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- MedChemExpress(MCE)
- 美国
- HY-18712
- 2025年12月05日
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- 详细信息
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
926259-99-6
- 规格：
10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥660.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥600.0 |
| 规格： | 10 mg | 产品价格： | ￥850.0 |
| 规格： | 50 mg | 产品价格： | ￥2800.0 |
| 规格： | 100 mg | 产品价格： | ￥4288.0 |
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BG45
CAS No. : 926259-99-6
MCE 国际站：BG45
产品活性：BG45 是一种有效的 HDAC3 抑制剂，抑制 HDAC3、HDAC1、HDAC2 和 HDAC6 的 IC50 值分别为 0.289、2、2.2 和 >20 μM。BG45 选择性靶向多发性骨髓瘤 (MM) 细胞，诱导 caspase 依赖性凋亡 (apoptosis)。
研究领域：Cell Cycle/DNA Damage | Epigenetics | Apoptosis
作用靶点：HDAC | Apoptosis | Caspase
In Vitro: BG45 (1.875-30 µM; 48 and 72 h) targets multiple myeloma (MM) cells and inhibits cell growth in a dose-dependent manner.
BG45 (15 µM; 0-48 h; MM.1S cells) induces apoptosis via caspase-3/PARP cleavage.
BG45 (10 and 20 µM; 12 h; MM.1S cells) induces acetylation of histone H2A, H3, and H4 in a dose-dependent manner.
BG45 (10 and 20 µM; 10 h; MM.1S cells) induces multiple myeloma (MM) cells toxicity is associated with hyperacetylation of histones and STAT3 and downregulation of p-STAT3.
In Vivo: BG45 (15-50 mg/kg; i.p.; 5 days a week for 3 weeks; CB17 SCID mice with MM.1S xenograft model) inhibits human multiple myeloma (MM) cells growth and enhances bortezomib (HY-10227) induced cytotoxicity in vivo.
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