| Nemadectin |
![]() Last updated: 16/09/2025 |
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(Also known as: S541A; LL-F28249 aplha) |
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A naturally occurring substance with broad-spectrum antiparasitic properties | |
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Shown to be efficacy against the natural canine-infecting helminths and ivermectin-resistant Haemonchus contortus in sheep | |
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Dogs; Sheep |
| Approval status |
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Not approved | |
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Not approved |
| Chemical structure |
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Nemadectin exhibits extensive stereoisomerism, including both optical and geometrical isomerism, due to its large, complex ring system and multiple stereocentres. | |
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C₃₆H₅₂O₈ | |
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CC1CC(=CCC2CC(CC3(O2)CC(C(C(O3)C(=CC(C)C)C)C)O)OC(=O)C4C=C(C(C5C4(C(=CC=C1)CO5)O)O)C)C | |
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C[C@@H]\1C/C(=C/C[C@@H]2C[C@@H](C[C@@]3(O2)C[C@@H]([C@@H]([C@H](O3)/C(=C/C(C)C)/C)C)O)OC(=O)[C@@H]4C=C([C@H]([C@@H]5[C@]4(/C(=C/C=C1)/CO5)O)O)C)/C | |
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YNFMRVVYUVPIAN-AQUURSMBSA-N | |
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InChI=1S/C36H52O8/c1-20(2)13-24(6)32-25(7)30(37)18-35(44-32)17-28-16-27(43-35)12-11-22(4)14-21(3)9-8-10-26-19-41-33-31(38)23(5)15-29(34(39)42-28)36(26,33)40/h8-11,13,15,20-21,25,27-33,37-38,40H,12,14,16-19H2,1-7H3/b9-8+,22-11+,24-13+,26-10+/t21-,25-,27+,28-,29-,30-,31+,32+,33+,35-,36+/m0/s1 | |
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Yes |
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| Common Name | Relationship | Link |
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| nemadectin | - | ![]() |
| General status |
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Antiparasitic | ||||||||||||||
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Micro-organism derived substance | ||||||||||||||
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Natural | ||||||||||||||
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[Glutamate-gated chloride channels (GluCl), Agonist] | ||||||||||||||
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102130-84-7 | ||||||||||||||
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None allocated | ||||||||||||||
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No | ||||||||||||||
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612.80 | ||||||||||||||
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(1'R,2R,4S,4'S,5S,6S,8'R,10'E,13'R,14'E,16'E,20'R,21'R,24'S)-4,21',24'-trihydroxy-5,11',13',22'-tetramethyl-6-[(2E)-4-methyl-2-penten-2-yl]-3,4,5,6-tetrahydro-2'H-spiro[pyran-2,6'-[3,7,19]trioxatetracyclo[15.6.1.1~4,8~.0~20,24~]pentacosa[10,14,16,22]tetraen]-2'-one | ||||||||||||||
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White solid | ||||||||||||||
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Current | |||
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1980s, first isolated; 1990s, use in research; 2013, not approved UK | |||
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Usually supplied in a solid formulation | |||
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Nemadectin is commercially produced through a fermentation process using Streptomyces cyaneogriseus subspecies noncyanogenus The production involves cultivating this microorganism under controlled conditions optimised for yield, including nutrient-rich media and precise temperature and pH settings. After fermentation, the compound is extracted and purified for use. | |||
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As microbial-based products tend to use fermentation-based production processes rather than chemical synthesis, they typically have a lower fossil fuel input in formulation and active ingredient creation, and also have reduced downstream emissions due to biodegradability and minimal soil disruption, their life-cycle GHG emissions are expected to be low. Whilst hard and precise data is not available, broad estimates suggest that typically emissions are likely to be below 5 kg CO₂e/kg. |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. | ||||||||||
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| Known metabolites |
None
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| Terrestrial ecotoxicology |
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| Aquatic ecotoxicology |
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Mainly excreted in the faeces | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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| Health issues |
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Possible liver toxicant at high doses | ||||||||||||||||||||||||||||
| Handling issues |
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IMDG Transport Hazard Class 6.1 | |||
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Not listed (Not listed) | |||
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UN2588 | |||
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Packaging Group III (minor danger) | |||
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nemadectin | ||
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nemadectin | ||
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nemadectina | ||
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| Record last updated: | 16/09/2025 |
| Contact: | aeru@herts.ac.uk |
| Please cite as: | Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |
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