货号:A568246
同义名:
Saponaretin; Homovitexin
Isovitexin是一种从Vitex trifolia L.种子中提取的天然产物,具有潜在的抗氧化活性,表现出强的抗高血糖作用,并在体内抑制α-葡萄糖苷酶。


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|---|---|---|---|---|---|---|---|
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| 产品名称 | JNK ↓ ↑ | JNK1 ↓ ↑ | JNK2 ↓ ↑ | JNK3 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Mulberroside A | ✔ | 99%+ | |||||||||||||||||
| Loureirin B | ✔ | Potassium Channel,Calcium Channel | 99%+ | ||||||||||||||||
| Ginsenoside Re | ✔ | NF-κB | 98% | ||||||||||||||||
| (+)-(3R,8S)-Falcarindiol | ✔ | ERK,STAT | 99%+ | ||||||||||||||||
| trans-Zeatin | ✔ | ERK,p38 MAPK | 95+% | ||||||||||||||||
| Urolithin B | ✔ | ERK,NF-κB | 95% | ||||||||||||||||
| Cucurbitacin IIb | ✔ | NF-κB | 99% | ||||||||||||||||
| Astragaloside IV | ✔ | mTOR,Akt,NF-κB | 98% | ||||||||||||||||
| m-PEG25-NHS ester | ✔ | 95% | |||||||||||||||||
| NDMC101 | ✔ | 99%+ | |||||||||||||||||
| DB07268 |
++++
JNK1, IC50: 9 nM |
99%+ | |||||||||||||||||
| SP600125 |
+
MKK4, IC50: 0.4 μM |
+++
JNK1, IC50: 40 nM |
+++
JNK2, IC50: 40 nM |
+++
JNK3, IC50: 90 nM |
98% | ||||||||||||||
| JNK-IN-7 |
++++
JNK1, IC50: 1.5 nM |
++++
JNK2, IC50: 2 nM |
++++
JNK3, IC50: 0.7 nM |
99% | |||||||||||||||
| JNK-IN-8 |
++++
JNK1, IC50: 4.7 nM |
+++
JNK2, IC50: 18.7 nM |
++++
JNK3, IC50: 1 nM |
99%+ | |||||||||||||||
| 3,3',5-Triiodo-L-thyronine |
++
JNK1, Kd: 240 nM |
++
JNK2, Kd: 290 nM |
+++
JNK3, Kd: 66 nM |
98% | |||||||||||||||
| IQ-1S free acid |
+
JNK1, IC50: 390 nM |
++
JNK2, IC50: 360 nM |
+++
JNK3, IC50: 87 nM |
99% | |||||||||||||||
| BI-78D3 |
++
JNK, IC50: 280 nM |
++
JNK, IC50: 280 nM |
++
JNK, IC50: 280 nM |
++
JNK, IC50: 280 nM |
99%+ | ||||||||||||||
| Bentamapimod |
+++
JNK1, IC50: 80 nM |
+++
JNK2, IC50: 90 nM |
++
JNK3, IC50: 230 nM |
98% | |||||||||||||||
| Resveratrol |
+
JNK1, IC50: 50 μM |
98% | |||||||||||||||||
| Indirubin-3′-oxime | ✔ | 99%+ | |||||||||||||||||
| SU3327 |
+
JNK, IC50: 0.7 μM |
+
JNK, IC50: 0.7 μM |
+
JNK, IC50: 0.7 μM |
+
JNK, IC50: 0.7 μM |
99%+ | ||||||||||||||
| JNK Inhibitor VIII |
++++
JNK1, Ki: 2 nM JNK1, IC50: 45 nM |
++++
JNK2, Ki: 4 nM JNK2, IC50: 160 nM |
+++
JNK3, Ki: 52 nM |
98% | |||||||||||||||
| Doramapimod | ✔ | 99%+ | |||||||||||||||||
| RPI-1 | ✔ | 99% | |||||||||||||||||
| TCS JNK 5a |
++
JNK2, pIC50: 6.5 |
++
JNK3, pIC50: 6.7 |
98% | ||||||||||||||||
| SP 600125, negative control |
+
JNK2, IC50: 18 μM |
+
JNK3, IC50: 24 μM |
97% | ||||||||||||||||
| 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 | Isovitexin, a natural product isolated and purified from the seeds of Vitex trifolia L., exhibits a potential antioxidant activity, shows a strong antihyperglycemic action, and inhibits α-glucosidase in vivo. |
| Concentration | Treated Time | Description | References | |
| Rat bone marrow mesenchymal stem cells (BMSCs) | 150μmol/L | To validate the restorative effects of Isovitexin on osteogenic differentiation, results showed that Isovitexin restored mitochondrial function and inhibited ferroptosis by upregulating SIRT3 expression. | Bone Res. 2025 Jan 26;13(1):18 | |
| A549 cells | 256 μg/ml | 2 hours | To determine whether isovitexin could block S. aureus internalization into the lung epithelial cells. Results showed that isovitexin significantly decreased the amount of intracellular S. aureus. | J Microbiol Biotechnol. 2022 Oct 28;32(10):1284-1291 |
