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21. 发明授权

US06521600B1 Compound, WF002, production thereof and use thereof 失效
标题翻译：化合物，WF002，其制备及其用途
公开(公告)号：US06521600B1
公开(公告)日：2003-02-18
申请号：US09720331
申请日：2001-01-18
申请人： Yasuhiro Hori , Masami Ezaki , Yasuhisa Tsurumi , Shigehiro Takase , Motohiro Hino
发明人： Yasuhiro Hori , Masami Ezaki , Yasuhisa Tsurumi , Shigehiro Takase , Motohiro Hino
IPC分类号： A61K317028
CPC分类号： C12R1/645 , C07J63/008 , C12P19/60 , Y10S435/911
摘要： The present invention provides a new bioactive compound of formula (I), which has an antimicrobial activity against pathogenic microorganisms, and a process for production thereof. Also provided are a pharmaceutical composition comprising the compound and pharmaceutically acceptable carrier, a use of the WF002 as a medicament and use of the compound for manufacture of the medicament for treatment of infectious disease.
摘要翻译：本发明提供了具有抗病原微生物的抗微生物活性的新的式（I）生物活性化合物及其生产方法。还提供了包含该化合物和药学上可接受的载体的药物组合物，该WF002作为药物的用途以及该化合物用于制备用于治疗感染性疾病的药物的用途。

22. 发明授权

US4767768A Nitro aliphatic compounds, process for preparation thereof and use thereof 失效
标题翻译：硝基脂族化合物，其制备方法和用途
公开(公告)号：US4767768A
公开(公告)日：1988-08-30
申请号：US559260
申请日：1983-12-08
申请人： Masanori Okamoto , Morita Iwami , Shigehiro Takase , Itsuo Uchida , Kazuyoshi Umehara , Masanobu Kohsaka , Hiroshi Imanaka
发明人： Masanori Okamoto , Morita Iwami , Shigehiro Takase , Itsuo Uchida , Kazuyoshi Umehara , Masanobu Kohsaka , Hiroshi Imanaka
IPC分类号： C07D207/416 , A61K31/15 , A61K31/16 , A61K31/215 , A61K31/26 , A61K31/445 , A61K31/495 , A61P7/02 , A61P9/08 , A61P9/12 , C07C43/23 , C07C45/41 , C07C57/03 , C07C205/51 , C07C233/02 , C07C233/09 , C07C233/20 , C07C233/49 , C07C235/28 , C07C249/04 , C07C251/32 , C07C251/38 , C07C251/40 , C07C251/60 , C07C255/10 , C07C255/19 , C07C255/23 , C07C255/64 , C07C291/12 , C07D207/40 , C07D207/404 , C07D295/18 , C07D295/185 , C07C103/22 , C07C103/34
CPC分类号： C07D207/404 , C07C205/44 , C07C205/51 , C07C255/00 , C07C43/23 , C07C45/41 , C07C57/03 , C07D295/185
摘要： New Nitro aliphatic compounds and their pharmaceutically acceptable salts are disclosed.
摘要翻译：公开了新的硝基脂族化合物及其药学上可接受的盐。

23. 发明授权

US07741085B2 Compound WS727713 失效
标题翻译：化合物WS727713
公开(公告)号：US07741085B2
公开(公告)日：2010-06-22
申请号：US11547729
申请日：2005-03-22
申请人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
发明人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
IPC分类号： C12P1/04 , A61K38/12
CPC分类号： C12R1/01 , A61K8/99 , A61K35/74 , A61K2800/85 , A61Q5/065 , A61Q19/00 , C07G17/00 , C12P1/06
摘要： The present invention relates to a compound WS727713, useful as a modulator of melanocortin receptors, and a process for its production by culturing in a culture medium the actinomycetes strain of the genus Pseudonocardia, deposit number FERM BP-7570 and recovering the compound.
摘要翻译：本发明涉及可用作黑皮质素受体的调节剂的化合物WS727713，以及通过在培养基中培养假诺卡氏菌属的放线菌菌株FERM BP-7570并回收该化合物来生产的方法。

