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529605 InSolution™ PP1 Analog - CAS 221243-82-9 - Calbiochem

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Overview

Replacement Information

Key Spec Table

CAS #Empirical Formula
221243-82-9C₁₉H₁₉N₅
Description
OverviewA potent, reversible, ATP-competitive, and cell-permeable inhibitor of Src-family tyrosine kinases that is >800 times more selective for the I338G mutant v-Src (IC50 = 1.5 nM) compared to wild-type v-Src (IC50 = 1.0 µM). Also inhibits wild-type Fyn (IC50 = 600 nM). A 10 mM (1 mg/315 µl) solution of PP1 Analog (Cat. No. 529579) in DMSO.
Catalogue Number529605
Brand Family Calbiochem®
References
ReferencesBishop, A.C., et al. 2000. Nature 407, 395.
Bishop, A.C., et al. 1999 J. Am. Chem. Soc. 121, 627.
Product Information
CAS number221243-82-9
Declaration

Not available for sale in the United States.

FormLiquid
FormulationA 10 mM (1 mg/315 µl) solution of PP1 Analog (Cat. No. 529579) in DMSO.
Hill FormulaC₁₉H₁₉N₅
Chemical formulaC₁₉H₁₉N₅
Hygroscopic Hygroscopic
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Purity≥97% by HPLC
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
R PhraseR: 36/38

Irritating to eyes and skin.
Product Usage Statements
Storage and Shipping Information
Ship Code Dry Ice Only
Toxicity Irritant
Storage ≤ -70°C
Protect from Light Protect from light
Hygroscopic Hygroscopic
Avoid freeze/thaw Avoid freeze/thaw
Do not freeze Ok to freeze
Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalogue Number GTIN
529605 0

Documentation

InSolution™ PP1 Analog - CAS 221243-82-9 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

InSolution™ PP1 Analog - CAS 221243-82-9 - Calbiochem Certificates of Analysis

TitleLot Number
529605

References

Reference overview
Bishop, A.C., et al. 2000. Nature 407, 395.
Bishop, A.C., et al. 1999 J. Am. Chem. Soc. 121, 627.
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.

Revision09-January-2012 RFH
DescriptionA potent, reversible, ATP-competitive, and cell-permeable inhibitor of Src-family tyrosine kinases that is >800 times more selective for the I338G mutant v-Src (IC50 = 1.5 nM) compared to wild-type v-Src (IC50 = 1.0 µM). Also inhibits wild-type Fyn (IC50 = 600 nM). A 10 mM (1 mg/315 µl) solution of PP1 Analog (Cat. No. 529579) in DMSO.
FormLiquid
FormulationA 10 mM (1 mg/315 µl) solution of PP1 Analog (Cat. No. 529579) in DMSO.
Intert gas (Yes/No) Packaged under inert gas
CAS number221243-82-9
Chemical formulaC₁₉H₁₉N₅
Structure formulaStructure formula
Purity≥97% by HPLC
Storage Protect from light
Avoid freeze/thaw
≤ -70°C
Hygroscopic
Do Not Freeze Ok to freeze
Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
Toxicity Irritant
ReferencesBishop, A.C., et al. 2000. Nature 407, 395.
Bishop, A.C., et al. 1999 J. Am. Chem. Soc. 121, 627.