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692000 ZM 336372 - CAS 208260-29-1 - Calbiochem

A potent, cell-permeable, reversible, ATP-competitive and specific inhibitor of the protein kinase c-Raf (IC₅₀ = 70 nM).

ZM 336372 - CAS 208260-29-1 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: N-[5-(3-Dimethylaminobenzamido)-2-methylphenyl]-4-hydroxybenzamide

Primary Target: Protein kinase c-Raf
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692000
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개요

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주요 사양표

CAS #Empirical Formula
208260-29-1C₂₃H₂₃N₃O₃

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692000-1MGCN
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      		 Plastic ampoule 1 mg
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      Description
      OverviewA potent, cell-permeable, reversible, ATP-competitive and specific inhibitor of the protein kinase c-Raf (IC50 = 70 nM). Inhibits c-Raf with ten-fold increased potency compared to B-Raf, but does not inhibit many other protein kinases (even at 50 µM) with the exception of SAPK2a/p38α (IC50 = 2 µM) and SAPK2b/p38β2 (IC50 = 2 µM). The inhibition of c-Raf by ZM 336372 is competitive with respect to ATP.
      Catalogue Number692000
      Brand Family Calbiochem®
      SynonymsN-[5-(3-Dimethylaminobenzamido)-2-methylphenyl]-4-hydroxybenzamide
      References
      ReferencesHall-Jackson, C.A., et al. 1999. Chem. Biol. 6, 559.
      Product Information
      CAS number208260-29-1
      ATP CompetitiveY
      DeclarationSold under license of PCT Application W098/22,103.
      FormOff-white solid
      Hill FormulaC₂₃H₂₃N₃O₃
      Chemical formulaC₂₃H₂₃N₃O₃
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetProtein kinase c-Raf
      Primary Target IC<sub>50</sub>70 nM against protein kinase c-Raf
      Purity≥95% 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 -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 3 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      카탈로그 번호 GTIN
      692000-1MGCN 04055977274561

      Documentation

      ZM 336372 - CAS 208260-29-1 - Calbiochem MSDS

      타이틀

      물질안전보건자료(MSDS) 

      ZM 336372 - CAS 208260-29-1 - Calbiochem Certificates of Analysis

      TitleLot Number
      692000

      References

      참고문헌 보기
      Hall-Jackson, C.A., et al. 1999. Chem. Biol. 6, 559.

      Posters

      Title
      Human Kinome & InhibitorSelect™ Libraries
      Data Sheet

      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.

      Revision13-January-2010 RFH
      SynonymsN-[5-(3-Dimethylaminobenzamido)-2-methylphenyl]-4-hydroxybenzamide
      DescriptionA potent, cell-permeable, reversible, ATP-competitive and specific inhibitor of c-Raf (IC50 = 70 nM). Inhibits c-Raf with ten-fold greater potency compared to B-Raf. Has no significant effect on many other protein kinases tested (even at 50 µM) with the exception of SAPK2a/p38α (IC50 = 2 µM) and SAPK2b/p38β2 (IC50 = 2 µM).
      FormOff-white solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number208260-29-1
      Chemical formulaC₂₃H₂₃N₃O₃
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (200 mg/ml)
      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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesHall-Jackson, C.A., et al. 1999. Chem. Biol. 6, 559.