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574714 Syk Inhibitor IV, BAY 61-3606 - CAS 732983-37-8 - Calbiochem

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574714
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概要

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主要スペック表

CAS #Empirical Formula
732983-37-8C₂₀H₁₈N₆O₃ • HCl • H₂O

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574714-2MGCN
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      ガラスビン 2 mg
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      Description
      OverviewA cell-permeable imidazopyrimidine compound that acts a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (IC50 = 10 nM) with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src even at concentrations as high as 4.7 µM. Shown to inhibit Syk-mediated cellular functions in vitro and exhibit good oral bioavailability and in vivo effacacy in the treatment of various allgery and asthma conditions in rat models.
      Catalogue Number574714
      Brand Family Calbiochem®
      Synonyms2-(7-(3,4-Dimethoxyphenyl)-imidazo[1,2-c]pyrimidin-5-ylamino)-nicotinamide, HCl, BAY 61-3606
      References
      ReferencesYamamoto, N., et al. 2003. J. Pharm. Exp. Ther. 306, 1174.
      Product Information
      CAS number732983-37-8
      ATP CompetitiveY
      FormYellow solid
      Hill FormulaC₂₀H₁₈N₆O₃ • HCl • H₂O
      Chemical formulaC₂₀H₁₈N₆O₃ • HCl • H₂O
      Hygroscopic Hygroscopic
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      ApplicationSyk Inhibitor IV, BAY 61-3606, CAS 732938-37-8, is a cell-permeable, potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (IC50 = 10 nM).
      Biological Information
      Primary TargetSyk
      Primary Target IC<sub>50</sub>10 nM
      Purity≥97% by HPLC
      Physicochemical Information
      Cell permeableY
      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
      Hygroscopic Hygroscopic
      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
      574714-2MGCN 04055977189698

      Documentation

      Syk Inhibitor IV, BAY 61-3606 - CAS 732983-37-8 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      Syk Inhibitor IV, BAY 61-3606 - CAS 732983-37-8 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      574714

      参考資料

      参考資料の概要
      Yamamoto, N., et al. 2003. J. Pharm. Exp. Ther. 306, 1174.
      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.

      Revision03-September-2020 JSW
      Synonyms2-(7-(3,4-Dimethoxyphenyl)-imidazo[1,2-c]pyrimidin-5-ylamino)-nicotinamide, HCl, BAY 61-3606
      DescriptionA cell-permeable imidazopyrimidine compound that acts a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (IC50 = 10 nM) with no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src even at concentrations as high as 4.7 µM. Shown to inhibit Syk-mediated cellular functions in vitro and exhibit good oral bioavailability and in vivo effacacy in the treatment of various allgery and asthma conditions in rat models.
      FormYellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number732983-37-8
      Chemical formulaC₂₀H₁₈N₆O₃ • HCl • H₂O
      Structure formulaStructure formula
      Purity≥97% by HPLC
      SolubilityDMSO (10 mg/ml) or H₂O (20 mg/ml)
      Storage Protect from light
      +2°C to +8°C
      Hygroscopic
      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
      ReferencesYamamoto, N., et al. 2003. J. Pharm. Exp. Ther. 306, 1174.