1975 IC50
13 μM
Compound: 4
Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay
Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
Neutrophil IC50
> 10 μg/mL
Compound: 5
Inhibition of FMLP/CB-induced elastase release in human neutrophils after 5 mins by spectrophotometry
Inhibition of FMLP/CB-induced elastase release in human neutrophils after 5 mins by spectrophotometry
[PMID: 24997688]
Neutrophil IC50
> 10 μg/mL
Compound: 5
Inhibition of FMLP/CB-induced superoxide anion generation in human neutrophils by ferricytochrome c reduction method
Inhibition of FMLP/CB-induced superoxide anion generation in human neutrophils by ferricytochrome c reduction method
[PMID: 24997688]
RAW264.7 IC50
0.1 μM
Compound: 14
Inhibition of LPS-induced NO production in mouse RAW264.7 cells measured after 24 hrs
Inhibition of LPS-induced NO production in mouse RAW264.7 cells measured after 24 hrs
[PMID: 20515062]
RAW264.7 IC50
14.9 μM
Compound: 5
Inhibition of NO production in LPS/IFN-gamma activated mouse RAW264.7 cells after 24 hrs by Griess assay
Inhibition of NO production in LPS/IFN-gamma activated mouse RAW264.7 cells after 24 hrs by Griess assay
[PMID: 24997688]
RAW264.7 IC50
2.5 μM
Compound: 15
Inhibition of LPS-induced NO production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
Inhibition of LPS-induced NO production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
[PMID: 27276091]
RAW264.7 IC50
9.89 μM
Compound: 19
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production pretreated for 30 mins before LPS challenge measured 24 hrs after LPS challenge by Griess reaction method
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production pretreated for 30 mins before LPS challenge measured 24 hrs after LPS challenge by Griess reaction method
[PMID: 21924800]
SGC-7901 IC50
22 μM
Compound: 4
Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay
Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
U-937 IC50
2.2 μM
Compound: 4
Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay
Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay
[PMID: 26316467]
分子量

250.33

Formula

C15H22O3

CAS 号
性状

固体

颜色

White to off-white

结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

溶解性数据
细胞实验: 

DMSO 中的溶解度 : 25 mg/mL (99.87 mM; 超声助溶; 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 3.9947 mL 19.9736 mL 39.9473 mL
5 mM 0.7989 mL 3.9947 mL 7.9895 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, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 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, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.9947 mL 19.9736 mL 39.9473 mL 99.8682 mL
5 mM 0.7989 mL 3.9947 mL 7.9895 mL 19.9736 mL
10 mM 0.3995 mL 1.9974 mL 3.9947 mL 9.9868 mL
15 mM 0.2663 mL 1.3316 mL 2.6632 mL 6.6579 mL
20 mM 0.1997 mL 0.9987 mL 1.9974 mL 4.9934 mL
25 mM 0.1598 mL 0.7989 mL 1.5979 mL 3.9947 mL
30 mM 0.1332 mL 0.6658 mL 1.3316 mL 3.3289 mL
40 mM 0.0999 mL 0.4993 mL 0.9987 mL 2.4967 mL
50 mM 0.0799 mL 0.3995 mL 0.7989 mL 1.9974 mL
60 mM 0.0666 mL 0.3329 mL 0.6658 mL 1.6645 mL
80 mM 0.0499 mL 0.2497 mL 0.4993 mL 1.2484 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:
2-Desoxy-4-epi-pulchellin
目录号:
HY-N1725
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