Name | Sardomozide HCl |
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Synonyms |
Sardomozide
(1E)-1-[(Diaminomethylene)hydrazono]-4-indanecarboximidamide 1H-Indene-4-carboximidamide, 1-[2-(diaminomethylene)hydrazinylidene]-2,3-dihydro-, (1E)- Sardomozide dihydrochloride |
Description | Sardomozide dihydrochloride is an S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM. |
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Related Catalog | |
Target |
IC50: 5 nM (SAMDC)[1] |
In Vitro | Sardomozide is a S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM in cell assay. Following treatment for 48 h with 3 μM Sardomozide, intracellular SAMDC activity is reduced to 10% of control[1]. When the CHO/664 cells are grown in the presence of Sardomozide and during treatment with DENSPM, vacuole formation is not observed, and these cells are growth-inhibited and contain levels of DENSPM similar to the parental CHO cells[2]. |
Cell Assay | The parent CHO cell line is chronically exposed to increasing levels of Sardomozide for at least eight passages beginning at 0.1 μM. Cell lines are serially exposed to increasing concentrations until a panel of sublines is obtained resistant to 1 (CHO/1). 3 (CHO/3), 10 (CHO/10), 30 (CHO/30), and 100 (CHO/100) μM Sardomozide for comparative studies[2]. |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 490.6±55.0 °C at 760 mmHg |
Molecular Formula | C11H16Cl2N6 |
Molecular Weight | 303.19 |
Flash Point | 250.5±31.5 °C |
LogP | -0.49 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.768 |
Storage condition | 2-8℃ |