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509106 Sphingosine Kinase-2 Inhibitor, K145 - Calbiochem

A cell permeable, selective, sphingosine competitive inhibitor of spingosine Kinase -2 (IC₅₀ = 4.3 µM).

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: SphK2 Inhibitor, K145

Primary Target: Sphk2
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509106
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Overview

Replacement Information

Key Specifications Table

Empirical Formula
C₁₈H₂₄N₂O₃S

Pricing & Availability

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      		 Glass bottle 10 mg
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      Description
      OverviewA cell permeable, orally bioavailable thiazolidine-2,4-dione derivative that acts as a selective, sphingosine competitive inhibitor of spingosine Kinase -2 (SphK2; IC50 = 4.3 µM; Ki = 6.4 µM), but does not affect the activities of sphingosine kinase-1, ceremide kinase, and ceramide synthase even at high concentration (~10 micro;M). Shown to inhibit the growth of U937 human leukemic monocyte lymphoma cells by inducing apoptosis and inhibiting the phosphorylation of ERK and Akt. Blocks the growth of U937 cells in nude mice and inhibits the growth of JC tumor cells in BALB/c mice without any apparent toxicity.

      Please note that the molecular weight for this compound is batch-specific due to variable water content.
      Catalogue Number509106
      Brand Family Calbiochem®
      SynonymsSphK2 Inhibitor, K145
      References
      ReferencesLiu, K., et al. 2013. PLos One 8, e56471.
      Product Information
      FormOff-white powder
      Hill FormulaC₁₈H₂₄N₂O₃S
      Chemical formulaC₁₈H₂₄N₂O₃S
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetSphk2
      Primary Target IC<sub>50</sub>4.3 µ
      Purity≥95% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage +2°C to +8°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 2 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      Sphingosine Kinase-2 Inhibitor, K145 - Calbiochem SDS

      Title

      Safety Data Sheet (SDS) 

      References

      Reference overview
      Liu, K., et al. 2013. PLos One 8, e56471.
      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.

      Revision18-April-2014 JSW
      SynonymsSphK2 Inhibitor, K145
      DescriptionA cell permeable, orally bioavailable thiazolidine-2,4-dione derivative that acts as a selective, sphingosine competitive inhibitor of spingosine Kinase -2 (SphK2; IC50 = 4.3 µM; Ki = 6.4 µM), but does not affect the activities of sphingosine kinase-1, ceremide kinase, and ceramide synthase even at high concentration (~10 micro;M). Shown to inhibit the growth of U937 human leukemic monocyte lymphoma cells by inducing apoptosis and inhibiting the phosphorylation of ERK and Akt. Blocks the growth of U937 cells in nude mice and inhibits the growth of JC tumor cells in BALB/c mice without any apparent toxicity.
      FormOff-white powder
      Intert gas (Yes/No) Packaged under inert gas
      Chemical formulaC₁₈H₂₄N₂O₃S
      Purity≥95% by HPLC
      SolubilityDMSO (100 mg/ml) or H₂O (2.5 mg/ml)
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 2 months at -20°C.
      Toxicity Standard Handling
      ReferencesLiu, K., et al. 2013. PLos One 8, e56471.