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Troponin-IN-1 is a troponin inhibitor that protects H9c2 cardiomyocytes from OGD/R injury by reducing LDH leakage, pyroptosis, and reactive oxygen species (ROS) accumulation. In LPS-induced RAW264.7 cells, it suppresses NO production and the release of IL-1β, TNF-α, and IL-18. Troponin-IN-1 functions through the caspase-1/GSDMD/IL-18 signaling pathway and reduces myocardial infarction size in a LAD-induced myocardial ischemia/reperfusion (MI/R) male rat model. It is a valuable compound for studying myocardial ischemia/reperfusion injury.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Troponin-IN-1 is a troponin inhibitor that protects H9c2 cardiomyocytes from OGD/R injury by reducing LDH leakage, pyroptosis, and reactive oxygen species (ROS) accumulation. In LPS-induced RAW264.7 cells, it suppresses NO production and the release of IL-1β, TNF-α, and IL-18. Troponin-IN-1 functions through the caspase-1/GSDMD/IL-18 signaling pathway and reduces myocardial infarction size in a LAD-induced myocardial ischemia/reperfusion (MI/R) male rat model. It is a valuable compound for studying myocardial ischemia/reperfusion injury. |
| In vitro | Troponin-IN-1 (Compound 19) at concentrations of 0.1-10 μM during a 24-hour period can increase the viability of H9c2 myocardial cells subjected to OGD/R injury, decrease LDH leakage, and inhibit the accumulation of reactive oxygen species (ROS). At 10-50 μM, Troponin-IN-1 reduces pyroptosis in H9c2 cells, preserves cell morphology, and blocks pyroptosis by inhibiting the caspase-1/GSDMD/IL-18 signaling pathway. With a pre-treatment of 6.25-100 μM for 30 minutes, Troponin-IN-1 inhibits NO production induced by LPS in RAW264.7 cells (IC 50 = 13.49 μM), and reduces the release of IL-1β, TNF-α, and IL-18. |
| In vivo | Troponin-IN-1 (Compound 19) administered intraperitoneally at 20-80 mg/kg once daily for 7 days, with the final dose given 1 hour before surgery, can reduce myocardial infarction size induced by LAD in male Sprague-Dawley rats with MI/R. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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