货号:A147405
同义名:
Diferuloylmethane; Natural Yellow 3
Curcumin (Diferuloylmethane) 是一种天然酚类化合物,是乙酰转移酶 p300/CREB 结合蛋白的特异性抑制剂,抑制组蛋白/非组蛋白的乙酰化和组蛋白乙酰转移酶依赖的染色质转录。Curcumin 对 NF-κB 和 MAPKs 有抑制作用,具有抗炎、抗氧化、抗增殖和抗血管生成等药理作用。
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描述 | Curcumin, a polyphenol found in turmeric (curcuma longa), has health benefits such as antioxidant, anti-inflammatory, and anticancer properties, improvement of brain function, and control of obesity and diabetes. And dietary curcumin (80 mg kg−1) administered to mice on a high-fat diet significantly lowered the fasting blood glucose levels and TNF-α concentrations, and inhibited the lowering of glucose tolerance[3]. Moreover, cur(curcumin) inhibited hypoxia-induced HIF1α expression and tissue damage by demonstrating the improved morphology of astrocytes and remarkable reduction in vacuolation[4]. |
Concentration | Treated Time | Description | References | |
CHO cells | 10 µM | 24 h | Curcumin significantly reduced the secretion of Aβ40 and Aβ42 | Cells. 2020 Feb 3;9(2):349. |
SH-SY5Y cells | 10 µM | 24 h | Curcuminsignificantly reduced the secretion of Aβ40 | Cells. 2020 Feb 3;9(2):349. |
ARPE-19 cells | 0.01 mM | 24 h | To evaluate the effect of curcumin on cell proliferation, results showed that 0.01 mM curcumin significantly increased cell proliferation. | Int J Mol Sci. 2022 Nov 25;23(23):14771. |
ARPE-19 cells | 0.05 mM | 24 h | To evaluate the effect of curcumin on cell proliferation, results showed that 0.05 mM curcumin significantly decreased cell viability and triggered S-phase cell cycle arrest. | Int J Mol Sci. 2022 Nov 25;23(23):14771. |
ARPE-19 cells | 0.1 mM | 24 h | To evaluate the effect of curcumin on cell proliferation, results showed that 0.1 mM curcumin significantly decreased cell viability and triggered S-phase cell cycle arrest. | Int J Mol Sci. 2022 Nov 25;23(23):14771. |
Human cervical cancer cells (HeLa) | 5–50 μM | 72 h | To compare the cytotoxicity of free curcumin and FA-CLAP nanocurcumin on HeLa cells. Results showed that FA-CLAP nanocurcumin exhibited higher cytotoxicity at doses of 15 μM, 25 μM, and 50 μM. | J Nanobiotechnology. 2014 Jul 15;12:25. |
Human cervical cancer cells (HeLa) | 25 μM | 2 h | To study the cellular uptake of FA-CLAP nanocurcumin. Results showed that FA-CLAP nanocurcumin exhibited better cellular uptake than free curcumin. | J Nanobiotechnology. 2014 Jul 15;12:25. |
4T1 breast cancer cells | 6 µg/mL | 1, 2, and 4 h | To evaluate the cellular uptake of CUR/IR780@SMEDDS, results showed that the uptake of CUR/IR780@SMEDDS in 4T1 cells increased over time and further increased with NIR laser irradiation. | Int J Nanomedicine. 2019 May 7;14:3311-3330. |
Lewis Lung Carcinoma cells | 10, 20, 50, 100 µM | 24 and 48 h | To evaluate the effect of curcumin on tumor cell proliferation, results showed that curcumin significantly reduced tumor cell proliferation | Br J Cancer. 2012 Sep 25;107(7):1083-92. |
BZR human lung epithelial tumour cells | 10, 20, 50 µM | 48 h | To evaluate the effect of curcumin on tumor cell proliferation, results showed that curcumin significantly reduced tumor cell proliferation | Br J Cancer. 2012 Sep 25;107(7):1083-92. |
IEC-6 cells | 17.4 µg/ml | 24 h | To evaluate the cytotoxicity of Curcumin on IEC-6 cells, the results showed that SP@Curcumin had significantly lower cytotoxicity than free Curcumin. | Sci Adv. 2021 Nov 26;7(48):eabi9265. |
CT26 cells | 17.4 µg/ml | 4 h | To evaluate the antitumor effect of SP@Curcumin on CT26 cells, the results showed that SP@Curcumin combined with X-ray significantly enhanced the tumor cell killing effect. | Sci Adv. 2021 Nov 26;7(48):eabi9265. |
Microglia | 4 μM | 24 h | To assess the cytotoxicity of curcumin on microglia and hUC-MSC to determine the optimal concentration. | J Neuroinflammation. 2023 Feb 24;20(1):49. |
Administration | Dosage | Frequency | Description | References | ||
Rats | Sprague Dawley rats | Oral | 75 mg/kg | Single dose | To evaluate the oral bioavailability of CUR/IR780@SMEDDS in rats, results showed that CUR/IR780@SMEDDS significantly improved the oral absorption of curcumin and IR780, with relative bioavailability of 743.7% and 307.0%, respectively. | Int J Nanomedicine. 2019 May 7;14:3311-3330. |
C57Bl/6 mice | Lung tumor model | Oral | 3 mg/kg | 5 days per week, until the end of the experiment | To evaluate the effect of curcumin on lung tumor growth, results showed that curcumin significantly reduced the size of lung tumors | Br J Cancer. 2012 Sep 25;107(7):1083-92. |
C57BL/6 mice | Cisplatin-induced acute kidney injury model | Gavage | 100 mg/kg | Once daily for 3 days | To observe the protective effect of curcumin on cisplatin-induced acute kidney injury, results showed that curcumin significantly reduced serum creatinine and BUN levels, and decreased tubular cell necrosis and inflammation. | J Cell Mol Med. 2021 Sep;25(18):8775-8788. |
Balb/c mice | Colon cancer model | Oral | 1.2 mg/ml | Every 3 days for 15 days | To evaluate the chemoradiotherapeutic effect of SP@Curcumin in a colon cancer model, the results showed that SP@Curcumin significantly inhibited tumor growth and improved the survival rate of mice. | Sci Adv. 2021 Nov 26;7(48):eabi9265. |
Mice | MCAO model | Intraperitoneal injection | 100 mg/kg | Once every 24 hours for 3 days | To evaluate the functional recovery and neuroprotective effects of combined curcumin and hUC-MSC therapy in MCAO mice. | J Neuroinflammation. 2023 Feb 24;20(1):49. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.71mL 0.54mL 0.27mL |
13.57mL 2.71mL 1.36mL |
27.15mL 5.43mL 2.71mL |
CAS号 | 458-37-7 |
分子式 | C21H20O6 |
分子量 | 368.38 |
SMILES Code | O=C(CC(/C=C/C1=CC=C(O)C(OC)=C1)=O)/C=C/C2=CC=C(O)C(OC)=C2 |
MDL No. | MFCD00008365 |
别名 | Diferuloylmethane; Natural Yellow 3; UNIIIT942ZTH98.; NSC32982; C.I. 75300; curcumin I; Indian Saffron; Turmeric yellow |
运输 | 蓝冰 |
InChI Key | VFLDPWHFBUODDF-FCXRPNKRSA-N |
Pubchem ID | 969516 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, room temperature |
溶解方案 |
DMSO: 105 mg/mL(285.03 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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