| porcine ovarian granulosa cells (GCs) | 40 mmol/L | 12 hours | Promoted the proliferation of porcine GCs and enhanced the enzyme activity of UCHL1. | J Anim Sci Biotechnol. 2024 Jun 11;15(1):85 |
| HuH7 cells | 30 µM | 72 hours | Evaluate the effect on cholesterol biosynthesis, showing a reduction in cholesterol biosynthesis (-5.7%, not statistically significant) | Antioxidants (Basel). 2021 Jun 29;10(7):1042 |
| MC3T3-E1 cells | 150 μmol/L | 24 hours | To investigate the effects of Isovitexin on glucocorticoid-induced oxidative stress and osteonecrosis, results showed that Isovitexin effectively regulated mitophagy, preserved mitochondrial homeostasis, suppressed ferroptosis, and restored osteogenic capacity by promoting SIRT3 expression. | Bone Res. 2025 Jan 26;13(1):18 |
| HPAECs (Human Pulmonary Artery Endothelial Cells) | 25 or 50 μg/ml | 24 hours | Isovitexin inhibited LPS-induced IL-6 production in HPAECs. | Int J Biol Sci. 2016 Jan 1;12(1):72-86 |
| RAW 264.7 cells | 25 or 50 μg/ml | 24 hours | Isovitexin significantly reduced LPS-induced pro-inflammatory cytokine secretion, iNOS and COX-2 expression, and decreased ROS generation. | Int J Biol Sci. 2016 Jan 1;12(1):72-86 |
| Administration | Dosage | Frequency | Description | References | ||
| SD rats | Glucocorticoid-induced osteonecrosis of the femoral head model | Intraperitoneal injection | 15 mg/kg | Every two days for 4 weeks | To validate the preventive effects of Isovitexin on femoral head necrosis, results showed that Isovitexin significantly improved femoral head necrosis by upregulating SIRT3 expression and modulating mitophagy-mediated ferroptosis. | Bone Res. 2025 Jan 26;13(1):18 |
| Mice | S. aureus pneumonia model | Intraperitoneal injection | 100 mg/kg | Every 12 hours | To evaluate the protective effect of isovitexin against S. aureus pneumonia. Results showed that isovitexin significantly improved the survival rate of infected mice, reduced the bacterial load in lung tissues, and alleviated pathological injury and inflammation in lung tissues. | J Microbiol Biotechnol. 2022 Oct 28;32(10):1284-1291 |
| Sprague-Dawley rats | Acute gouty arthritis model | Intraperitoneal injection | 100 mg/kg | Once daily for 1 week | Isovitexin significantly reduced the ankle joint swelling index, alleviated inflammatory cell infiltration, ameliorated synovial cell proliferation, decreased levels of TNF-α, IL-1β, and IL-6, and remarkably decreased the expression of TLR4, MyD88, and p-NF-κB-p65 | Pharm Biol. 2021 Dec;59(1):1326-1333 |
| BALB/c mice | LPS-induced acute lung injury model | Intraperitoneal injection | 50 or 100 mg/kg | Single dose, lasting 12 hours | Isovitexin pretreatment attenuated histopathological changes, infiltration of polymorphonuclear granulocytes and endothelial activation, decreased the expression of ICAM-1 and VCAM-1, reduced the levels of MPO and MDA, and increased the content of GSH and SOD in ALI. | Int J Biol Sci. 2016 Jan 1;12(1):72-86 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.31mL 0.46mL 0.23mL |
11.56mL 2.31mL 1.16mL |
23.13mL 4.63mL 2.31mL |
|
| CAS号 | 38953-85-4 |
| 分子式 | C21H20O10 |
| 分子量 | 432.38 |
| SMILES Code | OC1=C(C2=O)C(OC(C3=CC=C(O)C=C3)=C2)=CC(O)=C1[C@@H]([C@@H]([C@@H](O)[C@@H]4O)O)O[C@@H]4CO |
| MDL No. | MFCD00076044 |
| 别名 | Saponaretin; Homovitexin |
| 运输 | 蓝冰 |
| InChI Key | MYXNWGACZJSMBT-VJXVFPJBSA-N |
| Pubchem ID | 162350 |
| 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: 25 mg/mL(57.82 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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