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Home > Natural Products > Chalcones (Find 47 items)

Chalcones

Phlorizin

(60-81-1)
Sodium-glucose cotransporter 1 (SGLT1) is a high affinity, low capacity transporter abundant in the small intestine, with some expression in the kidney as well. SGLT2 is a low affinity, high capacity transporter in the kidney that accounts for approximately 90% of glucose reabsorption into the blood stream. Selective inhibition of SGLT2 is a potential strategy for reducing plasma glucose levels as a treatment for diabetes. Phlorizin is a natural product, first isolated from the bark of apple tre

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Hesperidin methylchalcone

(24292-52-2)
Hesperidin Methylchalcone is a flavonoid agent used in the treatment of venous insufficiency.

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Cardamonin

(19309-14-9)
Chalone analog that display anti-inflammatory activity. Inhibits NO and PGE 2 production from LPS- and IFN- γ -induced RAW cells and inhibits TXB 2 production via the COX-1 and COX-2 pathways. Inhibits NF- κ B activation via inhibition of I κ B α degradation and phosphorylation, I κ B kinase activation and NF- κ B nuclear translocation.

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Isobavachalcone

(20784-50-3)
Isobavachalcone(Corylifolinin) is a chalcone constituent of Angelica keiskei, induces apoptosis in neuroblastoma.IC50 value:Target: Isobavachalcone inhibits platelet aggregation. Inhibitor of Epstein-Barr virus early antigen (EBV-EA) induction. Isobavachalcone exhibits potent inhibitory effect on skin tumor promotion. Potent inhibitor of MMP-2. Displays DNA strand-scission (cleaving) activity. Isobavachalcone hows antifungal activity.

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Butein

(487-52-5)
Butrin, isobutrin, and butein from medicinal plant Butea monosperma selectively inhibit nuclear factor-κB in activated human mast cells: suppression of tumor necrosis factor-α, interleukin (IL)-6, and IL-8. Anti-inflammatory agent

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4,4'-DIHYDROXY-2-METHOXYCHALCONE

(34221-41-5)
Echinatin is a chalcone isolated from the Chinese herbal medicine Gancao with hepatoprotective and anti-inflammatory effects. Echinatin may undergo an electron transfer (ET) and a proton transfer (PT) to cause the antioxidant action in aqueous solution[1]. Echinatin can be quickly absorbed and eliminated and extensively distributed with an absolute bioavailability of approximately 6.81% in Rat[2].

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Anthracite

(8029-10-5)

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Trilobatin

(4192-90-9)
Trilobatin, a natural sweetener derived from Lithocarpus polystachyus Rehd[1], Trilobatin is an HIV-1 entry inhibitor targeting the HIV-1 Gp41 envelope[2]. Neuroprotective effects[1]. Trilobatin is also a SGLT1/2 inhibitor that selectively induces the proliferation of human hepatoblastoma cells[3].

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Chalcone, also known as diphenylpropenone, styryl phenyl ketone, benzylidene acetophenone, is a common class of compounds in natural products and has corresponding pharmaceutical activity. The main purpose is to be used as an organic synthesis reagent and indicator.

Frequently Asked Questions

What are Chalcones and why are they important in pharmaceutical research?

Chalcones are organic compounds belonging to the flavonoid family, characterized by an open-chain structure with two aromatic rings linked by an α,β-unsaturated carbonyl system. They serve as key precursors in the synthesis of flavonoids and isoflavonoids, which exhibit a wide range of biological activities. Due to their anti-inflammatory, anticancer, antimicrobial, and antioxidant properties, chalcones are widely studied in drug discovery and development.

What are the common applications of Chalcones in medicinal chemistry?

In medicinal chemistry, chalcones are primarily used as scaffolds for developing new therapeutic agents. Their structural simplicity and ease of modification allow researchers to synthesize derivatives with enhanced pharmacological effects. Common applications include the development of anticancer drugs, antiviral agents, anti-diabetic compounds, and neuroprotective molecules. Additionally, chalcone-based compounds are explored for their potential in treating malaria and tuberculosis.

How are Chalcones synthesized in laboratory settings?

Chalcones are typically synthesized via the Claisen-Schmidt condensation reaction, which involves the base-catalyzed aldol condensation between an aromatic aldehyde and an acetophenone derivative. This method is favored for its high yield, simplicity, and scalability. Alternative green chemistry approaches—such as solvent-free reactions, microwave-assisted synthesis, or use of solid-supported catalysts—are also employed to improve sustainability and reduce environmental impact.

What factors should buyers consider when sourcing high-quality Chalcone compounds?

When sourcing chalcone compounds, buyers should evaluate several critical factors:1. Purity and analytical data (e.g., HPLC, NMR, MS reports) to ensure compound integrity.2. Supplier compliance with regulatory standards such as ISO or GMP, especially for pharmaceutical applications.3. Availability of custom synthesis services for specific derivatives.4. Stability and proper storage conditions of the product.5. Technical support and documentation for research or industrial use.Choosing a reputable supplier with transparent quality control enhances reliability and reproducibility in downstream applications.

Are Chalcones safe for use in drug development?

Chalcones themselves are not drugs but chemical intermediates or lead compounds used in preclinical research. Their safety profile depends on the specific derivative and its intended application. While many chalcone analogs show promising bioactivity with low toxicity in vitro and in animal models, thorough toxicological evaluation—including genotoxicity, hepatotoxicity, and pharmacokinetic studies—is required before clinical use. Regulatory approval for any chalcone-derived drug candidate must follow standard FDA or EMA guidelines.

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