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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C30H41FN4O12 |
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| Molecular Weight | 668.66 | CAS No. | 210344-95-9 | ||||||||
| Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (149.55 mM) | ||||||||
| Water | Insoluble | ||||||||||
| Ethanol | Insoluble | ||||||||||
| In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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| Description | Z-DEVD-FMK (Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and also shows potent inhibition on caspase-6, caspase-7, caspase-8, and caspase-10. | |
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| In vitro | Z-DEVD-FMK (1–200 μM) inhibits D4-GDI cleavage and apoptosis in a concentration-dependent manner. This compound reduces ceramide-induced cardiomyocyte death and significantly inhibits the activation of caspase 3. It (100μM) attenuates OxyHb-induced cell detachment, reduced caspase-2 and -3 activities, abolishes OxyHb-induced DNA ladders, and prevents OxyHb-induced cleavage of PARP in cultured brain microvessel endothelial cells. This chemical (100 μM) blocks MPP+-induced increases in caspase-3 enzyme activity. It dose dependently blocks 6-OHDA-induced apoptotic cell death with IC50 of 18 μM. | |
| In vivo | Z-DEVD-FMK, before and after injury, markedly reduces post-traumatic apoptosis, and significantly improved neurological recovery. |
| Kinase Assay:[5] |
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| Cell Assay:[5] |
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| Animal Study:[2] |
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, , Mol Carcinog, 2016, 56(1):218-231

Data from [ , , Oncotarget, 2017, 8(2):3396-3411 ]

Data from [ , , INTERNATIONAL JOURNAL OF ONCOLOGY, 2016, 48:1710-1720. ]
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