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  • α-己基肉桂醛

    alpha-Hexylcinnamaldehyde

    α-己基肉桂醛
    产品编号 CFN70003
    CAS编号 101-86-0
    分子式 = 分子量 C15H20O = 216.3
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Phenols
    植物来源
    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
    α-己基肉桂醛 CFN70003 101-86-0 10mg QQ客服:1413575084
    α-己基肉桂醛 CFN70003 101-86-0 20mg QQ客服:1413575084
    α-己基肉桂醛 CFN70003 101-86-0 50mg QQ客服:1413575084
    α-己基肉桂醛 CFN70003 101-86-0 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
  • Aarhus University (Denmark)
  • Molecular Biology Institute of Barcelona (IBMB)-CSIC (Spain)
  • University of East Anglia (United Kingdom)
  • University of Pretoria (South Africa)
  • Washington State University (USA)
  • Lund University (Sweden)
  • University of Eastern Finland (Finland)
  • Monash University Sunway Campus (Malaysia)
  • Tohoku University (Japan)
  • University of the Basque Country (Spain)
  • University Medical Center Mainz (Germany)
  • University of Minnesota (USA)
  • Heinrich-Heine-University Düsseldorf (Germany)
  • Stanford University (USA)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Front Pharmacol.2021, 12:765521.
  • J Microbiol Biotechnol.2022, 32(2):141-148.
  • Nat Prod Sci.2019, 25(3):238
  • Int J Mol Sci.2023, 25(1):283.
  • Analytical Methods2018, 10(27)
  • Heliyon.2022, 8(12):e12031.
  • Fitoterapia.2021, 153:104995.
  • Applied Biological Chemistry2023, 66:8
  • Environ Toxicol.2023, tox.23999.
  • Food Chem.2021, 337:128023.
  • Sci Rep.2019, 9(1):4646
  • Ind Crops Prod.2014, 62:173-178
  • PLoS One.2017, 12(3):e0173585
  • Bioorg Chem.2024, 145:107182.
  • J Chromatogr Sci.2020, 58(6):485-493.
  • Horticulture Research2022, uhac276.
  • Life Sci.2018, 209:498-506
  • Front Pharmacol.2017, 8:673
  • Food Funct.2020, 11(2):1322-1333.
  • Front Pharmacol.2021, 12:690113.
  • Indian J Pharm Sci.2022, 84(3):144-151
  • The Journal of Agromedicine and Medical Sciences2018, 4(1)
  • VNU Journal of Science2023, 39(2):24-33.
  • ...
  • 生物活性
    Description: alpha-Hexylcinnamaldehyde and p-tert-butyl-alpha-methylhydrocinnamic aldehyde are synthetic aldehydes, characterized by a typical floral scent, which makes them suitable to be used as fragrances in personal care (perfumes, creams, shampoos, etc.) and household products, and as flavouring additives in food and pharmaceutical industry. alpha-Hexylcinnamaldehyde is a weak allergen.
    In vitro:
    Regulatory Toxicology & Pharmacology, 2014, 68(1):16-22.
    Genotoxicity assessment of some cosmetic and food additives.[Pubmed: 24239523]
    alpha-Hexylcinnamaldehyde (HCA) and p-tert-butyl-alpha-methylhydrocinnamic aldehyde (BMHCA) are synthetic aldehydes, characterized by a typical floral scent, which makes them suitable to be used as fragrances in personal care (perfumes, creams, shampoos, etc.) and household products, and as flavouring additives in food and pharmaceutical industry. The aldehydic structure suggests the need for a safety assessment for these compounds. Here, HCA and BMHCA were evaluated for their potential genotoxic risk, both at gene level (frameshift or base-substitution mutations) by the bacterial reverse mutation assay (Ames test), and at chromosomal level (clastogenicity and aneuploidy) by the micronucleus test.
    METHODS AND RESULTS:
