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Shikonin

Cat. No.:YN360943

  • CAS No. :517-89-5

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    • 参考文献
    • 产品名称: Shikonin
      CAS No.: 517-89-5
      Chemical Name: 5,8-dihydroxy-2-[(1R)-1-hydroxy-4-methyl-3-penten-1-yl]-1,4-naphthalenedione
      Synonyms:紫草素; C.I. 75535; Isoarnebin 4
      分子量:288.30
      分子式:C₁₆H₁₆O₅
      SMILES:O=C1C([C@H](O)C/C=C(C)/C)=CC(C2=C1C(O)=CC=C2O)=O
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: Shikonin 是中草药紫草的主要成分。Shikonin 是一种有效的 TMEM16A 氯化物通道 (chloride channel) 抑制剂,IC50为 6.5 μM。Shikonin 是一种特异的丙酮酸激酶 M2 (PKM2) 抑制剂,还可以抑制TNF-α和NF-κB途径。Shikonin 通过抑制糖酵解降低外泌体 (exosome) 的分泌。
      IC50和靶点: [{name:"TMEM16A chloride channel:6.5 μM (IC50)'}, 'PKM2', 'NF-κB']
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Kamei, R., Kitagawa, Y., Kadokura, M., et al.Shikonin stimulates glucose uptake in 3T3-L1 adipocytes via an insulin-independent tyrosine kinase pathwayBiochem. Biophys. Res. Commun.292(3),642-651(2002)

      Nigorikawa, K., Yoshikawa, K., Sasaki, T., et al.A naphthoquinone derivative, shikonin, has insulin-like actions by inhibiting both phosphatase and tensin homolog deleted on chromosome 10 and tyrosine phosphatasesMol. Pharmacol.70(3),1143-1149(2006)

      Chen, J., Xie, J., Jiang, Z., et al.Shikonin and its analogs inhibit cancer cell glycolysis by targeting tumor pyruvate kinase-M2Oncogene30(42),4297-4306(2011)

      Han, W., Li, L., Qiu, S., et al.Shikonin circumvents cancer drug resistance by induction of a necroptotic deathMol. Cancer Ther.6(5),1641-1649(2007)

      Chen, X., Yang, L., Zhang, N., et al.Shikonin, a component of chinese herbal medicine, inhibits chemokine receptor function and suppresses human immunodeficiency virus type 1Antimicrob. Agents Chemother.47(9),2810-2816(2003)

      Kim, Y.O., Hong, S.J., and Yim, S.V.The efficacy of shikonin on cartilage protection in a mouse model of rheumatoid arthritisKorean J. Physiol. Pharmacol.14(4),199-204(2010)

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