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公开(公告)号:EP0345735B1
公开(公告)日:1993-06-02
申请号:EP89110234.5
申请日:1989-06-06
发明人: Nishio, Maki , Sawada, Yosuke , Miyaki, Takeo , Oki, Toshikazu
IPC分类号: C07H15/244 , C12P19/56 , A61K31/70 , C12R1/03
CPC分类号: C12R1/03 , C07H15/244 , C12P19/56 , Y10S435/825
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2.
公开(公告)号:EP0479505A1
公开(公告)日:1992-04-08
申请号:EP91308869.6
申请日:1991-09-27
发明人: Sawada, Yosuke , Saitoh, Kyoichiro , Hatori, Masami , Miyaki, Takeo , Oki, Toshikazu , Tomita, Koji
IPC分类号: C07H15/244 , A61K31/70 , C12P19/56 , C12N1/20
CPC分类号: C07H15/244
摘要: The present invention relates to novel antifungal antibiotics herein designated as pradimicin L and pradimicin FL, and derivatives thereof. Pradimicins L and FL are produced by Actinomadura verrucosospora subsp. neohibisca strain R103-3, ATCC No. 53930.
摘要翻译: 本发明涉及本文中称为普拉定霉素L和普拉定霉素FL的新型抗真菌抗生素及其衍生物。 Pradimicins L和FL由Actinomadura verrucosospora subsp。 新罗非鱼菌株R103-3,ATCC No.53930。
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公开(公告)号:EP0368349B1
公开(公告)日:1993-09-15
申请号:EP89120904.1
申请日:1989-11-10
IPC分类号: C07H15/244 , A61K31/70 , C12P19/56 , C12N1/20
CPC分类号: C07H15/244 , C12P19/56
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公开(公告)号:EP0423818A1
公开(公告)日:1991-04-24
申请号:EP90120104.6
申请日:1990-10-19
发明人: Sawada, Yosuke , Ueki, Tomokazu , Yamamoto, Satoshi , Tomita, Koji , Fukagawa, Yasuo , Oki, Toshikazu
CPC分类号: B82Y5/00 , A61K47/50 , A61K47/6899 , C12N9/16 , C12R1/465
摘要: The present invention relates to an arylsulfatase of microbial origin. The enzyme may be linked to an antibody against a tumor-associated antigen and the resulting conjugate used in conjuction with a sulfated prodrug of a 4′-demethylepipodophyllotoxin glucoside derivative, particularly etoposide in cancer chemotherapy.
摘要翻译: 本发明涉及微生物来源的芳基硫酸酯酶。 该酶可以与针对肿瘤相关抗原的抗体连接,所得到的缀合物与4分钟的硫酸化前药结合使用 - 甲氧基表鬼臼毒素葡糖苷衍生物,特别是癌症化学疗法中依托泊苷。
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公开(公告)号:EP0368349A3
公开(公告)日:1991-04-24
申请号:EP89120904.1
申请日:1989-11-10
IPC分类号: C07H15/244 , A61K31/70 , C12P19/56 , C12N1/20
CPC分类号: C07H15/244 , C12P19/56
摘要: Disclosed are antibiotics BU-3608 FA-1 and FA-2 and alkyl derivatives thereof (I). These compounds are useful as antifungal agents. BU-3608 FA-1 and FA-2 are produced from Actinomadura hibisca in a medium containing a source of D-serine.
wherein the serine is D-serine; R¹ and R² are independently H or C₁₋₆ alkyl; and R³ is H or β-D-xylosyl; or a pharmaceutically acceptable salt thereof.-
公开(公告)号:EP0423818B1
公开(公告)日:1998-01-14
申请号:EP90120104.6
申请日:1990-10-19
发明人: Sawada, Yosuke , Ueki, Tomokazu , Yamamoto, Satoshi , Tomita, Koji , Fukagawa, Yasuo , Oki, Toshikazu
CPC分类号: B82Y5/00 , A61K47/50 , A61K47/6899 , C12N9/16 , C12R1/465
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公开(公告)号:EP0485725A1
公开(公告)日:1992-05-20
申请号:EP91116627.0
申请日:1991-09-27
发明人: Sawada, Yosuke , Ueki, Tomokazu , Tsuno, Takashi , Oki, Toshikazu
CPC分类号: C07C65/40
摘要: The present invention relates to a novel α-glucosidase inhibitor, pradimicin Q, having the following formula
and its pharmaceutically acceptable base salts.摘要翻译: 本发明涉及具有下式(CHEM)的新型α-葡萄糖苷酶抑制剂,普拉定霉素Q及其药学上可接受的碱盐。
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8.
公开(公告)号:EP0345735A2
公开(公告)日:1989-12-13
申请号:EP89110234.5
申请日:1989-06-06
发明人: Nishio, Maki , Sawada, Yosuke , Miyaki, Takeo , Oki, Toshikazu
IPC分类号: C07H15/244 , C12P19/56 , A61K31/70 , C12R1/03
CPC分类号: C12R1/03 , C07H15/244 , C12P19/56 , Y10S435/825
摘要: Disclosed herein are antibiotic BU-3608 D and E isolated from Actinomadura hibisca. These compounds are active antifungal agents.
摘要翻译: 本文公开了从放线菌(Actinomadura hibisca)分离的抗生素BU-3608D和E(I)。 这些化合物是活性抗真菌剂。
其中R 1是H或甲基 -
公开(公告)号:EP0345735A3
公开(公告)日:1991-04-24
申请号:EP89110234.5
申请日:1989-06-06
发明人: Nishio, Maki , Sawada, Yosuke , Miyaki, Takeo , Oki, Toshikazu
IPC分类号: C07H15/244 , C12P19/56 , A61K31/70 , C12R1/03
CPC分类号: C12R1/03 , C07H15/244 , C12P19/56 , Y10S435/825
摘要: Disclosed herein are antibiotic BU-3608 D and E isolated from Actinomadura hibisca. These compounds are active antifungal agents.
摘要翻译: 本文公开了从马杜拉马杜拉放线菌(Actinomadura hibisca)分离的抗生素BU-3608D和E. 这些化合物是有效的抗真菌剂。
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公开(公告)号:EP0368349A2
公开(公告)日:1990-05-16
申请号:EP89120904.1
申请日:1989-11-10
IPC分类号: C07H15/244 , A61K31/70 , C12P19/56 , C12N1/20
CPC分类号: C07H15/244 , C12P19/56
摘要: Disclosed are antibiotics BU-3608 FA-1 and FA-2 and alkyl derivatives thereof (I). These compounds are useful as antifungal agents. BU-3608 FA-1 and FA-2 are produced from Actinomadura hibisca in a medium containing a source of D-serine.
wherein the serine is D-serine; R¹ and R² are independently H or C₁₋₆ alkyl; and R³ is H or β-D-xylosyl; or a pharmaceutically acceptable salt thereof.摘要翻译: 公开了抗生素BU-3608FA-1和FA-2及其烷基衍生物(I)。 这些化合物可用作抗真菌剂。 BU-3608 FA-1和FA-2由含有D-丝氨酸源的培养基中的放线菌(Ininomadura hibisca)生产。
,其中丝氨酸是D-丝氨酸; R 1和R 2独立地是H或C 1-6烷基; 且R 3为H或β-D-木糖基; 或其药学上可接受的盐。
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