1. Apoptosis Cytoskeleton Cell Cycle/DNA Damage
  2. Apoptosis Microtubule/Tubulin
  3. Tubulin inhibitor 14

Tubulin inhibitor 14 是一种有效的醌氧化还原酶 2 (NQO2) 抑制剂,其 IC50 为 1.0 μM。Tubulin inhibitor 14 也可抑制微管蛋白聚合和内皮细胞毛细血管样管的形成。Tubulin inhibitor 14 是一种微管稳定剂,具有潜在的肿瘤选择性、抗血管生成和血管破坏特征。

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Tubulin inhibitor 14 Chemical Structure

Tubulin inhibitor 14 Chemical Structure

CAS No. : 2767446-34-2

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Tubulin inhibitor 14 is a potent NQO2 (quinone oxidoreductase 2) inhibitor with an IC50 of 1.0 μM. Tubulin inhibitor 14 also inhibits tubulin polymerization and the formation of endothelial cell capillary-like tubes. Tubulin inhibitor 14 is a microtubule-destabilizing agent with potential tumor-selectivity and antiangiogenic and vascular disrupting features[1].

IC50 & Target

IC50: 1.0 μM (NQO2)[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
A549 IC50
0.27 μM
Compound: 4
Antiproliferative activity against human A549 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human A549 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
A549 IC50
0.44 μM
Compound: 4
Antiproliferative activity against human A549 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human A549 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
HCT-116 IC50
0.13 μM
Compound: 4
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
HCT-116 IC50
0.13 μM
Compound: 4
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human HCT-116 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
HepG2 IC50
0.86 μM
Compound: 4
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
HepG2 IC50
1.44 μM
Compound: 4
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human HepG2 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
MCF7 IC50
0.41 μM
Compound: 4
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
MCF7 IC50
0.5 μM
Compound: 4
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
MDA-MB-231 IC50
0.07 μM
Compound: 4
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
MDA-MB-231 IC50
0.09 μM
Compound: 4
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
SNU-423 IC50
0.25 μM
Compound: 4
Antiproliferative activity against human SNU-423 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
Antiproliferative activity against human SNU-423 cells assessed as inhibition of cell proliferation incubated for 96 hrs by Sulforhodamine B assay
[PMID: 35290041]
SNU-423 IC50
0.36 μM
Compound: 4
Antiproliferative activity against human SNU-423 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
Antiproliferative activity against human SNU-423 cells assessed as inhibition of cell proliferation incubated for 24 hrs followed by 72 hrs of compound-free incubation by Sulforhodamine B assay
[PMID: 35290041]
体外研究
(In Vitro)

Tubulin inhibitor 14 (compound 4) (0-20 μM, 96 h) inhibits cancer cells proliferation [1].
Tubulin inhibitor 14 (1-5 μM, 24 or 48 h) causes G2/M cell cycle arrest[1].
Tubulin inhibitor 14 (0.5-1 μM, 24 h) induces SNU423 cell apoptosis[1].
Tubulin inhibitor 14 (0.5-1 μM, 24 h) disrupts the cytoskeleton network in endothelial cells[1].

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

Cell Proliferation Assay[1]

Cell Line: MDA-MB-231, HepG2, SNU423, A549, HCT116
Concentration: 0 μM, 0.1 μM, 0.5 μM, 1 μM, 5 μM, 10 μM, and 20 μM
Incubation Time: 96 h
Result: Inhibited cell proliferation with IC50 values of 0.41 μM (MCF-7) , 0.07 μM (MDA-MB-231), 1.44 μM (HepG2), 0.25 μM (SNU423), 0.27 μM (A549), and 0.13 μM (HCT116).

Cell Cycle Analysis[1]

Cell Line: HepG2 cells
Concentration: 1, 2, 5 μM
Incubation Time: 24 h, 48 h
Result: Caused G2/M cell cycle arrest.

Apoptosis Analysis[1]

Cell Line: SNU423 cells
Concentration: 0.5, 1 μM
Incubation Time: 24 h
Result: Induced SNU423 cell apoptosis.

Immunofluorescence[1]

Cell Line: HUVECs
Concentration: 0.5, 1 μM
Incubation Time: 24 h
Result: Disrupted the cytoskeleton network in endothelial cells.
分子量

257.23

Formula

C15H9F2NO

CAS 号
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
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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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Tubulin inhibitor 14
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