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  • 桧木醇

    Hinokitiol

    桧木醇
    产品编号 CFN93995
    CAS编号 499-44-5
    分子式 = 分子量 C10H12O2 = 164.2
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Phenols
    植物来源 The herbs of Platycladus orientalis
    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
    桧木醇 CFN93995 499-44-5 10mg QQ客服:2056216494
    桧木醇 CFN93995 499-44-5 20mg QQ客服:2056216494
    桧木醇 CFN93995 499-44-5 50mg QQ客服:2056216494
    桧木醇 CFN93995 499-44-5 100mg 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
  • Universitas islam negeri Jakarta (Indonesia)
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  • Hamdard University (India)
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  • Institute of Pathophysiology Medical University of Vienna (Austria)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Ethnopharmacol.2019, 235:406-414
  • Int. J. of Pha. and Phy. Res.2015, 7(1):144-149
  • Earth Environ. Sci. 2021, 905:012080.
  • Front. Physiol.2022, 790345.
  • Tissue Cell.2022, 78:101901.
  • Antioxidants (Basel).2020, 9(4):284.
  • Process Biochemistry2019, 85:106-115
  • Phytochemistry2018, 15:83-92
  • Front Microbiol.2023, 14:1232039.
  • Pak J Pharm Sci.2019, 32(6):2879-2885
  • Org Biomol Chem.2017, 15(31):6483-6492
  • Int J Mol Sci.2021, 22(21):11447.
  • Plant Methods.2017, 13:108
  • Biomed Sci Letters.2020, 26:319-326
  • Emirates Journal of Food and Agriculture.2022, 34(6): 528-536.
  • J Cosmet Dermatol.2022, 21(1):396-402.
  • Drug Chem Toxicol.2020, 1-14.
  • J Integr Plant Biol.2023, 13564.
  • Front. Plant Sci.2022, 13:757852.
  • Appl. Sci.2021, 11(1),14.
  • J Ethnopharmacol.2017, 198:91-97
  • Korean Journal of Pharmacognosy2017, 48(4):320-328
  • Int Immunopharmacol.2021, 101(Pt A):108181.
  • ...
  • 生物活性
    Description: Hinokitiol has antibacterial effect , it can inhibit all Staphylococcus aureus isolates with MICs of 1.56-3.13 mg/L, it also has antifungal activity against 51 Malassezia pachydermatis strains, it is an inexpensive and safe treatment with anti-inflammatory and deodorant effects that can be recommended as an effective remedy for canine otitis externa. beta-thujaplicin (Hinokitiol) has ability to extract mitochondrial Mg and the prevention of the effects of beta-thujaplicin by an excess of Mg in the medium, suggests a common mode of action of beta-thujaplicin as a lipophilic chelator of Mg and other divalent cations.
    Targets: Antifection
    In vitro:
    J. Antimicrob. Chemoth., 2003, 51(1):113-22.
    Antibacterial effect of β-thujaplicin on staphylococci isolated from atopic dermatitis: relationship between changes in the number of viable bacterial cells and clinical improvement in an eczematous lesion of atopic dermatitis[Pubmed: 12493795]
    beta-Thujaplicin (Hinokitiol) is a tropolone-related compound purified from the wood of Chamaecyparis obtusa, Sieb. et Zucc. and Thuja plicata D. Don.
    METHODS AND RESULTS:
    All Staphylococcus aureus isolates were inhibited by beta-Thujaplicin with MICs of 1.56–3.13 mg/L. However, a paradoxical zone phenomenon occurred, with each isolate producing regrowth at higher β-thujaplicin concentrations. Other antimicrobial agents showed a wide range of MICs. The combination of beta-Thujaplicin and zinc oxide inhibited the paradoxical zone phenomenon, and enhanced killing activity against clinically isolated staphylococci. Large numbers of viable bacterial cells, especially S. aureus cells, were detected in the skin surface of atopic dermatitis, in comparison with those in healthy volunteers. The number of cells increased as the severity of the skin condition worsened. Topical application of β-thujaplicin resulted in a reduction in the number of bacterial cells on the skin surface, and an improvement in skin condition after treatment.
