Streptomycetal antibiotic
    3.
    发明授权
    Streptomycetal antibiotic 失效
    链霉菌抗生素

    公开(公告)号:US4179498A

    公开(公告)日:1979-12-18

    申请号:US717336

    申请日:1976-08-24

    CPC classification number: C07D477/20 C12P17/184 C12R1/58 Y10S435/902

    Abstract: A novel antibiotic designated herein MM 17880 may be obtained from the cultivation of strains of Streptomyces olivaceus and related organisms. In addition to being potent antibacterial agents, MM 17880 and its salts inhibit .beta.-lactamase obtained from many organisms so that it shows a synergistic antibacterial effect when combined with .beta.-lactam antibiotics.

    Abstract translation: 本文定义的新型抗生素MM 17880可以从橄榄油链霉菌和相关生物的菌株的培养获得。 除了有效的抗菌剂外,MM 17880及其盐抑制从许多生物体获得的β-内酰胺酶,因此当与β-内酰胺抗生素结合时,其显示出协同的抗菌作用。

    Streptomycetal antibiotic
    4.
    发明授权
    Streptomycetal antibiotic 失效
    链霉菌抗生素

    公开(公告)号:US4163051A

    公开(公告)日:1979-07-31

    申请号:US725864

    申请日:1976-09-23

    CPC classification number: C07D477/20

    Abstract: A novel antibiotic designated herein MM 17880 may be obtained from the cultivation of strains of Streptomyces olivaceus and related organisms. In addition to being potent antibacterial agents, MM 17880 and its salts inhibit .beta.-lactamase obtained from may organisms so that it shows a synergistic antibacterial effect when combined with .beta.-lactam antibiotics.

    Abstract translation: 本文定义的新型抗生素MM 17880可以从橄榄油链霉菌和相关生物的菌株的培养获得。 除了有效的抗菌剂外,MM 17880及其盐可抑制从有机体获得的β-内酰胺酶,以便与β-内酰胺抗生素组合时显示出协同的抗菌作用。

    .beta.-Lactam antibiotic, its preparation and use
    5.
    发明授权
    .beta.-Lactam antibiotic, its preparation and use 失效
    β-内酰胺抗生素,其制备和用途

    公开(公告)号:US4421760A

    公开(公告)日:1983-12-20

    申请号:US274464

    申请日:1981-06-17

    Applicant: Stephen J. Box

    Inventor: Stephen J. Box

    CPC classification number: C07D477/20 C12P17/184 C12R1/58

    Abstract: The compound of the formula (VI): ##STR1## pharmaceutically acceptable salts and pharmaceutically acceptable esters thereof, are useful for their antibacterial activity and for their .beta.-lactamase inhibitory activity. They may be combined in a synergistically effective amount with a penicillin or cephalosporin for the treatment of bacterial infections in humans and animals.

    Abstract translation: 式(VI)的化合物:其药学上可接受的盐和药学上可接受的酯可用于其抗菌活性和β-内酰胺酶抑制活性。 它们可以以协同有效量与青霉素或头孢菌素组合用于治疗人和动物的细菌感染。

    Process for producing antibiotics
    6.
    发明授权
    Process for producing antibiotics 失效
    生产抗生素的方法

    公开(公告)号:US4221870A

    公开(公告)日:1980-09-09

    申请号:US916768

    申请日:1978-06-19

    Applicant: Stephen J. Box

    Inventor: Stephen J. Box

    CPC classification number: C12R1/465 C12P17/184 Y10S435/886

    Abstract: This invention provides a process for the preparation of salts of the .beta.-lactamase inhibitory antibiotics MM4550A, MM13902 and MM17880, which are the compounds of the formulae (I)-(III), respectively: ##STR1## which process comprises cultivating a strain of Streptomyces gedanensis and isolating a salt of at least one of MM4550A, MM13902 and MM17880.

    Abstract translation: 本发明提供了分别制备式(I) - (III)化合物的β-内酰胺酶抑制性抗生素MM4550A,MM13902和MM17880的盐的方法: (III),该方法包括培养一种链霉菌(Streptomyces gedanensis)菌株并分离MM4550A,MM13902和MM17880中的至少一种的盐。

    Streptomycetal antibiotic
    7.
    发明授权
    Streptomycetal antibiotic 失效
    链霉菌抗生素

    公开(公告)号:US4162304A

    公开(公告)日:1979-07-24

    申请号:US725677

    申请日:1976-09-22

    CPC classification number: C07D477/20

    Abstract: A novel antibiotic designated herein MM 17880 may be obtained from the cultivation of strains of Streptomyces olivaceus and related organisms. In addition to being potent antibacterial agents, MM 17880 and its salts inhibit .beta.-lactamase obtained fromm many organisms so that it shows a synergistic antibacterial effect when combined with .beta.-lactam antibiotics.

    Abstract translation: 本文定义的新型抗生素MM 17880可以从橄榄油链霉菌和相关生物的菌株的培养获得。 除了有效的抗菌剂外,MM 17880及其盐抑制了许多生物体获得的β-内酰胺酶,因此当与β-内酰胺抗生素结合时,其显示出协同的抗菌作用。

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