Maduramicin

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Maduramicin
Maduramicin.svg
Clinical data
Other namesMaduramycin
AHFS/Drugs.com International Drug Names
ATCvet code
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
Formula C47H80O17
Molar mass 917.140 g·mol−1
3D model (JSmol)
  • O=C(O)C[C@@]1(O)O[C@H]([C@H](OC)[C@@H](OC)[C@@H]1C)[C@H](C)[C@H]7O[C@]6(O[C@](C)([C@@H]5O[C@](C)([C@@H]4O[C@@H]([C@H]2O[C@@](O)(C)[C@H](C)C[C@@H]2C)C[C@@H]4O[C@H]3O[C@@H](C)[C@H](OC)[C@@H](OC)C3)CC5)CC6)C[C@H](O)[C@H]7C

Maduramicin (maduramycin) is an antiprotozoal agent used in veterinary medicine to prevent coccidiosis. [1] [2] It is a natural chemical compound first isolated from the actinomycete Actinomadura rubra . [3]

Related Research Articles

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<span class="mw-page-title-main">Carbamate</span> Chemical group (>N–C(=O)–O–)

In organic chemistry, a carbamate is a category of organic compounds with the general formula R2NC(O)OR and structure >N−C(=O)−O−, which are formally derived from carbamic acid. The term includes organic compounds, formally obtained by replacing one or more of the hydrogen atoms by other organic functional groups; as well as salts with the carbamate anion H2NCOO.

<i>Actaea</i> (plant) Genus of plants

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<span class="mw-page-title-main">Anammox</span> Anaerobic ammonium oxidation, a microbial process of the nitrogen cycle

Anammox, an abbreviation for "anaerobic ammonium oxidation", is a globally important microbial process of the nitrogen cycle that takes place in many natural environments. The bacteria mediating this process were identified in 1999, and were a great surprise for the scientific community. In the anammox reaction, nitrite and ammonium ions are converted directly into diatomic nitrogen and water.

<span class="mw-page-title-main">Coccidia</span> Subclass of protists

Coccidia (Coccidiasina) are a subclass of microscopic, spore-forming, single-celled obligate intracellular parasites belonging to the apicomplexan class Conoidasida. As obligate intracellular parasites, they must live and reproduce within an animal cell. Coccidian parasites infect the intestinal tracts of animals, and are the largest group of apicomplexan protozoa.

<span class="mw-page-title-main">Quaternary ammonium cation</span> Polyatomic ions of the form N(–R)₄ (charge +1)

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Coccidiosis is a parasitic disease of the intestinal tract of animals caused by coccidian protozoa. The disease spreads from one animal to another by contact with infected feces or ingestion of infected tissue. Diarrhea, which may become bloody in severe cases, is the primary symptom. Most animals infected with coccidia are asymptomatic, but young or immunocompromised animals may suffer severe symptoms and death.

<i>Eimeria</i> Genus of single-celled organisms

Eimeria is a genus of apicomplexan parasites that includes various species capable of causing the disease coccidiosis in animals such as cattle, poultry and smaller ruminants including sheep and goats. Eimeria species are considered to be monoxenous because the life cycle is completed within a single host, and stenoxenous because they tend to be host specific, although a number of exceptions have been identified. Species of this genus infect a wide variety of hosts. Thirty-one species are known to occur in bats (Chiroptera), two in turtles, and 130 named species infect fish. Two species infect seals. Five species infect llamas and alpacas: E. alpacae, E. ivitaensis, E. lamae, E. macusaniensis, and E. punonensis. A number of species infect rodents, including E. couesii, E. kinsellai, E. palustris, E. ojastii and E. oryzomysi. Others infect poultry, rabbits and cattle. For full species list, see below.

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<span class="mw-page-title-main">SHARON Wastewater Treatment</span>

SHARON is a sewage treatment process. A partial nitrification process of sewage treatment used for the removal of ammonia and organic nitrogen components from wastewater flow streams. The process results in stable nitrite formation, rather than complete oxidation to nitrate. Nitrate formation by nitrite oxidising bacteria (NOB) is prevented by adjusting temperature, pH, and retention time to select for nitrifying ammonia oxidising bacteria (AOB). Denitrification of waste streams utilizing SHARON reactors can proceed with an anoxic reduction, such as anammox.

