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Amentoflavone

Catalog No.: GN10484Purity:>98.00%Synonyms: Didemethyl Ginkgetin, NSC 295677
Amentoflavone is an orally active phenolic compound with anti-inflammatory, anti-oxidation, anti-microbial, and anti-cancer activities.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


Amentoflavone
Cas No.: 1617-53-4
10mM (in 1mL DMSO)In Stock
$58.00
1
1mgIn Stock
$22.00
1
5mgIn Stock
$49.00
1
10mgIn Stock
$77.00
1
25mgIn Stock
$112.00
1
50mgIn Stock
$173.00
1
100mgIn Stock
$273.00
1

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제품 설명 (Description)

Amentoflavone is an orally active phenolic compound with anti-inflammatory, anti-oxidation, anti-microbial, and anti-cancer activities [1]. Amentoflavone exerts anti-SARS-CoV-2 effect via binding to the main protease (Mpro/3CLpro), spike protein receptor binding domain (RBD), and RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2 [2]. Amentoflavone has been widely used to inhibit the growth of malignant tumors, induce apoptosis of tumor cells, and suppress angiogenesis[3].

In vitro, Amentoflavone treatment for 48 hours significantly inhibited the proliferation of HepG2, T24, and A549 cells, with IC50 values of 9.13, 10.67, and 8.36µM, respectively[4]. Treatment with 5µM Amentoflavone for 24 hours significantly induced cell cycle arrest and autophagy in BV-2 cells, and increased the expression of CDK2, p27Kip1, and p53/p-p53[5]. Treatment with 60µM Amentoflavone for 1 hour significantly inhibited the nuclear translocation of p65 and the activation of NF-κB in RAW 264.7 cells induced by lipopolysaccharide (LPS), and reduced NO production[6].

In vivo, Amentoflavone treatment via oral administration at a dose of 25mg/kg daily for 3 days prevented pilocarpine-induced epilepsy in mice, inhibited the activation and expression of NF-κB, and suppressed the hyperexcitability of hippocampal neurons [7]. Oral administration of Amentoflavone at a dose of 100mg/kg weekly for 2 weeks significantly inhibited tumor growth and prolonged the survival of CT26 xenograft tumor-bearing mice[8].

References:
[1] Yu S, Yan H, Zhang L, et al. A review on the phytochemistry, pharmacology, and pharmacokinetics of amentoflavone, a naturally-occurring biflavonoid[J]. Molecules, 2017, 22(2): 299.
[2] Xiong X, Tang N, Lai X, et al. Insights into amentoflavone: A natural multifunctional biflavonoid[J]. Frontiers in Pharmacology, 2021, 12: 768708.
[3] Tuli H S, Joshi H, Vashishth K, et al. Chemopreventive mechanisms of amentoflavone: recent trends and advancements[J]. Naunyn-Schmiedeberg's Archives of Pharmacology, 2023, 396(5): 865-876.
[4] Wang C G, Yao W N, Zhang B, et al. Lung cancer and matrix metalloproteinases inhibitors of polyphenols from Selaginella tamariscina with suppression activity of migration[J]. Bioorganic & medicinal chemistry letters, 2018, 28(14): 2413-2417.
[5] Liu Z, Wang F, Ma H, et al. Amentoflavone induces cell cycle arrest, apoptosis, and autophagy in BV-2 cells[J]. Frontiers in Bioscience-Landmark, 2020, 25(5): 798-816.
[6] Woo E R, Lee J Y, Cho I J, et al. Amentoflavone inhibits the induction of nitric oxide synthase by inhibiting NF-κB activation in macrophages[J]. Pharmacological Research, 2005, 51(6): 539-546.
[7] Zhang Z, Sun T, Niu J, et al. Amentoflavone protects hippocampal neurons: anti-inflammatory, antioxidative, and antiapoptotic effects[J]. Neural regeneration research, 2015, 10(7): 1125-1133.
[8] Fang Y J, Chen C H, Ku H J, et al. Amentoflavone inhibits colorectal tumor growth, stemness, and metastasis, prolonging survival through GLI-1/IL6/STAT3 axis targeting[J]. Biomedicine & Pharmacotherapy, 2025, 191: 118435.

실험 프로토콜 (Protocol)

Cell experiment [1]:

Cell lines

A549 cells

Preparation Method

A549 cells were cultured in DMEM medium supplemented with 10% fetal bovine serum, 100U/ml penicillin, and 100μg/ml streptomycin at 37°C with 5% CO2 and 95% saturated atmospheric humidity. Cells were seeded into 96-well microplates at a density of 5×104 cells/ml for 12h. Various concentrations of Amentoflavone (0, 1, 5, 10, 20, 50, and 100µM) were added to each well. At the end of the incubation period (48h at 37°C), cell viability was analyzed.

Reaction Conditions

0, 1, 5, 10, 20, 50, and 100µM; 48h

Applications

Amentoflavone treatment significantly induced cell death of A549 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

BALB/c mice

Preparation Method

BALB/c mice (5 weeks old) were maintained under a 12h light and 12h dark cycle at a temperature of 25°C and humidity of 50%±10%, free with water and diet. CT26 cells were suspended in 100μl of serum-free RPMI-1640 medium, which containing 30μl matrigel. Cells were subcutaneously injected into the right thigh (1×107) or rectum (1×106) of the mouse with 29-gauge needles and holding a cotton swab over the injection site for 1min. When the average tumor volume of the mice reached 100mm3, mice were randomly divided into a control group (1% DMSO/week), Amentoflavone (100mg/kg/week) group. DMSO and Amentoflavone were given by gavage for 2 weeks. During the treatment, the tumor volume of each group was evaluated by electronic caliper, and the calculation was followed by the formula (tumor volume=0.523×length×width2). Mouse body weight was measured every week.

Dosage form

10mg/kg/week for 2 weeks; p.o.

Applications

Amentoflavone treatment inhibited tumor growth in mice with CT26 xenografts, without affecting body weight.

References:
[1] Wang C G, Yao W N, Zhang B, et al. Lung cancer and matrix metalloproteinases inhibitors of polyphenols from Selaginella tamariscina with suppression activity of migration[J]. Bioorganic & medicinal chemistry letters, 2018, 28(14): 2413-2417.
[2] Fang Y J, Chen C H, Ku H J, et al. Amentoflavone inhibits colorectal tumor growth, stemness, and metastasis, prolonging survival through GLI-1/IL6/STAT3 axis targeting[J]. Biomedicine & Pharmacotherapy, 2025, 191: 118435.

제품 문서 (Product Documents)

Purity:>98.00%Appearance:A solid

화학적 특성 (Chemical Properties)

CAS 번호
1617-53-4
동의어
Didemethyl Ginkgetin, NSC 295677
화학명
8-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILES
C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O
분자식
C30H18O10
분자량
538.46
용해도
≥ 26.9mg/mL in DMSO
보관
Store at 2-8°C,protect from light
일반 주의사항
제품의 용해도 데이터에 따라 적절한 용매를 선택하십시오. 조제 후에는 반복적인 동결·해동을 피할 수 있도록 저장 용액을 소분하십시오.
저장 용액은 -80°C 보관 시 6개월 이내, -20°C 보관 시 1개월 이내에 사용하십시오.
용해도를 높이려면 튜브를 37°C로 데운 뒤 적절한 시간 동안 초음파 처리하십시오.
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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