| S7242 |
Erastin
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Erastin is a ferroptosis activator by acting on mitochondrial VDAC, exhibiting selectivity for tumor cells bearing oncogenic RAS. Solutions are unstable and should be fresh-prepared.
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Exp Cell Res, 2026, 454(1):114825
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Nature, 2025, 10.1038/s41586-025-09741-1
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Cell, 2025, S0092-8674(25)00751-2
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| S4701 |
2-DG (2-Deoxy-D-glucose)
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2-DG (2-Deoxy-D-glucose), an analog of glucose, is a glycolytic inhibitor with antiviral activity. 2-Deoxy-D-glucose induces apoptosis and inhibits Herpes Simplex Virus type-1 (HSV-1) receptor expression.
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Signal Transduct Target Ther, 2025, 10(1):341
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Nat Commun, 2025, 16(1):212
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Cancer Commun (Lond), 2025, 10.1002/cac2.70036
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| S8452 |
BAY-876
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BAY-876 is a potent and selective GLUT1 inhibitor (IC50=0.002 μM) with a selectivity factor of >100 against GLUT2, GLUT3, and GLUT4.
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BMC Cancer, 2025, 25(1):716
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Am J Pathol, 2024, S0002-9440(24)00116-0
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Cancer Cell Int, 2024, 24(1):19
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| E1080 |
HG106
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HG106, a potent SLC7A11 inhibitor, leads to enhanced ROS generation, ER stress, and ultimately growth arrest specifically in KRAS-mutant lung adenocarcinoma (LUAD).
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J Lipid Res, 2025, S0022-2275(25)00138-5
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J Cell Mol Med, 2025, 29(14):e70693
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Biochem Biophys Res Commun, 2025, 766:151887
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| E0805 |
KL-11743
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KL-11743 is a potent glucose-competitive inhibitor of the class I glucose transporters with IC50s of 115, 137 and 90 nM for GLUT1, GLUT2, and GLUT3.
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Sci Rep, 2024, 14(1):15340
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| S6829 |
DTT (Dithiothreitol)
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DTT (Dithiothreitol), a small-molecule redox reagent, is a standard agent for reducing disulfide bonds between and within biological molecules.Solutions are best fresh-prepared.
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Methods Mol Biol, 2016, 1449:469-79
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