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219334 β-Catenin/Tcf Inhibitor V, BC21 - CAS 691005-38-6 - Calbiochem

219334
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
691005-38-6C₃₂H₃₆Cl₂Cu₂N₂O₂

价格及供货情况

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219334-10MGCN
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      玻璃瓶 10 mg
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      Description
      OverviewA cell-permeable dimeric copper complex that competitively binds β-catenin and disrupts β-catenin/Tcf4 interaction reversibly (IC50 = 5.0 µM), and acts as a Wnt signaling inhibitor. Shown to induce preferential growth arrest in β-catenin overexpressing HCT116 colon cancer and HEK293 cells (≤ 10 µM), and downregulate mRNA expressions of c-Myc and cyclin D1. Reported to inhibit PP2C and proteasomal activities at higher concentrations (~50 µM).
      Catalogue Number219334
      Brand Family Calbiochem®
      SynonymsCopper, di-µ-chlorobis[1-[(1-piperidinyl-κN)methyl]-2-naphthalenolato-κO]di-(9Cl), Wnt Pathway Inhibitor XV
      References
      ReferencesTian, W., et al. 2012. Biochemistry 51, 724.
      Rogers, J.P., et al. 2006. J. Med. Chem. 49, 1658.
      Daniel, K.G., et al. 2004. Biochem. Pharmacol. 67, 1139.
      Product Information
      CAS number691005-38-6
      FormDark brown solid
      Hill FormulaC₃₂H₃₆Cl₂Cu₂N₂O₂
      Chemical formulaC₃₂H₃₆Cl₂Cu₂N₂O₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥95% by Elemental Analysis
      Physicochemical Information
      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, freeze (≥-70°C). Stock solutions are stable for up to 12 months at ≥-70°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      产品目录编号 GTIN
      219334-10MGCN 04055977202137

      Documentation

      β-Catenin/Tcf Inhibitor V, BC21 - CAS 691005-38-6 - Calbiochem MSDS

      职位

      物料安全数据表 (MSDS) 

      β-Catenin/Tcf Inhibitor V, BC21 - CAS 691005-38-6 - Calbiochem 分析证书

      标题批号
      219334

      参考

      参考信息概述
      Tian, W., et al. 2012. Biochemistry 51, 724.
      Rogers, J.P., et al. 2006. J. Med. Chem. 49, 1658.
      Daniel, K.G., et al. 2004. Biochem. Pharmacol. 67, 1139.
      数据表

      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.

      Revision03-February-2017 JSW
      SynonymsCopper, di-µ-chlorobis[1-[(1-piperidinyl-κN)methyl]-2-naphthalenolato-κO]di-(9Cl), Wnt Pathway Inhibitor XV
      DescriptionA cell-permeable dimeric copper complex that competitively binds β-catenin and disrupts β-catenin/Tcf4 interaction reversibly (IC50 = 5.0 µM), and acts as a Wnt signaling inhibitor. Shown to induce preferential growth arrest in β-catenin overexpressing HCT116 colon cancer and HEK293 cells (≤ 10 µM), and downregulate mRNA expressions of c-Myc and cyclin D1. Reported to inhibit PP2C and proteasomal activities at higher concentrations (~50 µM).
      FormDark brown solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number691005-38-6
      Chemical formulaC₃₂H₃₆Cl₂Cu₂N₂O₂
      Structure formulaStructure formula
      Purity≥95% by Elemental Analysis
      SolubilityDMSO (0.5 mg/ml). Poorly soluble in water.
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution aliquot, freeze (≥-70°C). Stock solutions are stable for up to 12 months at ≥-70°C.
      Toxicity Standard Handling
      ReferencesTian, W., et al. 2012. Biochemistry 51, 724.
      Rogers, J.P., et al. 2006. J. Med. Chem. 49, 1658.
      Daniel, K.G., et al. 2004. Biochem. Pharmacol. 67, 1139.