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  • 忍冬苷

    Lonicerin

    忍冬苷
    产品编号 CFN95055
    CAS编号 25694-72-8
    分子式 = 分子量 C27H30O15 = 594.5
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Flavonoids
    植物来源 The herbs of Lonicera hypoglauca
    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
    忍冬苷 CFN95055 25694-72-8 1mg QQ客服:1457312923
    忍冬苷 CFN95055 25694-72-8 5mg QQ客服:1457312923
    忍冬苷 CFN95055 25694-72-8 10mg QQ客服:1457312923
    忍冬苷 CFN95055 25694-72-8 20mg 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
  • University of Vigo (Spain)
  • University of Fribourg (Switzerland)
  • University of Lodz (Poland)
  • Ateneo de Manila University (Philippines)
  • Martin Luther University of Halle-Wittenberg (Germany)
  • Instituto de Investigaciones Agropecuarias (Chile)
  • Universiti Malaysia Pahang (Malaysia)
  • University of Illinois (USA)
  • Nicolaus Copernicus Uniwersity (Poland)
  • Medizinische Universit?t Wien (Austria)
  • Universiti Sains Malaysia (Malaysia)
  • University of Perugia (Italy)
  • University of British Columbia (Canada)
  • Kyushu University (Japan)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Food Sci Technol.2019, 56(5):2712-2720
  • J Agric Food Chem.2020, 68(43):12164-12172.
  • Metabolites.2023, 13(5):625.
  • Front Pharmacol.2018, 9:756
  • Antioxidants.2022, 11(3):592.
  • Mol Divers.2022, s11030-022-10586-3.
  • Compounds.2023, 3(1), 169-179.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2021, 1187:123012.
  • J Agric Food Chem.2018, 66(1):351-358
  • Evidence-based Compl.&Alternative Med.2023, 5417813
  • Comp. & Mathematical Methods in Med.2022, 5475559.
  • J Pharmaceutical Research Int.2021, 33(41A):275-284.
  • Molecules.2020, 25(18),4089.
  • LWT-Food Sci Technol2020, 109163
  • Integr Cancer Ther.2018, 17(3):832-843
  • Int J Mol Sci.2023, 24(5):4505.
  • Sustainable Chemistry & Pharmacy2022, 30:100883.
  • Nutrients.2022, 14(16):3393.
  • J of Food Quality2020, 8851285.
  • Int J Mol Sci.2019, 21(1):E265
  • Appl Biochem Biotechnol.2022, s12010-022-04166-2.
  • Planta Med.2023, 2192-2281
  • J Integr Plant Biol.2023, 13564.
  • ...
  • 生物活性
    Description: Lonicerin has antioxidant, anti-arthritic and antifungal activities, it can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.
    Targets: Antifection
    In vitro:
    J Sep Sci. 2008 Oct;31(20):3519-26.
    Rapid and simple method for screening of natural antioxidants from Chinese herb Flos Lonicerae Japonicae by DPPH-HPLC-DAD-TOF/MS.[Pubmed: 18830958 ]
    A rapid and simple method has been developed for the screening and identification of natural antioxidants of Flos Lonicerae Japonicae (FLJ), derived from the flower buds of Lonicera japonica.
    METHODS AND RESULTS:
    The hypothesis is that upon reaction with 1,1-diphenyl-2-picrylhydrazyl (DPPH), the peak areas (PAs) of compounds with potential antioxidant effects in the HPLC chromatograms will be significantly reduced or disappeared, and the identity confirmation could be achieved by HPLC-DAD-TOF/MS hyphenated technique. Using the proposed approach, about 14 compounds in the FLJ extract were found to possess a potential antioxidant activity. They were identified as chlorogenic acid (1), 1-O-caffeoylquinic acid (1-O-CQA, 2), caffeic acid (4), 4-O-CQA (5), rutin (7), isoquercitrin (8), luteolin-7-O-glucoside (9), Lonicerin (10), 4,5-O-dicaffeoylquinic acid (4,5-O-diCQA, 11), 3,5-O-diCQA (12), 1,3-O-diCQA (13), 3,4-O-diCQA (14), 1,4-O-diCQA (16), and luteolin (17). In addition, the free radical scavenging capacities of the available identified compounds were also investigated by HPLC assay.
