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  • 洋椿苦素

    Cedrelone

    洋椿苦素
    产品编号 CFN99368
    CAS编号 1254-85-9
    分子式 = 分子量 C26H30O5 = 422.5
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The barks of Cedrela toona
    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
    洋椿苦素 CFN99368 1254-85-9 1mg QQ客服:2159513211
    洋椿苦素 CFN99368 1254-85-9 5mg QQ客服:2159513211
    洋椿苦素 CFN99368 1254-85-9 10mg QQ客服:2159513211
    洋椿苦素 CFN99368 1254-85-9 20mg QQ客服:2159513211
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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
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • Medical University of Gdansk (Poland)
  • Ateneo de Manila University (Philippines)
  • National Hellenic Research Foundation (Greece)
  • Universidad Miguel Hernández (Spain)
  • University of East Anglia (United Kingdom)
  • Sri Ramachandra University (India)
  • Universidad Industrial de Santander (Colombia)
  • University of the Basque Country (Spain)
  • Universiti Malaysia Pahang (Malaysia)
  • University of Brasilia (Brazil)
  • Texas A&M University (USA)
  • University of Wollongong (Australia)
  • Kamphaengphet Rajabhat University (Thailand)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Environ Toxicol.2023, 38(5):1174-1184.
  • HIV Med.2021, 22(8):690-704.
  • J Ethnopharmacol.2016, 192:370-381
  • Int J Mol Sci.2023, 24(4):3682.
  • LWT - Food Science and Technology2022, 164:113627
  • Molecules.2019, 24(11):E2102
  • Int J Mol Sci.2023, 24(18):14077.
  • J Cell Biochem.2024, 125(4):e30537.
  • Dermatologica Sinica2024, 42(1):p19-30.
  • Heliyon.2023, 9(6):e16138.
  • J Bone Miner Res.2017, 32(12):2415-2430
  • Food Analytical Methods2020, 13,1603-1612(2020)
  • Aquaculture2019, 510:392-399
  • Integr Med Res.2021, 10(3):100723.
  • J AOAC Int.2023, 106(1):56-64.
  • PLoS One.2015, 10(5):e0127060
  • Evid-Based Compl Alt2020, 7202519:13
  • Molecules.2022, 27(4):1412.
  • Molecules.2018, 23(9):E2121
  • Pol J Microbiol.2021, 70(1):117-130.
  • Molecules2022, 27(12):3903.
  • The Thai Journal of Pharmaceutical Sciences2023, 47(3):3.
  • Chemistry of Vegetable Raw Materials2019, 3:119-127
  • ...
  • 生物活性
    Description: Cedrelone exhibits antifeedant activity, it has insecticidal activity, it inhibits arval growth of P. saucia, and the molting of the milkweed bug, Oncopeltus fasciatus. Cedrelone and its derivatives exert antimicrobial activities, bromohydroxy cedrelone and Michael adduct show good antifungal activity. Cedrelone is also a very potent inducer of apoptosis, it can cause cell cycle arrest, it shows significant cytotoxicity against cancer cell lines, such as -60, SMMC-7721, A-549, MCF-7 and SW480.
    Targets: MMP(e.g.TIMP) | Antifection
    In vitro:
    Anticancer Agents Med Chem. 2013 Dec;13(10):1645-53.
    Effects of limonoid cedrelone on MDA-MB-231 breast tumor cells in vitro.[Pubmed: 23869780]
    Cancer is the second leading cause of death, preceded only by cardiovascular diseases, and there is epidemiological evidence that demonstrate this tendency is emerging worldwide.
    METHODS AND RESULTS:
    Brazil has an extensive vegetal biodiversity with more than 55,000 species listed. Such biodiversity collaborates with the finding of compounds which could be the basis for the design of new anti-tumor drugs, with fewer side effects than the conventional chemotherapy used currently. Cedrelone is a limonoid isolated from Trichilia catigua (Meliaceae) which is a native Brazilian plant. This study demonstrates that Cedrelone inhibits proliferation, adhesion, migration and invasion of breast tumor cells from the line MDA-MB-231. The effects of cell migration and invasion on MDA-MB-231 cell may be explained, at least in part, by the ability of Cedrelone to inhibit MMP activity. We also demonstrate that Cedrelone is able to induce apoptosis in MDA-MB-231 cells.
    CONCLUSIONS:
    There are only a few works investigating the effect of limonoids in cellular processes closely related to tumor progression such as adhesion, migration and invasion. To the best of our knowledge, this is the first work describing the effects of a limonoid on tumor and non-tumor cell adhesion process.
    Photochem Photobiol. 2000 Oct;72(4):464-6.
    Photooxidation of cedrelone, a tetranortriterpenoid from Toona ciliata.[Pubmed: 11045715]

