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    • 13. 发明授权
    • Anti-trypanosomiasis agent
    • 抗锥虫病药
    • US07795285B2
    • 2010-09-14
    • US11576426
    • 2005-09-29
    • Masataka IharaKiyosei TakasuKhanitha PudhomHiroshi KitaguchiMasayuki KawakamiKozo Sato
    • Masataka IharaKiyosei TakasuKhanitha PudhomHiroshi KitaguchiMasayuki KawakamiKozo Sato
    • A01N43/78
    • C07D417/14A61K31/428A61K31/4439A61K31/4709Y02A50/414
    • The present invention is to provide an anti-trypanosomiasis agent having a high selective toxicity, and high preventing or treating effect against trypanosomiasis, comprising a compound shown by the following general formula (1) as an active ingredient (wherein R1 and R2 each independently represents a hydrogen atom, halogen atom, hydroxyl group, oxygen atom, C1-5 alkyl group, C1-5 alkoxy group, C5-8 aryl group, C5-8 aryloxy group, C2-6 alkoxycarbonyl group or C2-6 alkylaminocarbonyl group, and may be bound to each other; R3, R4, and R5 each independently represents a C1-5 alkyl group or C5-8 aryl group; R6 and R7 each independently represents a hydrogen atom, halogen atom, hydroxyl group, oxygen atom, C1-8 alkyl group, C1-5 alkoxy group, C5-8 aryl group, C5-8 aryloxy group, or C2-6 alkoxycarbonyl group, and may be bound to each other; Y and Z each independently represents an atom group necessary to form a 5- or 6-membered heterocycle; m and n each represent 0 or 1; Q represents a physiologically acceptable anion; k represents an integer of 0 to 2, necessary to make the electric charge of the whole molecule 0).
    • 本发明提供具有高选择性毒性和对锥虫病的高预防或治疗作用的抗锥虫病药,其包含由以下通式(1)表示的化合物作为活性成分(其中R 1和R 2各自独立地表示 氢原子,卤素原子,羟基,氧原子,C 1-5烷基,C 1-5烷氧基,C 5-8芳基,C 5-8芳氧基,C 2-6烷氧基羰基或C 2-6烷基氨基羰基, 可以相互结合; R3,R4和R5各自独立地表示C1-5烷基或C5-8芳基; R6和R7各自独立地表示氢原子,卤素原子,羟基,氧原子,C1- 8个烷基,C 1-5烷氧基,C 5-8芳基,C 5-8芳氧基或C 2-6烷氧基羰基,并且可以彼此结合; Y和Z各自独立地表示形成 5-或6-元杂环; m和n各自表示0或1; Q表示物理 生理上可接受的阴离子 k表示0〜2的整数,使整个分子的电荷为0)。
    • 15. 发明申请
    • Anti-Trypanosomiasis Agent
    • 抗锥虫病药
    • US20080045574A1
    • 2008-02-21
    • US11576426
    • 2005-09-29
    • Masataka IharaKiyosei TakasuKhanitha PudhomHiroshi KitaguchiMasayuki KawakamiKozo Sato
    • Masataka IharaKiyosei TakasuKhanitha PudhomHiroshi KitaguchiMasayuki KawakamiKozo Sato
    • A61K31/426A61P33/00
    • C07D417/14A61K31/428A61K31/4439A61K31/4709Y02A50/414
    • The present invention is to provide an anti-trypanosomiasis agent having a high selective toxicity, and high preventing or treating effect against trypanosomiasis, comprising a compound shown by the following general formula (1) as an active ingredient (wherein R1 and R2 each independently represents a hydrogen atom, halogen atom, hydroxyl group, oxygen atom, C1-5 alkyl group, C1-5 alkoxy group, C5-8 aryl group, C5-8 aryloxy group, C2-6 alkoxycarbonyl group or C2-6 alkylaminocarbonyl group, and may be bound to each other; R3, R4, and R5 each independently represents a C1-5 alkyl group or C5-8 aryl group; R6 and R7 each independently represents a hydrogen atom, halogen atom, hydroxyl group, oxygen atom, C1-8 alkyl group, C1-5 alkoxy group, C5-8 aryl group, C5-8 aryloxy group, or C2-6 alkoxycarbonyl group, and may be bound to each other; Y and Z each independently represents an atom group necessary to form a 5- or 6-membered heterocycle; m and n each represent 0 or 1; Q represents a physiologically acceptable anion; k represents an integer of 0 to 2, necessary to make the electric charge of the whole molecule 0).
