2. Metabolic Enzyme/Protease Apoptosis
  3. MMP Apoptosis
  4. Nudol

Nudol 是一种具有抗癌活性的菲 (phenanthrene) 化合物。Nudol 抑制细胞增殖，诱导细胞凋亡 (apoptosis)。Nudol 抑制 MMP-2 和 MMP-9 活性 (Ki 值分别为 988.9 nM 和 1.76 μM)。Nudol 可用于骨肉瘤等癌症的研究。

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Nudol Chemical Structure

Nudol Chemical Structure

CAS No. : 86630-46-8

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Nudol 相关抗体

Top Publications Citing Use of Products

查看 MMP 亚型特异性产品:

查看所有亚型
MMP-1 MMP-2 MMP-3 MMP-8 MMP-9 MMP-13 MMP-14 MMP-17 ADAM10 ADAM17 MMP-7 MMP-12 MMP-10 MMP ADAM8

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Nudol is a phenanthrene compound that has anti-cancer activity. Nudol inhibits cell proliferation, induces cell apoptosis. Nudol inhibits MMP-2M and MMP-9 activity (Ki: 988.9 nM, 1.76 μM, respectively). Nudol can be used in the research of cancers, such as osteosarcoma[1][2].

IC50 & Target[2]

MMP-2

988.9 nM (Ki)

MMP-9

1.76 μM (Ki)

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
A549 IC50
> 10 μM
Compound: 15
Cytotoxicity against human A549 cells assessed as decrease in cell viability after 6 days by MTT assay
Cytotoxicity against human A549 cells assessed as decrease in cell viability after 6 days by MTT assay
[PMID: 27310249]
HeLa IC50
> 10 μM
Compound: 15
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 6 days by MTT assay
Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 6 days by MTT assay
[PMID: 27310249]
HSC-T6 IC50
> 100 μM
Compound: 13
Antiproliferative activity against rat HSC-T6 cells after 48 hrs by MTT assay
Antiproliferative activity against rat HSC-T6 cells after 48 hrs by MTT assay
[PMID: 18052323]
MCF7 IC50
> 10 μM
Compound: 15
Cytotoxicity against human MCF7 cells assessed as decrease in cell viability after 6 days by MTT assay
Cytotoxicity against human MCF7 cells assessed as decrease in cell viability after 6 days by MTT assay
[PMID: 27310249]
Neutrophil IC50
> 10 μM
Compound: 11
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as elastase substrate preincubated for 5 mins followed by fMLP/CB-induction
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as elastase substrate preincubated for 5 mins followed by fMLP/CB-induction
[PMID: 27525452]
Neutrophil IC50
1.7 μM
Compound: 11
Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/cytochalasin B-induced superoxide anion generation by measuring superoxide dismutase-inhibitable reduction of ferricytochrome c preincubated for 5 mins followed by FMLP/cytochal
Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/cytochalasin B-induced superoxide anion generation by measuring superoxide dismutase-inhibitable reduction of ferricytochrome c preincubated for 5 mins followed by FMLP/cytochal
[PMID: 27525452]
体外研究
(In Vitro)

Nudol (0-40 μM, 24-72 h) decreases cell viability in several cancer cell lines[1].
Nudol (0-20 μM, 24/48 h) suppresses the cell migration and causes cell cycle arrest at G2/M phase in U2OS cells[1].
Nudol (20 μM, 48 h) induces cell apoptosis through the caspase-dependent pathway in U2OS cells[1].
Nudol (compound 4) inhibits MMP-2 and MMP-9 activity with Ki values of 988.9 nM and 1.76 μM respectively[2].

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

Nudol 相关抗体:

Cell Viability Assay[1]

Cell Line: U2OS, MG63, MDA-MB-231, MCF-7, and A549 cells
Concentration: 0, 10, 20, 30, 40 μM
Incubation Time: 24, 48, and 72 h
Result: Decreased the cell viability of osteosarcoma cells in dose- and time-dependent manners.

Cell Cycle Analysis[1]

Cell Line: U2OS cells
Concentration: 0, 5, 10, 20 μM
Incubation Time: 24, 48, and 72 h
Result: Triggered G2/M phase arrest by decreasing cell cycle-related proteins (CDK1, CDK2, CDK4, and CDK10).

Western Blot Analysis[1]

Cell Line: U2OS cells
Concentration: 0, 5, 10, 20, 40 μM
Incubation Time: 24, 48, and 72 h
Result: Increased the protein level of cytochrome c.
Down-regulated anti-apoptotic Bcl-2, accompanied by an increased level of pro-apoptotic Bax.
分子量

270.28

Formula

C16H14O4
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

Nudol 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:

Nudol86630-46-8MMPApoptosisMatrix metalloproteinasesAnti-proliferationphenanthreneanti-tumoranti-cancerosteosarcomaU2OSapoptosisInhibitorinhibitorinhibit

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