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A process for the preparation of an antibiotic complex, called Bu2231, or components and acid addition salts thereof.

机译:一种制备称为Bu2231的抗生素复合物或其组分和酸加成盐的方法。

摘要

New complex glycopeptide antibiotics Bu-2231A (I) and Bu-2231b (II) are obtd. by culturing Streptoalloteichus hindustanus ATCC 31158 or its mutants, and sepd. the product (Bu-2231) into (I) AND (II) in the form of Cu complexes. (I) and (II), in both the Cu-complex and Cu-free form, are broad-spectrum antibacterials with higher activity than bleomycin NIHJ and phleomycin 616 against a wide range of Gram-positive, Gram-negative and acid-resistant microorganisms. They are also antifungal agents (for medical or agricultural use), and inhibit the growth of Walker 256 carcinosarcoma and Lewis carcinoma in rats.
机译:新的复合糖肽抗生素Bu-2231A(I)和Bu-2231b(II)被淘汰。通过培养印度斯坦链球菌ATCC 31158或其突变体和sepd。产物(Bu-2231)以铜络合物的形式分为(I)和(II)。 (I)和(II)以铜络合物和无铜形式存在,是广谱抗菌剂,对博克霉素NIHJ和phleomycin 616具有更高的活性,可抵抗多种革兰氏阳性,革兰氏阴性和耐酸微生物。它们还是抗真菌剂(用于医疗或农业用途),并抑制大鼠中Walker 256癌肉瘤和Lewis癌的生长。

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