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539162 Proteasome Inhibitor II - Calbiochem

The Proteasome Inhibitor II controls the biological activity of Proteasome. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

Proteasome Inhibitor II - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: (Benzyloxycarbonyl)-Leu-Leu-phenylalaninal, Z-LLF-CHO

Primary Target: MPC
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Overview

Replacement Information

Key Spec Table

Empirical Formula
C₂₉H₃₉N₃O₅

Products

Catalogue NumberPackaging Qty/Pack
539162-1MGCN Plastic ampoule 1 mg
539162-5MGCN Plastic ampoule 5 mg
Description
OverviewA potent, cell-permeable, and reversible proteasome inhibitor. Inhibits the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex (MPC; Ki = 460 nM). Does not inhibit the peptidyl-glutamyl peptide hydrolyzing activity of MPC even at concentrations of 200 µM. Also blocks the decay of IκB-α and IκB-β proteins in exponentially growing WEHI 231 cells.
Catalogue Number539162
Brand Family Calbiochem®
Synonyms(Benzyloxycarbonyl)-Leu-Leu-phenylalaninal, Z-LLF-CHO
References
ReferencesSchauer, S.L., et al. 1998. J. Immunol. 160, 4398.
Orlowski, M., et al. 1997. Biochemistry 36, 13946.
Orlowski, M., et al. 1993. Biochemistry 32, 1563.
Product Information
ATP CompetitiveN
FormWhite lyophilized solid
Hill FormulaC₂₉H₃₉N₃O₅
Chemical formulaC₂₉H₃₉N₃O₅
ReversibleY
Quality LevelMQ100
Applications
Biological Information
Primary TargetMPC
Primary Target K<sub>i</sub>460 nM against the pituitary multicatalytic proteinase complex (MPC)
Purity≥95% by HPLC
Physicochemical Information
Cell permeableY
Peptide SequenceZ-Leu-Leu-Phe-CHO
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 Moisture Protect from moisture
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalogue Number GTIN
539162-1MGCN 04055977269451
539162-5MGCN 04055977269468

Documentation

Proteasome Inhibitor II - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

Proteasome Inhibitor II - Calbiochem Certificates of Analysis

TitleLot Number
539162

References

Reference overview
Schauer, S.L., et al. 1998. J. Immunol. 160, 4398.
Orlowski, M., et al. 1997. Biochemistry 36, 13946.
Orlowski, M., et al. 1993. Biochemistry 32, 1563.

Brochure

Title
Caspases and other Apoptosis Related Tools Brochure
Proteasomes Technical Bulletin
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.

Revision04-September-2008 RFH
Synonyms(Benzyloxycarbonyl)-Leu-Leu-phenylalaninal, Z-LLF-CHO
DescriptionA potent and cell-permeable proteasome inhibitor. Inhibits the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex (MPC; Ki = 460 nM). Does not inhibit the peptidylglutamyl-peptide hydrolyzing (PGPH) activity of MPC even at concentrations of 200 µM. Also blocks the decay of IκB-α and IκB-β proteins in exponentially growing WEHI 231 cells.
FormWhite lyophilized solid
Chemical formulaC₂₉H₃₉N₃O₅
Peptide SequenceZ-Leu-Leu-Phe-CHO
Purity≥95% by HPLC
SolubilityDMSO (5 mg/ml)
Storage Protect from moisture
-20°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months.
Toxicity Standard Handling
ReferencesSchauer, S.L., et al. 1998. J. Immunol. 160, 4398.
Orlowski, M., et al. 1997. Biochemistry 36, 13946.
Orlowski, M., et al. 1993. Biochemistry 32, 1563.