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Biochemicals

Monensin sodium salt, Na+ ionophore (ab120499)

Price and availability

43 555 ₸

Availability

Order now and get it on Thursday February 25, 2021

Key features and details

  • Na+ ionophore
  • CAS Number: 22373-78-0
  • Soluble in ethanol to 100 mM
  • Form / State: Solid
  • Source: Streptomyces cinnamonensis

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Overview

  • Product name

    Monensin sodium salt, Na+ ionophore
  • Description

    Na+ ionophore
  • Biological description

    Na+ ionophore. Forms lipophilic complexes with monovalent cations to induce Na+ influx and H+/K+ efflux. Increases intracellular Ca2+ levels. Exhibits diverse biological actions; displays antibacterial properties and modulates ion gradients and intracellular pH. Apoptosis inducer.

  • CAS Number

    22373-78-0
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    4-[2-[5-Ethyl-5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]- 3-methyloxolan-2-yl]oxolan-2-yl]- 9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]-3-methoxy-2-methylpentanoic acid sodium salt
  • Molecular weight

    692.86
  • Molecular formula

    C36H61NaO11
  • Storage instructions

    Store at +4°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.

    Toxic, refer to SDS for further information.

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

  • SMILES

    OC[C@]1(O)O[C@@H]([C@@H](C)C[C@H]1C)[C@H]2C[C@H](C)[C@@H](O2)[C@]3(CC)CC[C@@H](O3)[C@]5(C)CC[C@]4(C[C@H](O)C[C@](C)(O4)[C@@H](C)[C@@H](OC)C(C)C(=O)O)O5
  • Source

    Streptomyces cinnamonensis

  • Research areas

    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Ion Channels
    • Ionophores, Indicators & Chelators
    • Biochemicals
    • Pharmacology
    • Signaling
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Heart disease
    • Signaling
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Signaling
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Signaling
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Cancer
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Diabetes
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Diabetes
    • Signaling
    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
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    • Apoptosis & cell cycle
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    • Research Area
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    • Biochemicals
    • Research Area
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    • Biochemicals
    • Research Area
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    • Biochemicals
    • Research Area
    • Obesity
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    • Apoptosis & cell cycle
    • Other
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Apoptosis & cell cycle
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    • Biochemicals
    • Research Area
    • Respiratory disease
    • Apoptosis & cell cycle
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    • Biochemicals
    • Research Area
    • Respiratory disease
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    • Biochemicals
    • Research Area
    • Stroke
    • Apoptosis & cell cycle
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    • Biochemicals
    • Research Area
    • Stroke
    • Signaling
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    • Biochemicals
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