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  • Aflastatin A

    Aflastatin A

    Aflastatin A
    产品编号 CFN00102
    CAS编号 179729-59-0
    分子式 = 分子量 C62H115NO24 = 1258.57
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 From Streptomyces sp.
    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
    Aflastatin A CFN00102 179729-59-0 1mg QQ客服:1457312923
    Aflastatin A CFN00102 179729-59-0 5mg QQ客服:1457312923
    Aflastatin A CFN00102 179729-59-0 10mg QQ客服:1457312923
    Aflastatin A CFN00102 179729-59-0 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 Parma (Italy)
  • Medical University of South Carolina (USA)
  • S.N.D.T. Women's University (India)
  • Chang Gung University (Taiwan)
  • Agricultural Research Organization (ARO) (Israel)
  • University of Dicle (Turkey)
  • Institute of Chinese Materia Medica (China)
  • Universidad Veracuzana (Mexico)
  • Universiti Kebangsaan Malaysia (Malaysia)
  • Universidad de La Salle (Mexico)
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  • Funda??o Universitária de Desenvolvimento (Brazil)
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  • Copenhagen University (Denmark)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Antioxidants (Basel).2024, 13(3):340.
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  • Mol Neurobiol.2022, 02873-9.
  • Plants2022, 11(3),294.
  • Free Radic Biol Med.2021, 166:104-115.
  • Pest Manag Sci.2019, 75(9):2530-2541
  • Evid Based Complement Alternat Med.2018, 2018:4580627
  • Nature Ecology & Evolution2020, doi: 10.1038
  • Int J Mol Sci.2021, 22(16):8641.
  • Antioxidants (Basel).2021, 10(11): 1802.
  • FASEB J.2019, 33(2):2026-2036
  • Phytomedicine.2023, 120:155063.
  • Primary and Industrial.2018, 52(11)
  • Int J Mol Sci.2023, 24(14):11496.
  • Appl. Sci.2020, 10(20),7374.
  • Journal of Plant Growth Regulation2022, 10705-2.
  • Molecules2022, 27(3),1140.
  • Pharmacognosy Magazine2017, 13(52):868-874
  • Plants (Basel).2020, 9(11):1555.
  • Phytother Res.2022, 10.1002:ptr.7626.
  • Applied Biological Chemistry2020, 63:37.
  • Molecules.2021, 26(19):6032.
  • Molecules2022, 27(11):3606.
  • ...
  • 生物活性
    Description: Aflastatin A exhibits antimicrobial activity against some bacteria, yeasts and fungi, it is a specific inhibitor of aflatoxin production by Aspergillus parasiticus, inhibits a very early step in aflatoxin biosynthesis prior to the transcription of aflR and can influence glucose metabolism in the fungus. Aflastatin A has antitumor activity. Aflastatin A inhibits an early step in melanin production, which suppresses the expression of PKS1.
    Targets: Antifection | PKS1
    In vitro:
    J Antibiot (Tokyo). 2001 Aug;54(8):650-7.
    Effects of aflastatin A, an inhibitor of aflatoxin production, on aflatoxin biosynthetic pathway and glucose metabolism in Aspergillus parasiticus.[Pubmed: 11592501]
    Aflastatin A inhibits aflatoxin production by Aspergillus parasiticus via an unknown mechanism.
    METHODS AND RESULTS:
    We found that aflastatin A clearly inhibited production of norsolorinic acid, an early biosynthetic intermediate of aflatoxin, at a concentration of 0.25 microg/ml. Reverse-transcriptase polymerase chain reaction (RT-PCR), and real-time quantitative PCR (TaqMan PCR) experiments indicated that the transcription of genes encoding aflatoxin biosynthetic enzymes (pksA, ver-1, and omtA) and a gene encoding a regulatory protein for expression of the biosynthetic enzymes (aflR) were significantly reduced by the addition of aflastatin A. We also found that aflastatin A elevated the glucose consumption and ethanol accumulation by A. parasiticus, and repressed transcription of genes involved in ethanol utilization.