    METHODS AND RESULTS:
    Cedrelone, a tetranortriterpenoid on photolysis by UV light yields a true photooxidation product 3 [14 beta,15beta,22beta,23beta-diepoxy-6-hydroxy-1,5, 20(22)-meliatriene-2,7,21-trione] whose structure is well established by NMR studies and confirmed by X-ray crystallography, along with product 4 [14 beta,15beta-epoxy-6,23-dihydroxy-1,5,20(22)-meliatriene-2,7, 21-trione]. Addition of rose bengal increases the rate of photooxidation whereas DABCO decreases rate of photolysis proving the involvement of singlet oxygen in the photooxygenation.
    CONCLUSIONS:
    Both the photoproducts exhibited antifeedant activity.
    Int. J. Drug Develop.Res.,2012, 4(4):385-92.
    Semisynthetic Modification of Cedrelone and its Antimicrobial Activity.[Reference: WebLink]

    METHODS AND RESULTS:
    Cedrelone was isolated from Toona ciliata heart wood and the compound was modified with various chemical reagents and the resultant product was characterized by IR, 1H NMR, 13C NMR and Mass spectra. The synthesized compounds were screened for antimicrobial activities and the zone of inhibition was ascertained by disc diffusion method. The microorganisms selected for the study was Gram positive organisms such as a) Staphylococcus aureus (ATCC 9144), b) Staphylococcus epidermitis (ATCC 155), c) Bacillus subtilis (ATCC 6633), d) Bacillus cereus (ATCC 11778), e) Micrococcus luteus (ATCC 46789) and Gram negative organisms a) Escherichia coli (ATCC 25922), b) Pseudomonas aeruginosa (ATCC 9027). Fungi organism a) Candida albicans (ATCC 1091), b) Aspergillus niger (ATCC 6275).
    CONCLUSIONS:
    Cedrelone and its derivatives exerted pronounced inhibitory response against all the species of bacterial organism tested, except E. coli. Bromohydroxy Cedrelone and Michael adduct showed good antifungal activity.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3669 mL 11.8343 mL 23.6686 mL 47.3373 mL 59.1716 mL
    5 mM 0.4734 mL 2.3669 mL 4.7337 mL 9.4675 mL 11.8343 mL
    10 mM 0.2367 mL 1.1834 mL 2.3669 mL 4.7337 mL 5.9172 mL
    50 mM 0.0473 mL 0.2367 mL 0.4734 mL 0.9467 mL 1.1834 mL
    100 mM 0.0237 mL 0.1183 mL 0.2367 mL 0.4734 mL 0.5917 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
    割舌树内酰胺A; Walsuralactam A CFN96441 1370556-82-3 C26H31NO5 = 437.53 5mg QQ客服:215959384
    洋椿苦素; Cedrelone CFN99368 1254-85-9 C26H30O5 = 422.5 5mg QQ客服:2159513211
    11beta-羟基洋椿苦素; 11beta-Hydroxycedrelone CFN98345 283174-18-5 C26H30O6 = 438.5 5mg QQ客服:2159513211
    Walsuronoid B; Walsuronoid B CFN97517 942582-15-2 C26H30O6 = 438.5 5mg QQ客服:1413575084
    1,3-Diacetylvilasinin; 1,3-Diacetylvilasinin CFN97682 78012-28-9 C30H40O7 = 512.64 5mg QQ客服:1413575084
    川楝素; Toosendanin CFN99908 58812-37-6 C30H38O11 = 574.62 20mg QQ客服:2056216494

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