Swertiamarin

Synonyms: Swertiamaroside

Swertiamarin (Swertiamaroside) is a common secoiridoid found among the members of Gentianaceae with anti-inflammatory, anticancer, hypoglycemic and hypolipidemic activities.

Swertiamarin Chemical Structure

Swertiamarin Chemical Structure

CAS: 17388-39-5

Selleck's Swertiamarin has been cited by 1 publication

Purity & Quality Control

Batch: S392701 DMSO] 74 mg/mL] false] ] ] false] ] ] false Purity: 99.76%
99.76

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Biological Activity

Description Swertiamarin (Swertiamaroside) is a common secoiridoid found among the members of Gentianaceae with anti-inflammatory, anticancer, hypoglycemic and hypolipidemic activities.
In Vivo
In vivo Pharmacokinetic analysis shows that Swertiamarin is absorbed very fast, with very short plasma half-life of 1.3 h, and is completely eliminated from systemic circulation after 4-5 h. Swertiamarin treatment has no significant effect on adipogenesis, or the mRNA expression of PPAR-g and GLUT-4; however, there is a significant increase in the mRNA expression of adiponectin[1]. On treatment, the compound exerts an antiinflammatory effect on macrophages and neutrophils by suppressing the release of free radicals, iNOS expression, and proinflammatory cytokines. Swertiamarin acts as an anti-inflammatory agent by suppressing proinflammatory mediators (Th1) and inducing anti-inflammatory mediators (Th2)[2]. Swertiamarin decreases serum cholesterol levels and reduces the oxidation of LDL. In addition, swertiamarin has also shown to have the ability in increasing the HDL levels and reduction in the ratio of LDL/HDL cholesterol. Swertiamarin has shown to modulate 5-HT2 receptor and hypolipidemic potential in animal models of depression, diabetes and obesity[3].
Animal Research Animal Models Swiss albino mice
Dosages 2, 5, and 10 mg/kg b.w.
Administration orally

Chemical Information & Solubility

Molecular Weight 374.34 Formula

C16H22O10

CAS No. 17388-39-5 SDF --
Smiles C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 74 mg/mL ( (197.68 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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