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  • 松香酸

    Abietic acid

    松香酸
    产品编号 CFN90587
    CAS编号 514-10-3
    分子式 = 分子量 C20H30O2 = 302.45
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The herbs of Pinus massoniana.
    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
    松香酸 CFN90587 514-10-3 10mg QQ客服:1413575084
    松香酸 CFN90587 514-10-3 20mg QQ客服:1413575084
    松香酸 CFN90587 514-10-3 50mg QQ客服:1413575084
    松香酸 CFN90587 514-10-3 100mg QQ客服:1413575084
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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
  • Medizinische Universit?t Wien (Austria)
  • University of Otago (New Zealand)
  • Weizmann Institute of Science (Israel)
  • University of East Anglia (United Kingdom)
  • University of Ioannina (Greece)
  • University of Hawaii Cancer Center (USA)
  • University of Malaya (Malaysia)
  • Center for protein Engineering (CIP) (Belgium)
  • University of Amsterdam (Netherlands)
  • University of Perugia (Italy)
  • Funda??o Universitária de Desenvolvimento (Brazil)
  • Istanbul University (Turkey)
  • University of Minnesota (USA)
  • VIT University (India)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Appl Biol Chem2023, 66:455−461
  • Nat Prod Sci.2018, 24(3):206
  • Plant Cell, Tissue and Organ Culture (PCTOC)2020, 143, 45-60(2020)
  • Biomedicines.2022, 10(2):463.
  • Pharmacological Reports2020, 1-9
  • Int Immunopharmacol.2019, 71:22-31
  • Drug Des Devel Ther.2020, 14:969-976.
  • Polytechnic University of Catalonia2017, 105826
  • Molecules.2016, 21(10)
  • Nature Ecology & Evolution2020, doi: 10.1038
  • Nutrients.2018, 10(12)
  • Phytomedicine.2019, 65:153089
  • J Nat Prod.2022, doi: 10.1021
  • Int. J. of Food Properties2017, S108-S118
  • Clin Transl Oncol.2019, 10.1007
  • J Holistic Integrative Pharm.2023, 4(1):14-28
  • J Sep Sci.2022, 45(18):3556-3566.
  • J Med Food.2022, 25(3):272-280.
  • Antibiotics.2022, 11(4), 510.
  • Biorxiv.2020, doi: 10.1101.
  • Int. J. Mol. Sci.2023, 24(20),15294.
  • Nutr Metab (Lond).2019, 16:31
  • Antioxidants (Basel).2020, 9(6):466.
  • ...
  • 生物活性
    Description: Abietic acid, an abietane diterpenoid, inhibited soybean 5-lipoxygenase with an IC50 of 29.5 ± 1.29 μM.Abietic acid acts as a PPARα/γ dual activator to inhibit UVB-induced MMP-1 expression and age-related inflammation by suppressing NF-κB and the MAPK/AP-1 pathway and can be a useful agent for improving skin photoageing. Abietic acid can be used not only for anti-inflammation but also for regulating lipid metabolism and atherosclerosis.
    Targets: NF-kB | p65 | PPAR | MMP(e.g.TIMP) | MAPK | AP-1 | NO | PGE | COX | IL Receptor
    In vitro:
    J Clin Biochem Nutr. 2010 Mar;46(2):119-25.
    Tetrahydroabietic Acid, a Reduced Abietic Acid, Inhibits the Production of Inflammatory Mediators in RAW264.7 Macrophages Activated with Lipopolysaccharide.[Pubmed: 20216944 ]
    Abietic acid (AA), the main component of the rosin fraction of oleoresin synthesized by conifer species, has been reported to have anti-inflammatory effects. AA is a weak contact allergen; however, compounds resulting from its oxidation by air elicit stronger allergic response. Hydrogenation of the conjugated double bonds of AA, as in tetrahydroabietic acid (THAA), decreases its susceptibility to air oxidation and would thus reduce the allergenicity of AA. The aim of this study was to investigate whether THAA could exert anti-inflammatory effects to the same extent as AA in RAW264.7 macrophages activated with the endotoxin lipopolysaccharide (LPS).
