GLPBio

Fucoxanthin (all-trans-Fucoxanthin)

Catalog No.: GC31364Purity:>98.00%
Fucoxanthin (all-trans-Fucoxanthin) هو كاروتينويد بحري ويظهر أنشطة مضادة للسمنة ومضادة لمرض السكري ومضاد للأكسدة ومضادة للالتهابات ومضادة للسرطان.

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


Fucoxanthin (all-trans-Fucoxanthin)
Cas No.: 3351-86-8
10mM (in 1mL DMSO)In Stock
$100.00
1
1mgIn Stock
$23.00
1
2mgIn Stock
$34.00
1
5mgIn Stock
$69.00
1
10mgIn Stock
$117.00
1
25mgIn Stock
$233.00
1
50mgIn Stock
$350.00
1
100mgIn Stock
$525.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    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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الوصف (Description)

Fucoxanthin (all-trans-Fucoxanthin) is a naturally occurring carotenoid widely distributed in edible brown seaweed and diatoms[1]. Fucoxanthin is highly unsaturated, its molecular structure is unstable and very active. Fucoxanthin has four isomers, namely all-trans Fucoxanthin (the main isomer in the natural environment), 9′-cis Fucoxanthin, 13-cis Fucoxanthin, and 13′-cis Fucoxanthin[2]. Fucoxanthin can be used in research on obesity, anti-diabetes, antioxidants, inflammation, and cancer[3]. Fucoxanthin can effectively inhibit the activity of Mycobacterium tuberculosis aromatic amine N-acetyltransferase (TBNAT), with an IC50 value of 4.8µM[4].

In vitro, treatment of B16-F10 cells with Fucoxanthin (0-30μM) for 24h inhibited cell invasion, migration and adhesion in a dose-dependent manner, and inhibited the expression of transfer factors MMP-9, CD44 and CXCR4[5]. Treatment of cervical cancer HeLa and SiHa cells with Fucoxanthin (0-25µM) for 24h inhibited cell proliferation and induced cell cycle arrest at the G0/G1 phase[6]. Treatment of RAW264.7 cells with Fucoxanthin (0-100µg/mL) for 24h inhibited the expression of intracellular TNF-α, PGE2, iNOS and COX-2 proteins in a dose-dependent manner[7].

In vivo, oral administration of Fucoxanthin (25, 50mg/kg) to mice with cadmium chloride-induced renal injury for 14 days promoted the recovery of renal function, renal cell microstructure and ultrastructure, significantly reduced blood urea nitrogen (BUN), kidney injury marker 1 (KIM1) and neutrophil gelatinase-associated lipocalin (NGAL) levels in mice, and increased peroxidase (POD), superoxide dismutase (SOD), catalase (CAT) and ascorbate peroxidase (APX) levels[8].

References:
[1] Din N A S, Mohd Alayudin A S, Sofian-Seng N S, et al. Brown algae as functional food source of fucoxanthin: A review[J]. Foods, 2022, 11(15): 2235.
[2] Pajot A, Hao Huynh G, Picot L, et al. Fucoxanthin from algae to human, an extraordinary bioresource: Insights and advances in up and downstream processes[J]. Marine drugs, 2022, 20(4): 222.
[3] Miyashita K, Beppu F, Hosokawa M, et al. Nutraceutical characteristics of the brown seaweed carotenoid fucoxanthin[J]. Archives of biochemistry and biophysics, 2020, 686: 108364.
[4] Šudomová M, Shariati M A, Echeverría J, et al. A microbiological, toxicological, and biochemical study of the effects of fucoxanthin, a marine carotenoid, on Mycobacterium tuberculosis and the enzymes implicated in its cell wall: A link between mycobacterial infection and autoimmune diseases[J]. Marine drugs, 2019, 17(11): 641.
[5] Chung T W, Choi H J, Lee J Y, et al. Marine algal fucoxanthin inhibits the metastatic potential of cancer cells[J]. Biochemical and biophysical research communications, 2013, 439(4): 580-585.
[6] Ye G, Wang L, Yang K, et al. Fucoxanthin may inhibit cervical cancer cell proliferation via downregulation of HIST1H3D[J]. Journal of International Medical Research, 2020, 48(10): 0300060520964011.
[7] Shiratori K, Ohgami K, Ilieva I, et al. Effects of fucoxanthin on lipopolysaccharide-induced inflammation in vitro and in vivo[J]. Experimental eye research, 2005, 81(4): 422-428.
[8] Yang H, Xing R, Liu S, et al. Role of Fucoxanthin towards Cadmium-induced renal impairment with the antioxidant and anti-lipid peroxide activities[J]. Bioengineered, 2021, 12(1): 7235-7247.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