    CONCLUSIONS:
    The results indicated that the compounds with PAs significantly decreasing were natural antioxidants, whereas those with PAs not changing presented no activities, which accordingly indicated that this newly proposed method could be widely applied for rapid screening and identification of natural antioxidants from complex matrices including Chinese herbal medicines.
    J Ethnopharmacol . 2019 Jul 15;239:111909.
    Lonicerin, an anti-algE flavonoid against Pseudomonas aeruginosa virulence screened from Shuanghuanglian formula by molecule docking based strategy[Pubmed: 31026553]
    Abstract Ethnopharmacological relevance: The Shuanghuanglian formula (SF) is a famous antimicrobial and antiviral traditional Chinese medicine that is made of Lonicera japonica Thunb., Scutellaria baicalensis Georgi, and Forsythia suspensa (Thunb.) Vahl. According to the Chinese Pharmacopoeia, the SF is commonly administered in the forms of oral liquid, tablets, and injection. It has long been used to treat acute respiratory tract infections, especially lung infection. Aim of the study: In the light of the increasing incidence of multidrug resistance to conventional antibiotics, the aim of this study was to screen potential anti-virulence agents against Pseudomonas aeruginosa from the extract of the SF. Materials and methods: The SF was used for effective compounds screening via the combination of the molecule docking approach and ultra-high-performance liquid chromatography-quadrupole/time of flight mass spectrometry. Fifty-one anti-virulence-related proteins were docked, 26 identified compounds were from SF. Subsequently, the top-scoring screened compound was assessed via bioactive-related assays, including the quantification of alginate biosynthesis, anti-biofilm assays, and the A549 human lung cells infection. Result: A flavonoid Lonicerin was found to be bonded with the active site of the alginate secretion protein (AlgE) with the highest score in molecule docking. Furthermore, we validated that Lonicerin could significantly reduce alginate secretion (25 μg/mL) and biofilm formation (12.5 μg/mL) at a sub-MIC concentration without inhibiting the proliferation of P. aeruginosa or influencing the expression of AlgE, which suggested that Lonicerin may directly inhibit AlgE. In addition, Lonicerin was proven to inhibit the infection of P. aeruginosa in the A549 cells. Conclusion: This work reported on the first potential AlgE antagonist that was derived from herbal resources. Lonicerin was proven to be an effective inhibitor in-vitro of P. aeruginosa infection. Keywords: AlgE; Alginate; Lonicerin; Molecule docking; Pseudomonas aeruginosa.
    In vivo:
    Arch Pharm Res. 2011 May;34(5):853-9.
    Antiarthritic effect of lonicerin on Candida albicans arthritis in mice.[Pubmed: 21656372 ]
    Fungal arthritis is a potentially serious disease resulting in rapid destruction of the joint. Among the various Candida species, Candida albicans is the most commonly associated with fungal arthritis.
    METHODS AND RESULTS:
    In the present study, we examined the effect of Lonicerin, a flavonoid isolated from Lonicerae Flos, on an arthritis caused by C. albicans cell wall (CACW) in mice. To examine the effect, an emulsified mixture of CACW and complete Freund's adjuvant (CACW/CFA) was injected into BALB/c mice via hind footpad route on days -3, -2, and -1. On Day 0, mice with the swollen footpad received Lonicerin at 1 or 2 mg/dose/time intraperitoneally 3 times every other day. The footpad-swelling was measured for 20 days. Results showed that the Lonicerin treatment reduced the edema at all dose levels, and, furthermore, there was app. 54% edema reduction in animals given the 2 mg-dose at the peak (day 10) of septic arthritis (p < 0.05). Since the peak, the edema was reduced in similar rates. This antiarthritic activity appeared to be mediated by Lonicerin's ability to suppress T cell proliferation, nitric oxide production from macrophages, and shift of cellular immunity from Th1- toward Th2-type responses, all of which are beneficial to treat arthritis. In addition, the flavonoid had anticandidal activity (p < 0.01).
