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112252 Acidic Mammalian Chitinase Inhibitor, Bisdionin F - CAS 917877-86-2 - Calbiochem

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112252
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
917877-86-2C₁₆H₁₈N₈O₄

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      ガラスビン 5 mg
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      Description
      OverviewA cell-permeable, competitive Acidic Mammalian Chitinase (AMCase) Inhibitor (IC50 = 0.92 µM and Ki = 0.42 µM for hAMCase, and IC50= 2.2 µM for mAMCase, in vitro) that demonstrates 20-fold selectivity for hAMCase over hCHIT1. It is shown to decrease chitinase enzymatic activity (5 mg/kg, i.p.) in the lungs of control PBS- and OVA-challenged mice. Furthermore, it attenuates lung chitinase activity, reduces eosinophil influx, and improves ventilatory function, in vivo, in a murine model of allergic inflammation. It also causes neutrophilia in the lungs of OVA-challenged mice.
      Catalogue Number112252
      Brand Family Calbiochem®
      SynonymsAMCase Inhibitor, 3,7-dimethyl-1-(3-(3-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)propyl)-1H-purine-2,6(3H,7H)-dione
      References
      ReferencesSutherland, T.E., et al. 2011. Chem. Biol. 18, 569.
      Product Information
      CAS number917877-86-2
      FormOff-white powder
      Hill FormulaC₁₆H₁₈N₈O₄
      Chemical formulaC₁₆H₁₈N₈O₄
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥95% 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 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 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
      112252-5MGCN 04055977208030

      Documentation

      Acidic Mammalian Chitinase Inhibitor, Bisdionin F - CAS 917877-86-2 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      Acidic Mammalian Chitinase Inhibitor, Bisdionin F - CAS 917877-86-2 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      112252

      参考資料

      参考資料の概要
      Sutherland, T.E., et al. 2011. Chem. Biol. 18, 569.
      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.

      Revision08-June-2012 JSW
      SynonymsAMCase Inhibitor, 3,7-dimethyl-1-(3-(3-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)propyl)-1H-purine-2,6(3H,7H)-dione
      DescriptionA cell-permeable, competitive Acidic Mammalian Chitinase (AMCase) Inhibitor (IC50 = 0.92 µM and Ki = 0.42 µM for hAMCase, and IC50= 2.2 µM for mAMCase, in vitro) that demonstrates 20-fold selectivity for hAMCase over hCHIT1. It is shown to decrease chitinase enzymatic activity (5 mg/kg, i.p.) in the lungs of control PBS- and OVA-challenged mice. Furthermore, it attenuates lung chitinase activity, reduces eosinophil influx, and improves ventilatory function, in vivo, in a murine model of allergic inflammation. It also causes neutrophilia in the lungs of OVA-challenged mice.
      FormOff-white powder
      Intert gas (Yes/No) Packaged under inert gas
      CAS number917877-86-2
      Chemical formulaC₁₆H₁₈N₈O₄
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (5 mg/ml; clear, nearly colorless solution)
      Storage Protect from light
      +2°C to +8°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
      ReferencesSutherland, T.E., et al. 2011. Chem. Biol. 18, 569.