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196876 BAY 41-2272 - CAS 256376-24-6 - Calbiochem

A cell-permeable pyrazolopyridinylpyrimidine compound that acts as a selective and potent stimulator of soluble guanylate cyclase (effective dose ~ 0.1 nM to 100 µM using recombinant soluble guanylate cyclase).

BAY 41-2272 - CAS 256376-24-6 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: 5-Cyclopropyl-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-4-ylamine

Primary Target: Soluble guanylate cyclase
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196876
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
256376-24-6C₂₀H₁₇FN₆

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      Description
      OverviewA cell-permeable pyrazolopyridinylpyrimidine compound that acts as a selective and potent stimulator of soluble guanylate cyclase (effective dose ~ 0.1 nM to 100 µM using recombinant soluble guanylate cyclase). The mode of activation is NO-independent and appears to be mediated through direct binding to the α1 and α2 subunits. Shown to be effective in treating numerous cardiovascular conditions in animal models. Inhibits phenylephrine-induced constriction of rabbit aortic rings (IC50 = 304 nM) and blocks collagen-induced aggregation of human platelets (IC50 = 36 nM). Does not inhibit phosphodiesterases.
      Catalogue Number196876
      Brand Family Calbiochem®
      Synonyms5-Cyclopropyl-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-4-ylamine
      References
      ReferencesBoerrigter, G., et al. 2003. Circulation 107, 686.
      Kalsi, J.S., et al. 2003. J Urol. 169, 761.
      Koglin, M., et al. 2002. Biochem. Biophys. Res. Commun. 292, 1057.
      Becker, E.M., et al. 2001. BMC Pharmacol. 1, 13.
      Stasch, J.P., et al. 2001. Nature 410, 212.
      Product Information
      CAS number256376-24-6
      ATP CompetitiveN
      FormWhite solid
      Hill FormulaC₂₀H₁₇FN₆
      Chemical formulaC₂₀H₁₇FN₆
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetSoluble guanylate cyclase
      Primary Target IC<sub>50</sub>304 nM inhibiting phenylephrine-induced constriction of rabbit aortic rings; 36 nM in blocking collagen-induced aggregation of human platelets
      Purity≥98% 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
      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
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      产品目录编号 GTIN
      196876-5MGCN 04055977206593

      Documentation

      BAY 41-2272 - CAS 256376-24-6 - Calbiochem MSDS

      职位

      物料安全数据表 (MSDS) 

      BAY 41-2272 - CAS 256376-24-6 - Calbiochem 分析证书

      标题批号
      196876

      参考

      参考信息概述
      Boerrigter, G., et al. 2003. Circulation 107, 686.
      Kalsi, J.S., et al. 2003. J Urol. 169, 761.
      Koglin, M., et al. 2002. Biochem. Biophys. Res. Commun. 292, 1057.
      Becker, E.M., et al. 2001. BMC Pharmacol. 1, 13.
      Stasch, J.P., et al. 2001. Nature 410, 212.
      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.

      Revision05-April-2011 RFH
      Synonyms5-Cyclopropyl-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-4-ylamine
      DescriptionA cell-permeable pyrazolopyridinylpyrimidine compound that acts as a selective and potent stimulator of soluble guanylate cyclase (effective dose ~0.1 nM to 100 µM using recombinant soluble guanylate cyclase). The mode of activation is NO-independent and appears to be mediated through direct binding to the α1 and α2 subunits. Shown to be effective in treating numerous cardiovascular conditions in animal models. Inhibits phenylephrine-induced constriction of rabbit aortic rings (IC50 = 304 nM) and blocks collagen-induced aggregation of human platelets (IC50 = 36 nM). Does not inhibit phosphodiesterases.
      FormWhite solid
      CAS number256376-24-6
      Chemical formulaC₂₀H₁₇FN₆
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (10 mg/ml)
      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
      ReferencesBoerrigter, G., et al. 2003. Circulation 107, 686.
      Kalsi, J.S., et al. 2003. J Urol. 169, 761.
      Koglin, M., et al. 2002. Biochem. Biophys. Res. Commun. 292, 1057.
      Becker, E.M., et al. 2001. BMC Pharmacol. 1, 13.
      Stasch, J.P., et al. 2001. Nature 410, 212.