1. Apoptosis Metabolic Enzyme/Protease Immunology/Inflammation NF-κB
  2. Ferroptosis Glutathione Peroxidase Reactive Oxygen Species (ROS)
  3. Ferroptosis-IN-23

Ferroptosis-IN-23 是一种铁死亡 (Ferroptosis) 抑制剂。Ferroptosis-IN-23 通过同时激活 Steap4 与谷胱甘肽过氧化物酶 4 (GPX4) 发挥协同作用,进而维持铁代谢稳态。Ferroptosis-IN-23 可逆转神经元铁死亡,抑制细胞中脂质 ROS 积累。Ferroptosis-IN-23 抑制斑马鱼铁死亡,缓解帕金森病斑马鱼模型的神经元凋亡,ROS 积累,多巴胺能神经元损伤。Ferroptosis-IN-23 可用于帕金森病的研究。

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Ferroptosis-IN-23

Ferroptosis-IN-23 Chemical Structure

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查看 Glutathione Peroxidase 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Ferroptosis-IN-23 is an inhibitor of ferroptosis. Ferroptosis-IN-23 exerts a synergistic effect by simultaneously activating Steap4 and glutathione peroxidase 4 (GPX4), thereby maintaining iron metabolism homeostasis. Ferroptosis-IN-23 reverses neuronal ferroptosis and inhibits lipid ROS accumulation in cells. Ferroptosis-IN-23 inhibits ferroptosis in zebrafish, alleviates neuronal apoptosis, ROS accumulation, and dopaminergic neuron damage in a zebrafish model of Parkinson's disease. Ferroptosis-IN-23 can be used for research on Parkinson's disease[1].

体外研究
(In Vitro)

Ferroptosis-IN-23 (Compound 8h) (10 μM; 48 h) 可强效逆转 RSL3 (HY-100218A)、Erastin (HY-15763)、Ammonium iron(III) citrate (FAC) (HY-B1645) 诱导的 HT-22 海马神经元铁死亡[1]
Ferroptosis-IN-23 (5-20 μM; 48 h) 以剂量依赖方式抑制 HT-22 海马神经元细胞中由 RSL3 诱导的脂质 ROS 积累[1]
Ferroptosis-IN-23 (10-20 μM; 48 h) 在 Steap4 沉默的 HT-22 海马神经元细胞中逆转 RSL3 诱导的铁死亡的能力,其中 10 μM 浓度可将细胞活力恢复至 60.4%,表明 Steap4 对其抗铁死亡活性有贡献,但并非必需条件[1]

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

Cell Viability Assay[1]

Cell Line: RSL3-treated HT-22 hippocampal neuronal cells
Concentration: 10 μM (after 4 h pre-treatment with 0.1 μM RSL3)
Incubation Time: 48 h
Result: Reversed RSL3-induced ferroptosis, restoring HT-22 cell viability to 74.3% relative to the control group.

Cell Viability Assay[1]

Cell Line: erastin-treated HT-22 hippocampal neuronal cells
Concentration: 10 μM (after 4 h pre-treatment with 0.3 μM erastin)
Incubation Time: 48 h
Result: Significantly reversed erastin-induced ferroptosis in HT-22 cells, with superior activity relative to a comparator compound.

Cell Viability Assay[1]

Cell Line: FAC-treated HT-22 hippocampal neuronal cells
Concentration: 10 μM (after 4 h pre-treatment with 6 mM FAC)
Incubation Time: 48 h
Result: Reversed FAC-induced ferroptosis in HT-22 cells.

Cell Viability Assay[1]

Cell Line: Steap4-silenced, RSL3-treated HT-22 hippocampal neuronal cells
Concentration: 10-20 μM (after 4 h pre-treatment with 0.1 μM RSL3 in Steap4-silenced cells)
Incubation Time: 48 h
Result: Restored cell viability to 60.4% relative to the control group at 10 μM, while 20 μM showed further improved viability.
体内研究
(In Vivo)

Ferroptosis-IN-23 (2-8 μM; 72 h) 可通过减少 ROS 积累、脂质过氧化并恢复铁稳态及 GPX4 功能,呈剂量依赖性地抑制 RSL3 诱导的野生型 AB 品系斑马鱼铁死亡[1]
Ferroptosis-IN-23 (2-8 μM; 72 h) 可呈剂量依赖性缓解 6-OHDA (HY-B1081A) 诱导的野生型 AB 品系斑马鱼 (帕金森病模型) 的神经元凋亡与 ROS 积累[1]
Ferroptosis-IN-23 (2-8 μM; 96 h) 可剂量依赖性地保护 Tg (vmat2: GFP) 品系斑马鱼免受 MPTP (HY-15608) 诱导的多巴胺能神经元损伤,该斑马鱼是帕金森病模型[1]

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

Animal Model: wild-type AB strain (2 hours post-fertilization)[1]
Dosage: 2 μM; 4 μM; 8 μM
Administration: 72 h
Result: Significantly reduced the number of apoptotic brain cells induced by RSL3.
Dose-dependently reduced RSL3-induced reactive oxygen species (ROS) accumulation in zebrafish brains.
Dose-dependently decreased RSL3-induced increases in lipid peroxidation (LPO) and malondialdehyde (MDA) levels.
Dose-dependently reduced RSL3-induced upregulation of hepcidin (HEPC) expression and restored ferroportin (FPN) expression.
Dose-dependently reversed RSL3-induced downregulation of glutathione peroxidase 4 (GPX4a and GPX4b) expression.
Dose-dependently restored RSL3-induced downregulation of Steap4 expression.
Animal Model: wild-type AB strain (2 hours post-fertilization)[1]
Dosage: 2 μM; 4 μM; 8 μM
Administration: immersion; daily replenishment; 72 hours, followed by 24 hours of co-exposure with 6-OHDA
Result: Significantly reduced the number of apoptotic brain cells induced by 6-OHDA.
Dose-dependently reduced 6-OHDA-induced ROS accumulation in zebrafish brains.
Animal Model: Tg(vmat2: GFP) strain (1 day post-fertilization)[1]
Dosage: 2 μM; 4 μM; 8 μM
Administration: immersion; daily replenishment; 96 hours with concurrent MPTP exposure
Result: Dose-dependently reversed MPTP-induced shortening of dopaminergic neuron regions, with recovery toward control levels.
分子量

370.36

Formula

C19H18N2O6

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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  • 稀释计算器

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  • 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:
Ferroptosis-IN-23
目录号:
HY-181665
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