HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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快速发货 顺丰冷链运输,1-2 天到达
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| 描述 | Vascular Endothelial Growth Factors (VEGFs) and their receptors (VEGF-Rs) are important regulators for angiogenesis and lymphangiogenesis. VEGFs and VEGF-Rs are not only expressed on endothelial cells but also on various subtypes of solid tumors and leukemias contributing to the growth of the malignant cells[2]. VEGF rapidly induced tyrosine phosphorylation of type 1 and type 2 VEGF receptors. Physical association between VEGF-receptor 2 (VEGF-R2) and insulin receptor substrate (IRS-1) and phosphatidylinositol 3'-kinase (PI3K) was induced by VEGF, which augmented PI3K activity in VEGF-R2 immunoprecipitates[3]. In a human melanoma xenograft mouse model, blockade of both VEGF-R2 and Tie-2 pathways or the VEGF receptor pathway alone resulted in a significant inhibition of tumor growth and tumor angiogenesis (92.2 % and 74.4 %)[4]. (Z)-Guggulsterone inhibits the growth of human prostate cancer cells by causing apoptosis. Z-guggulsterone inhibits angiogenesis by suppressing the vascular endothelial growth factor (VEGF)-VEGF-R2–Akt signaling axis. In HUVEC, Z-guggulsterone (10, 20 μM; 24 or 48 hours) induces a reduction in the level of VEGF-R2 protein. In tumor volume and wet tumor weight, Z-guggulsterone (p.o.; 1 mg; 5 times/week) causes a statistically significant reduction[5]. |
| Concentration | Treated Time | Description | References | |
| AML12 cells | 10 µM | 12 h | To evaluate the inhibitory effect of (Z)-Guggulsterone on viral replication, results showed that (Z)-Guggulsterone significantly reduced the fluorescence of VSV-GFP. | Acta Pharm Sin B. 2024 Aug;14(8):3513-3527. |
| Huh7 cells | 10 µM | 16 h | To evaluate the inhibitory effect of the FXR inhibitor (Z)-Guggulsterone on viral infection, results showed that (Z)-Guggulsterone significantly reduced the ratio of VSV-GFP positive cells. | Acta Pharm Sin B. 2024 Aug;14(8):3513-3527. |
| CD18/HPAF cells | 5–100 µM | 24–72 h | GS treatment resulted in dose- and time-dependent growth inhibition and decreased colony formation. | Cancer Lett. 2013 Dec 1;341(2):166-77. |
| 4T1 mouse breast cancer cells | 50 µM | Z-guggulsterone obliterated the anti-apoptotic effect of DC by blocking the farnesoid X receptor (FXR) and reduced the expression level of Flk-1. | Breast Cancer Res. 2008;10(6):R106 | |
| Barrett's esophagus-derived cells (CP-18821) | 20 μM | 48 h | To evaluate the effect of (Z)-Guggulsterone on apoptosis in Barrett's esophagus cells. Results showed that (Z)-Guggulsterone significantly increased the percentage of apoptotic cells (15.1% ± 3.5% vs 6.9% ± 0.8%, p = 0.02) and further confirmed by caspase 3 activity assay (177 ± 15 vs 53 ± 7; p = 7·10-4). | Mol Cancer. 2006 Oct 20;5:48. |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | VSV infection model | Intraperitoneal injection | 10 mg/kg | Once daily for 5 days | To evaluate the effect of (Z)-Guggulsterone on the survival rate and lung tissue damage in virus-infected mice, results showed that (Z)-Guggulsterone significantly extended the survival rate and reduced inflammatory lesions in the lungs. | Acta Pharm Sin B. 2024 Aug;14(8):3513-3527. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.20mL 0.64mL 0.32mL |
16.00mL 3.20mL 1.60mL |
32.01mL 6.40mL 3.20mL |
|
| CAS号 | 39025-23-5 |
| 分子式 | C21H28O2 |
| 分子量 | 312.45 |
| SMILES Code | C[C@@]1(CC[C@]([H])([C@](C)2CC3)[C@](CCC2=CC3=O)([H])[C@]1([H])CC/4=O)C4=C\C |
| MDL No. | MFCD01310757 |
| 别名 | Z-Guggulsterone |
| 运输 | 蓝冰 |
| InChI Key | WDXRGPWQVHZTQJ-OSJVMJFVSA-N |
| Pubchem ID | 6450278 |
| 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: 9 mg/mL(28.8 mM),配合低频超声,并水浴加热至45℃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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