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Chemical Structure
Chemical Structure
Chemical Structure

Selamectin [220119-17-5]

Research Use Only
CDX-S0051
Chemodex
CAS Number220119-17-5
Product group Chemicals
Estimated Purity>99%
Molecular Weight770
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Selamectin [220119-17-5]
  • Delivery Days Customer
    10
  • CAS Number
    220119-17-5
  • Certification
    Research Use Only
  • Estimated Purity
    >99%
  • Hazard Information
    Non-hazardous
  • Molecular Formula
    C43H63NO11
  • Molecular Weight
    770
  • Scientific Description
    Avermectin derivative prepared by hydrolysis and oximation of doramectin. Selamectin is a potent nematocide used for the treatment of parasites that acts as agonist of the GABA (gamma-aminobutyric acid) neurotransmitter in nerve cells and also binds to glutamate-gated chloride channels in nerve and muscle cells of invertebrates. In both cases it blocks the transmission of neuronal signals of the parasites, which are either paralyzed and expelled out of the body, or they starve. It also affects the reproduction of some parasites by diminishing oviposition or inducing an abnormal oogenesis. The substance fights both internal and surface parasitic infection. Compound can be used as analytical reference material. Antiviral effective against 2019-nCoV - Chemical. CAS: 220119-17-5. Formula: C43H63NO11. MW: 770. Synthetic. Avermectin derivative prepared by hydrolysis and oximation of doramectin. Selamectin is a potent nematocide used for the treatment of parasites that acts as agonist of the GABA (gamma-aminobutyric acid) neurotransmitter in nerve cells and also binds to glutamate-gated chloride channels in nerve and muscle cells of invertebrates. In both cases it blocks the transmission of neuronal signals of the parasites, which are either paralyzed and expelled out of the body, or they starve. It also affects the reproduction of some parasites by diminishing oviposition or inducing an abnormal oogenesis. The substance fights both internal and surface parasitic infection. Compound can be used as analytical reference material.
  • SMILES
    O[C@@H]1[C@@H](OC)C[C@@](O[C@](C(C)/C=C/C=C(CO2)/[C@@](C2/C(C(C)=C3)=N\O)(O)[C@]3([H])C4=O)([H])/C(C)=C/C[C@]5([H])C[C@@](O4)([H])C[C@]6(CC[C@H](C)[C@](C7CCCCC7)([H])O6)O5)([H])O[C@H]1C
  • Storage Instruction
    2°C to 8°C,RT
  • UNSPSC
    12352200