| Name | SHIN1 |
|---|
| Description | SHIN1 is a human serine hydroxymethyltransferse 1 and 2 (SHMT1/2) inhibitor with IC50s of 5 and 13 nM, respectively, in an in vitro assay. |
|---|---|
| Related Catalog | |
| Target |
IC50: 5 nM (SHMT1), 13 nM (SHMT1)[1] |
| In Vitro | SHIN1 inhibits human SHIN1 SHMT1/2 with IC50s of 5 and 13 nM, respectively in an in vitro assay. SHIN1 inhibits the growth of SHMT2 deletion HCT-116 cells with an IC50 of 10 nM. SHIN1 inhibits SHMT1/2 in HCT-116 cells. SHIN1 is particularly active against B-cell malignancies. SHIN1 blocks cell growth through a progressive depletion of purines, leading to loss of nucleotide triphosphates[1]. |
| Cell Assay | For proliferation assays, HCT-116 cells are treated with SHIN1 (1, 10, 100, 1000, 10000 nM) for 24-72 hours. Cell number was counted directly using Trypan blue and the Countess system[1]. |
| References |
| Molecular Formula | C24H24N4O2 |
|---|---|
| Molecular Weight | 400.47 |
| Storage condition | 2-8℃ |