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Antibiotic rubradirin and method of making same

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专利汇可以提供Antibiotic rubradirin and method of making same专利检索,专利查询,专利分析的服务。并且An antibiotic rubradirin gives a red colour in acid solution and a green colour in alkaline solution, it is effective against gram positive and negative bacteria; it is soluble in ethyl acetate, 1-butanol, methyl ethyl ketone, methylene chloride, methanol and benzene and relatively insoluble in water; it has the following elemental analysis: C=57.31%, H=4.69%, N=5.25% and O=31.36%; molecular weight 1026\sB12; ultra-violet absorption spectrum (Fig. 2) showing maxima at 264 mm , a = 28.48; 337 mm , a = 34.73 and 515 mm , a = 1.58; and infra-red absorption spectrum as in Fig. 1. Rubradirin is produced by cultivating Streptomyces achromogenes var. rubradiris NRRL 3061 (N.C.I.B. 9516) in an aqueous nutrient medium containing an assimiliable source of carbon and nitrogen under aerobic conditions. The temperature is 18 DEG to 40 DEG C., pH 6 to 8 and duration of cultivation 2 to 10 days. Rubradirin may be recovered from the clarified broth by (a) extraction or (b) adsorption. Extraction from a broth of pH 3.2, by means of a solvent such as methylene chloride, may be followed by precipitation by a non-solvent such as Skellysolve B. Adsorption may be on strongly basic anion exchange resins, e.g. Amberlite IRS-400 or on silicic acid, alumina or "Florisil" (Registered Trade Mark), followed by elution with a solvent. Further purification may be by counter-current distribution, e.g. in the solvent system Skellysolve B, acetone and water (5 : 5 : 1). Rubradirin forms salts with organic and inorganic bases, e.g. alkali metal, alkaline earth metal and amine bases.,下面是Antibiotic rubradirin and method of making same专利的具体信息内容。

1. RUBRADIRIN, A COMPOUND WHICH (A) IS EFFECTIVE IN INHIBITING THE GROWTH OF VARIOUS GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA; (B) IS SOLUBLE IN ETHYL ACETATE, 1-BUTANOL, METHYL ETHYL KETONE, METHYLENE CHLORIDE, METHANOL, AND BENZENE; AND RELATIVELY INSOLUBLE IN WATER; (C) HAS THE ELEMENTAL ANALYSIS: C, 57.31; H, 4.69; N, 5.25; O, 31.36; (D) HAS A MOLECULAR WEIGHT OF 1026$12; (E) HAS A CHARACTERISTIC ULTRAVIOLET ABSORPTION SPECTRUM AS FOLLOWS: IN DIOXANE: 264 MU, A=28.48; 337 MU, A=34.73; 515 MU, A=1.58; AND AS SHOWN IN FIGURE II OF THE DRAWING; (F) HAS A CHARACTERISTIC INFRARED ABSORPTION SPECTRUM AS SHOWN IN FIGURE I OF THE ACCOMPANYING DRAWING; (G) HAS A MELTING POINT OF 205-215*C.; AND (H) HAS AN EMPIRICAL FORMULA C51H50O21N4.
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