| Name | Pyridostatin hydrochloride | 
|---|
| Description | Pyridostatin hydrochloride is a G-quadruplexe stabilizer, with a Kd of 490 nM. | 
|---|---|
| Related Catalog | |
| Target | Kd: 490 nM (G-quadruplexe)[1] | 
| In Vitro | Pyridostatin hydrochloride is a G-quadruplexe stabilizer, with a Kd of 490 nM[1]. Pyridostatin (PDS) shows neurotoxic activity against primary cortical neurons at 0.01-5 μM, causes DNA double-strand breaks (DSBs) at 1 μM, downregulates BRCA1 in neurons at 1, 2 or 5 μM[2]. Pyridostatin interacts with G-quadruplex motifs in SRC and alters mRNA levels of damaged genes[3]. | 
| Cell Assay | Cells are plated at equal confluence and either untreated or treated with 2 μM Pyridostatin continually for 72 h. Cells from individual plates are trypsinized and counted in a Coultercounter. Graphs represent total cell numbers at each time interval and error bars represent S.E.M. Data represent three independent experiments[3]. | 
| References | 
| Molecular Formula | C31H37Cl5N8O5 | 
|---|---|
| Molecular Weight | 778.94 | 
| Storage condition | 2-8℃ |