Kayaflavone
Based on 1 Customer Validation
Kayaflavone is a biflavonoid compound from the seed kernel of Torreya grandis. Kayaflavone exhibits anticancer activity and is cytotoxic to human tumor cell lines. Kayaflavone inhibits amyloid-β toxicity in PC-12 cells with an EC50 of 5.29 μM. Kayaflavone is predicted to bind to the catalytic site of the SARS-CoV-2 main protease (Mpro/3CLpro) and block enzyme activity, indicating potential antiviral activity. Kayaflavone can be used in cancer-related research, such as cervical cancer and breast cancer, as well as in research related to neurological diseases.
For research use only. We do not sell to patients.
- Purity : 96.0%
- CAS No.: 481-45-8
- Formula: C33H24O10
- Molecular Weight:580.54
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Storage:
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Biological Activity
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HeLa | IC50 |
3.26 μg/mL
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Cytotoxicity against human cervical carcinoma HeLa cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
Cytotoxicity against human cervical carcinoma HeLa cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
|
MGC-220077 |
| MCF7 | IC50 |
12.64 μg/mL
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Cytotoxicity against human breast cancer MCF-7 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
Cytotoxicity against human breast cancer MCF-7 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
|
MGC-220077 |
| PANC-1 | IC50 |
16.44 μg/mL
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Cytotoxicity against human pancreatic cancer PANC-1 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
Cytotoxicity against human pancreatic cancer PANC-1 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
|
MGC-220077 |
| HepG2 | IC50 |
8.67 μg/mL
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Cytotoxicity against human hepatocellular carcinoma HepG-2 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
Cytotoxicity against human hepatocellular carcinoma HepG-2 cells assessed by MTT colorimetric assay with absorbance at 570 nm after 48 hrs incubation.
|
MGC-220077 |
In Vitro
Kayaflavone (compound 2) (0.01-100 µg/mL; 48 h) exhibits cytotoxic activity against HeLa, MCF-7, PANC-1, and HepG-2 cells, with IC50 values of 3.26, 12.64, 16.44, and 8.67 µg/mL, respectively, among which the activity against HeLa is the strongest[1].
Kayaflavone (compound C9) (molecular docking simulation) yields a high predicted binding score (‑9.0351) against the SARS‑CoV‑2 main protease MPRO[2].
Kayaflavone (compound 15) inhibits amyloid-β toxicity in PC-12 cells, with an EC50 of 5.29 μM, and cell viability reaches 80.5% at 10 μM[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:HeLa, MCF-7, PANC-1, and HepG-2
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Concentration:0.01, 0.1, 1.0, 10.0, 100.0 µg/mL
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Incubation Time:48 h
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Result:Showed IC50 values of 3.26 µg/mL against HeLa, 12.64 µg/mL against MCF-7, 16.44 µg/mL against PANC-1, and 8.67 µg/mL against HepG-2.
Chemical Information
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CAS No. 481-45-8
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Appearance Solid
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Molecular Weight 580.54
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Formula C33H24O10
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Color Light yellow to yellow
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SMILES
O=C1C=C(C2=CC(C3=C(C=C(C4=C3OC(C5=CC=C(OC)C=C5)=CC4=O)O)OC)=C(OC)C=C2)OC6=C1C(O)=CC(O)=C6
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Protocols
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Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.
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Amyloid: Congo Red Amyloid Staining
Congo red amyloid staining is a histochemical method used to detect extracellular amyloid deposits in tissue sections based on the affinity of Congo red dye for β-pleated sheet-rich protein aggregates. When bound to amyloid, Congo red produces characteristic apple-green birefringence under polarized light microscopy, which is widely regarded as a diagnostic feature of amyloid deposition in histopathology. The diagnostic principle relies on the combination of dye binding (congophilia) and optical anisotropy under polarized illumination, which distinguishes amyloid from most non-amyloid eosinophilic extracellular deposits in routine histological evaluation. Amyloid identification by Congo red staining remains a cornerstone in diagnostic pathology despite the availability of adjunct methods such as immunohistochemistry and mass spectrometry, particularly because of its ability to localize deposits directly within tissue architecture. The specificity of Congo red-positive deposits is incre
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Breast Cancer Modeling
Breast cancer is a heterogeneous cancer, and it has been distinguished into four subtypes: luminal A, luminal B, HER2-positive and basal-like. Molecular mutations, epigenetic alterations, hormone exposure and immune microenvironment are related to the progression of breast cancer.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
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Alzheimer’s Disease Modeling
Alzheimer’s Disease (AD) is a neurodegenerative disorder characterized by a progressive decline in cognitive functions and loss of specific types of neurons and synapses. Alzheimer's symptoms can be simulated in mice by injecting drugs (such as Aβ) or genetically modified.
Purity & Documentation
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Data Sheet (274 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)