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  • 芦竹碱

    Gramine

    芦竹碱
    产品编号 CFN98111
    CAS编号 87-52-5
    分子式 = 分子量 C11H14N2 = 174.25
    产品纯度 >=98%
    物理属性 Cryst.
    化合物类型 Alkaloids
    植物来源 The herbs of Arundo donax L.
    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
    芦竹碱 CFN98111 87-52-5 10mg QQ客服:2056216494
    芦竹碱 CFN98111 87-52-5 20mg QQ客服:2056216494
    芦竹碱 CFN98111 87-52-5 50mg QQ客服:2056216494
    芦竹碱 CFN98111 87-52-5 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
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  • Instituto de Investigaciones Agropecuarias (Chile)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Appl. Sci.2020, 10,1304
  • J Ginseng Res.2020, 44(4):611-618.
  • J. of The Korean Society of Food Culture2017, 144-149
  • J Biomed Sci.2020, 27(1):60.
  • Front Pharmacol.2019, 10:1025
  • Environ Toxicol.2023, 23929.
  • Front Pharmacol.2023, 14:1095083.
  • Biomedicine & Pharmacotherapy2022, 153:113404.
  • Korean J Environ Agric.2018, 37(4):260-267
  • Planta Med.2019, 85(3):217-224
  • Antioxidants2022, 11(2),234.
  • SBRAS2016, 12
  • Biochem Biophys Res Commun.2017, 494(3-4):587-593
  • J Colloid Interface Sci.2022, 622:298-308.
  • Huazhong Agricultural University2022, pp34.
  • Journal of Third Military Medical University2019, 41(2):110-115
  • Antioxidants (Basel).2022, 11(8):1471.
  • J Pharmaceutical and Biomedical Analysis2022, 114631.
  • Chemistry of Natural Compounds2020, 56,423-426
  • Nat Commun.2019, 10(1):5169
  • Plant Foods Hum Nutr.2021, 76(4):472-477.
  • Front Plant Sci.2017, 8:723
  • Exp Biol Med (Maywood).2019, 244(16):1463-1474
  • ...
  • 生物活性
    Description: Gramine has anti-tumor, anti-viral and anti-inflammatory properties; it can activate of antioxidants and inactivative of SOD in M. aeruginosa, it also has phytotoxicity on M. aeruginosa may be due to oxidative damage via oxidation of ROS .
    Targets: SOD | ROS | Antifection
    In vitro:
    Chemosphere. 2014 Jun;104:212-20.
    Natural xenobiotics to prevent cyanobacterial and algal growth in freshwater: contrasting efficacy of tannic acid, gallic acid, and gramine.[Pubmed: 24332729]
    Allelochemical action against planktonic phototrophs is one central issue in freshwater ecology and quality management.
    METHODS AND RESULTS:
    To determine some basic mechanisms of this toxic action, we exposed the coccal green alga, Desmodesmus armatus, and the coccal cyanobacterium, Microcystis aeruginosa, in a batch culture well-supplied with carbon dioxide to increasing concentrations of the polyphenols tannic acid and gallic acid and the alkaloid gramine. The phototrophs were checked after 2d and at the end of the culture for biomass-based growth rates, cell volume, maximum quantum yield of photosystem II (ΦPSIImax), chlorophyll a content (chla) after 2d and at the end of the culture, and lipid peroxidation only at the end of the culture. During the culture, the pH rose from 7.64 to 10.95, a pH characteristic of eutrophic freshwater bodies during nuisance algal blooms. All xenobiotics reduced the growth rate, ΦPSIImax, and chla during the first 2d with M. aeruginosa being more sensitive to the polyphenols than D. armatus. The efficacy of the polyphenols declined with increasing pH, indicating potential polymerization and corresponding reduced bioavailability of the polyphenols. In contrast to the polyphenols, gramine increased its toxic action over time, independent of the prevailing pH. All exposures caused slight to severe lipid peroxidation (LPO) in the phototrophs. Hence, one mechanism of growth inhibition may be oxidative stress-mediated reduction in photosynthesis.
    CONCLUSIONS:
    The presented results suggest that in successful field trials with leachate, the prevailing environmental conditions may inactivate polyphenols and xenobiotics other than polyphenols may be more effective.
    Plant Cell Physiol. 2001 Oct;42(10):1103-11.
    Gramine increase associated with rapid and transient systemic resistance in barley seedlings induced by mechanical and biological stresses.[Pubmed: 11673626]
    Systemic acquired resistance (SAR) is one of the intriguing issues for studying the mechanism in signal transduction system in a whole plant. We found that SAR and increase of an antifungal compound were induced rapidly and transiently in barley (Hordeum vulgare L. cv. Goseshikoku) by mechanical and biological stresses. One of the major antifungal compounds was identified as an indole alkaloid, gramine (N,N-dimethyl-3-aminomethylindole), by mass spectrum and NMR analyses.
    METHODS AND RESULTS:
    Gramine is well known as a constitutive compound of barley, but it increased significantly in the primary and secondary leaves of barley seedlings within 12 h after pruning or inoculating with the powdery mildew fungi of barley (Blumeria graminis f.sp. hordei) and wheat (B. graminis f.sp. tritici). However, in the leaf detached from unwounded seedlings or in the leaf inoculated with the barley powdery mildew fungus, gramine did not increase at all. In the water droplets contacted with barley leaves, the amount of leaked gramine increased dependently upon the time after the seedling was injured mechanically. We also found a tight correlation between gramine increase and enhancement of resistance to the barley powdery mildew fungus in barley leaves treated with an endogenous elicitor. Furthermore, such a systemic resistance was not observed in a barley cultivar Morex that lacks the biosynthetic pathway of gramine.
    CONCLUSIONS:
    From these results, we conclude that gramine is the excellent marker in rapid and transient systemic acquired resistance in barley.
    In vivo:
    Steroids. 2015 Jun;98:92-9.
    Synthesis, spectroscopy, theoretical and biological studies of new gramine-steroids salts and conjugates.[Pubmed: 25777948]