B16-F10 cells

Preparation Method

100μL of 0.2% collagen-fragmented gelatin was applied to the upper side of the filter. Serum-free DMEM (with or without Fucoxanthin (0, 5,10, 30μM)) was added to the lower part of the chamber. The chamber was incubated at 37°C in a 5% CO2 atmosphere for 24h. After incubation, the filter insert was removed from the chamber wells and cells on the upper side of the filter were removed using a cotton swab. The filter was fixed, stained with hematoxylin and eosin, and mounted on a microscope slide. Cells located on the lower side of the filter were counted to determine whether they were invasive cells.

Reaction Conditions

0, 5,10, 30μM; 24h

Applications

Fucoxanthin resulted in a significant decrease in the number of invaded B16-F10 cells.

Animal experiment [2]:

Animal models

Kunming mice

Preparation Method

Total animals (N=120) were randomly divided into two groups of equal average body weight. The mice of the control group (N=20) were given pure water only, whereas the animals of the cadmium exposure group (N=100) were given CdCl2 orally at a dose of 30mg/kg/day for 30 days. In this study, Fucoxanthin was administered at 10, 25 and 50mg/kg/day. To evaluate ameliorative effects of Fucoxanthin on the kidney, the cadmium exposure group was divided into the following five subgroups: without Fucoxanthin treatment as a negative control group (NCG); positive control group (PCG) was mice received Shenfukang tablets orally at a dose of 50mg/kg/day for 14 days; low (F1), medium (F2), and high (F3) Fucoxanthin concentration treated mice were received Fucoxanthin orally at a dose of 10, 25, and 50mg/kg/day for 14 days, respectively. After the 14-day Fucoxanthin treatment, mice were sacrificed. Kidney tissues and peripheral blood samples were collected directly.

Dosage form

10, 25, 50mg/kg/day for 14 days; p.o.

Applications

High doses of Fucoxanthin administration significantly decreased BUN, KIM1, NGAL levels, increasing POD, SOD, CAT, and ascorbate APX levels. Fucoxanthin administration also promoted recovery of the renal functions, micro-structural organization, and ultra-structural organization in the renal cells. 

References:
[1]Chung T W, Choi H J, Lee J Y, et al. Marine algal fucoxanthin inhibits the metastatic potential of cancer cells[J]. Biochemical and biophysical research communications, 2013, 439(4): 580-585.
[2]Yang H, Xing R, Liu S, et al. Role of Fucoxanthin towards Cadmium-induced renal impairment with the antioxidant and anti-lipid peroxide activities[J]. Bioengineered, 2021, 12(1): 7235-7247.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
3351-86-8
SMILES
O=C(/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C([H])=[C@@]=C([C@@]1(O)C)C(C)(C[C@H](OC(C)=O)C1)C)C[C@]2(C3(C)C)[C@@](C)(C[C@@H](O)C3)O2
الصيغة الجزيئية
C42H58O6
الوزن الجزيئي
658.91
الذوبانية
DMSO : ≥ 50 mg/mL (75.88 mM);Water : < 0.1 mg/mL (insoluble)
التخزين
Store at 2-8°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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