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  • 曲酸

    Kojic acid

    曲酸
    产品编号 CFN94478
    CAS编号 501-30-4
    分子式 = 分子量 C6H6O4 = 142.11
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Miscellaneous
    植物来源 From the Aspergillus parasiticus.
    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
    曲酸 CFN94478 501-30-4 10mg QQ客服:1457312923
    曲酸 CFN94478 501-30-4 20mg QQ客服:1457312923
    曲酸 CFN94478 501-30-4 50mg QQ客服:1457312923
    曲酸 CFN94478 501-30-4 100mg 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 Auckland (New Zealand)
  • Northeast Normal University Changchun (China)
  • Medical University of Gdansk (Poland)
  • Lund University (Sweden)
  • Medizinische Universit?t Wien (Austria)
  • National Chung Hsing University (Taiwan)
  • University of Wollongong (Australia)
  • Sri Ramachandra University (India)
  • Pennsylvania State University (USA)
  • Massachusetts General Hospital (USA)
  • Sanford Burnham Medical Research Institute (USA)
  • Universidad de Ciencias y Artes de Chiapas (Mexico)
  • Helmholtz Zentrum München (Germany)
  • Melbourne University (Australia)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Pharm Anal.2016, 6(6):363-373
  • SRM Institute of Sci&Tech2022, 34(1): 32-37
  • Cells.2022, 11(6):931.
  • Biomol Ther (Seoul).2023, 31(1):40-47.
  • Exp Biol Med (Maywood).2019, 244(16):1463-1474
  • BMC Plant Biol.2022, 22(1):128.
  • Metabolites2023, 13(1), 3.
  • Food Chem.2017, 221:1135-1144
  • Pol J Microbiol.2021, 70(1):117-130.
  • J of Pharmaceutical Analysis2020, doi: 10.1016
  • J Colloid Interface Sci.2022, 622:298-308.
  • Sci Rep.2019, 9(1):4342
  • Metabolites.2020, 10(12):497.
  • Applied Biological Chemistry2022, 65(77).
  • Viruses.2021, 13(11):2118.
  • The Pharmaceutical Society of Japan2018, 138(4):571-579
  • Korea Institute of Oriental Medicine2020, doi: 10.21203.
  • Anal Chim Acta.2018, 1039:162-171
  • J Nat Prod.2023, 86(2):264-275.
  • Plant Growth Regulation2020, 90(2):383-392
  • Antioxidants (Basel).2021, 10(9):1487.
  • J Ethnopharmacol.2021, 267:113615.
  • Antioxidants (Basel).2020, 9(7):581.
  • ...
  • 生物活性
    Description: Kojic acid has been used as a food additive for preventing enzymatic browning of crustaceans and as a cosmetic agent for skin whitening. Kojic acid exhibits concentration-dependent scavenging activity on DPPH possessing strong antioxidant activity, it can reduce the mortality induced by gamma irradiation; it exhibits a competitive inhibition for the oxidation of chlorogenic acid and catechol by potato polyphenol oxidase (PPO) and of 4-methylcatechol and chlorogenic acid by apple PPO; it also has significant tyrosinase inhibitory activity.
    Targets: Tyrosinase
    In vitro:
    J Pharm Pharmacol. 1994 Dec;46(12):982-5.
    Kojic acid, a cosmetic skin whitening agent, is a slow-binding inhibitor of catecholase activity of tyrosinase.[Pubmed: 7714722]