    METHODS AND RESULTS:
    New gramine connections with bile acids (lithocholic, deoxycholic, cholic) and sterols (cholesterol, cholestanol) were synthesized. The structures of products were confirmed by spectral (NMR, FT-IR) analysis, mass spectrometry (ESI-MS) as well as PM5 semiempirical methods. Unexpectedly, the products of the reaction of gramine with cholesterol and cholestanol were symmetrical compounds consisting of two molecules of sterols connected by N(CH3)2 group. All new synthesized compounds interact in vitro with the human erythrocyte membrane and alter discoid erythrocyte shape inducing stomatocytosis or echinocytosis. Increase in the incorporation of the fluorescent dye merocyanine 540 (MC540) into the erythrocyte membrane indicates that new compounds at sublytic concentrations are capable of disturbing membrane phospholipids asymmetry and loosening the molecular packing of phospholipids in the bilayer. Gramine significantly decreases the membrane partitioning properties as well as haemolytic activity of lithocholic acid in its new salt. Moreover, both deoxycholic and cholic acids completely lost their membrane perturbing activities in the gramine salts. On the other hand, the capacity of new gramine-sterols connections to alter the erythrocyte membrane structure and its permeability is much higher in comparison with sterols alone.
    CONCLUSIONS:
    The dual effect of gramine on the bile acid and sterols cell membrane partitioning activity observed in our study should not be neglected in vivo.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 5.7389 mL 28.6944 mL 57.3888 mL 114.7776 mL 143.472 mL
    5 mM 1.1478 mL 5.7389 mL 11.4778 mL 22.9555 mL 28.6944 mL
    10 mM 0.5739 mL 2.8694 mL 5.7389 mL 11.4778 mL 14.3472 mL
    50 mM 0.1148 mL 0.5739 mL 1.1478 mL 2.2956 mL 2.8694 mL
    100 mM 0.0574 mL 0.2869 mL 0.5739 mL 1.1478 mL 1.4347 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
    1-甲氧基吲哚-3-羧酸; 1-Methoxyindole-3-carboxylic acid CFN96036 91913-76-7 C10H9NO3 = 191.2 5mg QQ客服:1457312923
    1-甲氧基-3-吲哚乙腈; Caulilexin C CFN96052 30536-48-2 C11H10N2O = 186.2 5mg QQ客服:3257982914
    N-甲基-5-羟色胺; N-Methylserotonin CFN91557 1134-01-6 C11H14N2O = 190.2 5mg QQ客服:1413575084
    芦竹碱; Gramine CFN98111 87-52-5 C11H14N2 = 174.25 20mg QQ客服:2159513211
    蟾蜍色胺; Bufotenine CFN91165 487-93-4 C12H16N2O = 204.3 10mg QQ客服:2159513211
    华蟾蜍色胺; Cinobufotenine CFN91166 60657-23-0 C13H19N2O = 219.3 10mg QQ客服:1413575084
    松果体素; Melatonin CFN90037 73-31-4 C13H16N2O2 = 232.28 20mg QQ客服:1413575084
    红豆碱; Abrine CFN90202 526-31-8; 21339-55-9 C12H14N2O2 = 218.25 20mg QQ客服:3257982914
    刺桐碱; Hypaphorine CFN90634 487-58-1 C14H18N2O2 = 246.3 20mg QQ客服:2159513211
    色氨酸; Tryptophan CFN90473 54-12-6 C11H12N2O2 = 204.22 5mg QQ客服:215959384

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