    In order to evaluate a primary and repairable DNA damage, the comet assay has been also included. In spite of their potential hazardous chemical structure, a lack of mutagenicity was observed for both compounds in all bacterial strains tested, also in presence of the exogenous metabolic activator, showing that no genotoxic derivatives were produced by CYP450-mediated biotransformations. Neither genotoxicity at chromosomal level (i.e. clastogenicity or aneuploidy) nor single-strand breaks were observed.
    CONCLUSIONS:
    These findings will be useful in further assessing the safety of HCA and BMHCA as either flavour or fragrance chemicals.
    In vivo:
    Toxicol Appl Pharmacol, 1999, 159(2):142-151.
    Selective Modulation of B-Cell Activation Markers CD86 and I-Ak on Murine Draining Lymph Node Cells Following Allergen or Irritant Treatment.[Reference: WebLink]
    It is well known that T cells are key effector cells in the development of allergic contact dermatitis. However, we and others have shown that mice exposed to contact allergens show a preferential increase in B lymphocytes in the draining lymph nodes (DLN) as seen by an increase in the percentage of B220 or IgG/IgM cells.
    METHODS AND RESULTS:
    The purpose of the present investigation was to determine whether chemical allergens, in contrast to irritants, would modulate B-cell activation markers, CD86 and I-Ak, on B cells isolated from DLN of treated mice using the local lymph node assay (LLNA) protocol. Mice were treated on the ears for 3 consecutive days with concentrations of allergens (1-chloro-2,4-dinitrobenzene, alpha-Hexylcinnamaldehyde, 4-ethoxymethylene-2-phenyl-2-oxazoline-5-one, and trinitrochlorobenzene), or irritants (benzalkonium chloride and sodium lauryl sulfate), which caused an increase in the number of DLN cells. The DLN were excised 72 h following the final chemical treatment, and the cells were prepared for analysis by flow cytometry. In mice treated with allergens an increase in the median intensity of I-AK and CD86 on B220 or IgG/IgM B cells was observed compared to mice treated with irritants or vehicles. Mice treated with allergens demonstrated an increase in the median intensity of CD86 on B220 B cells that was dose dependent and peaked at 72 h following the final allergen treatment. The increase in the median intensity of I-AK also was dose dependent but peaked at 96 h. Finally, T and B cells isolated from both allergen- and irritant-treated mice demonstrated an increase in [3H]thymidine incorporation compared to vehicle-treated and naı̈ve mice at 72 h following the final chemical treatment.
    CONCLUSIONS:
    The results suggest that B cells isolated from DLN of allergen-treated mice are activated and proliferating. Analysis of B-cell activation markers may be useful in differentiating allergen and irritant responses in the draining lymph nodes of chemically treated mice.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 4.6232 mL 23.116 mL 46.2321 mL 92.4642 mL 115.5802 mL
    5 mM 0.9246 mL 4.6232 mL 9.2464 mL 18.4928 mL 23.116 mL
    10 mM 0.4623 mL 2.3116 mL 4.6232 mL 9.2464 mL 11.558 mL
    50 mM 0.0925 mL 0.4623 mL 0.9246 mL 1.8493 mL 2.3116 mL
    100 mM 0.0462 mL 0.2312 mL 0.4623 mL 0.9246 mL 1.1558 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
    4',5-二甲基槲皮素; 4',5-Di-O-methyl quercetin CFN91810 100648-56-4 C17H14O7 = 330.3 5mg QQ客服:1413575084
    新化合物32; New compound 32 CFN95700 N/A C39H50O21 = 854.8 5mg QQ客服:1457312923
    5-表紫草氰苷; 5-Epilithospermoside CFN97404 84799-31-5 C14H19NO8 = 329.3 5 mg QQ客服:2159513211
    13-O-Cinnamoylbaccatin III ; 13-O-Cinnamoylbaccatin III CFN89044 220932-65-0 C40H44O12 = 716.77 5mg QQ客服:215959384

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