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US 4,375,464 AGranted
Antibiotic AY24,668 and process of preparation
AssigneeAyerst McKenna and Harrison Ltd.
InventorsSurendra N. Sehgal, Claude Vezina
Life of this patent
Estimating the term…
Abstract
Antibiotic AY24,668 is producible by culturing Streptomyces hygroscopicus NRRL 5491 in an aqueous nutrient medium. AY24,668 has antifungal properties. Methods for its preparation and use are disclosed.
Claims3
Solid AY24,668, an antibiotic which
- a. gives a colorless, crystalline compound with a melting point of 122.degree. to 124.degree. C., after recrystallization from diethyl ether;
- b. is soluble in diethyl ether, chloroform, acetone, methanol and dimethylformamide, very sparingly soluble in hexane and petroleum ether and substantially insoluble in water;
- c. shows a uniform spot on thin layer plates of silica gel;
- d. has a characteristic elemental analysis of about C, 67.75%, H, 8.93% N, 1.72%;
- e. exhibits the following characteristic absorption maxima in its ultraviolet absorption spectrum (95% ethanol):
- 267 nm (E.sub.1cm.sup.1% 421), 277 nm (E.sub.1cm.sup.1% 549) and 288 nm (E.sub.1cm.sup.1% 423);
- f. has a characteristic infrared absorption spectrum shown in accompanying FIG. 1;
- g. has a characteristic nuclear magnetic resonance spectrum as shown in accompanying FIG. 2;
- h. has a minimum inhibitory concentration of 0.36 to 10.0 .mu.g/ml against Candida albicans;
- and
- i. exhibits a LD.sub.50 (i.p., mice) of >900 mg/kg.
8 more elements
A pharmaceutical composition which comprises a pharmaceutically acceptable carrier and an antifungal effective amount of the antibiotic AY24,668 which
- a. is a solid giving a colorless, crystalline compound with a melting point of 122.degree. to 124.degree. C., after recrystallization from diethyl ether;
- b. is soluble in diethyl ether, chloroform, acetone, methanol and dimethylformamide, very sparingly soluble in hexane and petroleum ether and substantially insoluble in water;
- c. shows a uniform spot on thin layer plates of silica gel;
- d. has a characteristic elemental analysis of about C, 67.75%, H, 8.93% N, 1.72%;
- e. exhibits the following characteristic absorption maxima in its ultraviolet absorption spectrum (95% ethanol):
- 267 nm (E.sub.1cm.sup.1% 421), 277 nm (E.sub.1cm.sup.1% 549) and 288 nm (E.sub.1cm.sup.1% 423);
- f. has a characteristic infrared absorption spectrum shown in accompanying FIG. 1;
- g. has a characteristic nuclear magnetic resonance spectrum as shown in accompanying FIG. 2;
- h. has a minimum inhibitory concentration of 0.36 to 10.0 .mu.g/ml against Candida albicans;
- and
- i. exhibits a LD.sub.50 (i.p., mice) of >900 mg/kg.
8 more elements
A method of inhibiting the growth of pathogenic fungi in a mammal which comprises administering to the mammal an antifungally effective amount of the antibiotic AY24,668 which
- a. is a solid giving a colorless, crystalline compound with a melting point of 122.degree. to 124.degree. C., after recrystallization from diethyl ether;
- b. is soluble in diethyl ether, chloroform, acetone, methanol and dimethylformamide, very sparingly soluble in hexane and petroleum ether and substantially insoluble in water;
- c. shows a uniform spot on thin layer plates of silica gel;
- d. has a characteristic elemental analysis of about C, 67.75%, H, 8.93% N, 1.72%;
- e. exhibits the following characteristic absorption maxima in its ultraviolet absorption spectrum (95% ethanol):
- 267 nm (E.sub.1cm.sup.1% 421), 277 nm (E.sub.1cm.sup.1% 549) and 288 nm (E.sub.1cm.sup.1% 423);
- f. has a characteristic infrared absorption spectrum shown in accompanying FIG. 1;
- g. has a characteristic nuclear magnetic resonance spectrum as shown in accompanying FIG. 2;
- h. has a minimum inhibitory concentration of 0.36 to 10.0 .mu.g/ml against Candida albicans;
- and
- i. exhibits a LD.sub.50 (i.p., mice) of >900 mg/kg.
8 more elements
Dependencies are inferred from the claim text.