GIBH-130

目录号: GC30831纯度: >99.50%
GIBH-130是有效的神经炎症抑制剂。GIBH-130作用于活化的小胶质细胞,显著抑制IL-1β分泌,IC50为3.4nM。

GIBH-130
Cas No.: 1252608-59-5
规格价格库存数量操作
2mg¥594.00现货
1
5mg¥990.00现货
1
10mg¥1,710.00现货
1
50mg¥4,949.00现货
1
100mg¥8,550.00现货
1
10mM (in 1mL DMSO)¥785.00现货
1

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产品描述 Description

GIBH-130 is an effective inhibitor of neuroinflammation. GIBH-130 significantly suppresses the IL-1β secretion by activated microglia (IC50=3.4 nM).

GIBH-130 is a novel antineuroinflammatory agent that is identified through microglia-based phenotypic screenings. GIBH-130 (IC50 3.4 nM) is identified in screenings as one of the most effective inhibitors with an acceptable half-life. Pretreatment of microglia with GIBH-130 significantly reduces the production of these factors in response to Lipopolysaccharides (LPS) stimulation, and the extent of the reduction is dependent on the concentrations of GIBH-130. The IC50 values of GIBH-130 for NO and TNF-α inhibition are 46.24 and 40.82 μM, respectively. Notably, pretreatment with GIBH-130 significantly suppresses the IL-1β secretion by activated microglia (IC50=3.4 nM). The inhibitory efficiency of GIBH-130 at 20 nM is comparable to 20 μM minocycline against IL-1β release. IL-1β is one of the major cytokines during neuroinflammatory progression of AD. So, it is meaningful to explain the selectivity of GIBH-130 against IL-1β (IC50 value 3.4 nM) over NO and TNF-α (IC50 value 46.24 and 40.82 μM, respectively) [1].

GIBH-130 exhibits comparable in vivo efficacy of cognitive impairment relief to donepezil and memantine respectively in both β amyloid-induced and APP/PS1 double transgenic Alzheimer's murine models at a substantially lower dose (0.25 mg/kg). The pharmacokinetic properties of GIBH-130 are assessed in Sprague-Dawley rats. As a potential drug candidate targeting in CNS, GIBH-130 is found to be orally bioavailable in rats, with 74.91% bioavailability and 4.32 h half-life. In addition, GIBH-130 displays good penetration ability across blood-brain barrier (AUCBrain/Plasma=0.21)[1].

[1]. Zhou W, et al. Microglia-Based Phenotypic Screening Identifies a Novel Inhibitor of Neuroinflammation Effective in Alzheimer's Disease Models. ACS Chem Neurosci. 2016 Nov 16;7(11):1499-1507.

实验参考方法 Experimental Reference Method

Cell experiment:

The murine microglial cell line N9 (N9 cells) are cultured in DMEM supplemented with 10% FBS, 1 mM sodium pyruvate, 100 U/mL penicillin, and 100 μg/mL streptomycin. All cultures are maintained in a humidified CO2 incubator at 37°C and 5% CO2. Stock N9 cells are passaged 2-3 times/week with a 1:4 split ratio and used within 8 passages. N9 cells (5×104 cells/well) are plated into 96-well microtiter plates, followed by the treatment of Minocycline (20 μM) or various concentrations of the GIBH-130 (25, 50, and 100 μM) for 18 h. The NO production is stimulated by incubation with LPS (1 μg/mL) for 48 h. The levels of NO in the culture medium are measured using the nitric oxide detection kit[1].

Animal experiment:

Rats[1] Sprague-Dawley (SD) rats (half male and half female, 250–270 g) are used. Rats exposed to Aβ25-35 received oral (p.o.) GIBH-130 (0.0022, 0.02, or 0.18 mg/kg), Donepezil hydrochloride (0.9 mg/kg), Memantine hydrochloride (1.8 mg/kg) or distilled water via gavage after the Aβ25-35 injection. The sham-operated group receive a p.o. administration of distilled water (n=10 per group). All compounds are systemically administered in a volume of 0.01 mL per g body weight once daily after the day of surgery until the end of the behavioral testing. The behavioral tests started 8 days after the Aβ25-35 injection and are performed sequentially. Mice[1] APP/PS1 transgenic mice (half male and half female, 14 weeks age) and age-and-strained-matched wild type mice (C57BL/6J) are used. APP/PS1 transgenic mice are randomly divided into six groups: model group, GIBH-130 0.0031, 0.028, and 0.25 mg/kg group, Donepezil hydrochloride 1.3 mg/kg group, and Memantine hydrochloride 2.6 mg/kg group (n=10 per group). C57BL/6J mice are used as normal control group (n=10). The doses of GIBH-130 and the positive drugs used in this mouse model are equivalent to the rat model. All mice receive oral administration at 15 weeks of age and continuously for 25 weeks until the end of the behavioral tests. The model group and normal control group receive the same volume of distilled water (0.01 mL per g body weight).

References:

[1]. Zhou W, et al. Microglia-Based Phenotypic Screening Identifies a Novel Inhibitor of Neuroinflammation Effective in Alzheimer's Disease Models. ACS Chem Neurosci. 2016 Nov 16;7(11):1499-1507.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
1252608-59-5
SMILES
O=C(C1=NN=C(C2=CC=CC=C2)C=C1C)N3CCN(C4=NC=CC=N4)CC3
分子式
C20H20N6O
分子量
360.41 g/mol
溶解性
DMSO : 50 mg/mL (138.73 mM);Water : < 0.1 mg/mL (insoluble)
保存条件
Store at -20°C
General tips
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°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

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