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  • Conocarpan

    Conocarpan

    Conocarpan
    产品编号 CFN98208
    CAS编号 221666-27-9
    分子式 = 分子量 C18H18O2 = 266.3
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Lignans
    植物来源 The woods of Conocarpus erectus
    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
    Conocarpan CFN98208 221666-27-9 1mg QQ客服:2056216494
    Conocarpan CFN98208 221666-27-9 5mg QQ客服:2056216494
    Conocarpan CFN98208 221666-27-9 10mg QQ客服:2056216494
    Conocarpan CFN98208 221666-27-9 20mg QQ客服:2056216494
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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
  • Regional Crop Research Institute (Korea)
  • National Cancer Institute (USA)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • Shanghai University of TCM (China)
  • Aarhus University (Denmark)
  • University of Queensland (Australia)
  • Mahatma Gandhi University (India)
  • Tohoku University (Japan)
  • Srinakharinwirot University (Thailand)
  • Universidade Federal de Goias (UFG) (Brazil)
  • Cornell University (USA)
  • University of Otago (New Zealand)
  • Sanford Burnham Medical Research Institute (USA)
  • Istanbul University (Turkey)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Cell Mol Med.2023, 27(11):1592-1602.
  • Front Immunol.2018, 9:2655
  • Front Pharmacol.2021, 12:764297.
  • Nutrients.2019, 11(11):E2694
  • Molecules.2022, 27(5):1675
  • Phytother Res.2022, 10.1002:ptr.7602.
  • Mol Med Rep.2024, 29(2):26.
  • J Pharm Biomed Anal.2017, 140:274-280
  • Front Microbiol.2022, 13:835463.
  • Invest New Drugs.2017, 35(2):166-179
  • Spectrochim Acta A2019, 210:372-380
  • Curr Eye Res.2018, 43(1):27-34
  • Life (Basel).2021, 11(7):616.
  • Oncol Rep.2016, 35(3):1356-64
  • Appl. Sci. 2021, 11(1),14.
  • Oxid Med Cell Longev.2021, 2021:4883398.
  • Nat Prod Sci.2019, 25(3):238
  • TCI CO.2019, US20190151257A1
  • UDC.2020, 19(4).
  • Acta Chromatographica2021, 00960.
  • Front Plant Sci.2021, 12:673337.
  • Sci Rep. 2017, 12953(7)
  • Molecules.2019, 24(11):E2102
  • ...
  • 生物活性
    Description: Conocarpan has antinociceptive effects. Conocarpan is quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml, it also shows activity against M. tuberculosis (MIC=15.6 ug/ml). Conocarpan shows considerable activity against epimastigote forms of T. cruzi, with 50% inhibition concentrations (IC50) of 8.0 microg/ml.
    Targets: Antifection
    In vitro:
    Mem Inst Oswaldo Cruz. 2003 Dec;98(8):1115-20.
    Antibacterial activity of extracts and neolignans from Piper regnellii (Miq.) C. DC. var. pallescens (C. DC.) Yunck.[Pubmed: 15049100]
    The evaluation of the activity of the aqueous and ethyl acetate extracts of the leaves of Piper regnellii was tested against gram-positive and gram-negative bacteria.
    METHODS AND RESULTS:
    The aqueous extract displayed a weak activity against Staphylococcus aureus and Bacillus subtilis with minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of 1000 micrograms/ml. The ethyl acetate extract presented a good activity against S. aureus and B. subtilis with MIC and MBC at 15.62 micrograms/ml. In contrast to the relative low MICs for gram-positive bacteria, gram-negative bacteria were not inhibited by the extracts at concentrations < or = 1000 mg/ml. The ethyl acetate extract was fractionated on silica gel into nine fractions. The hexane and chloroform fractions were active against S. aureus (MIC at 3.9 micrograms/ml) and B. subtilis (MIC at 3.9 and 7.8 micrograms/ml, respectively). Using bioactivity-directed fractionation, the hexane fraction was rechromatographed to yield the antimicrobial compounds 1, 2, 5, and 6 identified as eupomatenoid-6, eupomatenoid-5, eupomatenoid-3, and Conocarpan, respectively.
    CONCLUSIONS:
    The pure compounds 1 and 2 showed a good activity against S. aureus with MIC of 1.56 micrograms/ml and 3.12 micrograms/ml, respectively. Both compounds presented MIC of 3.12 micrograms/ml against B. subtilis. The pure compound 6 named as Conocarpan was quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml. The antibacterial properties of P. regnellii justify its use in traditional medicine for the treatment of wounds, contaminated through bacteria infections.
    Phytomedicine. 2013 May 15;20(7):600-4.
    Anti-tuberculosis neolignans from Piper regnellii.[Pubmed: 23474218]
    The present study determined the anti-Mycobacterium tuberculosis activities of supercritical CO2 extracts, neolignans eupomatenoid-5 (1), Conocarpan (4) and eupomatenoid-3 (7) and their derivatives (2, 3, 5, 6, and 8) from Piper regnellii, as well as their cytotoxicities.
    METHODS AND RESULTS:
    The supercritical CO2 extract from leaves was purified by chromatographic methods, yielding compounds (1), (4) and (7), which were identified by (1)H NMR and comparison with literature data. Anti-M. tuberculosis activity (H37Rv and clinical isolates) was evaluated using a resazurin microtiter assay plate (REMA) to determine the MIC. The cytotoxicity assay was carried out in macrophages J774G.8 by sulforhodamine B colorimetric assay. The supercritical CO2 extracts from leaves and stems, and compound (4) showed activity against M. tuberculosis (MIC 15.6 μg/ml). Compound (1) showed the best activity (MIC 1.9 μg/ml), with good SI. Compounds (7) and (8) showed low activity against M. tuberculosis H37Rv. The derivative compounds did not show increased anti-M. tuberculosis activity.
    CONCLUSIONS:
    This is the first report, to our knowledge, to describe neolignans from P. regnellii with activity against M. tuberculosis, and compound (1) is a potential candidate for future antituberculosis drugs.
    In vivo:
    J Nat Med. 2010 Oct;64(4):402-8.
    Antinociceptive properties of conocarpan and orientin obtained from Piper solmsianum C. DC. var. solmsianum (Piperaceae).[Pubmed: 20473574 ]

