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  • 阿江榄仁酸

    Arjunolic acid

    阿江榄仁酸
    产品编号 CFN98690
    CAS编号 465-00-9
    分子式 = 分子量 C30H48O5 = 488.7
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The fruits of Terminalia chebula Retz.
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    阿江榄仁酸 CFN98690 465-00-9 1mg QQ客服:2932563308
    阿江榄仁酸 CFN98690 465-00-9 5mg QQ客服:2932563308
    阿江榄仁酸 CFN98690 465-00-9 10mg QQ客服:2932563308
    阿江榄仁酸 CFN98690 465-00-9 20mg QQ客服:2932563308
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Florida A&M University (USA)
  • Funda??o Universitária de Desenvolvimento (Brazil)
  • Florida International University (USA)
  • University of Bordeaux (France)
  • Cornell University (USA)
  • University of Medicine and Pharmacy (Romania)
  • University of Ioannina (Greece)
  • University of Madras (India)
  • Korea Institute of Oriental Medicine (Korea)
  • Seoul National University (Korea)
  • University of Perugia (Italy)
  • Uniwersytet Gdański (Poland)
  • Yale University (USA)
  • University of Wuerzburg (Germany)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Phytochemistry Letters2015, 243-247
  • J Pharm Biomed Anal.2016, 129:50-59
  • Food Chem.2016, 191:81-90
  • J Drug Target.2016, 24:1-28
  • Universidade Estadual Paulista2017, 11449
  • J Ethnopharmacol.2017, 198:205-213
  • J Ethnopharmacol.2017, 198:91-97
  • Phytomedicine.2017, 24:77-86
  • Phytomedicine.2018, 38:45-56
  • Mol Cells.2018, 41(8):771-780
  • J Nat Med.2018, 72(3):734-744
  • Journal of Life Science2018, 917-922
  • J of Health Science and Alternative Medicine2019, 1(1)
  • Industrial Crops and Products2019, 140:111612
  • Molecules.2019, 24(11):E2102
  • Molecules.2019, 24(7):E1290
  • Nat Prod Sci.2019, 25(3):238
  • Phytother Res.2019, 33(3):676-689
  • Int J Mol Med.2019, 43(6):2516-2522
  • J Food Sci Technol.2019, 56(5):2712-2720
  • J Agric Food Chem.2019, 67(27):7748-7754
  • Sci Rep.2019, 9(1):4646
  • Food Chem.2020, 313:126079
  • ...
  • 生物活性
    Description: Arjunolic acid has antioxidant, anti-inflammatory, antinociceptive and anticholinesterasic (AChE and BuChE) activities, it may as promising targets for the development of innovative multi-functional medicines for Alzheimer desease treatment.Arjunolic acid protects cardiac tissues from both extrinsic and intrinsic cell death pathways.Arjunolic acid exhibits better protection against histamine release than against acetylcholine release, anti-asthmatic and anaphylactic activity of it may be possibly due to membrane stabilizing potential and inhibition of antigen induced histamine and acetylcholine release. Arjunolic acid protects cardiac tissues from both extrinsic and intrinsic cell death pathways, it also has antitumor activity.
    Targets: TNF-α | IL Receptor | JNK | Caspase | NOS | p38MAPK | ROS | TGF-β/Smad | AChR | Histamine Receptor | Antifection
    In vitro:
    Biochimie. 2013 Jun;95(6):1098-109.
    Arjunolic acid: a new multifunctional therapeutic promise of alternative medicine.[Pubmed: 23402784]
    In recent years, a number of studies describing the effective therapeutic strategies of medicinal plants and their active constituents in traditional medicine have been reported. Indeed, tremendous demand for the development and implementation of these plant derived biomolecules in complementary and alternative medicine is increasing and appear to be promising candidates for pharmaceutical industrial research. These new molecules, especially those from natural resources, are considered as potential therapeutic targets, because they are derived from commonly consumed foodstuff and are considered to be safe for humans.
