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公开(公告)号:US4199514A
公开(公告)日:1980-04-22
申请号:US6461
申请日:1979-01-25
申请人: Satoshi Omura , Yuzuru Iwai , Juichi Awaya , Yoko Takahashi , Ruiko Oiwa
发明人: Satoshi Omura , Yuzuru Iwai , Juichi Awaya , Yoko Takahashi , Ruiko Oiwa
IPC分类号: A61K31/365 , A61P31/04 , C07D493/04 , C12P17/18
CPC分类号: C07D493/04 , Y10S435/886
摘要: A novel compound frenolicin B of the formula: ##STR1## is prepared by cultivating a microorganism belonging to genus Streptomyces, e.g. Streptomyces roseofulvus AM-3867, in a culture medium and isolating the compound formed and accumulated in the medium from the cultured product. Said frenolicin B is useful as an antibiotic.
摘要翻译: 通过培养属于链霉菌属(Streptomyces)属的微生物,例如,制备下式的新化合物富伦菌素B:
链霉菌AM-3867,在培养基中分离培养物中形成和积累的培养基中的化合物。 所述富伦菌素B可用作抗生素。 -
公开(公告)号:US4493845A
公开(公告)日:1985-01-15
申请号:US434818
申请日:1982-10-18
申请人: Satoshi Omura , Yoshitake Tanaka , Yuzuru Iwai , Yoko Takahashi , Akira Nakagawa
发明人: Satoshi Omura , Yoshitake Tanaka , Yuzuru Iwai , Yoko Takahashi , Akira Nakagawa
IPC分类号: C07H17/08 , A61K31/325 , A61K31/35 , A61K35/74 , A61P31/04 , C07G11/00 , C12P1/06 , C12P17/18 , C07D491/08
摘要: Antibiotic AM-3603 which is also designated as irumamycin is represented by the following formula: ##STR1## This substance is active upon certain Gram-positive bacteria, phytopathogenic fungi and dermatophytes, and is of interest in treating various diseases of humans and animals caused by infectious bacteria and fungi and also useful for agricultural purposes. Antibiotic AM-3603 may be prepared by fermentation, in which a microorganism capable of producing AM-3603 is cultured in a medium to accumulate AM-3603 in the cultured broths, from which AM-3603 is recovered. A preferred strain is Streptomyces sp. AM-3603 (FERM-P 5619; NRRL 12518).
摘要翻译: 也被称为伊马利霉素的抗生素AM-3603由下式表示:
该物质对某些革兰氏阳性菌,植物病原真菌和皮肤癣菌有活性,并且对于治疗人类和动物引起的各种疾病感兴趣 感染性细菌和真菌,也可用于农业目的。 抗生素AM-3603可以通过发酵制备,其中能够产生AM-3603的微生物在培养基中培养以在收集AM-3603的培养肉汤中积累AM-3603。 优选的菌株是链霉菌属(Streptomyces sp。)。 AM-3603(FERM-P 5619; NRRL 12518)。 -
公开(公告)号:US20090130717A1
公开(公告)日:2009-05-21
申请号:US12084878
申请日:2006-05-16
申请人: Satoshi Omura , Hiroshi Tomoda , Yong-pil Kim , Hideaki Hanaki , Atsuko Matsumoto , Yoko Takahashi
发明人: Satoshi Omura , Hiroshi Tomoda , Yong-pil Kim , Hideaki Hanaki , Atsuko Matsumoto , Yoko Takahashi
摘要: A microorganism represented by a strain K04-0144 belonging to Streptomyces sp. having ability to produce K04-0144 substance is cultured in the medium, and the isolated K04-0144A substance, K04-0144B substance and K04-0144C substance therefrom have strong antibacterial activities against Gram-positive bacteria including methicillin-resistant Streptococcus aureus (MRSA), consequently these are useful as the therapeutic agents for infectious disease caused by MRSA as well as infectious diseases caused by multidrug including β-lactam antibiotics resistant bacteria. Further, similarly, since the novel K04-0144D substance isolated from the cultured liquid has the action for enhancing the effect of β-lactam antibiotics, which are utilized as the antibacterial agents, in combination with them, it is useful as the therapeutic agent for infectious diseases caused by methicillin-resistant Staphylococcus aureus (MRSA) and multidrug including β-lactam antibiotics resistant bacteria.