    METHODS AND RESULTS:
    It was found that kojic acid, which is used in cosmetics for its excellent whitening effect, inhibits catecholase activity of tyrosinase in a non-classical manner. A decrease in the initial velocity to a steady-state inhibited velocity can be observed over a few minutes. This time-dependence, which is unaltered by prior incubation of the enzyme with the inhibitor, is consistent with a first-order transition.
    CONCLUSIONS:
    The kinetic data obtained correspond to those for a postulated mechanism that involves the rapid formation of an enzyme inhibitor complex that subsequently undergoes a relatively slow reversible reaction. Kinetic parameters characterizing this type of inhibition were evaluated by means of nonlinear regression of product accumulation curves.
    In vivo:
    Toxicol Sci. 2004 Sep;81(1):43-9.
    Enhancement of hepatocarcinogenesis by kojic acid in rat two-stage models after initiation with N-bis(2-hydroxypropyl)nitrosamine or N-diethylnitrosamine.[Pubmed: 15201437]
    Kojic acid (KA) has been used as a food additive for preventing enzymatic browning of crustaceans and as a cosmetic agent for skin whitening.
    METHODS AND RESULTS:
    In the present experiments, effects of KA on the induction of hepatic pre-neoplastic lesions in N-bis(2-hydroxypropyl)nitrosamine-initiated (experiment 1) and non-initiated (experiment 2) models, and its promoting influence in a medium-term liver bioassay (experiment 3) were investigated at dietary doses of up to 2% in male F344 rats. In experiment 1, 2% KA feeding induced significant increases in numbers (22.3 +/- 13.0 vs 8.5 +/- 3.4 in the 0%) and areas (0.37 +/- 0.29 vs 0.05 +/- 0.03 in the 0%) of glutathione-S-transferase P form (GST-P)-positive foci and toxic changes such as vacuolation of hepatocytes and microgranulomas. The development of GST-P-positive foci was pronounced in the animals with hepatocellular toxic changes. In experiment 2, numbers (0.65 +/- 0.57 vs 0.17 +/- 0.28 in the 0%) and areas (0.005 +/- 0.005 vs 0.0007 +/- 0.0012 in the 0%) of GST-P-positive foci and hepatocellular proliferating cell nuclear antigen (PCNA) expression (3.8 +/- 2.3 vs 2.6 +/- 0.7 in the 0%) were significantly increased by the 2% treatment. The PCNA-positive hepatocytes were abundantly localized around the vacuolated and granulomatous legions in both experiments 1 and 2. In experiment 3, significant increases in numbers (16.9 +/- 3.2 vs 8.4 +/- 2.7 in the 0%) and areas (1.62 +/- 0.39 vs 0.77 +/- 0.34 in the 0%) of GST-P-positive foci were again observed with 2% KA.
    CONCLUSIONS:
    These results demonstrate tumor-promoting and possible hepatocarcinogenic activity of KA at 2%, but the carcinogenic potential is likely to be weak. This study also indicated that enhanced replication of hepatocytes related to toxic changes might be involved as an underlying mechanism.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 7.0368 mL 35.184 mL 70.368 mL 140.736 mL 175.9201 mL
    5 mM 1.4074 mL 7.0368 mL 14.0736 mL 28.1472 mL 35.184 mL
    10 mM 0.7037 mL 3.5184 mL 7.0368 mL 14.0736 mL 17.592 mL
    50 mM 0.1407 mL 0.7037 mL 1.4074 mL 2.8147 mL 3.5184 mL
    100 mM 0.0704 mL 0.3518 mL 0.7037 mL 1.4074 mL 1.7592 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
    麦芽酚; Maltol CFN97949 118-71-8 C6H6O3 = 126.1 20mg QQ客服:215959384
    5-Hydroxymaltol 3-O-beta-D-glucoside; 5-Hydroxymaltol 3-O-beta-D-glucoside CFN95641 N/A C12H16O9 = 304.3 10mg QQ客服:2056216494
    曲酸; Kojic acid CFN94478 501-30-4 C6H6O4 = 142.11 20mg QQ客服:1413575084
    白屈菜酸; Chelidonic acid CFN94111 99-32-1 C7H4O6 = 184.10 20mg QQ客服:215959384
    去甲氧基茵陈色原酮; Demethoxycapillarisin CFN97716 61854-36-2 C15H10O6 = 286.24 5mg QQ客服:2056216494
    7-O-去甲氧基茵陈色原酮; Demethoxy-7-O-methylcapillarisin CFN96209 61854-37-3 C16H12O6 = 300.3 5mg QQ客服:2159513211
    茵陈色原酮; Capillarisin CFN90317 56365-38-9 C16H12O7 = 316.26 5mg QQ客服:2159513211
    Epimedonin B; Epimedonin B CFN92907 1616061-69-8 C20H16O6 = 352.34 5mg QQ客服:3257982914
    5,7-二羟基色原酮; 5,7-Dihydroxychromone CFN97761 31721-94-5 C9H6O4 = 178.14 20mg QQ客服:3257982914
    5,7-二羟基色原酮 7-芸香糖苷; 5,7-Dihydroxychromone 7-rutinoside CFN92369 52538-46-2 C21H26O13 = 486.4 5mg QQ客服:1413575084

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