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(-) -Asarinin

(-) -Asarinin is a tetrahydrofurofurano lignan with various biological activities. (-) -Asarinin induces apoptosis in cancer cells. (-) -Asarinin promotes mitochondrial ROS accumulation, inhibits the STAT3 signaling pathway and induces apoptosis in precancerous cells. (-) -Asarinin is a Src family kinase inhibitor that suppresses mast cell activation. (-) -Asarinin is a non-competitive Δ5-desaturase inhibitor with a Ki of 0.28 mM. (-) -Asarinin possesses pain relief, anti-viral, anti-allergic and anti-tuberculous bacilli, and anti-tumor effects[1][2][3][4].

Product Specifications

CAS Number

133-04-0

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Apoptosis; Bacterial; Reactive Oxygen Species (ROS) ; Src; STAT; Stearoyl-CoA Desaturase (SCD)

Type

Natural Products

Related Pathways

Anti-infection; Apoptosis; Immunology/Inflammation; JAK/STAT Signaling; Metabolic Enzyme/Protease; NF-κB; Protein Tyrosine Kinase/RTK; Stem Cell/Wnt

Applications

Cancer-programmed cell death

Field of Research

Cancer; Infection; Inflammation/Immunology; Neurological Disease

Assay Protocol

https://www.medchemexpress.com/asarinin.html

Purity

99.90

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

[H][C@]12[C@](CO[C@@H]2C3=CC=C(OCO4)C4=C3)([H])[C@H](C5=CC=C(OCO6)C6=C5)OC1

Molecular Formula

C20H18O6

Molecular Weight

354.35

Precautions

H302, H315, H319, H335

References & Citations

[1]Zhao M, et al. (-) -Asarinin alleviates gastric precancerous lesions by promoting mitochondrial ROS accumulation and inhibiting the STAT3 signaling pathway. Phytomedicine. 2024 Apr;126:155348. |[2]Jeong M, et al. (-) -Asarinin from the Roots of Asarum sieboldii Induces Apoptotic Cell Death via Caspase Activation in Human Ovarian Cancer Cells. Molecules. 2018 Jul 25;23 (8) :1849. |[3]Hou Y, et al. (-) -Asarinin inhibits mast cells activation as a Src family kinase inhibitor. Int J Biochem Cell Biol. 2020 Apr;121:105701.|[4]Sakayu Shimizu, et al. Inhibition of Δ5-desaturase in polyunsaturated fatty acid biosynthesis by (−) -asarinin and (−) -epiasarinin. Phytochemistry. Volume 31, Issue 3, March 1992, Pages 757-760.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, protect from light)

Scientific Category

Natural Products

Clinical Information

No Development Reported

Available Sizes

Frequently Asked Questions

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