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    veratridine-na-channel-opener-ab120279.pdf

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Biochemicals Chemical Type Biochemicals
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Veratridine, Na+ channel opener (ab120279)

  • Datasheet
  • SDS
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Chemical Structure - Veratridine, Na<sup>+</sup> channel opener (ab120279)

    Key features and details

    • Na+ channel opener
    • CAS Number: 71-62-5
    • Soluble in ethanol to 100 mM
    • Form / State: Solid
    • Source: Liliaceae sp.

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    Overview

    • Product name

      Veratridine, Na+ channel opener
    • Description

      Na+ channel opener
    • Biological description

      Alkaloid toxin found in Liliaceae plants. Causes persistent opening of the voltage-gated Na+ channel and reduces its single-channel conductance. Channel opener.
    • CAS Number

      71-62-5
    • Chemical structure

      Chemical Structure

    Properties

    • Chemical name

      3-Veratroylveracevine
    • Molecular weight

      673.80
    • Molecular formula

      C36H51NO11
    • PubChem identifier

      6610253
    • Storage instructions

      Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
    • Solubility overview

      Soluble in ethanol to 100 mM
    • Handling

      Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

      Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

    • SMILES

      COc1ccc(cc1OC)C(=O)OC4CC[C@@]7(C)C5CCC6[C@]8(O)C[C@H](O)[C@@]3(O)C(CN2CC(C)CCC2[C@@]3(C)O)[C@]8(O)C[C@@]67O[C@]45O
    • Source

      Liliaceae sp.

    • Research areas

      • Biochemicals
      • Chemical Type
      • Biochemicals
      • Biochemicals
      • Pharmacology
      • Ion Channels
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Diabetes
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Heart disease
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Hypertension
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Obesity
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Pain & inflammation
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Respiratory disease
      • Sodium
      • Blockers
      • Biochemicals
      • Research Area
      • Stroke
      • Sodium
      • Blockers

    Images

    • Chemical Structure - Veratridine, Na<sup>+</sup> channel opener (ab120279)
      Chemical Structure - Veratridine, Na+ channel opener (ab120279)
      2D chemical structure image of ab120279, Veratridine, Na+ channel opener

    Protocols

    To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

    Click here to view the general protocols

    Datasheets and documents

    • SDS download

    • Datasheet download

      Download

    References (5)

    Publishing research using ab120279? Please let us know so that we can cite the reference in this datasheet.

    ab120279 has been referenced in 5 publications.

    • Mohammed ZA  et al. An unbiased and efficient assessment of excitability of sensory neurons for analgesic drug discovery. Pain 161:1100-1108 (2020). PubMed: 31929383
    • Mohammed ZA  et al. Veratridine produces distinct calcium response profiles in mouse Dorsal Root Ganglia neurons. Sci Rep 7:45221 (2017). PubMed: 28338073
    • Sousa SR  et al. Discovery and mode of action of a novel analgesic ß-toxin from the African spider Ceratogyrus darlingi. PLoS One 12:e0182848 (2017). PubMed: 28880874
    • Henriques ST  et al. Interaction of Tarantula Venom Peptide ProTx-II with Lipid Membranes Is a Prerequisite for Its Inhibition of Human Voltage-gated Sodium Channel NaV1.7. J Biol Chem 291:17049-65 (2016). PubMed: 27311819
    • Zimmermann K  et al. Analgesic treatment of ciguatoxin-induced cold allodynia. Pain 154:1999-2006 (2013). PubMed: 23778293

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    Specific neuronal activator

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    Used at 15uM on primary culture of ENS for 45min. c-fos stained with ab222699 at 1/500 (red), counterstained with Hu C/D (green).

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    Submitted Jan 20 2021

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