| Name | Corin |
|---|
| Description | Corin is a dual inhibitor of histone lysine specific demethylase (LSD1) and histone deacetylase (HDAC), with a Ki(inact) of 110 nM for LSD1 and an IC50 of 147 nM for HDAC1. |
|---|---|
| Related Catalog | |
| Target |
IC50: 147 nM (HDAC1), Ki(inact): 110 nM (LSD1)[1]. |
| In Vitro | Corin is able to inhibit the deacetylation of semisynthetic, reconstituted nucleosomes by the CoREST ternary complex. Corin shows irreversible inhibition of HDAC1 activity. In Comparison to MS-275, corin appears to more potently (Corin EC50 95 nM vs. MS-275 EC50 420 nM) and efficaciously induce cellular H3K9 acetylation. Interestingly, Corin (1 μM) is non-toxic to primary human melanocytes in contrast to MS-275 (1 μM)[1]. |
| References |
| Molecular Formula | C26H28N4O2 |
|---|---|
| Molecular Weight | 428.53 |
| Storage condition | 2-8℃ |