4-bromo-N'-butylbenzohydrazide
- Product Name
- 4-bromo-N'-butylbenzohydrazide
- CAS No.
- 537672-41-6
- Chemical Name
- 4-bromo-N'-butylbenzohydrazide
- Synonyms
- UF 010;CS-2427;UF010, >98%;UF010 ,S5810;UF-010; UF 010;UF010 >=98% (HPLC);UF010, 10 mM in DMSO;4-bromo-N'-butylbenzohydrazide;4-Bromobenzoic acid 2-butylhydrazide;Benzoic acid, 4-bromo-, 2-butylhydrazide
- CBNumber
- CB53049247
- Molecular Formula
- C11H15BrN2O
- Formula Weight
- 271.15
- MOL File
- 537672-41-6.mol
4-bromo-N'-butylbenzohydrazide Property
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- insoluble in H2O; ≥10.65 mg/mL in DMSO; ≥20.85 mg/mL in EtOH
- form
- solid
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- 21273
- Product name
- UF010
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $44
- Updated
- 2024/03/01
- Product number
- 21273
- Product name
- UF010
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $78
- Updated
- 2024/03/01
- Product number
- 21273
- Product name
- UF010
- Purity
- ≥98%
- Packaging
- 25mg
- Price
- $172
- Updated
- 2024/03/01
- Product number
- 21273
- Product name
- UF010
- Purity
- ≥98%
- Packaging
- 50mg
- Price
- $321
- Updated
- 2024/03/01
- Product number
- B680880
- Product name
- 4-Bromo-2-butylhydrazideBenzoicAcid
- Packaging
- 10mg
- Price
- $65
- Updated
- 2021/12/16
4-bromo-N'-butylbenzohydrazide Chemical Properties,Usage,Production
Description
UF010 is a class I HDAC inhibitor with IC50 values of 0.06, 0.1, 0.5, and 1.5 μM for HDAC3, 2, 1, and 8, respectively. It is more than 6-fold selective for these class I HDACs over any additional HDACs. UF010 is reported to inhibit cancer cell proliferation with a mean GI50 value of 2.94 μM when screened against the NCI-60 panel of cancer cell lines and functions by blocking the G1/S phase of the cell cycle.
Uses
4-Bromo-2-butylhydrazide Benzoic Acid inhibits histone deacetylases (HDAC) as potential clinical anticancer therapies.
in vivo
UF010 (15 mg/kg, Intraperitoneal injection, single dose) contributes considerably to the inflammatory regulation of hippocampal neurons in postoperative cognitive dysfunction (POCD) mice[4]. UF010 (15 mg/kg, Intraperitoneal injection, single dose) has antitumor therapeutic efficacy in the 4T1-Luc tumor-bearing mouse model[5].
| Animal Model: | postoperative cognitive dysfunction (POCD) mice[4] |
| Dosage: | 15 mg/kg |
| Administration: | Intraperitoneal injection (i.p.) |
| Result: | Weakened the infiltration of CD4+ T cells and NK cells in hippocampal tissues. Reduced inflammatory parameters in serum and hippocampal tissues, such as interleukin 6 (IL-6), C-reactive protein (CRP), and tumor necrosis factor alpha (TNF-α) levels. Activated the NF-κB/p65, JAK/STAT and TLR/MyD88 pathways. |
| Animal Model: | 4T1-Luc tumor-bearing mouse model[5] |
| Dosage: | 15 mg/kg |
| Administration: | Intraperitoneal injection (i.p.) |
| Result: | Inhibited the tumor growth rate percentage to 55.56, 38.36, 39.52% at days 7, 14, and 21. Induced high levels of ROS generation, causing apoptosis-mediated tumor cell death. |
IC 50
HDAC1: 1.42 μM (); HDAC2: 0.32 μM (IC50); HDAC3: 256.7 nM (IC50); HDAC6: 18.93 μM (IC50); HDAC8: 3.97 μM (IC50); IL-6
References
[1]. wang y, stowe rl, pinello ce, et al. identification of histone deacetylase inhibitors with benzoylhydrazide scaffold that selectively inhibit class i histone deacetylases. chem biol, 2015, 22(2): 273-284.
4-bromo-N'-butylbenzohydrazide Preparation Products And Raw materials
Raw materials
Preparation Products
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