    METHODS AND RESULTS:
    This review highlights the beneficial role of Arjunolic acid, a naturally occurring chiral triterpenoid saponin, in various organ pathophysiology and the underlying mechanism of its protective action. Studies on the biochemistry and pharmacology suggest the potential use of Arjunolic acid as a novel promising therapeutic strategy. WHAT THE READERS WILL GAIN: The multifunctional therapeutic application of Arjunolic acid has already been documented by its various biological functions including antioxidant, anti-fungal, anti-bacterial, anticholinesterase, antitumor, antiasthmatic, wound healing and insect growth inhibitor activities. The scientific basis behind its therapeutic application as a cardioprotective agent in traditional medicine is justified by its ability to prevent myocardial necrosis and apoptosis, platelet aggregation, coagulation and lowering of blood pressure, heart rate, as well as cholesterol levels. Its antioxidant property coupled with metal chelating property (by its two hydroxyl groups) protects different organs from metal and drug-induced organ pathophysiology. Arjunolic acid also plays a beneficial role in the pathogenesis of diabetes and its associated complications. The mechanism of cytoprotection of Arjunolic acid, at least in part, results from the detoxification of reactive oxygen species (ROS) produced in the respective pathophysiology. In addition to its other biological functions, it also possesses vibrant insecticidal properties and it has the potential to be used as a structural molecular framework for the design of molecular receptors in the general area of supramolecular chemistry and nanochemistry. Esters of Arjunolic acid function as organogelators which has wide application in designing thermochromic switches and sensor devices. Arjunolic acid derived crown ether is an attractive candidate for the design of molecular receptors, biomimetics and supramolecular systems capable of performing some biological functions.
    CONCLUSIONS:
    This review would provide useful information about the recent progress of natural product research in the domain of clinical science. This review also aims to untie the multifunctional therapeutic application of Arjunolic acid, a nanometer-long naturally occurring chiral triterpenoid biomolecule.
    Biomed Pharmacother. 2016 Aug;82:28-34.
    Anti-tumor activity of arjunolic acid against Ehrlich Ascites Carcinoma cells in vivo and in vitro through blocking TGF-β type 1 receptor.[Pubmed: 27470335 ]
    We aimed to evaluate therapeutic potential of arjunolic acid (AA), in Terminalia Arjuna bark, on Ehrlich Ascites carcinoma (EAC) in-vivo and in-vitro. EAC was induced in fifty female Swiss albino mice.
    METHODS AND RESULTS:
    Two doses of AA was used 100 and 250mg/kg. Arjunulic acid reduced tumor volume and cells count. AA decreased EAC cells viability and increased cell toxicity. Moreover, AA reduced TNF-α, IL-1β, TGF-β, TGF-β type I receptor and latency-associated peptide levels associated with elevated IL-10 in-vivo and in-vitro.
    CONCLUSIONS:
    In conclusion, AA produced antitumor activity against EAC by increasing cytotoxicity and apoptosis and partially blocking the TGF-βR1 and affecting inflammatory cytokine levels.
    Nat. Prod. Sci., 2004, 10(5):240-3.
    Antiallergic and anti-asthmatic activities of the alcoholic extract of Terminalia arjuna and arjunolic acid.[Reference: WebLink]
    In the present study, the alcoholic extract of Terminalia arjuna (TA) and Arjunolic acid (AA) were studied for its anti-asthmatic and anaphylactic activity.
    METHODS AND RESULTS:
    Treatment with TA (250 & 500 mg/kg) and AA (50 & 100 mg/kg) has shown significant protection against mast cell disruption in rats induced by compound 48/80. TA and AA also protected the guinea pig against histamine as well as acetylcholine induced bronchospasm. Both TA & AA exhibited better protection against histamine release than against acetylcholine release.
    CONCLUSIONS:
    Anti-asthmatic and anaphylactic activity may be possibly due to membrane stabilizing potential and inhibition of antigen induced histamine and acetylcholine release.
    In vivo:
    Life Sci. 2014 Aug 28;111(1-2):18-26.
    Protective effects of arjunolic acid against cardiac toxicity induced by oral sodium nitrite: effects on cytokine balance and apoptosis.[Pubmed: 25064822]
    Sodium nitrite, a preservative used in meat products, helps in the production of free radicals, leading to increased lipid peroxidation, which plays a vital role in posing toxic effects in different body organs. On the other hand, arjunolic acid possesses antioxidant properties and plays protective roles against chemically induced organ pathophysiology. We investigated the effect of sodium nitrite on cardiac tissue in rats on the inflammatory cytokine balance and the type of induced apoptosis, and we analyzed the protective role of arjunolic acid.
