| Bioactivity | BRD9757 is a potent, capless and selective HDAC6 inhibitor with an IC50 of 30 nM. BRD9757 shows excellent selectivity toward HDAC6 versus the class I (>20-fold) and class II (>400-fold) HDACs[1]. |
| Invitro | BRD9757（化合物 14）对抗 HDAC1、HDAC2、HDAC3、HDAC4、HDAC5、HDAC7、HDAC8 和 HDAC9，IC50 值分别为 0.638 μM、1.79 μM、0.694 μM、21.80 μM、18.32 μM、12.61 μM、1.09 μM 和 >33.33 μM[1]。BRD9757（化合物 14；10-30 μM；24 小时）选择性地增加 Ac-tubulin 的水平，而不增加组蛋白乙酰化[1]。 Western Blot Analysis[1] Cell Line: |
| Name | BRD9757 |
| CAS | 1423058-85-8 |
| Formula | C6H9NO2 |
| Molar Mass | 127.14 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Florence F Wagner, et al. Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif. J Med Chem. 2013 Feb 28;56(4):1772-6. |