    • 本发明提供具有高选择性毒性和对锥虫病的高预防或治疗作用的抗锥虫病药,其包含由以下通式(1)表示的化合物作为活性成分(其中R 1, / O 2和R 2各自独立地表示氢原子,卤素原子,羟基,氧原子,C 1-5烷基,C 1-5 C 5〜8芳基,C 5〜8芳氧基,C 2-6烷氧基羰基或C 2-6个亚烷基氨基羰基,并且可以彼此结合; R 3,R 4和R 5 >各自独立地表示C 1-5烷基或C 5-8芳基; R 6和R 7, SUP各自独立地表示氢原子,卤素原子,羟基,氧原子,C 1-8烷基,C 1-5烷氧基,C 1〜 5-8芳基,C 5-8芳氧基,或C 1〜 并且可以相互结合; Y和Z各自独立地表示形成5-或6-元杂环所必需的原子团; m和n各自表示0或1; Q表示生理上可接受的阴离子; k表示0〜2的整数,使整个分子的电荷为0)。
    • 20. 发明授权
    • Process for image formation comprising a heating step
    • 用于图像形成的方法,包括加热步骤
    • US4639408A
    • 1987-01-27
    • US799996
    • 1985-11-20
    • Hiroshi KitaguchiMasatoshi Kato
    • Hiroshi KitaguchiMasatoshi Kato
    • C09B57/00G03C1/498G03C7/00G03C7/305G03C8/40G03C1/40G03C1/06G03C1/42G03C5/54
    • G03C8/408G03C1/49845G03C7/30511Y10S430/156Y10S430/158Y10S430/159Y10S430/16
    • A process for forming an image comprising a heating step is described, wherein a photographic material is heated in the presence of a compound represented by formula (I) ##STR1## wherein X represents an atomic group completing a carbocyclic aromatic ring or a heterocyclic aromatic ring; R.sup.1 is selected from groups represented by formulae (A), (B), and (C) ##STR2## in which R.sup.11 and R.sup.12 each represents a substituted or unsubstituted alkyl group, a cycloalkyl group, a substituted or unsubstituted alkenyl group, an aralkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heterocyclic group, an alkyloxy or aryloxy group, an alkylthio or arylthio group, or a substituted or unsubstituted amino group, or R.sup.11 and R.sup.12 together form a 5-membered or 6-membered ring; R.sup.2 represents a group selected from the groups represented by R.sup.11 ; R.sup.1 and R.sup.2 together form a 5-membered or 6-membered ring; Q represents a hydrogen atom, an alkyl group, or an aryl group; TIME represents a timing group; PUG represents a photographically useful group; and n represents 0 or an integer.
    • 描述了一种用于形成包括加热步骤的图像的方法,其中在由式(I)表示的化合物(I)的存在下照相材料加热,其中X表示完成碳环芳环或 杂环芳环; 其中R 11选自由式(A),(B)和(C)表示的基团,其中R 11和R 12各自表示取代或未取代的烷基 基团,环烷基,取代或未取代的烯基,芳烷基,取代或未取代的芳基,取代或未取代的杂环基,烷氧基或芳氧基,烷硫基或芳硫基,或取代或未取代的氨基 ,或R 11和R 12一起形成5元或6元环; R2表示选自由R11表示的基团的基团; R1和R2一起形成5元或6元环; Q表示氢原子,烷基或芳基; TIME代表一个时间组; PUG代表一个摄影有用的组; n表示0或整数。