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Curcumin/姜黄素 {[allProObj[0].p_purity_real_show]}

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。

Curcumin/姜黄素 化学结构 CAS号:458-37-7
Curcumin/姜黄素 化学结构
CAS号:458-37-7
Curcumin/姜黄素 3D分子结构
CAS号:458-37-7
Curcumin/姜黄素 化学结构 CAS号:458-37-7
Curcumin/姜黄素 3D分子结构 CAS号:458-37-7
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Curcumin/姜黄素 生物活性

靶点
  • p300/CBP

    p300, IC50:~25 μM

  • HDAC

  • NF-κB

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].

Curcumin/姜黄素 细胞实验

Cell Line
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.

Curcumin/姜黄素 动物实验

Species
Animal Model
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.

Curcumin/姜黄素 参考文献

[1]Cao A, Li Q, et al. Curcumin induces apoptosis in human gastric carcinoma AGS cells and colon carcinoma HT-29 cells through mitochondrial dysfunction and endoplasmic reticulum stress. Apoptosis. 2013 Nov;18(11):1391-402.

[2]Gao S, Duan X, et al. Curcumin attenuates arsenic-induced hepatic injuries and oxidative stress in experimental mice through activation of Nrf2 pathway, promotion of arsenic methylation and urinary excretion. Food Chem Toxicol. 2013 Sep;59:739-47.

[3]Tsuda T . Curcumin as a functional food-derived factor: degradation products, metabolites, bioactivity, and future perspectives. Food Funct. 2018 Feb 21;9(2):705-714. doi: 10.1039/c7fo01242j. PMID: 29206254.

[4]Daverey A, Agrawal SK. Curcumin Protects against White Matter Injury through NF-κB and Nrf2 Cross Talk. J Neurotrauma. 2020 May 15;37(10):1255-1265. doi: 10.1089/neu.2019.6749. Epub 2020 Feb 5. PMID: 31914858.

Curcumin/姜黄素 实验方案

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

Curcumin/姜黄素 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
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