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    Luteolin

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      Luteolin

      SKU
      L0087

      Category: Lipids, Fatty Acids

      Synonyms
      3',4',5,7-Tetrahydroxyflavone , Luteolol , BRN 0292084 , C.I. Natural Yellow 2 , Digitoflavone , Flacitran , Flavopurpol , Daphneflavonol , Argemexitin
      491-70-3
      CAS-Number
      C15H10O6
      Molecular Formula
      286.24
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (TLC)
      Appearance
      Yellow powder
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO (10mg/ml), DMF (20mg/ml), methanol, ethanol (5mg/ml)
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Transportation
      Not dangerous goods
      Description
      Luteolin is a hydroxylated flavone derivative that is a strong antioxidant and radical scavenger. It has multiple activities, such as anticancer, antimetastatic, anti-adipogenic, anti-inflammatory and neuroprotective. Luteolin has been described as a fatty acid synthase (FASN), 15-lipoxygenase, alpha-glucosidase, PPAR-γ, topoisomerase I, PI3K/Akt, RSK1/RSK2 and HDAC inhibitor.
      Smiles
      OC1=C2C(OC(C3=CC(O)=C(O)C=C3)=CC2=O)=CC(O)=C1
      InChi Key
      IQPNAANSBPBGFQ-UHFFFAOYSA-N
      References
      (1) Y.T. Huang, et al., Br. J. Pharmacol. 128, 999 (1999) , (2) J.S. Kim, et al., Biosci. Biotechnol. Biochem. 64, 2458 (2000) , (3) H. Ueda, et al., Biol. Pharm. Bull. 25, 1197 (2002) , (4) A.R. Chowdhury, et al., Biochem. J. 366, 653 (2002) , (5) L. Sartor, et al., Biochem. Pharmacol. 64, 229 (2002) , (6) C.D. Sadik, et al., Biochem. Pharmacol. 65, 773 (2003) , (7) D.T. Coleman, et al., Mol. Cancer Ther. 8, 214 (2009) , (8) K. Xu, et al., Molecules 14, 3486 (2009) , (9) H.S. Park, et al., Biofactors 35, 373 (2009) , (10) S. Attoub, et al., Eur. J. Pharmacol. 651, 18 (2011) , (11) H.Y. Kim, et al., Phytother. Res. 27, 1481 (2013) , (12) K.M. Reipas, et al., Oncotarget 4, 329 (2013)

      Luteolin is a hydroxylated flavone derivative that is a strong antioxidant and radical scavenger. It has multiple activities, such as anticancer, antimetastatic, anti-adipogenic, anti-inflammatory and neuroprotective. Luteolin has been described as a fatty acid synthase (FASN), 15-lipoxygenase, alpha-glucosidase, PPAR-γ, topoisomerase I, PI3K/Akt, RSK1/RSK2 and HDAC inhibitor.

      Artikelnummer: L0087 Kategorie: Lipids, Fatty Acids
      • Zusätzliche Informationen

      Zusätzliche Informationen

      Synonyms

      3',4',5,7-Tetrahydroxyflavone, Luteolol, BRN 0292084, C.I. Natural Yellow 2, Digitoflavone, Flacitran, Flavopurpol, Daphneflavonol, Argemexitin

      Purity

      ≥98% (TLC)

      Appearance

      Yellow powder

      CAS-Number

      491-70-3

      Molecular Formula

      C15H10O6

      Molecular Weight

      286.24

      Identity

      1H-NMR

      Solvents

      DMSO (10mg/ml), DMF (20mg/ml), methanol, ethanol (5mg/ml)

      Smiles

      OC1=C2C(OC(C3=CC(O)=C(O)C=C3)=CC2=O)=CC(O)=C1

      InChi Key

      IQPNAANSBPBGFQ-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Transportation

      Not dangerous goods

      References

      (1) Y.T. Huang, et al., Br. J. Pharmacol. 128, 999 (1999), (2) J.S. Kim, et al., Biosci. Biotechnol. Biochem. 64, 2458 (2000), (3) H. Ueda, et al., Biol. Pharm. Bull. 25, 1197 (2002), (4) A.R. Chowdhury, et al., Biochem. J. 366, 653 (2002), (5) L. Sartor, et al., Biochem. Pharmacol. 64, 229 (2002), (6) C.D. Sadik, et al., Biochem. Pharmacol. 65, 773 (2003), (7) D.T. Coleman, et al., Mol. Cancer Ther. 8, 214 (2009), (8) K. Xu, et al., Molecules 14, 3486 (2009), (9) H.S. Park, et al., Biofactors 35, 373 (2009), (10) S. Attoub, et al., Eur. J. Pharmacol. 651, 18 (2011), (11) H.Y. Kim, et al., Phytother. Res. 27, 1481 (2013), (12) K.M. Reipas, et al., Oncotarget 4, 329 (2013)

      Quantity

      10 mg, 50 mg, Bulk

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