1. Apoptosis Immunology/Inflammation
  2. TNF Receptor Interleukin Related Caspase SOD
  3. Hibiscetin

Hibiscetin is an orally active anti-inflammatory, antioxidant, antihyperglycemic, hypolipidemic, hepatoprotective and neuroprotective agent. Hibiscetin reduces the levels of TNF-α, IL-1β and IL-6. Hibiscetin inhibits lipid peroxidation, reduces MDA levels, and induces the activities of antioxidant enzymes CAT, GSH and SOD. Hibiscetin lowers blood glucose, reverses reduced insulin levels, regulates adipokine levels, and reduces elevated AST and ALT levels. Hibiscetin alleviates Rotenone (HY-B1756)-induced akinesia and catalepsy, normalizes neurotransmitter levels, and modulates the activities of activated caspase 3 and BDNF. Hibiscetin can be used in the research of type 2 diabetes, Parkinson's disease and Huntington's disease.

For research use only. We do not sell to patients.

Hibiscetin

Hibiscetin Chemical Structure

CAS No. : 577-24-2

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Description

Hibiscetin is an orally active anti-inflammatory, antioxidant, antihyperglycemic, hypolipidemic, hepatoprotective and neuroprotective agent. Hibiscetin reduces the levels of TNF-α, IL-1β and IL-6. Hibiscetin inhibits lipid peroxidation, reduces MDA levels, and induces the activities of antioxidant enzymes CAT, GSH and SOD. Hibiscetin lowers blood glucose, reverses reduced insulin levels, regulates adipokine levels, and reduces elevated AST and ALT levels. Hibiscetin alleviates Rotenone (HY-B1756)-induced akinesia and catalepsy, normalizes neurotransmitter levels, and modulates the activities of activated caspase 3 and BDNF. Hibiscetin can be used in the research of type 2 diabetes, Parkinson's disease and Huntington's disease[1][2][3][4].

IC50 & Target[1][4]

IL-6

 

IL-1β

 

TNF-α

 

Caspase 3

 

In Vitro

Hibiscetin exhibits high antioxidant activity, with the 8-OH position as the preferred site for radical attack[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Hibiscetin (10 mg/kg; p.o.; daily; 42 days) exerts significant antidiabetic, hypolipidemic, antioxidant, anti-inflammatory, and hepatoprotective effects in high-fat diet/Streptozotocin (HY-13753)-induced type 2 diabetic male Wistar rats[1].
Hibiscetin (10 mg/kg; p.o.; daily; 42 days) significantly improved lipid profile parameters in male Wistar rats[1].
Hibiscetin (10 mg/kg; p.o.; daily; 28 days) exerts anti-Parkinsonian activity in Rotenone (HY-B1756)-induced parkinsonism in rats, significantly reducing catalepsy and akinesia, restoring endogenous antioxidant and neurotransmitter levels, lowering oxidative/nitrative stress and neuroinflammatory cytokines, and improving neuronal histopathology[3].
Hibiscetin (10 mg/kg; p.o.; daily; 15 days) provides significant neuroprotection in 3-Nitropropionic acid (HY-W012875)-induced Huntington's disease in male Wistar rats by restoring body weight, normalizing oxidative stress markers, monoamine neurotransmitters, BDNF, caspase 3, and proinflammatory cytokine levels[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Wistar (male, 10-12 weeks old, 150-200 g, high-fat diet + Streptozotocin (HY-13753)-induced type 2 diabetes)[1]
Dosage: 10 mg/kg
Administration: p.o.; daily; 42 days
Result: Produced a significant reduction in body weight.
Significantly reduced elevated blood glucose levels and increased lowered serum insulin levels.
Significantly reduced elevated total cholesterol and triglyceride levels, increased lowered high-density lipoprotein cholesterol levels, and reduced elevated total protein levels.
Significantly reduced elevated hepatic malondialdehyde levels, and increased lowered superoxide dismutase, glutathione, and catalase activity.
Significantly reduced elevated serum tumor necrosis factor-α, interleukin-1β, and interleukin-6 levels.
Significantly increased lowered serum adiponectin and leptin levels, and reduced elevated serum resistin levels.
Significantly reduced elevated serum aspartate aminotransferase and alanine aminotransferase levels.
Animal Model: Wistar (male, 10-12 weeks old, 150-200 g)[1]
Dosage: 10 mg/kg
Administration: p.o.; daily; 42 days
Result: Produced a significant reduction in lipid profile parameters.
Animal Model: Wistar (male, 180 g)[4]
Dosage: 10 mg/kg
Administration: p.o.; daily; 15 days
Result: Restored body weight and reversed 3‑nitropropionic acid–induced weight loss.
Reduced brain lipid peroxidation and restored antioxidant biomarkers.
Normalized monoamine neurotransmitter levels.
Reduced cleaved caspase 3 activity and restored BDNF levels.
Reduced proinflammatory markers.
Molecular Weight

334.24

Formula

C15H10O9

CAS No.
SMILES

O=C1C(O)=C(OC=2C(O)=C(O)C=C(O)C12)C=3C=C(O)C(O)=C(O)C3

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Hibiscetin
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HY-N7773
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