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382190 Histone Lysine Methyltransferase Inhibitor - CAS 935693-62-2 - Calbiochem

The Histone Lysine Methyltransferase Inhibitor, also referenced under CAS 935693-62-2, controls the biological activity of Histone Lysine Methyltransferase. This small molecule/inhibitor is primarily used for Cancer applications.

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

同义词: HMTase Inhibitor, 2-(Hexahydro-4-methyl-1H-1,4-diazepin-1-yl)-6,7-dimethoxy-N-(1-(phenylmethyl)-4-piperidinyl)-4-quinazolinamine, BIX-01294, EHMT2/G9a Inhibitor I

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382190
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
935693-62-2C₂₈H₃₈N₆O₂

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      		 塑胶安瓿;塑胶针药瓶 5 mg
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      Description
      OverviewA cell-permeable diazepinyl-quinazolinamine, non-SAM (S-adenosylmethionine) analog-based HMTase (histone methyltransferase) inhibitor that selectively interferes with the G9a-catalyzed H3K9me2 (histone H3 Lys9 dimethylation) modification (IC50 = 1.7 µM) in a reversible manner. It inhibits the GLP-catalyzed H3K9me3 only at much higher concentrations (IC50 = 38 µM) and exhibits little activity against H3 methylations catalyzed by other HMTases (PRMT1, SET7/9, ESET, SUV39H1). Shown to effectively synergize with Oct3/4 and Klf4 in inducing reprogramming of primary murine fetal NPCs (Neural Progenitor Cells) into iPS (induced Pluripotent Stem) cells without additional viral transduction of Sox2 and c-Myc.
      Catalogue Number382190
      Brand Family Calbiochem®
      SynonymsHMTase Inhibitor, 2-(Hexahydro-4-methyl-1H-1,4-diazepin-1-yl)-6,7-dimethoxy-N-(1-(phenylmethyl)-4-piperidinyl)-4-quinazolinamine, BIX-01294, EHMT2/G9a Inhibitor I
      References
      ReferencesShi, Y., et al. 2008. Cell Stem Cell 2, 525.
      Kubicek, S., et al. 2007. Mol. Cell 25, 473.
      Product Information
      CAS number935693-62-2
      FormOff-white solid
      Hill FormulaC₂₈H₃₈N₆O₂
      Chemical formulaC₂₈H₃₈N₆O₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥97% 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 -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 up to 6 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      产品目录编号 GTIN
      382190-5MGCN 04055977212877

      Documentation

      Histone Lysine Methyltransferase Inhibitor - CAS 935693-62-2 - Calbiochem MSDS

      职位

      物料安全数据表 (MSDS) 

      Histone Lysine Methyltransferase Inhibitor - CAS 935693-62-2 - Calbiochem 分析证书

      标题批号
      382190

      参考

      参考信息概述
      Shi, Y., et al. 2008. Cell Stem Cell 2, 525.
      Kubicek, S., et al. 2007. Mol. Cell 25, 473.

      技术信息

      标题
      White Paper - The Message in the Marks: Deciphering Cancer Epigenetics
      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.

      Revision06-November-2009 RFH
      SynonymsHMTase Inhibitor, 2-(Hexahydro-4-methyl-1H-1,4-diazepin-1-yl)-6,7-dimethoxy-N-(1-(phenylmethyl)-4-piperidinyl)-4-quinazolinamine, BIX-01294, EHMT2/G9a Inhibitor I
      DescriptionA cell-permeable diazepinyl-quinazolinamine, non-SAM (S-adenosylmethionine) analog-based HMTase (histone methyltransferase) inhibitor that selectively interferes with the G9a-catalyzed H3K9me2 (histone H3 Lys9 dimethylation) modification (IC50 = 1.7 µM) in a reversible manner. It inhibits the GLP-catalyzed H3K9me3 only at much higher concentrartions (IC50 = 38 µM) and exhibits little activity against H3 methylations catalyzed by other HMTases (PRMT1, SET7/9, ESET, SUV39H1). Shown to effectively synergize with Oct3/4 and Klf4 in inducing reprogramming of primary murine fetal NPCs (Neural Progenitor Cells) into iPS (induced Pluripotent Stem) cells without additional viral transduction of Sox2 and c-Myc.
      FormOff-white solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number935693-62-2
      Chemical formulaC₂₈H₃₈N₆O₂
      Structure formulaStructure formula
      Purity≥97% by HPLC
      SolubilityDMSO (10 mg/ml) or Ethanol (10 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 up to 6 months at -20°C.
      Toxicity Standard Handling
      ReferencesShi, Y., et al. 2008. Cell Stem Cell 2, 525.
      Kubicek, S., et al. 2007. Mol. Cell 25, 473.