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ANTI-MRSA ANTIBIOTIC

机译:抗MRSA抗生素

摘要

PROBLEM TO BE SOLVED: To obtain a new compound useful as an antibiotic effective for infec tious diseases caused by various pathogenic bacteria including multiple drug- resistant bacteria of Staphylococcus aureus. ;SOLUTION: This new compound is such one as to be a white powdery acidic substance, soluble in chloroform and ethyl acetate and insoluble in hexane. This compound has such physicochemical properties as to have a specific rotatory power of [α]D22=-45±5° (c=1.0, DMSO), molecular weight of FAB-MS m/z 1110(M+H), have the main absorption peaks in its ultraviolet absorption spectrum at 213, 278-283, 310-320 nm in methanol, and have 1H-NMR spectrum (400 MHz, d6-DMSO) as shown in the figure. This compound is obtained by culturing bactera capable of producing the above-mentioned compound and belonging to the genus Kineosuporia [e.g. Kineosporia sp. AP11158(FERM BP-6653)] by shaking culture or the like in a liquid medium, and then, separating the compound from the cultured product.;COPYRIGHT: (C)2000,JPO
机译:要解决的问题:获得一种新的化合物,可用作对由各种病原菌(包括多种金黄色葡萄球菌耐药菌)引起的传染病有效的抗生素。 ;解决方案:这种新化合物是白色粉末状酸性物质,可溶于氯仿和乙酸乙酯,不溶于己烷。该化合物的理化性质为:[α] D22 = -45±5°(c = 1.0,DMSO),FAB-MS m / z 1110(M + H)的分子量,如图所示,其主要吸收峰在甲醇中的213、278-283、310-320 nm处具有紫外线吸收光谱,并具有1H-NMR光谱(400 MHz,d6-DMSO)。该化合物是通过培养能够产生上述化合物并属于运动型尿失球菌的细菌而获得的。 Kineosporia sp。 AP11158(FERM BP-6653)],方法是在液体培养基中振荡培养物等,然后从培养物中分离出化合物。;版权:(C)2000,JPO

著录项

  • 公开/公告号JP2000239292A

    专利类型

  • 公开/公告日2000-09-05

    原文格式PDF

  • 申请/专利权人 ASAHI CHEM IND CO LTD;

    申请/专利号JP19990042584

  • 发明设计人 ISHIKAWA SATORU;ISHIZAWA KENYA;

    申请日1999-02-22

  • 分类号C07G11/00;A61P31/04;

  • 国家 JP

  • 入库时间 2022-08-22 01:59:40

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