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Schisandrol B

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Chemical Structure| 58546-54-6 同义名 : 戈米辛A ;Gomisin A;TJN-101;Wuweizichun B;Gamma-Schisandrin;Besigomsin;Schizandrol B;Wuweizi alcohol-B
CAS号 : 58546-54-6
货号 : A134812
分子式 : C23H28O7
纯度 : 99%+
分子量 : 416.464
MDL号 : MFCD01941645
存储条件:

粉末 Sealed in dry,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 50 mg/mL(120.06 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

动物实验配方:
生物活性
描述 Gomisin A from the fruit of Schisandra chinensis has many pharmacological properties, including hepato-protective, anti-diabetic, and anti-oxidative stress. Gomisin A inhibited reactive oxygen species production even in the SIPS-HDF (stress-induced premature senescence-human diploid fibroblast) cells. Gomisin A was also able to attenuate the activity of senescence-associated β-galactosidase and the production of pro-inflammatory molecules in the SIPS as well as aged HDF cells. In addition, gomisin A promoted the autophagy and mitochondrial biogenesis factors through the translocation of nuclear factor erythroid 2-related factor-2, and inhibited aging progression in the SIPS-HDF cells[3]. Using human liver microsomes, a reversible inhibition assay revealed that Gom A ( Gomisin A) was a competitive inhibitor with a KI value of 1.10 µM, and the time- and NADPH-dependent CYP3A inhibition of Gom A was observed in a time-dependent inhibition assay (KI = 0.35 µM, kinact = 1.96 min-1)[4]. Both oral and intraperitoneal administration of G.A (50 mg/kg) inhibited lung metastasis of CT26 cells. G.A (Gomisin A) significantly decreased the viability of various CRC (colorectal cancer) cell lines, whereas it did not change the proliferation of normal colon cells. Moreover, the migration and invasion of CRC cells were reduced by G.A treatment. Especially, G.A decreased matrix metalloproteinase (MMP)-2 and MMP-9 expressions and activities[5].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.40mL

0.48mL

0.24mL

12.01mL

2.40mL

1.20mL

24.01mL

4.80mL

2.40mL

参考文献

[1]Jiang Y, Fan X, et al. Schisandrol B protects against acetaminophen-induced hepatotoxicity by inhibition of CYP-mediated bioactivation and regulation of liver regeneration. Toxicol Sci. 2015 Jan;143(1):107-15.

[2]Jin J, Bi H, et al. Enhancement of oral bioavailability of paclitaxel after oral administration of Schisandrol B in rats. Biopharm Drug Dispos. 2010 May;31(4):264-8.

[3]Kim JS, Jeong SH, Han SH, Yi HK. Gomisin A modulates aging progress via mitochondrial biogenesis in human diploid fibroblast cells. Clin Exp Pharmacol Physiol. 2018;45(6):547-555

[4]Zhai J, Zhang F, Gao S, et al. Time- and NADPH-Dependent Inhibition on CYP3A by Gomisin A and the Pharmacokinetic Interactions between Gomisin A and Cyclophosphamide in Rats. Molecules. 2017;22(8):1298. Published 2017 Aug 8

[5]Kee JY, Han YH, Mun JG, Park SH, Jeon HD, Hong SH. Gomisin A Suppresses Colorectal Lung Metastasis by Inducing AMPK/p38-Mediated Apoptosis and Decreasing Metastatic Abilities of Colorectal Cancer Cells. Front Pharmacol. 2018;9:986. Published 2018 Aug 29