373225 | Hdm2 E3 Ligase Inhibitor - CAS 414905-09-2 - Calbiochem

373225
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      Overview

      Key Spec Table

      Empirical FormulaCAS #
      C₁₀H₈F₆N₂O₃S414905-09-2

      Pricing & Availability

      Catalogue NumberAvailability Packaging Qty/Pack Price Quantity
      373225-5MG
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          5 mg
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          Description
          Overview A cell-permeable and reversible inhibitor of Hdm2 E3 ligase that selectively blocks Hdm2 E3-mediated ubiquitination. Has been shown to inhibit ubiquitination of p53 in vitro (IC50 = 12.7 µM using Ub-Ubc as the donor substrate). Exhibits little effect towards other ubiquitin-using enzymes (IC50 > 100 µM for E1, Nedd-4, and SCF) or the auto-ubiquitination activity of Hdm2. The inhibition is non-competitive with respect to either the donor or acceptor substrate.
          Catalogue Number 373225
          Brand Family Calbiochem®
          Synonyms N-((3,3,3-Trifluoro-2-trifluromethyl)propionyl)sulfanilamide, Mdm2 E3 Ligase Inhibitor, MDM2 Inhibitor V
          References
          References Lai, Z., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 14734.
          Product Information
          CAS number 414905-09-2
          Form Pale yellow solid
          Hill Formula C₁₀H₈F₆N₂O₃S
          Chemical formula C₁₀H₈F₆N₂O₃S
          Molar Mass 350.2
          Reversible Y
          Structure formula Image
          Applications
          Application The Hdm2 E3 Ligase Inhibitor, also referenced under CAS 414905-09-2, controls the biological activity of Hdm2 E3 Ligase. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
          Biological Information
          Primary Target ubiquitination of p53 in vitro
          Primary Target IC<sub>50</sub> 12.7 µM inhibiting ubiquitination of p53 in vitro using Ub-Ubc as the donor substrate
          Purity ≥95% by NMR
          Physicochemical Information
          Cell permeable Y
          Solubility DMSO
          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
          Special Instructions Following 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

          Documentation

          MSDS

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          Certificates of Analysis

          TitleLot Number
          373225
          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.

          Revision 07-July-2014 JSW
          Synonyms N-((3,3,3-Trifluoro-2-trifluromethyl)propionyl)sulfanilamide, Mdm2 E3 Ligase Inhibitor, MDM2 Inhibitor V
          Description A cell-permeable and reversible inhibitor of Hdm2 E3 ligase that selectively blocks Hdm2 E3-mediated ubiquitination. Has been shown to inhibit ubiquitination of p53 in vitro (IC50 = 12.7 µM using Ub-Ubc as the donor substrate). Exhibits little effect towards other ubiquitin-using enzymes (IC50 >100 µM for E1, Nedd-4, and SCF) or the auto-ubiquitination activity of Hdm2. The inhibition is non-competitive with respect to either the donor or acceptor substrate.
          Form Pale yellow solid
          Intert gas (Yes/No) Packaged under inert gas
          CAS number 414905-09-2
          Molar mass 350.2
          Chemical formula C₁₀H₈F₆N₂O₃S
          Structure formula
          Purity ≥95% by NMR
          Solubility DMSO (50 mg/ml)
          Storage +2°C to +8°C
          Protect from light
          Special Instructions Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Toxicity Standard Handling
          References Lai, Z., et al. 2002. Proc. Natl. Acad. Sci. USA 99, 14734.