324693 | Emetine, Dihydrochloride - CAS 316-42-7 - Calbiochem

324693
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      Overview

      Replacement Information

      Key Spec Table

      Empirical Formula CAS #
      C₂₉H₄₀N₂O₄ · 2HCl316-42-7

      Pricing & Availability

      Catalogue NumberAvailability Packaging Qty/Pack Price Quantity
      324693-250MG
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          250 mg
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          Description
          Overview Principal alkaloid of ipecac, isolated from the ground roots of Uragoga ipecacuanha. Irreversibly blocks protein synthesis in eukaryotes by inhibiting the movement of ribosomes along the mRNA. Induces hypotension by blocking adrenoreceptors. Interferes with cytometric analysis of DNA replication at the early S phase. Also identified as a specific inhibitor of HIF-2α protein stability and transcriptional activity (IC50 ≤1 µM.
          Catalogue Number 324693
          Brand Family Calbiochem®
          Synonyms 6ʹ,7ʹ,10,11-Tetramethoxyemetan, 2HCl
          References
          References Kong, H.S., et al. 2010. Mol. Pharmacol. in press.
          Khan, M.A. 1995. Prog. Neurobiol. 46, 541.
          Kokuho, T., et al. 1995. Immunobiology 193, 42.
          Lee, Y.S., and Wurster, R.D. 1995. Cancer Lett. 93, 157.
          Burhans, W.C., et al. 1991. EMBO J. 10, 4351.
          Filley, E.A., and Rook, G.A. 1991. Infect. Immun. 59, 2567.
          Landis, R.C., et al. 1991. J. Immunol. 146, 128.
          Schweighoffer, T., et al. 1991. Histochemistry 96, 93.
          Product Information
          CAS number 316-42-7
          ATP Competitive N
          Form White solid with a faint yellow cast
          Hill Formula C₂₉H₄₀N₂O₄ · 2HCl
          Chemical formula C₂₉H₄₀N₂O₄ · 2HCl
          Molar Mass 553.6
          Hygroscopic Hygroscopic
          Reversible N
          Structure formula Image
          Applications
          Biological Information
          Primary Target Movement of ribosomes along the mRNA
          Primary Target IC50 ≤1 µM as a specific inhibitor of HIF-2α protein stability and transcriptional activity
          Purity ≥98% by HPLC and Titration (dried basis) (perchloric acid method)
          Physicochemical Information
          Cell permeable N
          Solubility EtOH or H₂O
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          RTECS JY5250000
          Safety Information
          R Phrase R: 28-36/38

          Very toxic if swallowed.
          Irritating to eyes and skin.
          S Phrase S: 28-36/37-45


          Wear suitable protective clothing and gloves.
          In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Ambient Temperature Only
          Toxicity Highly Toxic
          Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping chargesmay be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
          Storage +2°C to +8°C
          Protect from Light Protect from light
          Hygroscopic Hygroscopic
          Do not freeze No
          Special Instructions Following 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

          Documentation

          MSDS

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          Certificates of Analysis

          TitleLot Number
          324693

          References

          Reference overview
          Kong, H.S., et al. 2010. Mol. Pharmacol. in press.
          Khan, M.A. 1995. Prog. Neurobiol. 46, 541.
          Kokuho, T., et al. 1995. Immunobiology 193, 42.
          Lee, Y.S., and Wurster, R.D. 1995. Cancer Lett. 93, 157.
          Burhans, W.C., et al. 1991. EMBO J. 10, 4351.
          Filley, E.A., and Rook, G.A. 1991. Infect. Immun. 59, 2567.
          Landis, R.C., et al. 1991. J. Immunol. 146, 128.
          Schweighoffer, T., et al. 1991. Histochemistry 96, 93.
          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.

          Revision 20-September-2010 JSW
          Synonyms 6ʹ,7ʹ,10,11-Tetramethoxyemetan, 2HCl
          Description Principle alkaloid of ipecac, isolated from the ground roots of Uragoga ipecacuanha. Irreversibly blocks protein synthesis in eukaryotes by inhibiting the movement of ribosomes along the mRNA. Induces hypotension by blocking adrenoreceptors. Inhibits cytometric analysis of DNA replication at the early S phase. Also identified as a specific inhibitor of HIF-2α protein stability and transcriptional activity (IC50 ≤1 µM.
          Form White solid with a faint yellow cast
          CAS number 316-42-7
          RTECS JY5250000
          Molar mass 553.6
          Chemical formula C₂₉H₄₀N₂O₄ · 2HCl
          Structure formula
          Purity ≥98% by HPLC and Titration (dried basis) (perchloric acid method)
          Solubility Ethanol or H₂O (20 mg/ml)
          Storage +2°C to +8°C
          Protect from light
          Hygroscopic
          Do Not Freeze No
          Special Instructions Following reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Toxicity Highly Toxic
          Merck USA index 14, 3559
          References Kong, H.S., et al. 2010. Mol. Pharmacol. in press.
          Khan, M.A. 1995. Prog. Neurobiol. 46, 541.
          Kokuho, T., et al. 1995. Immunobiology 193, 42.
          Lee, Y.S., and Wurster, R.D. 1995. Cancer Lett. 93, 157.
          Burhans, W.C., et al. 1991. EMBO J. 10, 4351.
          Filley, E.A., and Rook, G.A. 1991. Infect. Immun. 59, 2567.
          Landis, R.C., et al. 1991. J. Immunol. 146, 128.
          Schweighoffer, T., et al. 1991. Histochemistry 96, 93.