摘要翻译: 属于Streptomyces sp。的菌株K04-0144所代表的微生物 在培养基中培养生产K04-0144物质的能力,分离的K04-0144A物质,K04-0144B物质和K04-0144C物质对革兰氏阳性菌(包括耐甲氧西林金黄色葡萄球菌(MRSA))具有很强的抗菌活性, 因此,这些可用作由MRSA引起的感染性疾病的治疗剂以及由多种药物(包括β-内酰胺抗生素抗性细菌)引起的感染性疾病。 此外,类似地,由于从培养液体中分离的新型K04-0144D物质具有增强作为抗菌剂的β-内酰胺抗生素与其组合的作用,因此可用作治疗剂 由耐甲氧西林金黄色葡萄球菌(MRSA)引起的感染性疾病和包括β-内酰胺抗生素抗性细菌在内的多种药物。
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公开(公告)号:US20060287252A1
公开(公告)日:2006-12-21
申请号:US10571263
申请日:2004-02-09
申请人: Satoshi Omura , Akio Abe , Masato Iwatuki , Yoko Takahashi , Hiroshi Tomoda
发明人: Satoshi Omura , Akio Abe , Masato Iwatuki , Yoko Takahashi , Hiroshi Tomoda
IPC分类号: A61K38/04 , C12P21/04 , C12P17/00 , C07D403/02 , C07K5/04
CPC分类号: C12R1/465 , C07K5/1024 , C12P17/165
摘要: A microorganism belonging to the genus Streptomyces and being capable of producing substance K01-0509-A1 and/or substance K01-0509-A2 is cultured in a medium. Then, the substance K01-0509-A1 and/or the substance K01-0509-A2 having been thus accumulated in the liquid culture medium are collected from the medium. It is expected that the obtained substances are efficacious as drugs which are selectively effective on pathogenic gram-negative bacteria having the type III secretion system.
摘要翻译: 在培养基中培养属于链霉菌属的能够产生物质K01-0509-A1和/或物质K01-0509-A2的微生物。 然后,从介质中收集已经积累在液体培养基中的物质K01-0509-A1和/或物质K01-0509-A2。 预期所获得的物质作为对具有III型分泌系统的病原性革兰氏阴性细菌有选择性的药物是有效的。
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公开(公告)号:US20060089298A1
公开(公告)日:2006-04-27
申请号:US10508413
申请日:2003-01-17
申请人: Satoshi Omura , Hiroshi Tomoda , Masato Iwatsuki , Yoko Takahashi
发明人: Satoshi Omura , Hiroshi Tomoda , Masato Iwatsuki , Yoko Takahashi
摘要: The present invention is comprised of culturing a microorganism having ability to produce K01-B0171-B substance and/or K01-B0171-C substance in a medium, accumulating K01-B0171-B substance and/or K01-B0171-C substance in a culture fluid and isolating K01-B0171-B substance and/or, K01-B0171-C substance from the culture fluid. The obtained K01-B0171-B substance, K01-B0171-C substance or a composition of these substances is expected to be useful as a medicament of antituberculous agent.