24. 发明申请

US20070254829A1 Compound Ws727713 失效
标题翻译：化合物Ws727713
公开(公告)号：US20070254829A1
公开(公告)日：2007-11-01
申请号：US11547729
申请日：2005-03-22
申请人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
发明人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
IPC分类号： A61K38/00 , C07K14/00 , C12N1/21 , C12P1/04
CPC分类号： C12R1/01 , A61K8/99 , A61K35/74 , A61K2800/85 , A61Q5/065 , A61Q19/00 , C07G17/00 , C12P1/06
摘要： The present invention relates to a new compound useful as a modulator of melanxocortin receptors. In particular, the present invention relates to a compound WS727713, a process for production of the compound by culturing, in a culture medium, a WS727713-producing strain belonging to Pseudonocardia and recovering the compound from a culture broth, a pharmaceutical composition containing the compound, a use of the compound for manufacture of a medicament or a cosmetic for melanocortin receptor modulation, a use of the compound for manufacture of a medicament or a cosmetic for treating or preventing ishemia/reperfusion injury, brain and renal inflammatory diseases, hepatitis, sepsis/septic shock, hypoxic shock, acute respiratory distress syndrome (ARDS), rheumatic arthritis (RA), gouty arthritis, aortic regurgitation (AR), juvenile chronic arthritis, osteoarthritis, nephritis, induction of tolerance, contact hypersensitivity, inflammatory bowel disease (IBD), sexual dysfunction, transplantation, pain, disease progression of HIV, postinflammatory hypopigmentation, tinea versicolor, idiopathic guttate hypomelanosis, fever, functional bowel disease, obesity, satiety effect, diabetes mellitus, modulation of dermal exocrine function, canities (canities circumscripta), gray hair, pancreatitis, fibrotic disorders (hypertrophic scars, keloids, localized scleroderma, systematic sclerosis, sclerodermic graft versus host disease of the skin, cirrhosis of the liver, idiopathic and bleomycin induced lung fibrosis, cyclosporin induced nephropathy), uveitis (especially in Behçet's syndrome and sarcoidosis), vasculitis, microbial infections, celiac disease, vulvar vestibulitis syndrome, melonoma invasion, anorexia or the like.
摘要翻译：本发明涉及可用作黑皮皮素受体调节剂的新化合物。特别地，本发明涉及化合物WS727713，该化合物的生产方法是在培养基中培养属于假诺卡氏菌属的WS727713生产菌株并从培养液中回收该化合物，含有该化合物的药物组合物，该化合物用于制造用于黑皮质素受体调节的药物或化妆品的用途，该化合物用于制备用于治疗或预防缺血/再灌注损伤，脑和肾炎性疾病，肝炎，败血症的药物或化妆品的用途 /脓毒性休克，缺氧休克，急性呼吸窘迫综合征（ARDS），风湿性关节炎（RA），痛风性关节炎，主动脉瓣反流（AR），青少年慢性关节炎，骨关节炎，肾炎，耐受诱导，接触性超敏反应，炎性肠病），性功能障碍，移植，疼痛，艾滋病病毒进展，炎性色素沉着，花斑斑，乳糜泻黄斑病，发热，功能性肠病，肥胖症，饱腹感，糖尿病，皮肤外分泌功能的调节，阴毛（canence circumscripta），灰白色头发，胰腺炎，纤维化疾病（肥大性瘢痕，瘢痕疙瘩，局部硬皮病，系统性硬化症，硬皮病皮肤移植物抗宿主病，肝硬化，特发性和博来霉素引起的肺纤维化，环孢菌素诱导的肾病），葡萄膜炎（尤其是Behçet综合征和结节病），血管炎，微生物感染，乳糜泻，外阴前庭炎综合征，美黄酮侵袭，厌食症等。

