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Formononetin/刺芒柄花素 {[allProObj[0].p_purity_real_show]}

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。

Formononetin/刺芒柄花素 化学结构 CAS号:485-72-3
Formononetin/刺芒柄花素 化学结构
CAS号:485-72-3
Formononetin/刺芒柄花素 3D分子结构
CAS号:485-72-3
Formononetin/刺芒柄花素 化学结构 CAS号:485-72-3
Formononetin/刺芒柄花素 3D分子结构 CAS号:485-72-3
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Formononetin/刺芒柄花素 纯度/质量文件 产品仅供科研

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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。

Formononetin/刺芒柄花素 生物活性

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].

Formononetin/刺芒柄花素 细胞实验

Cell Line
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.

Formononetin/刺芒柄花素 动物实验

Species
Animal Model
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.

Formononetin/刺芒柄花素 临床研究

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 <<

Formononetin/刺芒柄花素 参考文献

[1]Zhang X, Bi L, et al. Formononetin induces apoptosis in PC-3 prostate cancer cells through enhancing the Bax/Bcl-2 ratios and regulating the p38/Akt pathway. Nutr Cancer. 2014;66(4):656-61.

[2]Chen J, Zeng J, et al. Formononetin induces cell cycle arrest of human breast cancer cells via IGF1/PI3K/Akt pathways in vitro and in vivo. Horm Metab Res. 2011 Sep;43(10):681-6.

[3]Huang D, Wang C, Duan Y, Meng Q, Liu Z, Huo X, Sun H, Ma X, Liu K. Targeting Oct2 and P53: Formononetin prevents cisplatin-induced acute kidney injury. Toxicol Appl Pharmacol. 2017 Jul 1;326:15-24. doi: 10.1016/j.taap.2017.04.013. Epub 2017 Apr 13. Erratum in: Toxicol Appl Pharmacol. 2022 Sep 1;450:116133. PMID: 28414026.

[4]El-Bakoush A, Olajide OA. Formononetin inhibits neuroinflammation and increases estrogen receptor beta (ERβ) protein expression in BV2 microglia. Int Immunopharmacol. 2018 Aug;61:325-337. doi: 10.1016/j.intimp.2018.06.016. Epub 2018 Jun 15. PMID: 29913427.

Formononetin/刺芒柄花素 实验方案

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

Formononetin/刺芒柄花素 技术信息

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

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
方案 二
方案 三
配制的工作液建议现用现配,短期内尽快用完。 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
方案 二
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