货号:A682906
同义名:
Schizandrin-C; Wuweizisu-C
Schisandrin C is a phytochemical lignan isolated from Schizandra chinensis Baill and shows anticancer-effects in human leukemia U937 cells.
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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+ |
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描述 | Schisandrin C is a phytochemical lignan isolated from Schizandra chinensis Baill and shows anticancer-effects in human leukemia U937 cells. |
Concentration | Treated Time | Description | References | |
THP-1 cells | 20 µM | 24 hours | To evaluate the activation of the cGAS-STING pathway by SC and its inhibitory effect on HBV replication. Results showed that SC significantly increased the phosphorylation of IRF3 and promoted IFN-β production, thereby inhibiting HBV replication. | Chin Med. 2024 Mar 18;19(1):48 |
Mouse C2C12 skeletal muscle cells | 2.5 µM and 5 µM | 24 hours | Schisandrin C enhanced glucose uptake at non-toxic concentrations and increased the protein expression of GLUT-4, IRS-1, AMPK, PI3K, and Akt. | Molecules. 2021 Oct 28;26(21):6509 |
Rat INS-1 pancreatic β-cells | 2.5 µM and 5 µM | 24 hours | Schisandrin C enhanced glucose-stimulated insulin secretion at non-toxic concentrations and increased the protein expression of PPARγ, PDX-1, IRS-2, PI3K, and Akt. | Molecules. 2021 Oct 28;26(21):6509 |
4T1 cells | 15 µM | 24 hours | Assess the cytotoxicity of SC on 4T1 cells, results showed SC exhibited minimal toxicity | Front Pharmacol. 2024 Aug 7;15:1369563 |
MC38 cells | 15 µM | 24 hours | Assess the cytotoxicity of SC on MC38 cells, results showed SC exhibited minimal toxicity | Front Pharmacol. 2024 Aug 7;15:1369563 |
HFL1 cells | 20 µM, 40 µM, 80 µM | 48 hours | To evaluate the inhibitory effects of Sch C on TGF-β1-induced differentiation and migration of HFL1 cells. Results showed Sch C significantly inhibited the expressions of α-SMA and FN, and reduced cell migration. | Sci Rep. 2023 Aug 18;13(1):13475 |
Administration | Dosage | Frequency | Description | References | ||
C57BL/6J mice | HBV infection model | Oral gavage | 20 mg/kg | Continuous for 20 days | To evaluate the inhibitory effect of SC alone and in combination with Lut on HBV replication. Results showed that SC alone significantly reduced the levels of HBsAg, HBeAg, and HBV DNA in serum, and the effect was enhanced when combined with Lut. | Chin Med. 2024 Mar 18;19(1):48 |
ICR mice | BLM-induced pulmonary fibrosis model | Oral | 50 mg/kg, 100 mg/kg, 200 mg/kg | Once daily for 28 days | To evaluate the protective effects of Sch C on BLM-induced pulmonary fibrosis. Results showed Sch C significantly improved pulmonary indexes, reduced ECM accumulation, and inhibited LOX expression. | Sci Rep. 2023 Aug 18;13(1):13475 |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.60mL 0.52mL 0.26mL |
13.01mL 2.60mL 1.30mL |
26.01mL 5.20mL 2.60mL |
CAS号 | 61301-33-5 |
分子式 | C22H24O6 |
分子量 | 384.42 |
SMILES Code | C[C@H]([C@H](C)C1)CC2=C(C3=C1C=C4OCOC4=C3OC)C(OC)=C5OCOC5=C2 |
MDL No. | MFCD00272170 |
别名 | Schizandrin-C; Wuweizisu-C |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, store in freezer, under -20°C |
溶解方案 |
DMSO: 7 mg/mL(18.21 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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