2. Cell Cycle/DNA Damage Epigenetics Apoptosis
  3. PARP Topoisomerase Apoptosis
  4. TOPOI/PARP-1-IN-1

TOPOI/PARP-1-IN-1 (化合物 B6) 是一种口服有效的、低细胞毒性的 TOPOI/PARP 双重抑制剂，其对 PARP1 的 IC50 值为 0.09 μM。TOPOI/PARP-1-IN-1 能有效抑制癌细胞的增殖和迁移。TOPOI/PARP-1-IN-1 还可导致细胞周期停滞于 G0/G1 期，并诱导细胞凋亡 (apoptosis)。TOPOI/PARP-1-IN-1 对小鼠的肿瘤生长抑制率 (TGI) 为 75.4%。

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TOPOI/PARP-1-IN-1 Chemical Structure

TOPOI/PARP-1-IN-1 Chemical Structure

CAS No. : 2948352-16-5

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TOPOI/PARP-1-IN-1 相关抗体

Top Publications Citing Use of Products

查看 PARP 亚型特异性产品:

查看所有亚型
PARP PARP1 PARP2 PARP3 PARP4 TNKS1/PARP5A TNKS2/PARP5B PARP7 PARP10 PARP14 PARP15 PARP12 PARP16

查看 Topoisomerase 亚型特异性产品:

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Topoisomerase Topo I Topo II

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

TOPOI/PARP-1-IN-1 (Compound B6) is an orally active, low cytotoxic TOPOI/PARP dual inhibitor with an IC50 value of 0.09 μM for PARP1. TOPOI/PARP-1-IN-1 can effectively inhibit the proliferation and migration of cancer cells. TOPOI/PARP-1-IN-1 also causes cell cycle arrest in the G0/G1 phase and induces apoptosis. The tumor growth inhibition rate (TGI) of TOPOI/PARP-1-IN-1 in mice is 75.4%[1].

IC50 & Target

IC50: 0.09 μM (PARP1)[1].
体外研究
(In Vitro)

TOPOI/PARP-1-IN-1 (1.25-5 μM; 48 h) 以浓度依赖的方式抑制 HGC-27 细胞的增殖和迁移[1]。
TOPOI/PARP-1-IN-1 (1.25-5 μM; 24 h) 以剂量依赖的方式诱导 HGC-27 细胞凋亡[1]。
TOPOI/PARP-1-IN-1 在 HGC-27 细胞中诱导 DNA 损伤，并抑制 TOPOI 蛋白的表达[1]。
TOPOI/PARP-1-IN-1 具有抗肿瘤活性，对 HeLa、A549、HepG-2 和 HGC-27 细胞的 IC50 值分别为 7.21 μM、9.48 μM、3.80 μM 和 2.49 μM[1]。

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

TOPOI/PARP-1-IN-1 相关抗体:

Cell Proliferation Assay[1]

Cell Line: HGC-27 cells
Concentration: 1.25, 2.5, 5 μM
Incubation Time: 48 h
Result: Demonstrated dose-dependent inhibitory effect of B6 on the clonogenicity of HGC-27 cells.

Apoptosis Analysis[1]

Cell Line: HGC-27 cells
Concentration: 1.25, 2.5, 5 μM
Incubation Time: 24 h
Result: Induced 15.5%, 43.1% and 76.0% of cell apoptosis when the concentrations were 1.25, 2.5, and 5 μM respectively.
体内研究
(In Vivo)

TOPOI/PARP-1-IN-1 (40 mg/kg; p.o.; once every two days, for a total of 17 days) 抑制异种移植小鼠模型中的 HGC-27 肿瘤生长[1]。

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

Animal Model: Female BALB/c nude mice (xenograft tumor model of HGC-2 cells)[1].
Dosage: 40 mg/kg
Administration: Oral administration; once every two days, for a total of 17 days
Result: Exhibited tumor growth inhibition rate (TGI) of 75.4% in mice.
分子量

718.52

Formula

C36H38Br2N4O2
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

TOPOI/PARP-1-IN-1 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:

TOPOI/PARP-1-IN-12948352-16-5PARPTopoisomeraseApoptosispoly ADP ribose polymerase HGC-27cancertumorHeLaA549HepG-2apoptosisTGIInhibitorinhibitorinhibit

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