GLPBio

Farnesol

Catalog No.: GC32387Purity:>99.00%Synonyms: Farnesol, FCI 119a, NSC 60597
Farnesol هو كحول سيسكيتيربين الذي ينظم الاتصال من خلية إلى خلية في المبيضات البيض ، وله نشاط في تثبيط البكتيريا.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


Farnesol
Cas No.: 4602-84-0
10mM (in 1mL DMSO)In Stock
$39.00
1
500mgIn Stock
$35.00
1
1gIn Stock
$42.00
1
5gIn Stock
$59.00
1
10gIn Stock
$70.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    641, 529–536 (2025)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    387(6734) (2025)
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الوصف (Description)

Farnesol, a C15 terpene alcohol that is ubiquitous in nature, is a component of plant essential oils and is a quorum sensing molecule in Candida albicans [1]. Farnesol exerts the pro-inflammatory effect by increasing the levels of IL-6, TNF-α, and COX-2 in macrophage cells[2]. Farnesol has been widely used in various cell models and animal models to inhibit tumor growth[3].

In vitro, Farnesol treatment for 24 hours significantly inhibited the viability of A549 cells and Caco-2 cells, with IC50 values of 4.6mM and 3.9mM, respectively[4]. Treatment with 20μM Farnesol for 48 hours significantly inhibited the growth of MCF-7 cells, induced the expression of THRβ1 mRNA and protein, and prevented the binding of THRβ1 to DNA[5]. Treatment of H460 cells with 250μM Farnesol for 24 hours induced endoplasmic reticulum stress and unfolded protein response, promoted cell apoptosis, accompanied by the activation of MEK1/2[6].

In vivo, Farnesol treatment via oral administration at a dose of 100mg/kg/day for 5 weeks restored the cytokine secretion capacity of peritoneal macrophages in asthmatic mice, and reduced the levels of IL-6, TNF-α and inducible nitric oxide synthase (iNOS)[7]. Oral administration of 50mg/kg Farnesol daily for 5 weeks significantly reduced tumor growth in a prostate cancer mouse model[8].

References:
[1] Chandran S S, Kealey J T, Reeves C D. Microbial production of isoprenoids[J]. Process biochemistry, 2011, 46(9): 1703-1710.
[2] Ghosh S, Howe N, Volk K, et al. Candida albicans cell wall components and farnesol stimulate the expression of both inflammatory and regulatory cytokines in the murine RAW264. 7 macrophage cell line[J]. FEMS Immunology & Medical Microbiology, 2010, 60(1): 63-73.
[3] Jung Y Y, Hwang S T, Sethi G, et al. Potential anti-inflammatory and anti-cancer properties of farnesol[J]. Molecules, 2018, 23(11): 2827.
[4] Yilmaz Öztürk B, Feyzullazade N, Dağ İ, et al. The investigation of in vitro effects of farnesol at different cancer cell lines[J]. Microscopy Research and Technique, 2022, 85(8): 2760-2775.
[5] Duncan R E, Archer M C. Farnesol induces thyroid hormone receptor (THR) β1 but inhibits THR-mediated signaling in MCF-7 human breast cancer cells[J]. Biochemical and biophysical research communications, 2006, 343(1): 239-243.
[6] Joo J H, Liao G, Collins J B, et al. Farnesol-induced apoptosis in human lung carcinoma cells is coupled to the endoplasmic reticulum stress response[J]. Cancer research, 2007, 67(16): 7929-7936.
[7] Ku C M, Lin J Y. Farnesol, a sesquiterpene alcohol in herbal plants, exerts anti‐inflammatory and antiallergic effects on ovalbumin‐sensitized and‐challenged asthmatic mice[J]. Evidence‐Based Complementary and Alternative Medicine, 2015, 2015(1): 387357.
[8] Park J S, Kwon J K, Kim H R, et al. Farnesol induces apoptosis of DU145 prostate cancer cells through the PI3K/Akt and MAPK pathways[J]. International journal of molecular medicine, 2014, 33(5): 1169-1176.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

Caco-2 cells

Preparation Method

The growth and maintenance of Caco-2 cells were carried out in a modified Dubecco Eagle medium (DMEM) containing 10% FBS and 1% antibiotics, and the cells were cultured at 37°C, 5% CO2 and humidity conditions. Adjust the cell concentration to 5×104 cells/ml, and inoculate it in 96-well plates at a volume of 100μl/well. Treat the cells with different concentrations of Farnesol (0.01, 0.025, 0.05, 0.1, 0.5, 1, 2, 5, and 10mM) for 24 hours, and then analyze the cell viability.

Reaction Conditions

0.01, 0.025, 0.05, 0.1, 0.5, 1, 2, 5, and 10mM; 24h

Applications

Farnesol treatment inhibited the cell viability of Caco-2 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

Male nude mice

Preparation Method

Five-week-old male nude mice weighing 20-30 grams were raised in a standard sterile environment with a temperature of 23±5℃ and a relative humidity of 40±10%. A density of 5×106 cells/ml of DU145 cells were injected subcutaneously into the lateral abdomen of the nude mice. All mice received oral treatment starting from the day of tumor implantation and continued for 5 weeks. The control group mice were orally administered 0.2ml of corn oil daily for 5 weeks. The treatment group mice were orally administered 50mg/kg of Farnesol daily for 5 weeks, and the tumor growth was analyzed.

Dosage form

50mg/kg/day for 5 weeks; p.o.

Applications

Farnesol treatment significantly decreased the tumor volume in the DU145 cell- xenograft mouse models.

References:
[1] Yilmaz Öztürk B, Feyzullazade N, Dağ İ, et al. The investigation of in vitro effects of farnesol at different cancer cell lines[J]. Microscopy Research and Technique, 2022, 85(8): 2760-2775.
[2] Park J S, Kwon J K, Kim H R, et al. Farnesol induces apoptosis of DU145 prostate cancer cells through the PI3K/Akt and MAPK pathways[J]. International journal of molecular medicine, 2014, 33(5): 1169-1176.

وثائق المنتج (Product Documents)

Purity:>99.00%Appearance:A Liquid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
4602-84-0
المرادفات
Farnesol, FCI 119a, NSC 60597
SMILES
C/C(C)=C\CC/C(C)=C/CC/C(C)=C/CO
الصيغة الجزيئية
C15H26O
الوزن الجزيئي
222.37
الذوبانية
DMF: 20 mg/ml,DMSO: 10 mg/ml,Ethanol: 30 mg/ml,Ethanol:PBS (pH 7.2) (1:3): 0.25 mg/ml
التخزين
4°C, protect from light
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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