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| 描述 | 10-Gingerol, a natural product isolated and purified from the rhizomes of Zingiber officinale Roscoe. with anti-neuroinflammatory capacity, effectively inhibits the growth of the oral pathogens, and inhibits exogenous ghrelin deacylation, induces [Ca2+]i rise by causing Ca2+ release from the endoplasmic reticulum and Ca2+ influx from non-L-type Ca2+ channels in SW480 cancer cells, and induces apoptosis accompanied by phosphorylation of the mitogen-activated protein kinase (MAPKs) family, c-Jun N-terminal kinase (JNK), p38 MAPK (p38), and extracellular signal-regulated kinase (ERK). | 
| Concentration | Treated Time | Description | References | |
| MCF-10A | 0, 25, 50, 100, 150, 200, 400, 800 μM | 48 h | 10-G showed low inhibition on non-tumor breast epithelial cell MCF-10A and did not enhance the cytotoxicity of paclitaxel. | Drug Des Devel Ther. 2023 Jan 20;17:129-142 | 
| SUM-159 | 0, 25, 50, 100, 150, 200, 400, 800 μM | 48 h | 10-G inhibited the proliferation of SUM-159 cells in a concentration-dependent manner and increased their sensitivity to paclitaxel. | Drug Des Devel Ther. 2023 Jan 20;17:129-142 | 
| MDA-MB-231 | 0, 25, 50, 100, 150, 200, 400, 800 μM | 48 h | 10-G inhibited the proliferation of MDA-MB-231 cells in a concentration-dependent manner and increased their sensitivity to paclitaxel. | Drug Des Devel Ther. 2023 Jan 20;17:129-142 | 
| rat bone marrow-derived osteoclast precursors | 2.5 μM | 6 days | 10-gingerol reduced the number of osteoclasts in TRAP staining. | Front Cell Dev Biol. 2021 Mar 3;9:588093 | 
| RAW264.7 cells | 2.5 μM | 6 days | 10-gingerol significantly suppressed RANKL-induced osteoclast differentiation in RAW264.7 cells, reducing the number of TRAP-positive multinucleated osteoclasts. | Front Cell Dev Biol. 2021 Mar 3;9:588093 | 
| MDA-MB-231/IR cells | 90 µM | 24 h | To evaluate the effects of 10-gingerol on the invasive ability of MDA-MB-231/IR cells. Results showed that 10-gingerol significantly reduced the number of invading MDA-MB-231/IR cells. | Molecules. 2020 Jul 10;25(14):3164 | 
| MDA-MB-231/IR cells | 90, 45 µM | 24 h | To evaluate the effects of 10-gingerol on the migratory ability of MDA-MB-231/IR cells. Results showed that 10-gingerol significantly inhibited the migratory ability of MDA-MB-231/IR cells. | Molecules. 2020 Jul 10;25(14):3164 | 
| MDA-MB-231/IR cells | 40, 20, 10, 5 µM | 10 days | To evaluate the effects of 10-gingerol on the clonogenic ability of MDA-MB-231/IR cells. Results showed that 10-gingerol significantly reduced the clonogenic ability of MDA-MB-231/IR cells. | Molecules. 2020 Jul 10;25(14):3164 | 
| MCF-10A cells | 200, 100, 50, 25, 12.5, 6.25 µM | 24 and 48 h | To evaluate the cytotoxic effects of 10-gingerol on normal mammary epithelial cells. Results showed that 10-gingerol exerted fewer cytotoxic effects in MCF-10A cells than the positive control docetaxel. | Molecules. 2020 Jul 10;25(14):3164 | 
| MDA-MB-231/IR cells | 200, 100, 50, 25, 12.5, 6.25 µM | 24 and 48 h | To evaluate the inhibitory effects of 10-gingerol on the proliferation of MDA-MB-231/IR cells. Results showed that 10-gingerol suppressed the proliferation of MDA-MB-231/IR cells in a dose and time-dependent manner. | Molecules. 2020 Jul 10;25(14):3164 | 
| HepG2 cells | 10 µM | 48 h | To investigate the effect of 10-Gingerol on CYP3A4 mRNA expression. Results showed that 10-Gingerol inhibited CYP3A4 mRNA expression by 61%±4%. | Acta Pharmacol Sin. 2013 Sep;34(9):1237-42 | 
| Administration | Dosage | Frequency | Description | References | ||
| NOD/SCID mice | Breast cancer xenograft model | Oral | 40 mg/kg | Once daily for 33 days | 10-G enhanced the anti-tumor effects of paclitaxel in the TNBC xenograft model without increasing hepatorenal toxicity. | Drug Des Devel Ther. 2023 Jan 20;17:129-142 | 
| 计算器 | ||||
| 存储液制备 | ![]()  | 
                        1mg | 5mg | 10mg | 
| 
                             1 mM 5 mM 10 mM  | 
                        
                             2.85mL 0.57mL 0.29mL  | 
                        
                             14.27mL 2.85mL 1.43mL  | 
                        
                             28.53mL 5.71mL 2.85mL  | 
                    |
| CAS号 | 23513-15-7 | 
| 分子式 | C21H34O4 | 
| 分子量 | 350.49 | 
| SMILES Code | CCCCCCCCC[C@H](O)CC(CCC1=CC=C(O)C(OC)=C1)=O | 
| MDL No. | MFCD01682694 | 
| 别名 | (S)-[10]-Gingerol | 
| 运输 | 蓝冰 | 
| 存储条件 | 
                                
                                    
                                             In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C  | 
                        
| 溶解方案 | 
                                
                                    
                                     DMSO: 105 mg/mL(299.58 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的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 
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