    METHODS AND RESULTS:
    The antinociceptive properties of some fractions and two pure compounds, Conocarpan and orientin, obtained from P. solmsianum leaves were investigated in several models of pain in mice. The results indicated that this plant exhibits a promising antinociceptive profile, as it produces active principles which are several times more active than some reference drugs used for comparison. The main compound tested, orientin, caused potent and dose-dependent effects against acetic acid-induced writhing and capsaicin- and glutamate-induced nociception, being more effective against the first one, with an ID(50) value of 6.5 mg/kg (14.5 micromol/kg). Orientin was about 20-fold more potent than acetylsalicylic acid and 3.5-fold more active than indomethacin.
    CONCLUSIONS:
    The antinociceptive effects of this plant may be attributed, at least partially, to the presence of Conocarpan and, in particular, to the flavonoid orientin.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.7552 mL 18.7758 mL 37.5516 mL 75.1033 mL 93.8791 mL
    5 mM 0.751 mL 3.7552 mL 7.5103 mL 15.0207 mL 18.7758 mL
    10 mM 0.3755 mL 1.8776 mL 3.7552 mL 7.5103 mL 9.3879 mL
    50 mM 0.0751 mL 0.3755 mL 0.751 mL 1.5021 mL 1.8776 mL
    100 mM 0.0376 mL 0.1878 mL 0.3755 mL 0.751 mL 0.9388 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
    Ailanthoidol; Ailanthoidol CFN89428 156398-61-7 C19H18O5 = 326.34 5mg QQ客服:1457312923
    (-)-白玉兰亭B; 玉兰脂B; Denudatin B CFN97599 87402-88-8 C21H24O5 = 356.42 5mg QQ客服:2056216494
    Conocarpan; Conocarpan CFN98208 221666-27-9 C18H18O2 = 266.3 5mg QQ客服:1457312923
    Conocarpan acetate; Conocarpan acetate CFN89302 56319-04-1 C20H20O3 = 308.37 5mg QQ客服:1457312923
    利卡灵A; Licarin A CFN98244 23518-30-1 C20H22O4 = 326.4 5mg QQ客服:1457312923
    去氢二异丁香酚; Dehydrodiisoeugenol CFN99750 2680-81-1 C20H22O4 = 326.39 20mg QQ客服:2056216494
    (-)-利卡灵B; (-)-Licarin B CFN99751 51020-87-2 C20H20O4 = 324.37 3mg QQ客服:1413575084
    Odoratisol A; Odoratisol A CFN90908 891182-93-7 C21H24O5 = 356.41 5mg QQ客服:1413575084
    粗毛淫羊藿苷; Acuminatin CFN98656 41744-39-2 C21H24O4 = 340.4 5mg QQ客服:215959384
    淫羊藿次甙E5; Icariside E5 CFN99373 126176-79-2 C26H34O11 = 522.6 5mg QQ客服:1457312923

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