25. 发明申请

US20120214731A1 COMPOUND WS 727713 失效
标题翻译：化合物WS 727713
公开(公告)号：US20120214731A1
公开(公告)日：2012-08-23
申请号：US13354308
申请日：2012-01-19
申请人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
发明人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
IPC分类号： A61K38/12 , A61P31/18 , A61P31/12 , A61P1/16 , A61P17/00 , A61P3/04 , A61P1/04 , A61P19/02 , A61P1/18 , A61P25/02 , A61P31/00 , A61P3/10
CPC分类号： C12R1/01 , A61K8/99 , A61K35/74 , A61K2800/85 , A61Q5/065 , A61Q19/00 , C07G17/00 , C12P1/06
摘要： The present invention relates to a new compound useful as a modulator of melanocortin receptors. In particular, the present invention relates to a compound WS727713, a process for production of the compound by culturing, in a culture medium, a WS727713-producing strain belonging to Pseudonocardia and recovering the compound from a culture broth, a pharmaceutical composition containing the compound, and uses of the compound.
摘要翻译：本发明涉及可用作黑皮质素受体调节剂的新化合物。特别地，本发明涉及化合物WS727713，该化合物的生产方法是在培养基中培养属于假诺卡氏菌属的WS727713生产菌株并从培养液中回收该化合物，含有该化合物的药物组合物，以及化合物的用途。

26. 发明申请

US20110015121A1 CYCLIC COMPOUND AND SALT THEREOF 有权
标题翻译：环状化合物及其盐
公开(公告)号：US20110015121A1
公开(公告)日：2011-01-20
申请号：US12922337
申请日：2009-03-13
申请人： Ikuko Nakamura , Koji Yoshikawa , Keisuke Ohsumi , Ryuichi Kanasaki , Shigehiro Takase
发明人： Ikuko Nakamura , Koji Yoshikawa , Keisuke Ohsumi , Ryuichi Kanasaki , Shigehiro Takase
IPC分类号： A61K38/12 , C07K7/64 , A61P31/00 , C12P21/04
CPC分类号： A61K36/06 , C07K7/64 , C12N1/14 , C12P21/02 , C12R1/645
摘要： A compound useful as an antifungal agent, particularly a therapeutic agent for deep-seated mycoses, is provided. A fungus Acremonium persicinum was collected, and cyclic compounds were isolated from culture liquids thereof. The present inventors confirmed that the cyclic compounds or salts thereof have a potent antifungal activity and are useful as medicaments, particularly an antifungal agent, and thus the present invention was completed. The cyclic compound and the salt thereof according to the present invention can be used as an agent for preventing or treating mycoses, particularly deep-seated mycoses.
摘要翻译：提供了可用作抗真菌剂的化合物，特别是用于深层真菌病的治疗剂。收集真菌Acremonium persicinum，从其培养液中分离出环状化合物。本发明人证实，环状化合物或其盐具有有效的抗真菌活性，可用作药物，特别是抗真菌剂，因此完成了本发明。根据本发明的环状化合物及其盐可用作预防或治疗真菌病，特别是深层真菌病的药剂。

27. 发明申请

US20080214447A1 Cyclic Peptide Compound 失效
标题翻译：环状肽化合物
公开(公告)号：US20080214447A1
公开(公告)日：2008-09-04
申请号：US11719921
申请日：2005-11-21
申请人： Motoo Kobayashi , Satoshi Sasamura , Hideyuki Muramatsu , Yasuhisa Tsurumi , Shigehiro Takase , Kazuki Okada
发明人： Motoo Kobayashi , Satoshi Sasamura , Hideyuki Muramatsu , Yasuhisa Tsurumi , Shigehiro Takase , Kazuki Okada
IPC分类号： A61K38/12 , C07K7/64 , A61P31/12 , C12P21/04
CPC分类号： C07K7/645
摘要： A cyclic peptide compound of the following general formula (I): Wherein R1, R2 and R3 are defined in the description, or a salt thereof. The compound (I) is useful for the prophylactic and/or therapeutic treatment of hepatitis C.
摘要翻译：下列通式（I）的环肽化合物：其中R 1，R 2和R 3 3定义在说明书中，或其盐。化合物（I）可用于预防和/或治疗丙型肝炎。

