| Name | Sirt1/2-IN-2 |
|---|
| Description | Sirt1/2-IN-2 (compound hsa55) is a dual inhibitor of SIRT1/2 with IC50s of 1.8 μM (SIRT1) and 2.4 μM (SIRT2), respsectivley. Sirt1/2-IN-2 completely blocks p53 deacetylation, and increase of p53 and α-tubulin acetylation. Sirt1/2-IN-2 induces apoptosis and shows anti-proliferation activity against human leukemia cell lines[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 1.8 μM (SIRT1), 2.4 μM (SIRT2), 65 μM (SIRT3)[1] |
| References |
| Molecular Formula | C18H14N4O3S2 |
|---|---|
| Molecular Weight | 398.46 |