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420132 JAK2 Inhibitor II - CAS 1837-91-8 - Calbiochem

The JAK2 Inhibitor II, also referenced under CAS 1837-91-8, controls the biological activity of JAK2. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: 1,2,3,4,5,6-Hexabromocyclohexane

Primary Target: JAK2 autophosphorylation
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420132
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개요

Replacement Information

주요 사양표

CAS #Empirical Formula
1837-91-8C₆H₆Br₆

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420132-25MGCN
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      		 Plastic ampoule 25 mg
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      Description
      OverviewA cell-permeable hexabromocyclohexane compound that interacts with a solvent-accessible pocket near the activation loop of JAK2 and acts as a specific, reversible, and direct inhibitor of JAK2 autophosphorylation (maximal inhibition at 50 µM in BSC-40 cells overexpressing JAK2). Reduces growth hormone-mediated JAK2 activation in γ2A cells that stably express growth hormone receptor and JAK2. Does not block EGFR autophosphorylation in murine fibroblasts.
      Catalogue Number420132
      Brand Family Calbiochem®
      Synonyms1,2,3,4,5,6-Hexabromocyclohexane
      References
      ReferencesSandberg, E.M., et al. 2005. J. Med. Chem. 48, 2526.
      Product Information
      CAS number1837-91-8
      ATP CompetitiveN
      FormOff-white solid
      Hill FormulaC₆H₆Br₆
      Chemical formulaC₆H₆Br₆
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetJAK2 autophosphorylation
      Purity≥ 97% by GC
      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
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      카탈로그 번호 GTIN
      420132-25MGCN 04055977188103

      Documentation

      JAK2 Inhibitor II - CAS 1837-91-8 - Calbiochem MSDS

      타이틀

      물질안전보건자료(MSDS) 

      JAK2 Inhibitor II - CAS 1837-91-8 - Calbiochem Certificates of Analysis

      TitleLot Number
      420132

      References

      참고문헌 보기
      Sandberg, E.M., et al. 2005. J. Med. Chem. 48, 2526.

      Technical Info

      Title
      JAK/STAT Signaling Research Focus
      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.

      Revision02-December-2010 RFH
      Synonyms1,2,3,4,5,6-Hexabromocyclohexane
      DescriptionA cell-permeable, specific, reversible, and direct inhibitor of JAK2 autophosphorylation (maximal inhibition at 50 µM in BSC-40 cells overexpressing JAK2 that interacts with a solvent-accessible pocket near the activation loop of JAK2. Reduces growth hormone-mediated JAK2 activation in γ2A cells that stably express growth hormone receptor and JAK2. Does not block EGFR autophosphorylation in murine fibroblasts.
      FormOff-white solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number1837-91-8
      Chemical formulaC₆H₆Br₆
      Structure formulaStructure formula
      Purity≥ 97% by GC
      SolubilityDMSO (5 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
      ReferencesSandberg, E.M., et al. 2005. J. Med. Chem. 48, 2526.