Sophora Flavescens
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Sophora Flavescens

Sophora flavescens, commonly known as Kushen, is a prominent species in the Fabaceae family that has held significant importance in traditional Chinese medicine (TCM) since the Qin and Han dynasties. The root of this plant has been widely used in traditional medicine across various countries, including China, Japan, Korea, India, and some parts of Europe. In TCM, Sophora flavescens is highly regarded for its therapeutic properties and is frequently combined with other medicinal plants in various prescriptions. It is traditionally used to treat a wide range of ailments, including fever, dysentery, hematochezia (blood in stool), jaundice, oliguria (reduced urine output), vulvar swelling, asthma, eczema, inflammatory disorders, ulcers, and conditions associated with skin burns.

The medicinal efficacy of Sophora flavescens can be attributed to its rich phytochemical profile. Over 200 compounds have been identified from this plant, including flavonoids, alkaloids, terpenoids, volatile oils, and fatty acids. These compounds contribute to its diverse pharmacological activities, making it a valuable resource in the treatment of various health conditions.

Typical Active Ingredients

Matrine

Matrine is a naturally occurring alkaloid derived from plants of the genus Sophora, particularly Sophora flavescens. Known for its diverse pharmacological effects, matrine exhibits strong anticancer properties by inhibiting cell proliferation and inducing apoptosis, both in vitro and in vivo. These antitumor effects are believed to be mediated through the upregulation of Fas/FasL expression and the activation of caspase-3, a critical enzyme in the apoptosis pathway. In addition to its anticancer activities, matrine also functions as an autophagy inhibitor, demonstrating significant anti-inflammatory, immunosuppressive, and anti-fibrotic effects. Furthermore, it shows potential in combating Candida-related infections by regulating the yeast-to-hypha transition, highlighting its versatility as a therapeutic agent.

Sophoraflavanone G

Sophoraflavanone G is a prenylated flavonoid primarily found in Sophora flavescens. This natural compound has attracted considerable interest due to its wide range of pharmacological activities. Notably, Sophoraflavanone G exhibits potent anti-inflammatory and antimicrobial properties. Its ability to inhibit mutans streptococci makes it a promising candidate for the development of novel oral hygiene products, such as gargle solutions or toothpaste. Additionally, Sophoraflavanone G acts as a novel small-molecule inhibitor by disrupting the NF-κB and MAPK signaling pathways, further underscoring its therapeutic potential.

Sophoridine

Sophoridine is a bioactive quinolizidine alkaloid found in various Chinese medicinal herbs, particularly within the Fabaceae family, such as Sophora flavescens Alt, Sophora alopecuroides L, and Sophora viciifolia Hance. This natural compound has garnered significant attention for its broad spectrum of pharmacological activities, including anti-cancer, anti-inflammatory, anti-viral, anti-arrhythmia, and analgesic effects. Notably, sophoridine exhibits neuroprotective properties, as demonstrated in studies involving rats with permanent middle cerebral artery occlusion (pMCAO).

Kurarinone

Kurarinone, a potent bioactive compound derived from Sophora flavescens, is recognized for its diverse pharmacological properties. It has demonstrated significant anti-tumor, estrogenic, and anti-inflammatory effects, along with a notable ability to suppress immune responses. Kurarinone's potential in treating chronic inflammatory skin diseases is particularly promising, as it appears to inhibit the differentiation of pathogenic CD4(+) T-cells, thereby reducing the overall immune response. Moreover, Kurarinone enhances the efficacy of TNF-related apoptosis-inducing ligand (TRAIL) in inducing tumor cell apoptosis by suppressing NF-κB-dependent cFLIP expression. Additionally, it may interfere with intercellular signal transduction by down-regulating Smad3 expression, which could contribute to the amelioration of renal interstitial fibrosis. These multifaceted activities make Kurarinone a valuable candidate for further research and therapeutic development.

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