    METHODS AND RESULTS:
    THAA and AA inhibited the production of nitric oxide (NO) and prostaglandin E(2) by suppressing the expression of inducible NO synthase and cyclooxygenase-2, respectively, in LPS-activated RAW264.7 macrophages. They also inhibited the LPS-induced production of interleukin (IL)-1beta, IL-6, and tumor necrosis factor-alpha.
    CONCLUSIONS:
    Both THAA and AA prevented the LPS-induced nuclear translocation of the nuclear factor-kappaB/p65 subunit, suggesting that THAA may inhibit the production of pro-inflammatory mediators through the same mechanism as AA. In comparison, the anti-inflammatory effects of THAA and AA were almost identical, indicating that THAA retains the anti-inflammatory activity of AA at least in LPS-activated RAW264.7 macrophages.
    In vivo:
    J Med Food. 2011 Sep;14(9):1052-6.
    Abietic acid has an anti-obesity effect in mice fed a high-fat diet.[Pubmed: 21812648]
    We investigated the anti-obesity effect of abietic acid in mice fed a high-fat diet with emphasis on changes in adipogenesis in epididymal adipose tissues.
    METHODS AND RESULTS:
    Male C57BL/6J mice were divided into four groups and fed a normal diet, a high-fat diet (HFD), or HFD plus oral administration of abietic acid (20 mg/kg of body weight/day [LA] or 40 mg/kg of body weight/day [HA]) for 8 weeks. Compared with the HFD group, mice orally administered 40 mg of abietic acid/kg of body weight/day exhibited significantly decreased body weight and adipose tissue weights. Serum triglyceride concentrations in the HA group were significantly lower than those in the HFD group, as were the levels of serum insulin and leptin. Hematoxylin and eosin staining revealed that epididymal adipose tissue mass was decreased by abietic acid administration. Abietic acid also inhibited the protein expression of sterol regulatory element-binding protein-1c, CCAAT/enhancer-binding protein α, and CD36 in epididymal adipose tissues, which are up-regulated by HFDs.
    CONCLUSIONS:
    These data demonstrate that abietic acid has an anti-obesity effect in mice mediated by the regulation of adipogenesis.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.3063 mL 16.5317 mL 33.0633 mL 66.1266 mL 82.6583 mL
    5 mM 0.6613 mL 3.3063 mL 6.6127 mL 13.2253 mL 16.5317 mL
    10 mM 0.3306 mL 1.6532 mL 3.3063 mL 6.6127 mL 8.2658 mL
    50 mM 0.0661 mL 0.3306 mL 0.6613 mL 1.3225 mL 1.6532 mL
    100 mM 0.0331 mL 0.1653 mL 0.3306 mL 0.6613 mL 0.8266 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
    Gelomulide N; Gelomulide N CFN96349 1005212-02-1 C24H32O7 = 432.5 5mg QQ客服:215959384
    Gelomulide B; Gelomulide B CFN96293 122537-60-4 C22H28O6 = 388.5 5mg QQ客服:3257982914
    岩大戟内酯B; Jolkinolide B CFN90245 37905-08-1 C20H26O4 = 330.42 20mg QQ客服:3257982914
    岩大戟内酯A; Jolkinolide A CFN92871 37905-07-0 C20H26O3 = 314.4 5mg QQ客服:2159513211
    月腺大戟素A; Ebracteolatanolide A CFN92873 212563-72-9 C20H28O4 = 332.4 5mg QQ客服:3257982914
    月腺大戟素D; Yuexiandajisu D CFN92874 866556-15-2 C20H30O5 = 350.4 5mg QQ客服:2056216494
    月腺大戟素E; Yuexiandajisu E CFN92875 866556-16-3 C20H30O5 = 350.4 5mg QQ客服:1457312923
    岩大戟内酯E; Jolkinolide E CFN92872 54494-34-7 C20H28O2 = 300.4 5mg QQ客服:1413575084
    ent-11alpha-Hydroxyabieta-8(14),13(15)-dien-16,12alpha-olide; ent-11alpha-Hydroxyabieta-8(14),13(15)-dien-16,12alpha-olide CFN89029 130466-20-5 C20H28O3 = 316.44 5mg QQ客服:2159513211
    Phlogacantholide B; Phlogacantholide B CFN89199 830347-16-5 C20H28O4 = 332.44 5mg QQ客服:3257982914

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