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208293 Calcium-activated Chloride Channel Inhibitor, CaCCinh-A01 - CAS 407587-33-1 - Calbiochem

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208293
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
407587-33-1C₁₈H₂₁NO₄S

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208293-10MGCN
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      ガラスビン 10 mg
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      Description
      OverviewAn aminothiophene that inhibits Calcium-activated Chloride Channel (CaCC) current influx induced by multiple calcium-elevating agonists (IC50 = 10 µM) without inhibiting calcium elevation, and CaMKII and CFTR activity. Inhibits CaCC chloride response following agonist stimulation in human bronchial and intestinal epithelial cells. Also demonstrates an inhibitory effect on TMEM16A channels (IC50 = 2.1 µM). Also available as a 100 mM solution in DMSO (Cat. No. 508628).
      Catalogue Number208293
      Brand Family Calbiochem®
      Synonyms6-tert-butyl-2-(furan-2-carboxamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid, CaCC Blocker I, TMEM16 Blocker I, ANO Blocker I, Anoctamin Blocker I
      References
      ReferencesFuente, R., et al. 2011, Mol Pharmacol. 73, 758.
      Namkung, W., et al. 2011, J Biol Chem. 286, 2365.
      Product Information
      CAS number407587-33-1
      FormOff-white solid
      Hill FormulaC₁₈H₂₁NO₄S
      Chemical formulaC₁₈H₂₁NO₄S
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥98% by HPLC
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage -20°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing 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
      Global Trade Item Number
      カタログ番号 GTIN
      208293-10MGCN 04055977203264

      Documentation

      Calcium-activated Chloride Channel Inhibitor, CaCCinh-A01 - CAS 407587-33-1 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      Calcium-activated Chloride Channel Inhibitor, CaCCinh-A01 - CAS 407587-33-1 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      208293

      参考資料

      参考資料の概要
      Fuente, R., et al. 2011, Mol Pharmacol. 73, 758.
      Namkung, W., et al. 2011, J Biol Chem. 286, 2365.
      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.

      Revision14-May-2012 JSW
      Synonyms6-tert-butyl-2-(furan-2-carboxamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid, CaCC Blocker I, TMEM16 Blocker I, ANO Blocker I, Anoctamin Blocker I
      DescriptionAn aminothiophene that inhibits Calcium-activated Chloride Channel (CaCC) current influx induced by multiple calcium-elevating agonists (IC50 = 10 µM) without inhibiting calcium elevation, and CaMKII and CFTR activity. Inhibits CaCC chloride response following agonist stimulation in human bronchial and intestinal epithelial cells. Also demonstrates an inhibitory effect on TMEM16A channels (IC50 = 2.1 µM).
      FormOff-white solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number407587-33-1
      Chemical formulaC₁₈H₂₁NO₄S
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (50 mg/ml; pale yellow solution)
      Storage Protect from light
      -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 at -20°C.
      Toxicity Standard Handling
      ReferencesFuente, R., et al. 2011, Mol Pharmacol. 73, 758.
      Namkung, W., et al. 2011, J Biol Chem. 286, 2365.