货号:A161040
同义名:
Calycosin-7-glucoside; Calycosin-7-O-beta-D-glucoside
Calycosin-7-O-β-D-葡萄糖苷是从黄芪中分离出来的异黄酮类化合物。它具有各种生物活性,包括神经保护、心脏保护、抗炎和抗氧化作用。


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| 描述 | Calycosin-7-O-β-D-glucoside, a melanin biosynthesis inhibitor, is isolated from the methanol extract of astragalus. |
| Concentration | Treated Time | Description | References | |
| Human mesenchymal stem cells | 1-10 µM | 21 days | Evaluate late osteogenic differentiation, results showed that Caly promoted the formation of mineralized nodules | Int J Mol Sci. 2021 Oct 21;22(21):11362. |
| Human mesenchymal stem cells | 1-10 µM | 24 hours | Evaluate cell migration ability, results showed that Caly significantly promoted the migration of MSCs | Int J Mol Sci. 2021 Oct 21;22(21):11362. |
| NHBE cells | 1000 µg/ml and 500 µg/ml | 24 hours | To evaluate the effect of AR on CSE-induced autophagy in NHBE cells, results showed that AR significantly reduced the number of autophagosomes and autolysosomes and increased cellular structural integrity. | Front Pharmacol. 2021 Jan 14;11:580978. |
| HT22 cells | 35, 70, 140 µM | 24 hours | To investigate the protective effect of CAG on OGD/R-injured HT22 cells and its potential mechanism. Results showed that CAG significantly reduced ROS levels, apoptosis rate, and improved cell viability. | Molecules. 2025 Jan 25;30(3):549. |
| B16F10 cells | 1–1000 µg/mL | 48 hours | To evaluate the effect of YQD on melanogenesis in B16F10 cells. Results showed that YQD increased melanin content in B16F10 cells in a dose-dependent manner, significantly enhanced cellular tyrosinase activity, and upregulated TRP-1 gene and protein expression. | Pharmaceuticals (Basel). 2023 Dec 11;16(12):1716. |
| Mouse liver microsomes | 100 ng/mL | 60 minutes | To study the effect of CYP450 enzyme-specific inhibitors on the metabolism of Calycosin-7-O-β-D-glucoside, results showed no significant effect. | Front Pharmacol. 2023 Apr 14;14:1175896. |
| Human mesenchymal stem cells | 1-10 µM | 7 days | Evaluate early osteogenic differentiation, results showed that Caly increased ALP expression and activity | Int J Mol Sci. 2021 Oct 21;22(21):11362. |
| Administration | Dosage | Frequency | Description | References | ||
| Sprague-Dawley (SD) rats | Rheumatoid arthritis model | Oral gavage | 0.648 g/100g/d | 7 consecutive days | To evaluate the therapeutic effect of Xinfeng Capsule on rheumatoid arthritis. Results showed that Xinfeng Capsule significantly improved joint histopathological damage, inhibited NF-κB pathway activation, and promoted synovial cell apoptosis. | Front Immunol. 2025 Mar 13;16:1556764 |
| Mice | Diabetic nephropathy model | Oral | 0.96 g/kg, 0.48 g/kg, and 0.24 g/kg | Once daily for 12 weeks | To investigate the effects of HQD on diabetic nephropathy and the tissue distribution difference of its active constituents between normal and diabetic nephropathy mouse models. Results showed that HQD significantly decreased fasting blood glucose, 24-h urinary protein, blood urea nitrogen, serum creatinine, and triglyceride levels in DN mice. | Front Pharmacol. 2022 Jun 21;13:934720 |
| Sprague-Dawley rats | Normal rat model | Oral | 10 mg/mL | Single dose, duration of 720 minutes | To evaluate the effect of APS on the pharmacokinetics of CAG, results showed that APS significantly increased the maximum concentration (Cmax) and area under the curve (AUC) of CAG. | Int J Nanomedicine. 2023 Nov 14;18:6705-6724 |
| Zebrafish | Zebrafish embryos | Aqueous exposure | 200–1200 µg/mL | Continuous exposure from 24 hpf to 84 hpf | To evaluate the effect of YQD on melanogenesis in zebrafish. Results showed that YQD significantly promoted melanin production in zebrafish, especially at concentrations of 400–1200 μg/mL, where melanin density was significantly higher than in the control group. | Pharmaceuticals (Basel). 2023 Dec 11;16(12):1716. |
| A/J mice | Lung cancer model | Oral | 5.2 g/kg/d and 2.6 g/kg/d | Once daily for 28 weeks | To evaluate the therapeutic effect of AR on the lung cancer model, results showed that AR significantly reduced the number of lung tumor nodules, improved lung tissue structural integrity, and inhibited autophagy by upregulating p53 expression and downregulating p-Bcl-2 expression. | Front Pharmacol. 2021 Jan 14;11:580978. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.24mL 0.45mL 0.22mL |
11.20mL 2.24mL 1.12mL |
22.40mL 4.48mL 2.24mL |
|
| CAS号 | 20633-67-4 |
| 分子式 | C22H22O10 |
| 分子量 | 446.4 |
| SMILES Code | O=C1C(C2=CC=C(OC)C(O)=C2)=COC3=C1C=CC(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)=C3 |
| MDL No. | MFCD08061493 |
| 别名 | Calycosin-7-glucoside; Calycosin-7-O-beta-D-glucoside |
| 运输 | 蓝冰 |
| InChI Key | WACBUPFEGWUGPB-MIUGBVLSSA-N |
| Pubchem ID | 5318267 |
| 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: 105 mg/mL(235.21 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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