<i>Actinomadura</i> Genus of bacteria

The genus Actinomadura is one of four genera of Actinomycetota that belong to the family Thermomonosporaceae. It contains aerobic, Gram-positive, non-acid-fast, non-motile, chemo-organotrophic actinomycetes that produce well-developed, non-fragmenting vegetative mycelia and aerial hyphae that differentiate into surface-ornamented spore chains. These chains are of various lengths and can be straight, hooked or spiral. The genus currently comprises over 70 species with validly published names with standing in nomenclature, although the species status of some strains remains uncertain, and further comparative studies are needed.

<span class="mw-page-title-main">Ammonia transporter</span>

Ammonia transporters are structurally related membrane transport proteins called Amt proteins in bacteria and plants, methylammonium/ammonium permeases (MEPs) in yeast, or Rhesus (Rh) proteins in chordates. In humans, the RhAG, RhBG, and RhCG Rhesus proteins constitute solute carrier family 42 whilst RhD and RhCE form the Rh blood group system. The three-dimensional structure of the ammonia transport protein AmtB from Escherichia coli has been determined by x-ray crystallography revealing a hydrophobic ammonia channel. The human RhCG ammonia transporter was found to have a similar ammonia-conducting channel structure. It was proposed that the erythrocyte Rh complex is a heterotrimer of RhAG, RhD, and RhCE subunits in which RhD and RhCE might play roles in anchoring the ammonia-conducting RhAG subunit to the cytoskeleton. Based on reconstitution experiments, purified RhCG subunits alone can function to transport ammonia. RhCG is required for normal acid excretion by the mouse kidney and epididymis.

<span class="mw-page-title-main">Dragendorff's reagent</span>

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Eimeria zuernii is a species of the parasite Eimeria that causes diarrheic disease known as eimeriosis in cattle, and mainly affects younger animals. The disease is also commonly referred to as coccidiosis. The parasite can be found in cattle around the globe.

Eimeria arlongi is a species of Eimeria that causes clinical coccidiosis in goats. It and Eimeria ninakohlyakimovae are two of the most pathogenic species for goats. It is particularly prevalent in goat kids in Iran. Issues with coccidiosis specifically due to Eimeria arloingi have also been reported in Egypt and Portugal. It is unclear whether this species is present in the Americas as most of the case reports of coccidiosis in these areas do not differentiate the species causing the disease. Infections with this species are commonly compounded by infections with other Eimeria species in "mixed infections." This species is closely related to Eimeria bovis and Eimeria zuernii which are both highly pathogenic in cattle' Infections with this species are characterized by lesions specifically in the jejunum, but also the ilium and cecum which results in diarrhea. Oocysts begin shedding between 16 and 18 days after the animal is infected which is when the parasite is spread. The shedding can last as long as 15 days. This parasite causes an immune response in its host that includes accumulation of fluid in body cavities, presence of large numbers of leukocytes in the small intestine, and necrosis of the tissue of the small intestine. Pale yellow plaques can be seen on the small intestine of severely affected kids at necropsy.

Eimeria bovis is a parasite belonging to the genus Eimeria and is found globally. The pathogen can cause a diarrheic disease in cattle referred to as either eimeriosis or coccidiosis. The infection predominantly cause disease in younger animals.

References

  1. Maduramicin Ammonium, Canadian Food Inspection Agency
  2. McDougald LR, Fuller AL, Mathis GF, Wang GT (1990). "Efficacy of maduramicin ammonium against coccidiosis in turkeys under laboratory and floor-pen conditions". Avian Diseases. 34 (3): 634–638. doi:10.2307/1591256. JSTOR   1591256. PMID   2241692.
  3. Fleck WF, Strauss DG, Meyer J, Porstendorfer G (1978). "Fermentation, isolation, and biological activity of maduramycin: a new antibiotic from Actinomadura rubra". Zeitschrift für Allgemeine Mikrobiologie. 18 (6): 389–398. doi:10.1002/jobm.3630180602 (inactive 2024-01-22). PMID   362738.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)