货号:A204811
同义名:
Biochanin B; Flavosil
Formononetin可作为芳香烃受体的激动剂(EC50 = 130 nM),具有预防乳腺癌、前列腺癌和结肠癌的作用。Formononetin 可以从 Ononis natrix L. 的树皮中提取。
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产品名称 | AhR ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
StemRegenin 1 |
++
Aryl hydrocarbon receptor (AhR), IC50: 127 nM |
99%+ | |||||||||||||||||
CH-223191 |
+++
AhR, IC50: 30 nM |
99%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Formononetin is the main compound of red clover plants, which belongs to herbal isoflavone. in vivo, formononetin could reduce the nephrotoxicity by decreasing the accumulation of cisplatin in renal tubular cells. After formononetin treatment (15, 50, 75 mg/kg), the levels of BUN(blood urea nitrogen) and creatinine were decreased in a dose-dependent manner. The mRNA level of Kim-1 in the kidneys was significantly elevated at 48 h[3]. Moreover, formononetin inhibits neuroinflammation by targeting NF-κB signalling pathway in BV2 microglia[4]. |
Concentration | Treated Time | Description | References | |
HCC827 OR | 10μM | 24 hours | Formononetin significantly inhibited the cell viability of HCC827 OR cells. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
H1299 | 10μM | 24 hours | Formononetin significantly inhibited the cell viability of H1299 cells. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
A549 | 10μM | 24 hours | Formononetin significantly inhibited the cell viability of A549 cells. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
H1975 | 10μM | 24 hours | Formononetin significantly inhibited the cell viability of H1975 cells. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
H3255 | 10μM | 24 hours | Formononetin significantly inhibited the cell viability of H3255 cells. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
Human umbilical vein endothelial cells | 10 μM | 24 hours | FN stabilizes NRF2 levels in HUVECs, protecting cells from oxaliplatin-induced damage. | Redox Biol. 2020 Sep;36:101677. |
Mouse dorsal root ganglion neurons | 10 μM | 24 hours | FN protects DRG neurons from oxaliplatin-induced damage by activating the NRF2-GSTP1 axis. | Redox Biol. 2020 Sep;36:101677. |
ND7/23 neuron cells | 10 μM | 24 hours | FN protects neurons from oxaliplatin-induced damage by activating the NRF2 pathway, increasing NRF2 protein levels and reducing ROS production. | Redox Biol. 2020 Sep;36:101677. |
BUMPT cells | 25 mg/kg | 3 days | Induced PRDM16 expression, peaking at 25 mg kg−1 | Adv Sci (Weinh). 2024 Feb;11(7):e2306704. |
Human aortic smooth muscle cells (HASMCs) | 1-5 μM | 24 hours | Inhibited oxLDL-induced foam cell formation and reduced lipid droplet accumulation | Theranostics. 2020 Jan 1;10(3):1090-1106. |
Peritoneal macrophages (PMs) | 1-5 μM | 24 hours | Inhibited oxLDL-induced foam cell formation and reduced lipid droplet accumulation | Theranostics. 2020 Jan 1;10(3):1090-1106. |
Hep3B cells | 20μM, 40μM | Formononetin treatment inhibited the binding of SLUG to the promoter of E-cadherin, upregulated the expression level of epithelial markers (E-cadherin, cytokeratin, and occludin), and downregulated the expression level of mesenchymal markers (Vimentin, N-cadherin, and myosin). | Theranostics. 2019 Jan 1;9(2):573-587. | |
PLC-PRF-5 cells | 20μM, 40μM | Formononetin treatment inhibited the binding of SLUG to the promoter of E-cadherin, upregulated the expression level of epithelial markers (E-cadherin, cytokeratin, and occludin), and downregulated the expression level of mesenchymal markers (Vimentin, N-cadherin, and myosin). | Theranostics. 2019 Jan 1;9(2):573-587. | |