    METHODS AND RESULTS:
    Sixty adult male Sprague-Dawley rats were injected with 80mg/kg sodium nitrite in the presence/absence of arjunolic acid (100 and 200mg/kg). Cardiac pro-inflammatory cytokines (TNF-α and IL-1β), c-reactive protein (CRP) and anti-inflammatory cytokines (IL-4 and IL-10) were measured by ELISA. Cardiac mitochondrial activity (cytochrome-C-oxidase), JNK activation and apoptosis (caspase-3, caspase-8 and caspase-9) were assessed. Sodium nitrite resulted in increased TNF-α (1.6-fold), IL-1β (3.7-fold) and CRP (2.4-fold) levels accompanied by 52%, 59% and 40% reductions in IL-10, IL-4 and cytochrome-C-oxidase, respectively, as well as enhanced JNK, caspase-3, caspase-8 and caspase-9 activities. Arjunolic acid markedly ameliorated these effects.
    CONCLUSIONS:
    Arjunolic acid attenuated sodium nitrite-induced cardiac damage in rats and restored the normal balance between pro- and anti-inflammatory cytokines. Moreover, arjunolic acid protected cardiac tissues from both extrinsic and intrinsic cell death pathways.
    J Biochem Mol Toxicol. 2014 Nov;28(11):515-21.
    Cisplatin-induced testicular toxicity in rats: the protective effect of arjunolic acid.[Pubmed: 25130312 ]

    METHODS AND RESULTS:
    In the present study, the effect of arjunolic acid on testicular damage induced by intraperitoneal injection of rats with 7 mg/kg cisplatin was studied. Cisplatin induced a significant reduction in testicular weights, plasma testosterone, and testicular reduced glutathione levels in addition to a significant elevation of testicular malondialdehyde levels and testicular gene expressions of inducible nitric oxide synthase (iNOS), tumor necrosis factor-α (TNF-α), and p38 mitogen-activated protein kinase (MAPK) when compared with the control group (p < 0.05). Lower tubular diameters and depletion of germ cells and irregular small seminiferous tubules with Sertoli cells only were observed in the cisplatin group. Arjunolic acid administration significantly corrected the changes in both biochemical and histopathological parameters.
    CONCLUSIONS:
    Arjunolic acid plays a significant protective role against cisplatin-induced testicular injury by attenuating oxidative stress parameters along with downregulation of iNOS, TNF-α, and p38-MAPK testicular expressions.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.0462 mL 10.2312 mL 20.4625 mL 40.9249 mL 51.1561 mL
    5 mM 0.4092 mL 2.0462 mL 4.0925 mL 8.185 mL 10.2312 mL
    10 mM 0.2046 mL 1.0231 mL 2.0462 mL 4.0925 mL 5.1156 mL
    50 mM 0.0409 mL 0.2046 mL 0.4092 mL 0.8185 mL 1.0231 mL
    100 mM 0.0205 mL 0.1023 mL 0.2046 mL 0.4092 mL 0.5116 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    Eucalyptolic acid; Eucalyptolic acid CFN92275 189272-68-2 C40H56O7 = 648.9 5mg QQ客服:3257982914
    脱氢山楂酸; Camaldulenic acid CFN96017 71850-15-2 C30H46O4 = 470.7 5mg QQ客服:2159513211
    阿江榄仁酸; Arjunic acid CFN98397 31298-06-3 C30H48O5 = 488.7 5mg QQ客服:1148253675
    阿江榄仁酸; Arjunolic acid CFN98690 465-00-9 C30H48O5 = 488.7 5mg QQ客服:3257982914
    阿江榄仁素; Arjungenin CFN95039 58880-25-4 C30H48O6 = 504.7 10mg QQ客服:2159513211
    3-O-香豆酰阿江榄仁酸; 3-O-Coumaroylarjunolic acid CFN96829 171864-20-3 C39H54O7 = 634.85 5mg QQ客服:215959384
    2,3-二羟基-12-齐墩果烯-28-酸; 2,3-Dihydroxy-12-oleanen-28-oic acid CFN98310 26563-68-8 C30H48O4 = 472.7 5mg QQ客服:215959384
    2,3,23-三羟基-12-齐墩果烯-28-酸; 2,3,23-Trihydroxy-12-oleanen-28-oic acid CFN99041 102519-34-6 C30H48O5 = 488.7 5mg QQ客服:3257982914
    2alpha,3alpha,24-三羟基-12-烯-28-齐墩果酸; 2,3,24-Trihydroxyolean-12-en-28-oic acid CFN99628 150821-16-2 C30H48O5 = 488.7 5mg QQ客服:1148253675
    贝萼皂苷元; 贝萼甙元; Bayogenin CFN90314 6989-24-8 C30H48O5 = 488.70 20mg QQ客服:2932563308

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