Antibiotics TKR1912-I and TKR1912-II and process for...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C549S485000, C424S116000, C435S171000

Reexamination Certificate

active

06380245

ABSTRACT:

TECHNICAL FIELD
The present invention relates to TKR1912-I and TKR1912-II, which are antibiotics of use as therapeutic agents for fungal infections diseases, a method for their production, and microorganisms producing said antibiotics.
BACKGROUND ART
Fungi are known to cause a variety of infectious diseases in man, animals, and plants. In man, for instance, they cause superficial mycosis affecting the skin, oral cavity, etc. and systemic mycosis affecting the viscera, brain, etc. They cause similar infections in pet and domestic animals as well. Furthermore, fungi inflict various hazardous effects on plants such as orchard trees and vegetables.
As the principal pathogenic fungi causing systemic mycosis in man, those of the genera Candida, Cryptococcus, and Aspergillus, among others, are known. As to superficial mycosis, candidal species affecting the skin, oral cavity, and vagina and trichophytons infecting the skin of the extremities are regarded as the major pathogenic fungi. Besides those fungi, many other fungi exist in the environment and are suspected to contaminate the animal and vegetable kingdoms.
As antimycotics of use for the prevention and treatment of such fungal infections and contaminations, only a very few are known. As therapeutic drugs for systemic mycosis in man and animals, for instance, amphotericin B, flucytosine, miconazole, and fluconazole can be mentioned. However, those compounds are not fully satisfactory in potency, toxic potential, or antifungal spectrum, thus being not impeccable as therapeutic drugs.
DISCLOSURE OF THE INVENTION
In view of the above-mentioned prior art, the present invention has for its object to provide a novel class of antibiotics which are of value as therapeutic agents for fungal infections.
In their search for a novel antibiotic, the inventors of the present invention isolated a large number of microorganisms from the natural kingdom, isolated the antibiotics they produced, and scrutinized their biological properties. As a result, they discovered that the culture broth of a strain of microorganism of the genus Aureobasidium contained an antibiotic having antifungal activity against pathogenic fungi inclusive of Candida albicans and Cryptococcus neoformans. Accordingly the inventors isolated this antibiotic and studied its physicochemical properties. As a result, they discovered that the above antibiotic is actually comprised of two novel substances having distinct physicochemical characteristics and named them TKR1912-I and TKR1912-II. The present invention provides the above-mentioned antibiotics TKR1912-I and TKR1912-II and a method for their production.


REFERENCES:
patent: 0 170 006 (1986-02-01), None
patent: 0 352 092 (1990-01-01), None
patent: 57-32286 (1982-02-01), None
patent: WO96/28456 (1996-09-01), None
XP-002138911, Takesako et al, Aureobasidins, New Antifungal Antibiotics Taxonomy, Fermentation, Isolation, and Properties, The Journal of Antibiotics, vol. 44, No. 9, Sep. 1991, pp. 919-924.
XP 000578251, Yoshikawa et al, Isolation, Structures, and Antifungal Activities of New Aureobasidins, The Journal of Antibiotics, vol. 46, No. 9, Sep. 1993, pp. 1347-1354.
XP-000907491, McCormack et al, Production Of Antibacterial Compounds by Phylloplane-Inhabiting Yeasts and Yeastlike Fungi, Applied and Environmental Microbiology, vol. 60, No. 3, Mar. 1994, pp. 927-931.

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