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| Names | |
|---|---|
| Other names 4″-Deoxy-4″-epi-methylamino-avermectin B1; Epi-methylamino-4″-deoxy-avermectin; MK 243; EMA; GWN 1972 | |
| Identifiers | |
3D model (JSmol) | |
| 8671728 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.217.470 |
| EC Number |
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| RTECS number |
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| UNII |
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| Properties | |
| C49H75NO13 | |
| Molar mass | 886.133 g·mol−1 |
| Appearance | White or faintly yellow powder |
| Melting point | 141 to 146 °C (286 to 295 °F; 414 to 419 K) |
| 30-50 ppm (pH 7) | |
| Pharmacology | |
| QP54AA06 (WHO) | |
| Legal status | |
| Hazards | |
| GHS labelling: | |
     | |
| Danger | |
| H301,H311,H318,H331,H370,H372,H410 | |
| P260,P261,P264,P270,P271,P273,P280,P301+P310,P302+P352,P304+P340,P305+P351+P338,P307+P311,P310,P311,P312,P314,P321,P322,P330,P337+P313,P361,P363,P391,P403+P233,P405,P501 | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Emamectin is the 4″-deoxy-4″-methylamino derivative ofabamectin, a 16-membered macrocycliclactone produced by the fermentation of the soilactinomyceteStreptomyces avermitilis.[1][2]It is generally prepared as thesalt withbenzoic acid, emamectin benzoate, which is a white or faintly yellow powder.[3] Emamectin is widely used in the US and Canada as an insecticide because of its chloride channel activation properties.[4]
Emamectin, produced by the bacteriumStreptomyces avermitilis, belongs to the avermectin family of compounds all of which exhibit toxicity for nematodes, arthropods, and several other pests. The benzoate salt of emamectin in particular has found widespread use as an insecticide and is approved by the EPA for use in prevention of emerald ash borer in ash trees.[5]Emamectin is derived from avermectin B1, also known as abamectin, a mixture of the natural avermectin B1a and B1b. Emamectin has also shown promising applications in the eradication of fish lice and in fish farming.[6]
Emamectin was invented by Regina D. Leseota, Pradip K. Mookerjee, John Misselbrook, and Robert F. Peterson Jr. and patented on September 25, 2001, approved August 22, 2002.[7] It was developed as a pesticide byMerck & Co. as investigative compound MK-0244[8][9]It was first marketed in 1997 in Palestine and Japan.[citation needed]
Emamectin is derived from abamectin by replacement of an epi-amino-methyl (NHCH3) group by a hydroxyl (-OH) group at the 4″-position. Emamectin, like abamectin, is a mixture of twohomologue compounds termed B1a and B1b which differ on the C-25 side-chain by one methylene (CH2) group. B1a contains asec-butyl group while B1b has an isopropyl group. Emamectin is a mixture, typically consisting of 10% B1b and 90% B1a.[10]
Avermectinbiosynthesis is classified into three stages: the formation of thepolyketide-derived initialaglycone, modification of the initial aglycone to produce avermectin aglycones, andglycosylation of avermectin aglycones to generate avermectins.[11]
Emamectin is widely used in controlling lepidopterous pests (order of insects that as larvae are caterpillars and as adults have four broad wings including butterflies, moths, andskippers) in agricultural products in the US, Japan, Canada, and recently Taiwan. The low-application rate of the active ingredient needed (about 15 g/ha (6 g/acre)) and broad-spectrum applicability as an insecticide has gained emamectin significant popularity among farmers.[10]
Emamectin has been shown to possess a greater ability to reduce the colonization success ofengraver beetles and associated wood borers in loblolly pines (Pinus taeda).[12] A 2006 study regarding bolt-injections of four types of pesticides found emamectin to be the greatest reducer against these species with respect to the amount of larval feeding, length, and number of egg galleries.[12] Formation of long vertical lesions in the phloem and xylem surrounding emamectin injection points were found indicating some level of tree-toxicity to the emamectin.[12]
A water-soluble preparation of emamectin inpolysorbate,acetone, andmethanol was shown to prevent the wilting ofJapanese black pines inoculated with pine-wood nematodes (Bursaphelenchus xylophilus).[2] Previous treatment ofB. xylophilus infections involved eradicating the local population of Japanese pine sawyers associated with the spread of the nematode.
Emamectin has also been successfully employed by fish farmers in the control of sea lice in Atlantic salmon.[13][14]The United Kingdom, Chile, Ireland, Iceland, Finland, the Faroe Islands, Spain, and Norway are currently registered to use emamectin in their fish feed.[13] Removal of the afflicting sea louse represents an increase in the integrity of their salmonid product due to the subsequent reduction of bacterial and viral pathogens possibly carried by the sea lice. Emamectin has shown efficacy against all life-cycle stages ofLepeophtheirus salmonis (salmon louse) andCaligus elongatus (sea louse), preventing maturation to the reproductive stage.[14]
A related dihydroxy avermectin B1 compound,ivermectin, is utilized orally in humans as an acaricide and insecticide for the treatment ofstrongyloidiasis andonchocerciasis. Veterinarians also employ ivermectin in the treatment of heartworms in dogs and other infestations.[10]
Emamectin, like other avermectins, is a hydrophobic 16-membered macrocyclic lactone.[2] Emamectin differs from avermectins B1a and B1b by the presence of a hydroxyl group at the 4″-epimethylamino group rather than the 4″-position. Avermectins are pentacyclic polyketide-derived compounds linked to a disaccharide of the methylated deoxysugaroleandrose.[11]
The determination of the active-site for avermectins is difficult due to poor solubility and lipophilicity of these compounds.
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Emamectin works as a chloride channel activator by bindinggamma aminobutyric acid (GABA) receptor and glutamate-gated chloride channels disrupting nerve signals within arthropods.[6][15]The compound stimulates the release of GABA from the synapses between nerve cells and while additionally increasing GABA's affinity for its receptor on the post-junction membrane of muscle cells in insects and arthropods.[14] The stronger binding of GABA increases the cells permeability to chloride ions within the cell due to the hypotonic concentration gradient.[14] Neurotransmission is thereby reduced by subsequent hyperpolarisation and the elimination of signal transduction.[14]
