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  • 3-乙酰氧基-8(17),13E-劳丹二烯-15-酸

    3-Acetoxy-8(17),13E-labdadien-15-oic acid

    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸
    产品编号 CFN97090
    CAS编号 63399-37-1
    分子式 = 分子量 C22H34O4 = 362.5
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The rhizomes of Cibotium barometz (L.) J.Sm.
    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
    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸 CFN97090 63399-37-1 1mg QQ客服:1413575084
    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸 CFN97090 63399-37-1 5mg QQ客服:1413575084
    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸 CFN97090 63399-37-1 10mg QQ客服:1413575084
    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸 CFN97090 63399-37-1 20mg 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
  • Universidade Federal de Goias (UFG) (Brazil)
  • University of Perugia (Italy)
  • Instituto Politécnico de Bragan?a (Portugal)
  • Sanford Burnham Prebys Medical Discovery Institute (USA)
  • Universidad Miguel Hernández (Spain)
  • University of Wollongong (Australia)
  • Lodz University of Technology (Poland)
  • University of Amsterdam (Netherlands)
  • Texas A&M University (USA)
  • Shanghai Institute of Organic Chemistry (China)
  • Copenhagen University (Denmark)
  • Auburn University (USA)
  • Northeast Normal University Changchun (China)
  • Periyar University (India)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Int J Mol Sci.2022, 23(24):16000.
  • Int J Mol Sci.2019, 20(8):E1855
  • Vietnam J. Chemistry2022, 60(2):211-222
  • Evid Based Complement Alternat Med.2018, 2018:1073509
  • Cell Prolif.2021, 54(8):e13083.
  • Biochem Pharmacol.2017, 130:10-20
  • United States Patent Application2020, 20200038363
  • Evid Based Complement Alternat Med.2016, 2016:4357656
  • Journal of Molecular Liquids2021, 334:116014.
  • JOTCSA.2023, 10(4); 893-902.
  • Molecules.2021, 26(9):2526.
  • Phytomedicine.2015, 22(11):1027-36
  • Phytother Res.2016, 30(12):2020-2026
  • VNU Journal of Science: Med.& Pharm. Sci.2022, 38(2):2588-1132.
  • Nanjing University of Chinese Medicine2022, 345930.
  • J Sep Sci.2018, 41(9):1938-1946
  • Indian J Pharm Sci.2022, 84(4): 874-882.
  • Biomed Chromatogr.2019, 8:e4774
  • J Pharm Biomed Anal2016, 118:183-194
  • Molecules2022, 27(3),1140.
  • Molecules.2018, 23(3):E615
  • Biochem Biophys Res Commun.2019, 518(4):732-738
  • J of Dentistry & Oral Health2019, 2641-1962
  • ...
  • 生物活性
    Description: ent-3-Acetoxy-labda-8(17),13-dien-15-oic acid have vasorelaxant and hypotensive actions, the mechanisms underlying the cardiovascular actions of the labdane involve the activation of the endothelial NO-cGMP pathway, the opening of K+ channels and the alteration on Ca2+ mobilization.
    Targets: Calcium Channel | cAMP | Potassium Channel | NO
    In vivo:
    Eur J Pharmacol. 2014 Mar 5;726:66-76.
    Mechanisms underlying the vascular and hypotensive actions of the labdane ent-3-acetoxy-labda-8(17),13-dien-15-oic acid.[Pubmed: 24463178 ]
    We investigated the mechanisms underlying the vasorelaxant and hypotensive actions of the labdane-type diterpene ent-3-acetoxy-labda-8(17),13-dien-15-oic acid (3-Acetoxy-8(17),13E-labdadien-15-oic acid,labda-15-oic acid).
    METHODS AND RESULTS:
    Vascular reactivity experiments were performed in aortic rings isolated from male Wistar rats. cAMP and cGMP were measured by enzyme immunoassay (EIA) whereas nitrate measurement was performed by chemiluminescence. Nitric oxide (NO) concentration ([NO]c) was measured in endothelial cells by flow cytometry. The cytosolic calcium concentration ([Ca2+]c) in vascular smooth muscle cells (VSMC) was measured by confocal microscopy. Blood pressure measurements were performed in conscious rats. Labda-15-oic acid inhibited the contraction induced by phenylephrine and serotonin in either endothelium-intact or endothelium-denuded rat aortic rings. The labdane significantly reduced CaCl2-induced contraction in a Ca2+-free solution containing KCl or phenylephrine. Labda-15-oic acid (0.1–300 μmol/l) concentration-dependently relaxed endothelium-intact and endothelium-denuded aortas pre-contracted with either phenylephrine or KCl. In endothelium-intact rings, the relaxation induced by labda-15-oic acid was affected by L-NAME, 7-nitroindazole, ODQ, hemoglobin, Rp-8-Br-Pet-cGMPS and thapsigargin. Blockade of K+ channels with 4-aminopyridine, apamin, charybdotoxin and glibenclamide affected the relaxation induced by labda-15-oic acid. The labdane increased cGMP and nitrate levels but did not affect cAMP levels in endothelium-intact aortas. Labda-15-oic acid increased [NO]c in endothelial cells and decreased [Ca2+]c in VSMC. The hypotension induced by intravenous administration of labda-15-oic acid (0.3–3 mg/kg) was partially reduced by L-NAME.
    CONCLUSIONS:
    In conclusion, the mechanisms underlying the cardiovascular actions of the labdane involve the activation of the endothelial NO-cGMP pathway, the opening of K+ channels and the alteration on Ca2+ mobilization.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.7586 mL 13.7931 mL 27.5862 mL 55.1724 mL 68.9655 mL
    5 mM 0.5517 mL 2.7586 mL 5.5172 mL 11.0345 mL 13.7931 mL
    10 mM 0.2759 mL 1.3793 mL 2.7586 mL 5.5172 mL 6.8966 mL
    50 mM 0.0552 mL 0.2759 mL 0.5517 mL 1.1034 mL 1.3793 mL
    100 mM 0.0276 mL 0.1379 mL 0.2759 mL 0.5517 mL 0.6897 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
    Coronadiene; Coronadiene CFN92778 1145689-64-0 C17H26O2 = 262.4 5mg QQ客服:3257982914
    15-去甲-14-氧代赖百当-8(17),12-二烯-18-酸; 15-Nor-14-oxolabda-8(17),12-dien-18-oic acid CFN99058 1039673-32-9 C19H28O3 = 304.4 5mg QQ客服:1413575084
    南亚松酸; Junicedric acid CFN89382 41787-69-3 C20H32O4 = 336.46 5mg QQ客服:1457312923
    Zerumin A; Zerumin A CFN92779 176050-48-9 C20H30O3 = 318.5 5mg QQ客服:215959384
    紫背金牛酸,粉背蕨酸; Alepterolic acid CFN97091 63399-38-2 C20H32O3 = 320.5 5mg QQ客服:3257982914
    3-乙酰氧基-8(17),13E-劳丹二烯-15-酸; 3-Acetoxy-8(17),13E-labdadien-15-oic acid CFN97090 63399-37-1 C22H34O4 = 362.5 5mg QQ客服:215959384
    ent-3beta,18-Dihydroxylabda-8(17),13E-dien-15-oic acid; ent-3beta,18-Dihydroxylabda-8(17),13E-dien-15-oic acid CFN89391 99624-39-2 C20H32O4 = 336.46 5mg QQ客服:3257982914
    9-羟基-13E-赖百当烯-15-酸; 9-Hydroxy-13E-labden-15-oic acid CFN99412 132915-47-0 C20H34O3 = 322.5 5mg QQ客服:1413575084
    二羟丙茶碱B; Coronarin B CFN99303 119188-38-4 C20H30O4 = 334.5 5mg QQ客服:215959384
    Metasequoic acid A; Metasequoic acid A CFN96361 113626-22-5 C20H30O2 = 302.5 5mg QQ客服:1413575084

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