    CONCLUSIONS:
    These results suggest that aflastatin A inhibits a very early step in aflatoxin biosynthesis prior to the transcription of aflR and can influence glucose metabolism in the fungus.
    J Antibiot (Tokyo). 1997 Feb;50(2):111-8.
    Aflastatin A, a novel inhibitor of aflatoxin production by aflatoxigenic fungi.[Pubmed: 9099219]
    Aflastatin A, a novel inhibitor of the production of aflatoxin by aflatoxigenic fungi, has been isolated from the solvent extract of mycelial cake of Streptomyces sp. and its molecular formula was determined as C62H115NO24.
    METHODS AND RESULTS:
    Aflastatin A completely inhibited aflatoxin production by Aspergillus parasiticus NRRL 2999 in liquid medium or on agar plate at a concentration of 0.5 microgram/ml. The mycelial growth of this fungus was not affected in the liquid medium at the same concentration, while the hyphal extension rate was reduced on the plate together with some morphological changes. The growth of the fungus was not completely inhibited even at a concentration of 100 micrograms/ml.
    CONCLUSIONS:
    Aflastatin A exhibits antimicrobial activity against some bacteria, yeasts and fungi as well as antitumor activity.
    Microbiology. 2001 Sep;147(Pt 9):2623-8.
    Inhibitory effect of aflastatin A on melanin biosynthesis by Colletotrichum lagenarium.[Pubmed: 11535802]
    Aflastatin A, a novel inhibitor of the production of aflatoxin by aflatoxigenic fungi, has been isolated from the solvent extract of mycelial cake of Streptomyces sp. and its molecular formula was determined as C62H115NO24.
    METHODS AND RESULTS:
    Aflastatin A completely inhibited aflatoxin production by Aspergillus parasiticus NRRL 2999 in liquid medium or on agar plate at a concentration of 0.5 microgram/ml. The mycelial growth of this fungus was not affected in the liquid medium at the same concentration, while the hyphal extension rate was reduced on the plate together with some morphological changes. The growth of the fungus was not completely inhibited even at a concentration of 100 micrograms/ml.
    CONCLUSIONS:
    Aflastatin A exhibits antimicrobial activity against some bacteria, yeasts and fungi as well as antitumor activity.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 0.7946 mL 3.9728 mL 7.9455 mL 15.8911 mL 19.8638 mL
    5 mM 0.1589 mL 0.7946 mL 1.5891 mL 3.1782 mL 3.9728 mL
    10 mM 0.0795 mL 0.3973 mL 0.7946 mL 1.5891 mL 1.9864 mL
    50 mM 0.0159 mL 0.0795 mL 0.1589 mL 0.3178 mL 0.3973 mL
    100 mM 0.0079 mL 0.0397 mL 0.0795 mL 0.1589 mL 0.1986 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
    Aflastatin A; Aflastatin A CFN00102 179729-59-0 C62H115NO24 = 1258.57 5mg QQ客服:215959384
    Amycomycin; Amycomycin CFN00104 344362-08-9 C65H115NO18 = 1198.62 5mg QQ客服:2159513211
    杀稻瘟菌素A; Blasticidin A CFN00110 100513-53-9 C58H107NO23 = 1186.48 5mg QQ客服:215959384
    红霉素; Erythroskyrin CFN00116 4987-27-3 C26H33NO6 = 455.55 5mg QQ客服:3257982914
    alpha-脂霉素; alpha-Lipomycin CFN00122 51053-40-8 C32H45NO9 = 587.71 5mg QQ客服:1413575084
    Lydicamycin; Lydicamycin CFN00123 133352-27-9 C47H74N4O10 = 855.12 5mg QQ客服:2159513211
    Oleficin; Oleficin CFN00128 12764-54-4 C34H47NO9 = 613.74 5mg QQ客服:215959384
    Physarorubinic acid A; Physarorubinic acid A CFN00131 196621-49-5 C18H19NO6 = 345.35 5mg QQ客服:2056216494
    Polycephalin C; Polycephalin C CFN00132 220422-37-7 C32H36N2O8 = 576.64 5mg QQ客服:2159513211
    Streptolydigin; Streptolydigin CFN00138 7229-50-7 C32H44N2O9 = 600.7 5mg QQ客服:3257982914

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