    CONCLUSIONS:
    These data suggest that Lonicerin alone, which has both anti-arthritic and antifungal activities, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.
    Front Biosci (Landmark Ed) . 2020 Jan 1;25(3):480-497.
    Lonicerin prevents inflammation and apoptosis in LPS-induced acute lung injury[Pubmed: 31585898]
    Abstract Acute lung injury (ALI) is a life-threatening condition caused by severe inflammation of lung tissues. We hypothesized that lipopolysaccharide induced acute lung inflammation and injury in mice might be controlled by lonicerin (LCR), a plant flavonoid that impacts immunity, oxidative stress, and cell proliferation. LCR reduced pathological changes including pulmonary edema, elevation of protein in bronchoalveolar lavage, inflammation, pro-inflammatory gene expression, expression of toll-like receptor 4/nuclear factor-kappa B, apoptosis, and significantly reduced mortality. Together, the results suggest that LCR might be a potential and effective candidate for the treatment of ALI that acts by inhibiting inflammation and apoptosis.
    Front Biosci (Landmark Ed) . 2020 Jan 1;25(3):480-497.
    Lonicerin prevents inflammation and apoptosis in LPS-induced acute lung injury[Pubmed: 31585898]
    Abstract Acute lung injury (ALI) is a life-threatening condition caused by severe inflammation of lung tissues. We hypothesized that lipopolysaccharide induced acute lung inflammation and injury in mice might be controlled by lonicerin (LCR), a plant flavonoid that impacts immunity, oxidative stress, and cell proliferation. LCR reduced pathological changes including pulmonary edema, elevation of protein in bronchoalveolar lavage, inflammation, pro-inflammatory gene expression, expression of toll-like receptor 4/nuclear factor-kappa B, apoptosis, and significantly reduced mortality. Together, the results suggest that LCR might be a potential and effective candidate for the treatment of ALI that acts by inhibiting inflammation and apoptosis.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.6821 mL 8.4104 mL 16.8209 mL 33.6417 mL 42.0521 mL
    5 mM 0.3364 mL 1.6821 mL 3.3642 mL 6.7283 mL 8.4104 mL
    10 mM 0.1682 mL 0.841 mL 1.6821 mL 3.3642 mL 4.2052 mL
    50 mM 0.0336 mL 0.1682 mL 0.3364 mL 0.6728 mL 0.841 mL
    100 mM 0.0168 mL 0.0841 mL 0.1682 mL 0.3364 mL 0.4205 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
    木犀草苷; 木犀草素-7-O-葡萄糖苷; Luteolin-7-O-glucoside CFN98565 5373-11-5 C21H20O11 = 448.38 20mg QQ客服:215959384
    木犀草素-7-O-葡萄糖醛酸苷; Luteolin-7-O-glucuronide CFN98512 29741-10-4 C21H18O12 = 462.36 20mg QQ客服:1457312923
    忍冬苷; Lonicerin CFN95055 25694-72-8 C27H30O15 = 594.5 10mg QQ客服:2056216494
    木犀草素 7-芸香糖苷; Luteolin 7-rutinoside CFN93556 20633-84-5 C27H30O15 = 594.52 20mg QQ客服:1413575084
    木犀草素 5-葡萄糖苷; Luteollin 5-glucoside CFN98568 20344-46-1 C21H20O11 = 448.38 5mg QQ客服:1413575084
    芫花叶苷; Yuanhuanin CFN95127 83133-14-6 C22H22O11 = 462.4 5mg QQ客服:1457312923
    芫花素-5-O-茜黄苷; Yuankanin CFN95128 77099-20-8 C27H30O14 = 578.5 5mg QQ客服:3257982914
    木犀草素-3'-葡萄糖醛酸苷; Luteolin-3-O-beta-D-glucuronide CFN93187 53527-42-7 C21H18O12 = 462.4 10mg QQ客服:2159513211
    木犀草素-7-二葡萄糖苷酸; Luteolin 7-diglucuronide CFN70468 96400-45-2 C27H26O18 = 638.5 5mg QQ客服:2056216494
    新化合物11; New compound 11 CFN95351 N/A C36H32O20 = 784.6 10mg QQ客服:215959384

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