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681629 W-7, Hydrochloride - CAS 61714-27-0 - Calbiochem

A cell-permeable and reversible calmodulin antagonist that inhibits myosin light chain kinase (IC₅₀ = 51 µM) and Ca2+-calmodulin-dependent phosphodiesterase (IC₅₀ = 28 µM).

W-7, Hydrochloride - CAS 61714-27-0 - Calbiochem: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。

同義語: N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide, HCl

Primary Target: Myosin light chain kinase
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681629
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
61714-27-0C₁₆H₂₁ClN₂O₂S · HCl

価格＆在庫状況

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681629-10MGCN
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      Description
      OverviewA cell-permeable and reversible calmodulin antagonist that inhibits myosin light chain kinase (IC50 = 51 µM) and Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 28 µM).
      Catalogue Number681629
      Brand Family Calbiochem®
      SynonymsN-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide, HCl
      References
      ReferencesCaulfield, M.P., et al. 1991. Neurosci. Lett. 125, 57.
      Asano, M. 1989. J. Pharmacol. Exp. Ther. 251, 764.
      Itoh, H., and Hidaka, H. 1984. J. Biochem. 96, 1721.
      Tanaka, T., et al. 1983. Pharmacol. 26, 249.
      Hidaka, H. 1981. Proc. Natl. Acad. Sci. USA 78, 4354.
      Product Information
      CAS number61714-27-0
      ATP CompetitiveN
      FormOff-white crystalline solid
      Hill FormulaC₁₆H₂₁ClN₂O₂S · HCl
      Chemical formulaC₁₆H₂₁ClN₂O₂S · HCl
      Hygroscopic Hygroscopic
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetMyosin light chain kinase
      Primary Target IC<sub>50</sub> 51 µM inhibiting myosin light chain kinase; 28 µM inhibiting Ca2+-calmodulin-dependent phosphodiesterase
      Purity≥98% by TLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSQK0786000
      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
      Hygroscopic Hygroscopic
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, refrigerate (4°C). Stock solutions are stable for up to 6 months at 4°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      681629-10MGCN 04055977260144

      Documentation

      W-7, Hydrochloride - CAS 61714-27-0 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      W-7, Hydrochloride - CAS 61714-27-0 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      681629

      参考資料

      参考資料の概要
      Caulfield, M.P., et al. 1991. Neurosci. Lett. 125, 57.
      Asano, M. 1989. J. Pharmacol. Exp. Ther. 251, 764.
      Itoh, H., and Hidaka, H. 1984. J. Biochem. 96, 1721.
      Tanaka, T., et al. 1983. Pharmacol. 26, 249.
      Hidaka, H. 1981. Proc. Natl. Acad. Sci. USA 78, 4354.
      データシート

      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.

      Revision06-January-2010 RFH
      SynonymsN-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide, HCl
      DescriptionA cell-permeable and reversible calmodulin antagonist that inhibits Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 28 µM) and myosin light chain kinase (IC50 = 51 µM).
      FormOff-white crystalline solid
      CAS number61714-27-0
      RTECSQK0786000
      Chemical formulaC₁₆H₂₁ClN₂O₂S · HCl
      Structure formulaStructure formula
      Purity≥98% by TLC
      SolubilityDMSO (5 mg/ml), DMF, or warm Ethanol
      Storage Protect from light
      +2°C to +8°C
      Hygroscopic
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, refrigerate (4°C). Stock solutions are stable for up to 6 months at 4°C.
      Toxicity Standard Handling
      ReferencesCaulfield, M.P., et al. 1991. Neurosci. Lett. 125, 57.
      Asano, M. 1989. J. Pharmacol. Exp. Ther. 251, 764.
      Itoh, H., and Hidaka, H. 1984. J. Biochem. 96, 1721.
      Tanaka, T., et al. 1983. Pharmacol. 26, 249.
      Hidaka, H. 1981. Proc. Natl. Acad. Sci. USA 78, 4354.

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      カテゴリー

      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Other Inhibitors of Biological Interest > Phosphodiesterase Inhibitors
      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Protein Phosphorylation / Dephosphorylation > Myosin Light Chain Kinase (MLCK) Inhibitors