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.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度 : 96.0%
- CAS 番号: 481-45-8
- 分子式: C33H24O10
- 分子量:580.54
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保管条件:
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
生物活性
製品説明
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.
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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.
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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 |
体外実験
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.
化学情報
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CAS 番号 481-45-8
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性状 Solid
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分子量 580.54
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分子式 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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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
プロトコル
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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.
純度とドキュメンテーション
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データシート (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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取扱説明書 (2659 KB)
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)