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WUWEIZISU C

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WUWEIZISU C Basic information

Product Name:
WUWEIZISU C
Synonyms:
  • SCHIZANDRIN C
  • WUWEIZISU C
  • ,8-dimethyl-
  • cycloocta(1,2-f:3,4-f’)bis(1,3)benzodioxole6,7,8,9-tetrahydro-1,13-dimethoxy-7
  • (6R,7S,13aS)-5,6,7,8-Tetrahydro-13,14-dimethoxy-6,7-dimethylcycloocta[1,2-f:3,4-f']bis[1,3]benzodioxole
  • (S)-(-)-Schisandrin C
  • Schisandrin C (Schizandrin-C
  • Schisandrin C (S)-(-)-Schisandrin C
CAS:
61301-33-5
MF:
C22H24O6
MW:
384.42
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • Miscellaneous Natural Products
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
61301-33-5.mol
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WUWEIZISU C Chemical Properties

Melting point:
122-123℃
Boiling point:
549.2±50.0 °C(Predicted)
Density 
1.232
solubility 
DMSO : 8.33 mg/mL (21.67 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
form 
powder
color 
White
LogP
5.623 (est)
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WUWEIZISU C Usage And Synthesis

Description

Schisandrin C is a lignan originally isolated from Schizandrae that has diverse biological activities. It decreases viability of U937 cells in a concentration-dependent manner and induces cell cycle arrest at the G1 phase when used at a concentration of 100 μM. Schisandrin C (5-20 μM) decreases hydrogen peroxide-induced cell death and production of reactive oxygen species (ROS) in C2C12 skeletal muscle cells. It also decreases levels of matrix metalloproteinase-2 (MMP-2), MMP-9, COX-2, VCAM-1, IL-1β, and TNF-α in hydrogen peroxide-stimulated C2C12 cells. Schisandrin C decreases lipoteichoic acid-induced production of nitric oxide (NO), prostaglandin E2 (PGE2; ), TNF-α, IL-1β, and IL-6 in mouse primary microglia. In vivo, schisandrin C (200 mg/kg) decreases serum alanine amino transferase (ALT) and aspartate amino transferase (AST) activity, increases hepatic mitochondrial and total glutathione (GSH) levels, and reduces liver injury in a mouse model of acetaminophen-induced liver injury partially via inhibition of the cytochrome P450 (CYP) isoforms CYP2E1, CYP1A2, and CYP3A11.

Uses

Schisandrin C potently inhibits proprotein convertase subtillsin-kexin type 9 (PCSK9) mRNA expression. Also, it displays strong protective effects in SH-SY5Y cells against serum and glucose deprivation (SGD) injury.

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