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  • 委陵菜酸

    Tormentic acid

    委陵菜酸
    产品编号 CFN99434
    CAS编号 13850-16-3
    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 herbs of Potentilla tormentilla
    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
    委陵菜酸 CFN99434 13850-16-3 1mg QQ客服:3257982914
    委陵菜酸 CFN99434 13850-16-3 5mg QQ客服:3257982914
    委陵菜酸 CFN99434 13850-16-3 10mg QQ客服:3257982914
    委陵菜酸 CFN99434 13850-16-3 20mg QQ客服:3257982914
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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
  • University of Hertfordshire (United Kingdom)
  • University of Dicle (Turkey)
  • Leibniz-Institut für Pflanzenbiochemie (IPB) (Germany)
  • Texas A&M University (USA)
  • Michigan State University (USA)
  • Universiti Putra Malaysia(UPM) (Malaysia)
  • Kitasato University (Japan)
  • Georgia Institute of Technology (USA)
  • Chungnam National University (Korea)
  • Wageningen University (Netherlands)
  • University of Pretoria (South Africa)
  • University of Malaya (Malaysia)
  • National Cancer Center Research Institute (Japan)
  • Gyeongsang National University (Korea)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Phytomedicine.2019, 61:152813
  • Molecules.2023, 28(2):727.
  • Oxid Med Cell Longev.2022, 2022:5888636.
  • ACS Omega.2021, 6(36):23460-23474.
  • Int J Vitam Nutr Res.2022, doi: 10.1024.
  • Molecules.2021, 26(6):1635.
  • Med Sci Monit.2019, 25:9499-9508
  • Neurochem Int.2023, 167:105537.
  • Institute of Food Science & Technology2021, 18 December.
  • Asian J of Pharmaceutical&Clinical 2018, 11(2)
  • J Sep Sci.2021, 44(22):4064-4081.
  • LWT-Food Sci Technol2020, 109163
  • Mol Biol Rep.2023, 50(5):4029-4038.
  • Int J Mol Sci.2015, 16(1):1232-51
  • Life Sci.2023, 332:122107.
  • ACS Pharmacol.Transl.Sci.2024, 4c00003.
  • iScience.2020, 23(2):100849.
  • Agronomy2023, 13(9), 2410.
  • Molecules.2024, 29(6):1392.
  • Pharmaceutics.2021, 13(7):1028.
  • Chem Biol Interact.2019, 298:1-7
  • Molecules.2022, 27(19):6651.
  • Process Biochemistry2019, 87:213-220
  • ...
  • 生物活性
    Description: Tormentic acid has anticancer, anti-inflammatory, anti-atherogenic , anti-allodynic, and hepatoprotective properties, it can inhibit markedly the neuropathic allodynia induced by partial ligation of the sciatic nerve. Tormentic acid potently inhibits the production of nitric oxide (NO) in RAW 264.7 cells, also suppresses the LPS-stimulated degradation and phosphorylation of inhibitor of kappa B-α (IκB-α), suggests that the anti-inflammatory activity of TA is associated with the down-regulation of iNOS, COX-2, and TNF-α through the negative regulation of the NF-κB pathway in RAW 264.7 cells.
    Targets: NO | HO-1 | GLUT | NOS | NF-kB | Bcl-2/Bax | Caspase | COX | IL Receptor | PGE | PPAR | TNF-α | AMPK
    In vivo:
    Int Immunopharmacol. 2014 Apr;19(2):365-72.
    Protective effect of tormentic acid from Potentilla chinensis against lipopolysaccharide/D-galactosamine induced fulminant hepatic failure in mice.[Pubmed: 24560903]
    A compound was isolated from Potentilla chinensis, and it was identified as Tormentic acid (TA) based on its physicochemical properties and spectral data.
    METHODS AND RESULTS:
    The hepatoprotective effect of Tormentic acid was evaluated using an acute liver failure model induced by lipopolysaccharide (LPS)/D-galactosamine (D-GalN). The results revealed that Tormentic acid significantly prevented LPS/D-GalN-induced fulminant hepatic failure, as evidenced by the decrease in serum aminotransferase and total bilirubin activities and the attenuation of histopathological changes. Tormentic acid alleviated the pro-inflammatory cytokines including TNF-α and NO/iNOS by inhibiting nuclear factor-κB (NF-κB) activity. Moreover, Tormentic acid strongly inhibited lipid peroxidation, recruited the anti-oxidative defense system, and increased HO-1 activity. In addition, Tormentic acid significantly attenuated increases in TUNEL-positive hepatocytes through decreasing the levels of cytochrome c, as well as caspases-3, 8 and 9, while augmenting the expression of Bcl-2.
    CONCLUSIONS:
    In conclusion, Tormentic acid protects hepatocytes against LPS/D-GalN-induced injury by blocking NF-κB signaling pathway for anti-inflammatory response and attenuating hepatocellular apoptosis. Consequently, Tormentic acid is a potential agent for preventing acute liver injury and may be a major bioactive ingredient of Potentilla chinensis.
    Eur J Pharmacol. 2002 Oct 25;453(2-3):203-8.
    Anti-allodynic action of the tormentic acid, a triterpene isolated from plant, against neuropathic and inflammatory persistent pain in mice.[Pubmed: 12398905]

