Acidic polycyclic ether antibiotic having anticoccidial and grow

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

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514 25, 536 168, 536 181, A61K 3171, C07H 1704

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051589370

DESCRIPTION:

BRIEF SUMMARY
BACKGROUND OF THE INVENTION

The present invention concerns a new acidic polycyclic ether antibiotic having the formula: ##STR1## wherein Me.dbd.CH.sub.3, having absolute stereochemistry as shown; pharmaceutically acceptable cationic salts thereof; nutrient feed compositions comprising said antibiotic for poultry, cattle or swine; its use as an anticoccidial agent in poultry, in the treatment or prevention of swine dysentery, or as a growth promotant in cattle or swine; a fermentation method for its preparation; and the Actinomadura sp. microorganism which produces said antibiotic in said fermentation method.
The compound (I) is a new member of the acidic polycyclic ether group of antibiotics. This family includes such well known agents as monensin (The Merck Index, 10th Ed., Merck and Co.,Inc., Rahway, N.J., 1983, monograph no. 6100), nigericin (loc. cit., monograph no. 6390), narasin (loc. cit., monograph no. 6271), lasalocid (loc. cit., monograph no. 5204), and salinomycin (loc. cit., monograph no. 8193). The subject has been reviewed by Westley, "Polyether Antibiotics", Adv. Appl. Microbiol., vol. 22, pp. 77-223 (1977). Most closely related structurally to the present compound is portmicin, an antibiotic independently reported by Hamill et al , U.S. Pat. No. 4,582,822 and by Kusakabe et al., European patent application 158,179; Tetrahedron Letters, vol. 28, pp. 3357-3360(1987); J. Antibiotics, vol. 40, pp. 237-238(1987). The latter compound possesses an alpha-hydrogen on the tetrahydrofuran B-ring where the present compound possesses an alpha-methyl group. These compounds are generally known as coccidiostats, as feed additive-growth promotants, and/or as agents useful against swine dysentery.


SUMMARY OF THE INVENTION

A culture of Actinomadura sp., ATCC 53708, when fermented under aerobic conditions in aqueous media, produces a new acidic polycyclic ether antibiotic, a compound having the formula (I), as specified above.
The present invention is directed to said compound of the formula (I), including the pharmaceutically-acceptable cationic salts thereof, and to a process for its preparation which comprises fermentation of said Actinomadura sp. ATCC 53708 in an aqueous nutrient medium comprising an assimilable source of carbon and nitrogen until a recoverable amount of said compound of the formula (I) is formed, preferably under submerged aerobic conditions For use as an anticoccidial agent, in the prevention or treatment of swine dysentery, and/or as a growth promotant, the compound (I) is not necessarily separated from the fermentation and isolated in substantially pure form, but is alternatively used in crude form, either in precipitated form admixed with mycelium (recovered by filtration of the fermentation medium), or in solids obtained by spray- or freeze-drying the entire fermentation medium.
Said pharmaceutically-acceptable cationic salts include, but are not limited to, those of sodium, potassium, calcium, ammonia, N,N'-dibenzylethylenediamine, N-methylglucamine (meglumine) and diethanolamine. The preferred cationic salts are those of potassium and sodium.
The present invention is also directed to nutrient feed compositions, one for cattle or swine which comprises the compound of the formula (I) in an amount effective to promote growth and/or improve the feed utilization of said cattle or swine, or to prevent or treat dysentery in swine; and the other for poultry which comprises the compound of the formula (I) in an amount effective to control coccidial infection in said poultry.
The present invention is further directed to a method for promoting growth and/or increasing the efficiency of feed utilization in swine or cattle which comprises administering to said swine or cattle a growth promoting or feed-utilization efficiency promoting amount of the compound of the formula (I), particularly in the form of a nutrient feed composition; to a method for preventing or treating dysentery in swine which comprises administering to said swine a compound of the formula (I) in an amount effective in pr

REFERENCES:
patent: 4148882 (1979-04-01), Celmer et al.
patent: 4195079 (1980-03-01), Celmer et al.
patent: 4582822 (1986-04-01), Hamill et al.
patent: 4992423 (1991-02-01), Cullen et al.
Current Chemotherapy and Infectious Disease, Proc. 11th ICC and 19th ICAAC, Am. Soc. Microbiol., 1980, pp. 469-470.
Kusakabe et al., J. Antibiotics (Japan), v. 60, pp. 237-238 (1987).
Chemical Abstracts 104:166918w (abstracting EP 169,011).

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