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ChemicalBook--->CAS DataBase List--->61301-33-5

61301-33-5

61301-33-5 Structure

61301-33-5 Structure
IdentificationBack Directory
[Name]

WUWEIZISU C
[CAS]

61301-33-5
[Synonyms]

WUWEIZISU C
,8-dimethyl-
SCHIZANDRIN C
WUWEIZISU C USP/EP/BP
(S)-(-)-Schisandrin C
Schisandrin C >=98% (HPLC)
Schisandrin C (Schizandrin-C
Schisandrin C (S)-(-)-Schisandrin C
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
Cycloocta[1,2-f:3,4-f']bis[1,3]benzodioxole, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, (6R,7S,13aS)-
[Molecular Formula]

C22H24O6
[MDL Number]

MFCD00272170
[MOL File]

61301-33-5.mol
[Molecular Weight]

384.42
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H302-H410
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P273-P391-P501
Hazard InformationBack Directory
[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; Item No. 14010), 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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