1. Apoptosis NF-κB Metabolic Enzyme/Protease Immunology/Inflammation
  2. Necroptosis Reactive Oxygen Species (ROS) Mitochondrial Metabolism
  3. NecroX-2

NecroX-2 is a potent inhibitor of caspase-independent necrosis. NecroX-2 exhibits antioxidant activity by scavenging DPPH radicals and peroxynitrite. NecroX-2 inhibits t-BHP-induced mitochondrial ROS/RNS generation, and protects t-BHP and Doxorubicin (HY-15142A)-induced cell death in vitro. NecroX-2 can be used for research on neurological diseases.

For research use only. We do not sell to patients.

NecroX-2

NecroX-2 Chemical Structure

CAS No. : 1120333-38-1

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Description

NecroX-2 is a potent inhibitor of caspase-independent necrosis. NecroX-2 exhibits antioxidant activity by scavenging DPPH radicals and peroxynitrite. NecroX-2 inhibits t-BHP-induced mitochondrial ROS/RNS generation, and protects t-BHP and Doxorubicin (HY-15142A)-induced cell death in vitro. NecroX-2 can be used for research on neurological diseases[1][2].

In Vitro

NecroX-2 displays in vitro antioxidant activity with an IC50 of 17 μM in the DPPH radical-scavenging assay, and exhibits in vitro peroxynitrite scavenging activity with an IC50 of 0.9 μM[1].
NecroX-2 (0.4-10 μM; 2 h) inhibits copper ion-induced LDL oxidation[1].
NecroX-2 (2 h) potently inhibits t-BHP-induced mitochondrial ROS/RNS generation in H9C2 cells with an IC25 < 0.1 μM[1].
NecroX-2 (0.1-10 μM; 30 min pretreat) provides dose-dependent cytoprotection against t-BHP-induced cell death in H9C2 cells[1].
NecroX-2 (0.063-1.0 μM; 30 min pretreat) protects primary rat hepatocytes from Doxorubicin-induced cell death in a dose-dependent manner, with an IC50 of 0.12 μM [1].
NecroX-2 (0.3 μM; 30 min) suppresses caspase-independent necrosis in Cd-exposed SH-SY5Y and PC12 neuronal cells[2].

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

Cell Cytotoxicity Assay[1]

Cell Line: H9C2 cells
Concentration: 0.1, 1, 10 μM
Incubation Time: 30 min
Result: Showed a dose-dependent cytoprotective effect against t-BHP-induced cell death, as measured by LDH assay.

Cell Viability Assay[1]

Cell Line: primary rat hepatocytes
Concentration: 0.063, 0.125, 0.25, 0.5, 1.0 μM
Incubation Time: 30 min pretreat
Result: Displayed a dose-dependent cytoprotective effect against Doxorubicin-induced cell death at concentrations from 0.063 to 1.0 μM, with an IC50 of 0.12 μM, as measured by WST-1 assay.
Molecular Weight

516.68

Formula

C25H32N4O4S2

CAS No.
SMILES

O=S(N1CCC(CC1)NC2=CC(CN3CCS(=O)(CC3)=O)=CC4=C2NC(C5=CC=CC=C5)=C4)(C)=O

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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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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NecroX-2
Cat. No.:
HY-179037
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