摘要翻译: 本发明包括在培养基中培养具有生产K01-B0171-B物质和/或K01-B0171-C物质的微生物的微生物,将K01-B0171-B物质和/或K01-B0171-C物质累积在 培养液并从培养液中分离K01-B0171-B物质和/或K01-B0171-C物质。 获得的K01-B0171-B物质,K01-B0171-C物质或这些物质的组合物预期可用作抗结核药物的药物。
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公开(公告)号:US20140206889A1
公开(公告)日:2014-07-24
申请号:US14342311
申请日:2012-08-31
申请人: Satoshi Omura , Yoko Takahashi , Takuji Nakashima , Kazuhiko Otoguro , Kazuro Shiomi , Masato Iwatsuki , Atsuko Matsumoto
发明人: Satoshi Omura , Yoko Takahashi , Takuji Nakashima , Kazuhiko Otoguro , Kazuro Shiomi , Masato Iwatsuki , Atsuko Matsumoto
IPC分类号: C07D493/16 , C12R1/01 , C12P17/18
CPC分类号: C07D493/16 , C07D493/18 , C12P17/181 , C12R1/01
摘要: [Problem]The present invention addresses the problem of providing an anti-trypanosomal drug having a novel skeleton, in order to solve issues that occur with conventional technologies.[Solution]The present invention is based on the discovery of a microbe that produces an anti-trypanosomal drug having a novel skeleton. Specifically, this invention provides: a compound indicated by formula (I) having a trypanosomal inhibitory activity; an analog thereof; a production method therefor; and a Lechevalieria sp. Kl0-0216 strain that produces said compound.
摘要翻译: 本发明解决提供具有新骨架的抗锥虫毒素药物的问题,以解决常规技术中出现的问题。 [解决方案]本发明是基于产生具有新骨架的抗锥虫药物的微生物的发现。 具体地,本发明提供:具有锥虫体抑制活性的式(I)表示的化合物; 其类似物; 一种生产方法; 和Lechevalieria sp。 产生所述化合物的Kl0-0216菌株。
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公开(公告)号:US07439225B2
公开(公告)日:2008-10-21
申请号:US10508413
申请日:2003-01-17
申请人: Satoshi Omura , Hiroshi Tomoda , Masato Iwatsuki , Yoko Takahashi
发明人: Satoshi Omura , Hiroshi Tomoda , Masato Iwatsuki , Yoko Takahashi
IPC分类号: A61K38/12
摘要: The present invention is comprised of culturing a microorganism having ability to produce K01-B0171-B substance and/or K01-B0171-C substance in a medium, accumulating K01-B0171-B substance and/or K01-B0171-C substance in a culture fluid and isolating K01-B0171-B substance and/or, K01-B0171-C substance from the culture fluid. The obtained K01-B0171-B substance, K01-B0171-C substance or a composition of these substances is expected to be useful as a medicament of antituberculous agent.
摘要翻译: 本发明包括在培养基中培养具有生产K01-B0171-B物质和/或K01-B0171-C物质的微生物的微生物,将K01-B0171-B物质和/或K01-B0171-C物质累积在 培养液并从培养液中分离K01-B0171-B物质和/或K01-B0171-C物质。 获得的K01-B0171-B物质,K01-B0171-C物质或这些物质的组合物预期可用作抗结核药物的药物。
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公开(公告)号:US09000194B2
公开(公告)日:2015-04-07
申请号:US14342311
申请日:2012-08-31
申请人: Satoshi Omura , Yoko Takahashi , Takuji Nakashima , Kazuhiko Otoguro , Kazuro Shiomi , Masato Iwatsuki , Atsuko Matsumoto
发明人: Satoshi Omura , Yoko Takahashi , Takuji Nakashima , Kazuhiko Otoguro , Kazuro Shiomi , Masato Iwatsuki , Atsuko Matsumoto
IPC分类号: C07D321/00 , C07D493/16 , C07D493/18 , C12P17/18 , C12R1/01
CPC分类号: C07D493/16 , C07D493/18 , C12P17/181 , C12R1/01
摘要: The present invention addresses the problem of providing an anti-trypanosomal drug having a novel skeleton, in order to solve issues that occur with conventional technologies.The present invention is based on the discovery of a microbe that produces an anti-trypanosomal drug having a novel skeleton. Specifically, this invention provides: a compound indicated by formula (I) having a trypanosomal inhibitory activity; an analog thereof; a production method therefor; and a Lechevalieria sp. K10-0216 strain that produces said compound.