28. 发明授权

US08598115B2 Cyclic compound and salt thereof 有权
标题翻译：环状化合物及其盐
公开(公告)号：US08598115B2
公开(公告)日：2013-12-03
申请号：US12922337
申请日：2009-03-13
申请人： Ikuko Nakamura , Koji Yoshikawa , Keisuke Ohsumi , Ryuichi Kanasaki , Shigehiro Takase
发明人： Ikuko Nakamura , Koji Yoshikawa , Keisuke Ohsumi , Ryuichi Kanasaki , Shigehiro Takase
IPC分类号： A61K38/12 , C12Q1/68
CPC分类号： A61K36/06 , C07K7/64 , C12N1/14 , C12P21/02 , C12R1/645
摘要： A compound useful as an antifungal agent, particularly a therapeutic agent for deep-seated mycoses, is provided. A fungus Acremonium persicinum was collected, and cyclic compounds were isolated from culture liquids thereof. The present inventors confirmed that the cyclic compounds or salts thereof have a potent antifungal activity and are useful as medicaments, particularly an antifungal agent, and thus the present invention was completed. The cyclic compound and the salt thereof according to the present invention can be used as an agent for preventing or treating mycoses, particularly deep-seated mycoses.
摘要翻译：提供了可用作抗真菌剂的化合物，特别是用于深层真菌病的治疗剂。收集真菌Acremonium persicinum，从其培养液中分离出环状化合物。本发明人证实，环状化合物或其盐具有有效的抗真菌活性，可用作药物，特别是抗真菌剂，因此完成了本发明。根据本发明的环状化合物及其盐可用作预防或治疗真菌病，特别是深层真菌病的药剂。

29. 发明授权

US08592378B2 Compound WS 727713 失效
标题翻译：化合物WS 727713
公开(公告)号：US08592378B2
公开(公告)日：2013-11-26
申请号：US13354308
申请日：2012-01-19
申请人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
发明人： Takanao Otsuka , Hirotsugu Ueda , Keiko Fujie , Hideyuki Muramatsu , Michizane Hashimoto , Shigehiro Takase
IPC分类号： A61K38/12
CPC分类号： C12R1/01 , A61K8/99 , A61K35/74 , A61K2800/85 , A61Q5/065 , A61Q19/00 , C07G17/00 , C12P1/06
摘要： The present invention relates to a new compound useful as a modulator of melanocortin receptors. In particular, the present invention relates to a compound WS727713, a process for production of the compound by culturing, in a culture medium, a WS727713-producing strain belonging to Pseudonocardia and recovering the compound from a culture broth, a pharmaceutical composition containing the compound, and uses of the compound.
摘要翻译：本发明涉及可用作黑皮质素受体调节剂的新化合物。特别地，本发明涉及化合物WS727713，该化合物的生产方法是在培养基中培养属于假诺卡氏菌属的WS727713生产菌株并从培养液中回收该化合物，含有该化合物的药物组合物，以及化合物的用途。

30. 发明授权

US06730776B1 WF14573 or its salt, production thereof and use thereof 失效
标题翻译： WF14573或其盐，其制备及其用途
公开(公告)号：US06730776B1
公开(公告)日：2004-05-04
申请号：US09646342
申请日：2000-09-18
申请人： Yasuhiro Hori , Shigehiro Takase , Yasuhisa Tsurumi , Michizane Hashimoto , Motohiro Hino
发明人： Yasuhiro Hori , Shigehiro Takase , Yasuhisa Tsurumi , Michizane Hashimoto , Motohiro Hino
IPC分类号： C07K750
CPC分类号： C07K7/56 , A61K38/00
摘要： The present invention provides a new antimicrobial compound WF14573, and a process for producing WF14573 by (a) culturing a WF14573A and/or B-producing microorganism in a nutrient medium and recovering WF14573A and/or B from the resultant cultured broth or (b) deacylating WF14573A and/or B in the presence of a microbial substance which is capable of deacylating WF14573A and/or B. Also provided are an antimicrobial agent comprising WF14573 and carrier(s), a pharmaceutical composition comprising an effective amount of WF14573 and pharmaceutically acceptable carrier(s), a method for killing microorganisms by applying WF14573 to the microorganisms, and use of WF14573 for the treatment of infectious diseases caused by pathogenic microorganisms.
摘要翻译：本发明提供了一种新的抗微生物化合物WF14573，以及（a）在营养培养基中培养WF14573A和/或产生B生物的微生物并从所得培养液中回收WF14573A和/或B或（b）生产WF14573的方法，在能够脱酰基WF14573A和/或B的微生物物质存在下脱酰基WF14573A和/或B。还提供了包含WF14573和载体的抗微生物剂，包含有效量的WF14573和药学上可接受的药物组合物载体，通过向微生物施用WF14573杀死微生物的方法，以及使用WF14573来治疗由病原微生物引起的感染性疾病。

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