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

506155
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Overview

Replacement Information

Key Spec Table

CAS #Empirical Formula
64984-31-2C₈H₇NO₂S

Products

Catalogue NumberPackaging Qty/Pack
506155-10MG Plastic ampoule 10 mg
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
Catalogue Number GTIN
506155-10MG 04055977272253

Documentation

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

Title

Safety Data Sheet (SDS) 

Pifithrin-μ - CAS 64984-31-2 - Calbiochem Certificates of Analysis

TitleLot Number
506155

References

Reference overview
Leu, J., et al. 2009. Mol. Cell 36, 15.
Strom, E., et al. 2006. Nat. Chem. Biol. 2, 474.

Brochure

Title
p53 And Related Products
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.

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.