摘要翻译: 本发明解决提供具有新骨架的抗锥虫药物的问题,以解决常规技术中出现的问题。 本发明基于产生具有新骨架的抗锥虫毒素的微生物的发现。 具体地,本发明提供:具有锥虫体抑制活性的式(I)表示的化合物; 其类似物; 一种生产方法; 和Lechevalieria sp。 产生所述化合物的K10-0216菌株。
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公开(公告)号:US07973147B2
公开(公告)日:2011-07-05
申请号:US12084878
申请日:2006-05-16
申请人: Satoshi Omura , Hiroshi Tomoda , Yong-pil Kim , Hideaki Hanaki , Atsuko Matsumoto , Yoko Takahashi
发明人: Satoshi Omura , Hiroshi Tomoda , Yong-pil Kim , Hideaki Hanaki , Atsuko Matsumoto , Yoko Takahashi
摘要: A microorganism represented by a strain K04-0144 belonging to Streptomyces sp. having ability to produce K04-0144 substance is cultured in the medium, and the isolated K04-0144A substance, K04-0144B substance and K04-0144C substance therefrom have strong antibacterial activities against Gram-positive bacteria including methicillin-resistant Streptococcus aureus (MRSA), consequently these are useful as the therapeutic agents for infectious disease caused by MRSA as well as infectious diseases caused by multidrug including β-lactam antibiotics resistant bacteria. Further, similarly, since the novel K04-0144D substance isolated from the cultured liquid has the action for enhancing the effect of β-lactam antibiotics, which are utilized as the antibacterial agents, in combination with them, it is useful as the therapeutic agent for infectious diseases caused by methicillin-resistant Staphylococcus aureus (MRSA) and multidrug including β-lactam antibiotics resistant bacteria.
摘要翻译: 属于Streptomyces sp。的菌株K04-0144所代表的微生物 在培养基中培养生产K04-0144物质的能力,分离的K04-0144A物质,K04-0144B物质和K04-0144C物质对革兰氏阳性菌(包括耐甲氧西林金黄色葡萄球菌(MRSA))具有很强的抗菌活性, 因此,这些可用作由MRSA引起的感染性疾病的治疗剂以及由多种药物(包括β-内酰胺抗生素抗性细菌)引起的感染性疾病。 此外,类似地,由于从培养液中分离的新型K04-0144D物质具有增强作为抗菌剂的β-内酰胺抗生素与其组合的作用,因此可用作治疗剂 用于由耐甲氧西林金黄色葡萄球菌(MRSA)引起的感染性疾病和包含β-内酰胺抗生素抗性细菌的多药物。
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10.
公开(公告)号:US20060014825A1
公开(公告)日:2006-01-19
申请号:US10492654
申请日:2002-10-11
申请人: Satoshi Omura , Hiroshi Tomoda , Yoko Takahashi
发明人: Satoshi Omura , Hiroshi Tomoda , Yoko Takahashi
IPC分类号: A61K31/365 , C12P17/02 , C07D313/00
CPC分类号: C07D313/00 , C07D315/00 , C12P17/08 , C12R1/465
摘要: The present invention relates to effective drugs for mycosis caused by so called fungi such as fungi and yeast. The present invention is comprised of culturing a microorganism belonging to genus Streptomyces and having ability to produce K99-5278A substance, K99-5278B substance and K99-5278C substance in a medium, accumulating K99-5278A substance, K99-5278B substance and K99-5278C substance in the cultured medium and isolating K99-5278A substance, K99-5278B substance and K99-5278C substance from the cultured mass. The thus obtained substances can be expected as a novel antifungal agent.
摘要翻译: 本发明涉及由所谓的真菌如真菌和酵母引起的用于真菌病的有效药物。 本发明包括培养属于链霉菌属的微生物,并且能够在培养基中生产K99-5278A物质,K99-5278B物质和K99-5278C物质,积累K99-5278A物质,K99-5278B物质和K99-5278C 培养基中的物质,并从培养物质中分离K99-5278A物质,K99-5278B物质和K99-5278C物质。 可以预期由此获得的物质作为新颖的抗真菌剂。
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