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Butein

Cat. No.:YN340192

  • CAS No. :487-52-5

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    • 参考文献
    • 产品名称: Butein
      CAS No.: 487-52-5
      Chemical Name: (2E)-1-(2,4-dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)-2-propen-1-one
      Synonyms:紫铆因; 2’,3,4,4’-tetrahydroxy Chalcone
      分子量:272.25
      分子式:C₁₅H₁₂O₅
      SMILES:OC1=CC=C(C(/C=C/C2=CC(O)=C(O)C=C2)=O)C(O)=C1
      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: Butein,可从Dalbergia odorifera T. Chen分离,是一种 cAMP 特异性的PDE抑制剂,对PDE4的IC50为 10.4 μM。Butein 是蛋白酪氨酸激酶抑制剂,对EGFR和p60c-src的IC50分别为 16 和 65 μM。Butein 通过 AKT 和 ERK/p38 MAPK 通路,靶向 FoxO3a 使 HeLa 细胞对 Cisplatin 敏感。Butein 还是一种SIRT1激活剂 (STAC)。
      IC50和靶点: [{name:"EGFR:16 μM (IC50, in HepG2 cells)"},{name: "PDE4:10.4 μM (IC50)"}]
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Yadav, V.R., Prasad, S., Sung, B., et al.The role of chalcones in suppression of NF-κB-mediated inflammation and cancerInt. Immunopharmacol.11(3),295-309(2011)

      Lee, E.H., Song, D.G., Lee, J.Y., et al.Inhibitory effect of the compounds isolated from Rhus verniciflua on aldose reductase and advanced glycation endproductsBiol. Pharm. Bull.31(8),1626-1630(2008)

      Gupta, S.C., Kim, J.H., Prasad, S., et al.Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticalsCancer Metastasis Rev.29(3),405-434(2010)

      Sogawa, S., Nihro, Y., Ueda, H., et al.3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitorsJ. Med. Chem.36(24),3904-3909(1993)

      Sharma, S.K., Parasuraman, P., Kumar, G., et al.Green tea catechins potentiate triclosan binding to enoyl-ACP reductase from Plasmodium falciparum (PfENR)J. Med. Chem.50(4),765-775(2007)

      Bonesi, M., Loizzo, M.R., Statti, G.A., et al.The synthesis and angiotensin converting enzyme (ACE) inhibitory activity of chalcones and their pyrazole derivativesBioorg. Med. Chem. Lett.20(6),1990-1993(2010)

      McArdle, B.M., Campitelli, M.R., and Quinn, R.J.A common protein fold topology shared by flavonoid biosynthetic enzymes and therapeutic targetsJ. Nat. Prod.69(1),14-17(2006)

      Wood, J.G., Rogina, B., Lavu, S., et al.Sirtuin activators mimic caloric restriction and delay ageing in metazoansNature430,686-689(2004)

      Szczepankiewicz, B.G., and Ng, P.Y.Sirtuin modulators: Targets for metabolic diseases and beyondCurr. Top. Med. Chem.8(17),1533-1544(2008)

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