    METHODS AND RESULTS:
    The inhibition observed was 82+/-9% and 100+/-11%, respectively. Interestingly, Tormentic acid did not inhibit paw oedema formation following Complete Freund's Adjuvant plantar injection. Tormentic acid (30 mg/kg, p.o.) and gabapentin (70 mg/kg, p.o.), given twice a day, inhibited markedly the neuropathic allodynia induced by partial ligation of the sciatic nerve, with inhibition of 91+/-19% and 71+/-16%, respectively. The anti-allodynic action of Tormentic acid was not associated with impairment of the motor activity of the animals.
    CONCLUSIONS:
    Together, the present results indicate that Tormentic acid or its derivatives might be of potential interest in the development of new clinically relevant drugs for the management of persistent neuropathic and inflammatory allodynia.
    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
    2-氧代果树酸; 2-氧代坡模醇酸; 2-Oxopomolic acid CFN98920 54963-52-9 C30H46O5 = 486.7 5mg QQ客服:1457312923
    2alpha,19alpha-Dihydroxy-3-oxo-urs-12-en-28-oic acid; 2alpha,19alpha-Dihydroxy-3-oxo-urs-12-en-28-oic acid CFN89112 176983-21-4 C30H46O5 = 486.69 5mg QQ客服:2159513211
    覆盆子酸; Fupenzic acid CFN99311 119725-20-1 C30H44O5 = 484.7 5mg QQ客服:2056216494
    Negundonorin A; Negundonorin A CFN96848 1401618-51-6 C29H40O5 = 468.63 5mg QQ客服:3257982914
    1-beta-羟基蔷薇酸; 1beta-Hydroxyeuscaphic acid CFN92609 120211-98-5 C30H48O6 = 504.7 5mg QQ客服:3257982914
    1,2,3,19-四羟基-12-乌苏烯-28-酸; 1,2,3,19-Tetrahydroxy-12-ursen-28-oic acid CFN99233 113558-03-5 C30H48O6 = 504.7 5mg QQ客服:2159513211
    1-羟基-2-氧代果树酸; 1-Hydroxy-2-oxopomolic acid CFN98080 217466-37-0 C30H46O6 = 502.7 5mg QQ客服:1457312923
    3-O-顺式对香豆酰委陵菜酸; 3-O-cis-p-Coumaroyltormentic acid CFN92211 121072-40-0 C39H54O7 = 634.9 5mg QQ客服:2056216494
    蔷薇酸; 野鸦椿酸; Euscaphic acid CFN98888 53155-25-2 C30H48O5 = 488.7 5mg QQ客服:3257982914
    2,3-Di-O-methylthiomethyleuscaphic acid; 2,3-Di-O-methylthiomethyleuscaphic acid CFN97578 N/A C34H56O5S2 = 609.0 5mg QQ客服:2056216494

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