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506155 Pifithrin-μ - CAS 64984-31-2 - Calbiochem

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506155
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
64984-31-2C₈H₇NO₂S

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506155-10MGCN
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      樹脂アンプル 10 mg
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      Description
      OverviewA cell-permeable sulfonamide that blocks p53 interaction with Bcl-xL and Bcl-2 proteins and selectively inhibits p53 translocation to mitochondria without affecting the transactivation function of p53. Effectively protects against γ radiation-induced cell death in vitro and animal lethality in vivo. Because Pifithrin-μ targets only the mitochondrial branch of the p53 pathway without affecting the important transcriptional functions of p53, it is superior to Pifithrin-α (Cat. No. 506132) in in vivo studies. Shown to selectively interact with inducible HSP70 and disrupt its functions.
      Catalogue Number506155
      Brand Family Calbiochem®
      SynonymsPhenylacetylenylsulfonamide, Hsp70 Inhibitor I
      References
      ReferencesLeu, J., et al. 2009. Mol. Cell 36, 15.
      Strom, E., et al. 2006. Nat. Chem. Biol. 2, 474.
      Product Information
      CAS number64984-31-2
      ATP CompetitiveN
      FormOff-white solid
      Hill FormulaC₈H₇NO₂S
      Chemical formulaC₈H₇NO₂S
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      ApplicationPifithrin-μ, CAS 64984-31-2, is a cell-permeable inhibitor of p53 interaction with Bcl-xL & Bcl-2. Inhibits p53 translocation to mitochondria without affecting the transactivation function of p53.
      Biological Information
      Primary Targetp53 interaction with Bcl-xL and Bcl-2 proteins
      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 Ambient Temperature Only
      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 3 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      506155-10MGCN 04055977272253

      Documentation

      Pifithrin-μ - CAS 64984-31-2 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      Pifithrin-μ - CAS 64984-31-2 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      506155

      参考資料

      参考資料の概要
      Leu, J., et al. 2009. Mol. Cell 36, 15.
      Strom, E., et al. 2006. Nat. Chem. Biol. 2, 474.

      カタログ

      タイトル
      p53 And Related Products
      データシート

      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.

      Revision13-October-2009 RFH
      SynonymsPhenylacetylenylsulfonamide, Hsp70 Inhibitor I
      DescriptionA cell-permeable sulfonamide that blocks p53 interaction with Bcl-xL and Bcl-2 proteins and selectively inhibits p53 translocation to mitochondria without affecting the transactivation function of p53. Effectively protects against γ radiation-induced cell death in vitro and animal lethality in vivo. Because Pifithrin-μ targets only the mitochondrial branch of the p53 pathway without affecting the important transcriptional functions of p53, it is superior to Pifithrin-α (Cat. No. 506132) in in vivo studies. Shown to selectively interact with inducible HSP70 and disrupt its functions.
      FormOff-white solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number64984-31-2
      Chemical formulaC₈H₇NO₂S
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (50 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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesLeu, J., et al. 2009. Mol. Cell 36, 15.
      Strom, E., et al. 2006. Nat. Chem. Biol. 2, 474.