551600 Quercetin, Dihydrate - CAS 6151-25-3 - Calbiochem

551600
View Pricing & Availability

Overview

Replacement Information

Key Specifications Table

Empirical FormulaCAS #
C₁₅H₁₀O₇ · 2H₂O 6151-25-3

Pricing & Availability

Catalog Number AvailabilityPackaging Qty/Pack Price Quantity
551600-100MG
Retrieving availability...
Limited AvailabilityLimited Availability
Stocked 
Discontinued
Limited Quantities Available
Available
    Remaining : Will advise
      Remaining : Will advise
      Will advise
      Contact Customer Service
      Contact Customer Service

      Glass bottle 100 mg
      Retrieving price...
      Price could not be retrieved
      Minimum Quantity needs to be mulitiple of
      Upon Order Completion More Information
      You Saved ()
       
      Request Pricing
      Description
      OverviewA cell-permeable and reversible inhibitor of PIM1 kinase (IC50 = 43 nM), PI 3-K (IC50 = 3.8 µM) and phospholipase A2 (IC50 = 2 µM). Also inhibits mitochondrial ATPase, phosphodiesterases, and protein kinase C. Induces apoptosis in K562, Molt-4, Raji, and MCAS tumor cell lines. Reported to activate sirtuins and promote the survival of eukaryotic cells.
      Catalogue Number551600
      Brand Family Calbiochem®
      Synonyms3,3ʹ,4ʹ,5,7-Pentahydroxyflavone
      References
      ReferencesBullock, A.N., et al. 2005. J. Med. Chem. 48, 7604.
      Howitz, K.T., et al. 2003. Nature 425, 191.
      Wei, Y.Q., et al. 1994. Cancer Res. 54, 4952.
      Shibasaki, F., et al. 1993. Biochem. J. 289, 227.
      Matter, W.F., et al. 1992. Biochem. Biophys. Res. Comm. 186, 624.
      Levy, J., et al. 1984. Biochem. Biophys. Res. Commun. 123, 1227.
      Graziani, Y., et al. 1983. Eur. J. Biochem. 135, 583.
      Gschwendt, M., et al. 1983. Biochem. Biophys. Res. Commun. 117, 444.
      Ruckstuhl, M., et al. 1979. Biochem. Pharmacol. 28, 535.
      Beretz, A., et al. 1978. Experientia 34, 1054.
      Product Information
      CAS number6151-25-3
      ATP CompetitiveN
      FormYellow solid
      Hill FormulaC₁₅H₁₀O₇ · 2H₂O
      Chemical formulaC₁₅H₁₀O₇ · 2H₂O
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetPI 3-kinase
      Primary Target IC<sub>50</sub>43 nM, 3.8 µM, 2 µM against PIM1 kinase, PI 3-K, and phospholipase A2, respectively
      Purity>95% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSLK8950000
      Safety Information
      R PhraseR: 25-40

      Toxic if swallowed.
      Limited evidence of a carcinogenic effect.
      S PhraseS: 36/37/39-45

      Wear suitable protective clothing, gloves and eye/face protection.
      In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Toxic & Carcinogenic / Teratogenic
      Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
      Storage +15°C to +30°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, store in the refrigerator (4°C). Stock solutions are stable for up to 3 months at 4°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      Quercetin, Dihydrate - CAS 6151-25-3 - Calbiochem SDS

      Title

      Safety Data Sheet (SDS) 

      Quercetin, Dihydrate - CAS 6151-25-3 - Calbiochem Certificates of Analysis

      TitleLot Number
      551600

      References

      Reference overview
      Bullock, A.N., et al. 2005. J. Med. Chem. 48, 7604.
      Howitz, K.T., et al. 2003. Nature 425, 191.
      Wei, Y.Q., et al. 1994. Cancer Res. 54, 4952.
      Shibasaki, F., et al. 1993. Biochem. J. 289, 227.
      Matter, W.F., et al. 1992. Biochem. Biophys. Res. Comm. 186, 624.
      Levy, J., et al. 1984. Biochem. Biophys. Res. Commun. 123, 1227.
      Graziani, Y., et al. 1983. Eur. J. Biochem. 135, 583.
      Gschwendt, M., et al. 1983. Biochem. Biophys. Res. Commun. 117, 444.
      Ruckstuhl, M., et al. 1979. Biochem. Pharmacol. 28, 535.
      Beretz, A., et al. 1978. Experientia 34, 1054.
      Data Sheet

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision19-June-2009 JSW
      Synonyms3,3ʹ,4ʹ,5,7-Pentahydroxyflavone
      DescriptionA cell-permeable inhibitor of PIM1 kinase (IC50 = 43 nM), PI 3-K (IC50 = 3.8 µM) and phospholipase A2 (IC50 = 2 µM). Also inhibits mitochondrial ATPase, phosphodiesterases, and protein kinase C. Induces apoptosis in K562, Molt-4, Raji, and MCAS tumor cell lines. Reported to activate sirtuins and promote the survival of eukaryotic cells.
      FormYellow solid
      CAS number6151-25-3
      RTECSLK8950000
      Chemical formulaC₁₅H₁₀O₇ · 2H₂O
      Structure formulaStructure formula
      Purity>95% by HPLC
      SolubilityAcetic Acid (1 mg/ml), Aqueous Alkali (1 mg/ml), or DMSO (5 mg/ml)
      Storage +15°C to +30°C
      Protect from light
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, store in the refrigerator (4°C). Stock solutions are stable for up to 3 months at 4°C.
      Toxicity Toxic & Carcinogenic / Teratogenic
      Merck USA index14, 8034
      ReferencesBullock, A.N., et al. 2005. J. Med. Chem. 48, 7604.
      Howitz, K.T., et al. 2003. Nature 425, 191.
      Wei, Y.Q., et al. 1994. Cancer Res. 54, 4952.
      Shibasaki, F., et al. 1993. Biochem. J. 289, 227.
      Matter, W.F., et al. 1992. Biochem. Biophys. Res. Comm. 186, 624.
      Levy, J., et al. 1984. Biochem. Biophys. Res. Commun. 123, 1227.
      Graziani, Y., et al. 1983. Eur. J. Biochem. 135, 583.
      Gschwendt, M., et al. 1983. Biochem. Biophys. Res. Commun. 117, 444.
      Ruckstuhl, M., et al. 1979. Biochem. Pharmacol. 28, 535.
      Beretz, A., et al. 1978. Experientia 34, 1054.