BUMPT cells | 20 µM | 30 minutes | Formononetin significantly reduced I/R-stimulated BUMPT cell apoptosis and inhibited the activation of p38MAPK and JNK by upregulating the PRDM16/S100A6/PKC-η/ROS signaling pathways. | MedComm (2020). 2024 Sep 21;5(10):e737. |
Administration | Dosage | Frequency | Description | References | ||
Nude mice | Xenograft model | Intraperitoneal injection | 10 mg/kg | Once daily until the endpoint of the experiment | Formononetin significantly inhibited the growth of xenograft tumors, including HCC827, H3255, H1975, A549, and H1299-derived tumors. | J Exp Clin Cancer Res. 2020 Apr 10;39(1):62. |
C57BL/6 male mice | Oxaliplatin-induced peripheral neuropathy model | Intraperitoneal injection | 10.0 mg/kg | Daily injections for two cycles (5 days of injection and 5 days of rest per cycle) | FN alleviates mechanical and cold sensitivity in mice by activating the NRF2 signaling pathway and reduces morphological damage in DRG neurons. | Redox Biol. 2020 Sep;36:101677. |
ApoE-deficient mice | High-fat diet-induced atherosclerosis model | Oral | 10 mg/kg/day | Once daily for 16 weeks | Formononetin significantly reduced atherosclerotic lesion size, enhanced plaque stability, reduced macrophage accumulation and calcification | Theranostics. 2020 Jan 1;10(3):1090-1106. |
Db/db diabetic mice | Diabetic kidney disease model | Intragastric administration | 25 mg/kg | Once a day for four weeks | Attenuated renal fibrosis, MAPK activation, and TGF-β1 expression | Adv Sci (Weinh). 2024 Feb;11(7):e2306704. |
Nude mice | Hepatocellular carcinoma xenograft model | Subcutaneous injection | 100 mg/kg | Every 2 days for 15 days | Formononetin treatment inhibited tumor volume, fluorescence intensity, tumor weight, and the formation of pulmonary metastatic nodules. IHC analysis showed that Formononetin treatment decreased the expression of SLUG, Vimentin, and Ki67, and increased the expression of E-cadherin. | Theranostics. 2019 Jan 1;9(2):573-587. |
C57BL/6J mice | Cecal ligation and puncture (CLP)-induced sepsis model | Tail vein injection | 20 mg/kg | Single dose, observed for 18 hours | To evaluate the protective effect of Formononetin/PLGA on sepsis-induced multi-organ injury. Results showed that Formononetin/PLGA inhibited ferroptosis by upregulating the PRDM16/NRF2/GPX4 axis, alleviating sepsis-induced kidney injury and other organ injuries. | Redox Biol. 2024 Dec;78:103417. |
Mice | Ischemia/reperfusion (I/R) and cisplatin-induced acute kidney injury (AKI) model | Oral administration | 25 mg/kg | 3 consecutive days | Formononetin significantly ameliorated the progression of I/R- and cisplatin-triggered AKI in mice by regulating the PRDM16/S100A6/PKC-η/ROS/p38MAPK and JNK axes. | MedComm (2020). 2024 Sep 21;5(10):e737. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT02174666 | Osteopenia Os... 展开 >>teoporosis 收起 << | Not Applicable | Unknown | September 2016 | Denmark ... 展开 >> Aarhus University Hospital Aarhus, Central Jutland Region, Denmark, 8000 收起 << |
NCT01497977 | Low Serum Lipid Levels | Phase 4 | Completed | - | Serbia ... 展开 >> Ultramedica Clinic, American Medical Academy Belgrade, Serbia, 11000 收起 << |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.73mL 0.75mL 0.37mL |
18.64mL 3.73mL 1.86mL |
37.28mL 7.46mL 3.73mL |
CAS号 | 485-72-3 |
分子式 | C16H12O4 |
分子量 | 268.26 |
SMILES Code | O=C1C(C2=CC=C(OC)C=C2)=COC3=C1C=CC(O)=C3 |
MDL No. | MFCD00016948 |
别名 | Biochanin B; Flavosil; Formononetol Formononetin; NSC 93360; Formononetol |
运输 | 蓝冰 |
InChI Key | HKQYGTCOTHHOMP-UHFFFAOYSA-N |
Pubchem ID | 5280378 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, room temperature |
溶解方案 |
DMSO: 35 mg/mL(130.47 mM),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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