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13156-500A fungal mycotoxin that inhibits the Lys9-specific histone methyltransferases SU(VAR)3-9 (IC<sub>50</sub> = 0.8 &muM), G9a (IC<sub>50</sub> = 2.5 &muM), and DIM5 (IC<sub>50 </sub>= 3 &muM).
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19405-1A mycotoxic cytochalasin that targets filamentous actin and demonstrates antibacterial and nematicidal effects as well as induces apoptosis in cancer cell lines.
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19405-5A mycotoxic cytochalasin that targets filamentous actin and demonstrates antibacterial and nematicidal effects as well as induces apoptosis in cancer cell lines.
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C2800-25 g
Thomas Scientific
Chalcone and its derivatives typically display a wide variety of biological activities, including suppressing inflammation, limiting oxidative damage, and inhibiting growth of cancer cells. (C08-0488-477)
Price: $134.22List Price: $149.14Chalcone is an enone on which a variety of structures are based. Chalcone derivatives typically exhibit anti-inflammatory, antioxidative, neuroprotective, analgesic, anticancer, and anti-parasitic activities. -
C2800-100 g
Thomas Scientific
Chalcone and its derivatives typically display a wide variety of biological activities, including suppressing inflammation, limiting oxidative damage, and inhibiting growth of cancer cells. (C08-0488-935)
Price: $300.43List Price: $333.82Chalcone is an enone on which a variety of structures are based. Chalcone derivatives typically exhibit anti-inflammatory, antioxidative, neuroprotective, analgesic, anticancer, and anti-parasitic activities. -
C2800-500 g
Thomas Scientific
Chalcone and its derivatives typically display a wide variety of biological activities, including suppressing inflammation, limiting oxidative damage, and inhibiting growth of cancer cells. (C08-0489-517)
Price: $633.55List Price: $703.94Chalcone is an enone on which a variety of structures are based. Chalcone derivatives typically exhibit anti-inflammatory, antioxidative, neuroprotective, analgesic, anticancer, and anti-parasitic activities. -
11314-1A potent, cell permeable inhibitor of PKC (IC50 = 660 nM) also inhibits BclXL function (IC50 = 1.5 &muM), inducing apoptosis in several cancer cell lines can have PKC-independent effects, activate p38 and JUNK signaling pathways, and induce
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11314-10A potent, cell permeable inhibitor of PKC (IC50 = 660 nM) also inhibits BclXL function (IC50 = 1.5 &muM), inducing apoptosis in several cancer cell lines can have PKC-independent effects, activate p38 and JUNK signaling pathways, and induce
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11314-5A potent, cell permeable inhibitor of PKC (IC50 = 660 nM) also inhibits BclXL function (IC50 = 1.5 &muM), inducing apoptosis in several cancer cell lines can have PKC-independent effects, activate p38 and JUNK signaling pathways, and induce
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10011286-1A bile acid and FXR ligand (EC50 = 13-34 &muM) that is a key regulator of cholesterol homeostasis exhibits toxicity that is linked to increased glutathione and increased oxidative stress excess CDCA contributes to liver and intestinal cancers.
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10011286-10A bile acid and FXR ligand (EC50 = 13-34 &muM) that is a key regulator of cholesterol homeostasis exhibits toxicity that is linked to increased glutathione and increased oxidative stress excess CDCA contributes to liver and intestinal cancers.
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10011286-25A bile acid and FXR ligand (EC50 = 13-34 &muM) that is a key regulator of cholesterol homeostasis exhibits toxicity that is linked to increased glutathione and increased oxidative stress excess CDCA contributes to liver and intestinal cancers.