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1、Product Data SheetProcyanidin B2Cat. No.: HY-N0796CAS No.: 29106-49-8分式: CHO分量: 578.52作靶点: Reactive Oxygen Species作通路: Immunology/Inflammation; Metabolic Enzyme/Protease; NF-B储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性数据体外实验 DMSO : 50 mg/mL (86.43 mM)* means soluble, bu

2、t saturation unknown.SolventMass1 mg 5 mg 10 mgConcentration制备储备液1 mM 1.7285 mL 8.6427 mL 17.2855 mL5 mM 0.3457 mL 1.7285 mL 3.4571 mL10 mM 0.1729 mL 0.8643 mL 1.7285 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;旦配成溶液,请分装保存,避免反复冻融造成的产品失效。储备液的保存式和期限:-80C, 6 months; -20C, 1 month。-80C 储存时,请在 6 个内使,-20C 储存时,请在 1 个内使。

3、体内实验请根据您的实验动物和给药式选择适当的溶解案。以下溶解案都请先按照 In Vitro 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 的储备液可以根据储存条件,适当保存;体内实验的作液,建议您现现配,当天使; 以下溶剂前显的百分 指该溶剂在您配制终溶液中的体积占;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的式助溶1. 请依序添加每种溶剂: 10% DMSO 40% PEG300 5% Tween-80 45% salineSolubility: 2.5 mg/mL (4.32 mM); Clear solution此案可获得 2.5 mg/mL (4.32

4、 mM,饱和度未知) 的澄清溶液。以 1 mL 作液为例,取 100 L 25.0 mg/mL 的澄 DMSO 储备液加到 400 L PEG300 中,混合均匀;向上述体系中加50 L Tween-80,混合均匀;然后继续加 450 L 理盐定容 1 mL。2. 请依序添加每种溶剂: 10% DMSO 90% (20% SBE-CD in saline)Solubility: 2.5 mg/mL (4.32 mM); Clear solutionPage 1 of 2 www.MedChemE此案可获得 2.5 mg/mL (4.32 mM,饱和度未知) 的澄清溶液。以 1 mL 作液为例,

5、取 100 L 25.0 mg/mL 的澄 DMSO 储备液加到 900 L 20% 的 SBE-CD 理盐溶液中,混合均匀。3. 请依序添加每种溶剂: 10% DMSO 90% corn oilSolubility: 2.5 mg/mL (4.32 mM); Clear solution此案可获得 2.5 mg/mL (4.32 mM,饱和度未知) 的澄 溶液,此案不适于实验周 期在半个以上的实验。以 1 mL 作液为例,取 100 L 25.0 mg/mL 的澄 DMSO 储备液加到 900 L 油中,混合均匀。BIOLOGICAL ACTIVITY物活性 Procyanidin B2种天

6、然 酮类物质,具有抗肿瘤,抗氧化等作。体外研究 Procyanidin B2 shows antiproliferative activity to MCF-7 cells, with an IC50 of 19.21 M. However, Procyanidin B2exhibits no effect on DNA-ladder formation1. Procyanidin B2 (0.1, 1, 2 M) inhibits the activation of pyrin domaincontaining 3 (NLRP3) inflammasome in human umbilica

7、l vein ECs (HUVECs), and the inhibition is via suppression ofAP-1 activity, and such effect can be abolished by overexpression of c-Jun. Procyanidin B2 (2 M for 12 h) alsoreduces ROS in HUVECs2.体内研究 Procyanidin B2 (40, 20, and 10 mg/kg, p.o.) protects against cerebral ischemia-induced infarct volume

8、 and brainedema in rats. Procyanidin B2 (40 mg/kg, p.o) also improves functional outcomes, regulates blood-brain barrier (BBB) permeability after cerebral ischemia. Moreover, Procyanidin B2 attenuates cerebral ischemia-induced tight junctiondegradation, mitochondrial depolarization and intracellular

9、 oxidative stress. Procyanidin B2 (40 mg/kg, p.o) increasesNrf2 activation and HO-1, GST, and NQO1 protein expression in normal brains in vivo3.PROTOCOLCell Assay 1 MCF-7 cells are grown in 5 mL of RPMI 1640 medium supplemented with 20% fetal bovine serum, penicillin (100U/mL) and streptomycin (100

10、g/mL). Cells are maintained at 37C in a humidified atmosphere of 5% CO2 in air andsubcultured every 3 days. Exponentially growing cells are plated at a seeding density of 2104 cells/mL, in 96-wellplates or in dishes. After overnight incubation to allow for attachment, the cells are exposed for 24 or

11、 48 h to variousconcentrations of Procyanidin B2 (0.5; 1.0; 5.0; 10.0; 25.0 and 50.0 M) diluted in distilled water. Two millimolarcyclophosphamide (CP) is used as the positive control and solutions are sterilised by filtration1.MCE has not independently confirmed the accuracy of these methods. They

12、are for reference only.Animal To observe the effect of Procyanidin B2 on infarct size or brain edema, 40 rats are randomLy separated into five Administration 3 groups, and each group is administered with vehicle (equivalent dose of 0.9% saline administered via gavage) or 40, 20, or 10 mg/kg of Procy

13、anidin B2, respectively. To elucidate the effect of Procyanidin B2 on blood-brain barrier(BBB) permeability, the rats (n = 6 per group for Evans blue extravasation and n = 4 per group for IgG leakage) arerandomLy separated into two groups: vehicle and Procyanidin B2 (40 mg/kg). Procyanidin B2 (40 mg

14、/kg) isadministered intragastrically once a day starting at 3 h after middle cerebral artery occlusion (MCAO). For otherobservations, including immunohistological staining and western blot analysis, rats are randomLy separated intothree groups: sham-operated, vehicle, and Procyanidin B2 (n = 4 per g

15、roup). Procyanidin B2 (40 mg/kg) isadministered intragastrically once a day starting at 3 h after MCAO. To elucidate the improvement in neurologicalfunction after ischemic stroke in rats, the rats (n = 8 per group) undergo neurobehavioral assays to evaluate thefunctional outcome after administration

16、 of Procyanidin B2 (40 mg/kg) once a day starting at 24 h after MCAO. Theneurological deficits are assessed at 1, 3, 7, 11, and 14 days after MCAO3.MCE has not independently confirmed the accuracy of these methods. They are for reference only.Page 2 of 3 www.MedChemE户使本产品发表的科研献 Int J Food Sci Nutr.

17、2020 Jan 27:1-11.See more customer validations on HYPERLINK www.MedChemE www.MedChemEREFERENCES1. Avelar MM, et al. Procyanidin b2 cytotoxicity to mcf-7 human breast adenocarcinoma cells. Indian J Pharm Sci. 2012 Jul;74(4):351-5.2. Yang H, et al. Procyanidin B2 inhibits NLRP3 inflammasome activation in human vascular endothelial cells. Biochem Pharmacol. 2014 Dec 15;92(4):599-606.3. Wu S, et al. Procyanidin B2 attenuates neurological deficits and blood-brain barrier disruption in a rat model of cerebral ischem

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