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  6. 3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside 

目录号: HY-N12694
产品使用指南 技术支持

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside 是一种可以从 Aphananthe aspera 茎皮中分离得到的鞣花酸苷类化合物，可以用于炎症和疼痛的研究。

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3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside Chemical Structure

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside Chemical Structure

CAS No. : 51768-39-9

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3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside is an ellagic acid glycoside compound that can be isolated from the stem bark of Aphananthe aspera and can be used for the research of inflammation and pain[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
Col2 ED50
> 5 μg/mL
Compound: 11
Cytotoxicity against human Col2 cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against human Col2 cells after 72 hrs by sulforhodamine B assay
[PMID: 18271551]
Erythrocyte IC50
0.18 mM
Compound: 10
Anticomplement activity in sheep erythrocytes assessed as concentration required for 50% hemolytic inhibition by classic pathway pretreated for 10 mins with guinea pig serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric me
Anticomplement activity in sheep erythrocytes assessed as concentration required for 50% hemolytic inhibition by classic pathway pretreated for 10 mins with guinea pig serum followed by erythrocyte addition measured after 30 mins by spectrophotometeric me
[PMID: 29631958]
Erythrocyte IC50
0.26 mM
Compound: 10
Anticomplement activity in rabbit erythrocytes assessed as concentration required for 50% hemolytic inhibition by alternative pathway pretreated for 10 mins with normal human serum followed by erythrocyte addition measured after 30 mins by spectrophotomet
Anticomplement activity in rabbit erythrocytes assessed as concentration required for 50% hemolytic inhibition by alternative pathway pretreated for 10 mins with normal human serum followed by erythrocyte addition measured after 30 mins by spectrophotomet
[PMID: 29631958]
KB ED50
> 5 μg/mL
Compound: 11
Cytotoxicity against human KB cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against human KB cells after 72 hrs by sulforhodamine B assay
[PMID: 18271551]
Lu1 ED50
> 5 μg/mL
Compound: 11
Cytotoxicity against human Lu1 cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against human Lu1 cells after 72 hrs by sulforhodamine B assay
[PMID: 18271551]
MCF7 ED50
> 5 μg/mL
Compound: 11
Cytotoxicity against human MCF7 cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 72 hrs by sulforhodamine B assay
[PMID: 18271551]
P388 ED50
> 5 μg/mL
Compound: 11
Cytotoxicity against mouse P388 cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against mouse P388 cells after 72 hrs by sulforhodamine B assay
[PMID: 18271551]
分子量

462.36

Formula

C21H18O12
CAS 号
结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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.

Keywords:

3-O-Methylellagic acid-4′-O-α-L-rhamnopyranoside51768-39-9OthersinflammationpainInhibitorinhibitorinhibit

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