Name | 4-Bromo-N'-butylbenzohydrazide |
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Synonyms |
4-Bromo-N'-butylbenzohydrazide
Benzoic acid, 4-bromo-, 2-butylhydrazide UF010 |
Description | UF010 is a potent and selective HADC inhibitor with IC50 ~0.06 μM, 0.1 μM, 0.5 μM and 1.5 μM for HDACs 3, 2, 1 and 8, respectively. It has > 6-fold selectivity over other HDACs.IC50 value: 0.06 μM (HDAC3), 0.1 μM (HDAC2), 0.5 μM (HDAC1), 1.5 μM(HDAC 8)Target: HDACin vitro: UF010 is a competitive inhibitor with a fast-on/slow-off HDAC-binding mechanism. UF010 induces accumulation of acetylated histones in HCT116 cells in vitro, arrests cells at G1/S transition. It inhibits proliferation of a range of cancer cell lines. UF010 activates tumor suppression mechanisms while inhibiting oncogenic pathways. |
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Related Catalog | |
Target |
HDAC3:0.06 μM (IC50) HDAC2:0.1 μM (IC50) HDAC1:0.5 μM (IC50) HDAC8:1.5 μM (IC50) HDAC6:9.1 μM (IC50) HDAC10:15.3 μM (IC50) HDAC11:44.5 μM (IC50) |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 326.7±34.0 °C at 760 mmHg |
Molecular Formula | C11H15BrN2O |
Molecular Weight | 271.154 |
Flash Point | 151.4±25.7 °C |
Exact Mass | 270.036774 |
LogP | 3.46 |
Appearance | white solid |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.550 |
Storage condition | -20℃ |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Precautionary Statements | P301 + P312 + P330 |
RIDADR | NONH for all modes of transport |