GSK-LSD1 2HCl - Names and Identifiers
GSK-LSD1 2HCl - Physico-chemical Properties
Molecular Formula | C14H20N2
|
Molar Mass | 216.32 |
Density | 1.07±0.1 g/cm3(Predicted) |
Boling Point | 347.4±42.0 °C(Predicted) |
Solubility | Soluble in DMSO |
Appearance | powder |
Color | white to beige |
pKa | 10.14±0.10(Predicted) |
Storage Condition | 2-8°C |
Use | GSK-LSD1 2HCl is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B). |
In vitro study | GSK-LSD1 induces gene expression changes in cancer cell lines with average EC50 of < 5 nM and inhibits cancer cell line growth with average EC50 of < 5 nM. |
GSK-LSD1 2HCl - Risk and Safety
GSK-LSD1 2HCl - Preparation solution concentration reference
| 1mg | 5mg | 10mg |
---|
1 mM | 3.457 ml | 17.287 ml | 34.573 ml |
5 mM | 0.691 ml | 3.457 ml | 6.915 ml |
10 mM | 0.346 ml | 1.729 ml | 3.457 ml |
5 mM | 0.069 ml | 0.346 ml | 0.691 ml |
Last Update:2024-01-02 23:10:35
GSK-LSD1 2HCl - Reference Information
biological activity | GSK-LSD1 2HCl is an irreversible selective LSD1 inhibitor with an IC50 of 16 nM, the selectivity was more than 1000-fold higher than that of other closely related FAD available enzymes (I. E., LSD2,MAO-A,MAO-B). |
Last Update:2024-04-10 22:29:15