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559408 SB 220025, Trihydrochloride - CAS 197446-75-6 - Calbiochem

559408
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559408-500UG
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      Description
      OverviewA cell-permeable, potent, reversible, ATP-competitive, and specific inhibitor of human p38 MAP Kinase (IC50 = 60 nM). Binds to an extended pocket in the active site of the enzyme. Exhibits over 2000-fold greater selectivity for p38 MAPK over ERK (p42/p44 MAP kinase), 500-fold over PKA, 50-fold over PKC, and >1000-fold over EGFR. Also acts as a potent inhibitor of angiogenesis and as an inhibitor of LPS-induced TNF-α production.
      Catalogue Number559408
      Brand Family Calbiochem®
      Synonyms5-(2-Amino-4-pyrimidinyl)-4-(4-fluorophenyl)-1-(4-piperidinlyl)imidazole, p38 MAP Kinase Inhibitor XIV
      References
      ReferencesJackson, J.R., et al. 1998. J. Pharmacol. Exp. Ther. 284, 687.
      Wang, Z., et al. 1998. Structure 6, 1117.
      Product Information
      CAS number197446-75-6
      FormWhite solid
      Hill FormulaC₁₈H₁₉FN₆ • 3HCl
      Chemical formulaC₁₈H₁₉FN₆ • 3HCl
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥98% by HPLC
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Standard Handling
      Storage -20°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      SB 220025, Trihydrochloride - CAS 197446-75-6 - Calbiochem SDS

      Title

      Safety Data Sheet (SDS) 

      References

      Reference overview
      Jackson, J.R., et al. 1998. J. Pharmacol. Exp. Ther. 284, 687.
      Wang, Z., et al. 1998. Structure 6, 1117.
      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.

      Revision23-September-2014 JSW
      Synonyms5-(2-Amino-4-pyrimidinyl)-4-(4-fluorophenyl)-1-(4-piperidinlyl)imidazole, p38 MAP Kinase Inhibitor XIV
      DescriptionA cell-permeable, potent, reversible, ATP-competitive, and specific inhibitor of human p38 MAP Kinase (IC50 = 60 nM). Binds to an extended pocket in the active site of the enzyme. Exhibits over 2000-fold greater selectivity for p38 MAPK over ERK (p42/p44 MAP kinase), 500-fold over PKA, 50-fold over PKC, and >1000-fold over EGFR. Also acts as a potent inhibitor of angiogenesis and as an inhibitor of LPS-induced TNF-α production.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number197446-75-6
      Chemical formulaC₁₈H₁₉FN₆ • 3HCl
      Purity≥98% by HPLC
      SolubilityH₂O (22 mg/ml)
      Storage -20°C
      Protect from light
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesJackson, J.R., et al. 1998. J. Pharmacol. Exp. Ther. 284, 687.
      Wang, Z., et al. 1998. Structure 6, 1117.