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Halofuginone hydrobromide
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Halofuginone hydrobromide图片
CAS NO:64924-67-0
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品名称
常山酮溴酸盐
RU-19110 hydrobromide
产品介绍
Halofuginone (RU-19110) hydrobromid,Febrifugine 的衍生物,是一种竞争性的脯氨酰-tRNA 合成酶 (prolyl-tRNA synthetase) 抑制剂,Ki为 18.3 nM。Halofuginone hydrobromid 是 I 型胶原 (type-I collagen) 合成的特异性抑制剂,并通过抑制TGF-β活性可减轻骨关节炎。Halofuginone hydrobromid 也是一种有效的肺血管扩张剂,可激活Kv通道并阻断电压门控、受体操作和存储操作的Ca2+channels通道。Halofuginone hydrobromid 具有抗疟疾、抗炎、抗癌、抗纤维化作用。
生物活性

Halofuginone (RU-19110) hydrobromid, a Febrifugine derivative, is a competitiveprolyl-tRNA synthetaseinhibitor with aKiof 18.3 nM[1][2]. Halofuginone hydrobromid is a specific inhibitor oftype-I collagensynthesis and attenuates osteoarthritis (OA) by inhibition ofTGF-βactivity[3][4]. Halofuginone hydrobromid is also a potent pulmonary vasodilator by activatingKv channelsand blocking voltage-gated, receptor-operated and store-operatedCa2+channels. Halofuginone hydrobromid has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects[5].

IC50& Target

Ki: 18.3±0.5 nM (prolyl-tRNA synthetase)[2]

体外研究
(In Vitro)

Halofuginone competitively inhibits prolyl-tRNA synthetase by occupying both the prolineand tRNA-binding pockets of prolyl-tRNA synthetase[1].
The IC50s of Halofuginone (1, 10, 100, 1000, 10000 nM; 48 hours) are 114.6 and 58.9 nM in KYSE70 and A549 cells, respectively.
The IC50s of Halofuginone (1, 10, 100, 1000 nM; 24 hours) for NRF2 protein are 22.3 and 37.2 nM in KYSE70 and A549 cells, respectively. The IC50of Halofuginone for global protein synthesis is 22.6 and 45.7 nM in KYSE70 and A549 cells, respectively[1].
Halofuginone increases voltage-gated K+(Kv) currents in pulmonary artery smooth muscle cells (PASMC) and K+currents through KCNA5 channels in HEK cells transfected with KCNA5 gene. Halofuginone (0.03-1μM) inhibits receptor-operated Ca2+entry (ROCE) in HEK cells transfected with calcium-sensing receptor gene and attenuated store-operated (SOCE) Ca2+entry in PASMC[5].

Cell Viability Assay[1]

Cell Line:KYSE70 cells from human oesophageal cancer harbouring a mutation in theNRF2gene and A549 cells harbouring theKEAP1gene mutation
Concentration:1, 10, 100, 1000, 10000 nM
Incubation Time:48 hours
Result:The IC50s were 114.6 and 58.9 nM in KYSE70 and A549 cells, respectively.

Western Blot Analysis[1]

Cell Line:KYSE70 cells from human oesophageal cancer harbouring a mutation in theNRF2gene and A549 cells harbouring theKEAP1gene mutation
Concentration:1, 10, 100, 1000 nM
Incubation Time:24 hours
Result:The IC50s for NRF2 protein were 22.3 and 37.2 nM in KYSE70 and A549 cells, respectively.
体内研究
(In Vivo)

Halofuginone (0.2, 0.5, 1 or 2.5 mg/kg; injected intraperitoneally every other day for 1 month) attenuates progression of OA in anterior cruciate ligament transection (ACLT) mice. Lower concentration (0.2 or 0.5 mg/kg) has minimal effects on subchondral bone and higher concentration (2.5 mg/kg) induces proteoglycan loss in articular cartilage[3].
Halofuginone (0.25 mg/kg; intraperitoneally injected; every day; 16 days) decreases NRF2 protein levels in tumors. While the tumor volumes do not change substantially between treatments with the vehicle, Halofuginone (0.25 mg/kg, intraperitoneally injected, every day) or cisplatin alone. Combined treatment with Halofuginone and Cisplatin significantly suppresses the tumor volume compared to treatment with Halofuginone or cisplatin alone[1].
Intraperitoneal administration of Halofuginone (0.3mg/kg, for 2 weeks) partially reverses the established pulmonary hypertension in mice[5].

Animal Model:3-month-old male C57BL/6J (WT) mice[3]
Dosage:0.2, 0.5, 1 or 2.5 mg/kg
Administration:Injected intraperitoneally every other day for 1 month
Result:Attenuated progression of OA in ACLT mice.
Animal Model:Male nude mice (BALB/C nu/nu mice) (6-8-week)[1]
Dosage:0.25 mg/kg
Administration:Intraperitoneally injected; every day; 16 days
Result:The combined treatment with Cisplatin significantly suppressed the tumor volume. NRF2 protein levels in tumors were indeed decreased.
Clinical Trial
分子量

495.59

性状

Solid

Formula

C16H18Br2ClN3O3

CAS 号

64924-67-0

中文名称

常山酮溴酸盐;卤夫酮溴酸盐;哈洛夫酮溴酸盐

结构分类
  • Alkaloids
  • Piperidine Alkaloids
来源
  • Plants
  • Saxifragaceae
  • Dichroa febrifugaLour
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : 50 mg/mL(100.89 mM;Need ultrasonic)

H2O : 2.6 mg/mL(5.25 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.0178 mL10.0890 mL20.1780 mL
5 mM0.4036 mL2.0178 mL4.0356 mL
10 mM0.2018 mL1.0089 mL2.0178 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: ≥ 2.5 mg/mL (5.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.04 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20%SBE-β-CDin saline)

    Solubility: ≥ 2.5 mg/mL (5.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.04 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 2.5 mg/mL (5.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.04 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在本网站选购。