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  • α-环氧蒎烷

    alpha-Pinene oxide

    α-环氧蒎烷
    产品编号 CFN70073
    CAS编号 1686-14-2
    分子式 = 分子量 C10H16O = 152.2
    产品纯度 >=98%
    物理属性 Oil
    化合物类型 Monoterpenoids
    植物来源 The essential oil of Lavandula stoechas
    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
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    产品名称 产品编号 CAS编号 包装 QQ客服
    α-环氧蒎烷 CFN70073 1686-14-2 10mg QQ客服:1457312923
    α-环氧蒎烷 CFN70073 1686-14-2 20mg QQ客服:1457312923
    α-环氧蒎烷 CFN70073 1686-14-2 50mg QQ客服:1457312923
    α-环氧蒎烷 CFN70073 1686-14-2 100mg QQ客服:1457312923
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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
  • Hamdard University (India)
  • Universidad de La Salle (Mexico)
  • University of Liège (Belgium)
  • Washington State University (USA)
  • Nanjing University of Chinese Medicine (China)
  • Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
  • Sapienza University of Rome (Italy)
  • Max Rubner-Institut (MRI) (Germany)
  • Institute of Chinese Materia Medica (China)
  • Universidade Federal de Pernambuco (UFPE) (Brazil)
  • Nicolaus Copernicus Uniwersity (Poland)
  • University of Minnesota (USA)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • MTT Agrifood Research Finland (Finland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Food Res Int.2017, 96:40-45
  • Int. J of Herbal Med.2023, 11(1): 06-14
  • Int J Mol Sci.2019, 20(11):E2734
  • Food Chem.2019, 275:746-753
  • Plants (Basel).2021, 10(12):2795.
  • Front Pharmacol.2021, 12:635510.
  • Sci Rep.2019, 9:12132
  • Nutrients2020, 12(3):811.
  • Asian J Beauty Cosmetol2019, 17(3):287-294
  • Phytomedicine.2022, 96:153877.
  • Plants2022, 11(3),294.
  • Front Pharmacol.2023, 14:1095083.
  • Emirates Journal of Food and Agriculture.2022, 34(6): 528-536.
  • Pharmaceuticals (Basel).2020, 13(9):262.
  • Evid Based Complement Alternat Med.2016, 2016:4357656
  • Anal Bioanal Chem.2018, 410(5):1561-1569
  • Univerzita Karlova2021, 20.500.11956.
  • Antioxidants (Basel).2022, 11(12):2327.
  • Food Chem.2021, 337:128023.
  • Evid Based Complement Alternat Med.2018, 2018:4580627
  • J Sep Sci.2018, 41(11):2488-2497
  • Phytother Res.2022, 10.1002:ptr.7626.
  • Fitoterapia.2015, 100:179-86
  • ...
  • 生物活性
    Description: alpha-Pinene oxide shows low levels of inhibition on bacterial activities in nature.
    In vitro:
    Applied Microbiology & Biotechnology, 2003, 60(5):534-40.
    Optimization of isonovalal production from alpha-pinene oxide using permeabilized cells of Pseudomonas rhodesiae CIP 107491.[Pubmed: 12536252]

    METHODS AND RESULTS:
    Optimization studies on the synthesis of isonovalal from alpha-pinene oxide by Pseudomonas rhodesiae CIP 107491 operated in a biphasic medium are presented. Three key parameters are identified. The first is the need for a permeabilization of cells by freezing them and then treating the thawed material with an organic solvent such as chloroform, toluene or diethyl ether. This operation allows both enzyme release into the aqueous phase outside the cells and an improvement in the transport properties of both substrate and product across the cell membrane, strongly increasing reaction rates. The second is that the enzyme alpha-pinene oxide lyase, which exhibits an irreversible inactivation by isonovalal (or a by-product), presents a constant turn-over, i.e., the total product synthesis is proportional to the biomass loading and is close to 108 mmol (16.4 g) isonovalal l(-1) g(-1) biomass. The third phenomenon is that the biphasic system used is not phase-transfer-limited, a feature attributed to the spontaneous formation of an oil-in-water emulsion.
    CONCLUSIONS:
    It is thus possible to carry out a very efficient process, allowing the recovery of 2.63 mol isonovalal l(-1) (400 g l(-1)) from 25 g biomass l(-1) in 2.5 h, corresponding to an average reaction rate as high as 0.70 mmol min(-1) g(-1) cells (160 g l(-1) h(-1)).
    Appl.environ.microbiol, 1998, 64(9):520-525.
    Effect of selected monoterpenes on methane oxidation, denitrification, and aerobic metabolism by bacteria in pure culture.[Pubmed: 9464387]

    METHODS AND RESULTS:
    Selected monoterpenes inhibited methane oxidation by methanotrophs (Methylosinus trichosporium OB3b, Methylobacter luteus), denitrification by environmental isolates, and aerobic metabolism by several heterotrophic pure cultures. Inhibition occurred to various extents and was transient. Complete inhibition of methane oxidation by Methylosinus trichosporium OB3b with 1.1 mM (-)-alpha-pinene lasted for more than 2 days with a culture of optical density of 0.05 before activity resumed. Inhibition was greater under conditions under which particulate methane monooxygenase was expressed. No apparent consumption or conversion of monoterpenes by methanotrophs was detected by gas chromatography, and the reason that transient inhibition occurs is not clear. Aerobic metabolism by several heterotrophs was much less sensitive than methanotrophy was; Escherichia coli (optical density, 0.01), for example, was not affected by up to 7.3 mM (-)-alpha-pinene. The degree of inhibition was monoterpene and species dependent. Denitrification by isolates from a polluted sediment was not inhibited by 3.7 mM (-)-alpha-pinene, gamma-terpinene, or beta-myrcene, whereas 50 to 100% inhibition was observed for isolates from a temperate swamp soil. The inhibitory effect of monoterpenes on methane oxidation was greatest with unsaturated, cyclic hydrocarbon forms [e.g., (-)-alpha-pinene, (S)-(-)-limonene, (R)-(+)-limonene, and gamma-terpinene].
    CONCLUSIONS:
    Lower levels of inhibition occurred with oxide and alcohol derivatives [(R)-(+)-limonene oxide, alpha-pinene oxide, linalool, alpha-terpineol] and a noncyclic hydrocarbon (beta-myrcene). Isomers of pinene inhibited activity to different extents. Given their natural sources, monoterpenes may be significant factors affecting bacterial activities in nature.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.5703 mL 32.8515 mL 65.703 mL 131.406 mL 164.2576 mL
    5 mM 1.3141 mL 6.5703 mL 13.1406 mL 26.2812 mL 32.8515 mL
    10 mM 0.657 mL 3.2852 mL 6.5703 mL 13.1406 mL 16.4258 mL
    50 mM 0.1314 mL 0.657 mL 1.3141 mL 2.6281 mL 3.2852 mL
    100 mM 0.0657 mL 0.3285 mL 0.657 mL 1.3141 mL 1.6426 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
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    去氢二松柏醇 4-O-葡萄糖苷; Dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside CFN89430 107870-88-2 C26H32O11 = 520.52 5mg QQ客服:1413575084

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