    CONCLUSIONS:
    The results of this study suggest that the degree of reduction in the number of viable bacterial cells in an eczematous lesion of atopic dermatitis is related to the degree of improvement in skin condition.
    J. Vet. Med. Sci., 2005, 67(12):1243-7.
    Effects of beta-thujaplicin on anti-Malassezia pachydermatis remedy for canine otitis externa.[Pubmed: 16397383]
    The antifungal activity of beta-thujaplicin(Hinokitiol) was evaluated against 51 Malassezia pachydermatis strains isolated from canine ear canals with or without otitis externa.
    METHODS AND RESULTS:
    For comparison, sensitivity tests were performed on M. pachydermatis isolates for nystatin, ketoconazole, and terbinafine HCl, all clinically available antifungal agents. The minimal inhibition concentrations over 50% of the tested isolates (MIC50) were 3.13 microg/ml for beta-thujaplicin and nystatin, 0.016 microg/ml for ketoconazole, and 1.56 microg/ml for terbinafine HCl. The antifungal effect for M. pachydermatis of beta-thujaplicin compared favorably with commercial antifungal agents. None of the 51 M. pachydermatis isolates showed resistance against any of the tested antibiotics investigated in this study. Ten representative isolates of M. pachydermatis were subcultured for 30 generations at concentrations close to the MIC levels of beta-thujaplicin, nystatin, ketoconazole, and terbinafine HCl, and examined to determine whether they had acquired resistance to each drug. As a result, M. pachydermatis was found to achieve resistance more easily for ketoconazole and terbinafine HCl than for beta-thujaplicin or nystatin. The MIC50 of beta-thujaplicin did not change during the course of subculture, and it is thought that the potential development of a resistant strain is low, even with continuous infusion for otitis externa therapy.
    CONCLUSIONS:
    beta-Thujaplicin(Hinokitiol) is an inexpensive and safe treatment with anti-inflammatory and deodorant effects that can be recommended as an effective remedy for canine otitis externa.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.0901 mL 30.4507 mL 60.9013 mL 121.8027 mL 152.2533 mL
    5 mM 1.218 mL 6.0901 mL 12.1803 mL 24.3605 mL 30.4507 mL
    10 mM 0.609 mL 3.0451 mL 6.0901 mL 12.1803 mL 15.2253 mL
    50 mM 0.1218 mL 0.609 mL 1.218 mL 2.4361 mL 3.0451 mL
    100 mM 0.0609 mL 0.3045 mL 0.609 mL 1.218 mL 1.5225 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
    原苏木素B; Protosappanin B CFN90135 102036-29-3 C16H16O6 = 304.30 20mg QQ客服:2056216494
    10-O-甲基原苏木素B; 10-O-Methylprotosappanin B CFN96304 111830-77-4 C17H18O6 = 318.3 5mg QQ客服:1413575084
    苏木素A二甲缩醛; Protosappanin A dimethyl acetal CFN96252 868405-37-2 C17H18O6 = 318.3 5mg QQ客服:215959384
    Alterlactone ; Alterlactone CFN96958 1030376-89-6 C15H12O6 = 288.25 5mg QQ客服:2056216494
    桧木醇; Hinokitiol CFN93995 499-44-5 C10H12O2 = 164.2 20mg QQ客服:3257982914
    6(1H)-Azulenone, 2,3-dihydro-1,4-dimethyl; 6(1H)-Azulenone, 2,3-dihydro-1,4-dimethyl CFN92790 71305-89-0 C12H14O = 174.2 5mg QQ客服:1457312923
    Perilloxin; Perilloxin CFN96321 263249-77-0 C16H18O4 = 274.3 5mg QQ客服:1413575084
    Dehydroperilloxin; Dehydroperilloxin CFN89219 263241-09-4 C16H16O4 = 272.3 5mg QQ客服:2056216494

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