DescriptionSources: http://www.ema.europa.eu/docs/en_GB/document_library/Maximum_Residue_Limits_-_Report/2009/11/WC500010750.pdfCurator's Comment: description was created based on several sources, including:
https://www.drugs.com/vet/surmax-100-premix-can.html | https://www.fda.gov/downloads/AnimalVeterinary/Products/ApprovedAnimalDrugProducts/FOIADrugSummaries/UCM504548.pdf | http://www.fao.org/3/a-i0659e/i0659e02.pdf
Sources: http://www.ema.europa.eu/docs/en_GB/document_library/Maximum_Residue_Limits_-_Report/2009/11/WC500010750.pdf
Curator's Comment: description was created based on several sources, including:
https://www.drugs.com/vet/surmax-100-premix-can.html | https://www.fda.gov/downloads/AnimalVeterinary/Products/ApprovedAnimalDrugProducts/FOIADrugSummaries/UCM504548.pdf | http://www.fao.org/3/a-i0659e/i0659e02.pdf
Avilamycin is an orthosomycin antibiotic complex produced by the fermentation of Streptomyces viridochromogenes. Avilamycin is intended for use as a veterinary medicine in chickens, turkeys, pigs and rabbits to control bacterial enteric infections. It exhibits good antimicrobial activity against important veterinary Gram-positive pathogens (e.g., Clostridium perfringens) and has no related molecules in its class in human use. Therefore, avilamycin has been developed for treating necrotic enteritis in poultry, and enteric disease in pig and rabbits. Avilamycin inhibits bacterial protein synthesis through a novel mechanism of action by binding to the 50S ribosomal subunit and preventing the association of IF2, which inhibits the formation of the mature 70S initiation complex, and the correct positioning of tRNA in the aminoacyl site. No adverse drug-related changes were observed.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Preventing | SURMAX Approved UseIt is indicated for the prevention of necrotic enteritis caused by Clostridium perfringens in growing broiler chickens. Launch Date2009 |
|||
| Preventing | SURMAX Approved UseIt is indicated for the reduction in incidence and overall severity of diarrhea in the presence of pathogenic Escherichia coli in groups of weaned pigs. Launch Date2009 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Effect of avilamycin and tylosin on the metabolizable energy in growing and finishing pigs]. | 1995 |
|
| [The effect of avilamycin and tylosin on the apparent digestibility of iron, zinc, copper, manganese and selenium in the beginning and ending performance of swine]. | 1994 |
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| Synthesis of a terminal A-B-C disaccharide fragment of flambamycin, curamycin, and avilamycin. | 1993-10-04 |
|
| Effect of various levels of avilamycin on the performance of growing-finishing swine. | 1987-10 |
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| Isolation and structural identification of nine avilamycins. | 1986-07 |
|
| Avilamycin, an inhibitor of the 30 S ribosomal subunits function. | 1973-10-15 |
Patents
Sample Use Guides
Pig: 6-8 mg/kg body weight per day during 21 days.
Chicken: 20 mg/kg body weight per day during 21 days.
Turkey: 20 mg/kg body weight per day during 21 days.
Rabbit: 5 mg/kg body weight per day during 28 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4585189
The binding of [14C]phenylalanyl-tRNA to washed ribosomes directed by poly U was assayed employing the filter technique. The results obtained indicated that 2.86*10-5 M of avilamycin inhibits this reaction to the extent of approximately 50%.
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