会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明授权
    • Heterocyclic spiro-derivative
    • 杂环螺衍生物
    • US06469023B1
    • 2002-10-22
    • US08875863
    • 1997-08-07
    • Makoto TakemuraYouichi KimuraHitoshi Ohki
    • Makoto TakemuraYouichi KimuraHitoshi Ohki
    • A61K3144
    • C07D401/04
    • The present invention provides an antibacterial compound useful as medicines, animal drugs, fisheries drugs or antibacterial preservatives and to an antibacterial agent or preparation which contains the same, more particularly a compound which possesses high safety and excellent activity against a broad range of bacterial species including quinolone-resistant strains. A quinolone derivative of the following formula (I) which has a group derived from the heterocyclic spiro-compound at the 7-positioned R2 and the halogenocyclopropyl group at the N1-position, prefereably a compound of pure isomer, and an antibacterial agent containing the derivative compound.
    • 本发明提供了可用作药物,动物药物,渔业药物或抗菌防腐剂的抗菌化合物,以及含有该抗菌剂或抗菌剂的抗菌剂或制剂,更具体地,涉及对广泛的细菌种类具有高安全性和优异活性的化合物,包括 喹诺酮耐药株。 下述式(I)的喹啉酮衍生物,其具有衍生自7-位R2上的杂环螺环化合物和N1位上的卤代环丙基的基团,优选纯异构体的化合物和含有 衍生化合物。
    • 2. 发明授权
    • Cycloalkylaminomethylpyrrolidine derivatives
    • 环烷基氨基甲基吡咯烷衍生物
    • US06194434B1
    • 2001-02-27
    • US09171637
    • 1998-10-22
    • Makoto TakemuraYouichi KimuraKatsuhiro KawakamiHitoshi Ohki
    • Makoto TakemuraYouichi KimuraKatsuhiro KawakamiHitoshi Ohki
    • A61K3147
    • C07D401/04
    • A quinolone derivative represented by formula (I): wherein R1 represents a cycloalkyl group; R2 represents a hydrogen atom, an amino group, a hydroxyl group, a thiol group, a halogenomethyl group, an alkyl group, an alkenyl group, an alkynyl group, or an alkoxyl group; R3 represents an amino group, a halogenomethyl group, a halogenomethoxyl group, an alkyl group, an alkenyl group, an alkynyl group, or an alkoxyl group; R4 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms; R5 represents a cycloalkyl group having 3 to 6 carbon atoms; the above R1 to R5 may be substituted; X represents a halogen atom or a hydrogen atom; and Y represents a hydrogen atom, a phenyl group, an acetoxymethyl group, a pivaloyloxymethyl group, an ethoxycarbonyl group, a choline group, a dimethylaminoethyl group, a 5-indanyl group, a phthalidinyl group, a 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl group, a 3-acetoxy-2-oxobutyl group, an alkyl group having 1 to 6 carbon atoms, an alkoxymethyl group having 2 to 7 carbon atoms, or a phenylalkyl group having 1 to 6 carbon atoms in the alkyl moiety thereof, or a salt thereof. The compound exhibits high and broad antimicrobial activity against various bacteria including bacteria resistant to drugs and high safety.
    • 由式(I)表示的喹诺酮衍生物:其中R1表示环烷基; R2表示氢原子,氨基,羟基,硫醇基,卤代甲基,烷基,烯基,炔基或烷氧基; R3表示氨基,卤代甲基,卤代甲氧基,烷基,烯基,炔基或烷氧基; R4表示氢原子或碳原子数1〜6的烷基。 R5表示碳原子数3〜6的环烷基; 上述R 1〜R 5可以被取代; X表示卤素原子或氢原子; Y表示氢原子,苯基,乙酰氧基甲基,新戊酰氧基甲基,乙氧基羰基,胆碱基,二甲基氨基乙基,5-二氢化茚基,苯酞基,5-烷基-2-氧代 - 1,3-二氧杂环戊烯-4-基甲基,3-乙酰氧基-2-氧代丁基,碳原子数1〜6的烷基,碳原子数2〜7的烷氧基甲基或碳原子数1〜6的苯基烷基 其烷基部分的原子,或其盐。 该化合物对各种细菌(包括对药物有抗性的细菌和高安全性)具有高而广的抗菌活性。
    • 4. 发明申请
    • Pyridobenzoxazine derivative
    • 吡啶并苯并恶嗪衍生物
    • US20070191356A1
    • 2007-08-16
    • US10587946
    • 2005-02-01
    • Makoto TakemuraHitoshi Ohki
    • Makoto TakemuraHitoshi Ohki
    • A61K31/535C07D265/38
    • C07D498/06A23K20/111A23K20/195A23K50/80A23L3/3544A61K31/5383
    • A quinolone antimicrobial agent having potent antimicrobial activity against gram positive and gram negative bacteria and having high safety is provided. A compound represented by the following formula (1): [Chemical formula 1] [wherein, R1: hydrogen, alkyl, cycloalkyl, or substituted carbonyl derived from amino acid, peptide or tripeptide; R2: hydrogen, alkyl, or cycloalkyl; R3: hydrogen, amino, halogen, or alkyl; R4: hydrogen, phenyl, acetoxymethyl, pivaloyloxymethyl, ethoxycarbonyl, choline, dimethylaminoethyl, 5-indanyl, phthalidinyl, 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl, 3-acetoxy-2-oxobutyl, alkyl, alkoxymethyl, or phenylalkyl; X, X1, X2: hydrogen or halogen] or salt thereof, or a hydrate thereof; and antimicrobial agent and therapeutic agent for infections, each containing the compound, salt thereof or a hydrate thereof.
    • 提供了对革兰氏阳性和革兰氏阴性细菌具有强抗微生物活性并具有高安全性的喹诺酮类抗微生物剂。 由下式(1)表示的化合物:[化学式1] [其中,R 1,H 2,氢,烷基,环烷基或衍生自氨基酸,肽或三肽的取代的羰基; R 2:氢,烷基或环烷基; 氢,氨基,卤素或烷基; 吡啶,二甲基氨基乙基,5-茚满基,邻苯二甲酰基,5-烷基-2-氧代-1,3-二氧杂环戊烯-4-基甲基,3-甲氧基羰基, 乙酰氧基-2-氧代丁基,烷基,烷氧基甲基或苯基烷基; X,X 1,X 2:氢或卤素]或其盐或其水合物; 和抗微生物剂和感染治疗剂,各自含有化合物,其盐或其水合物。
    • 5. 发明授权
    • Vehicle door
    • 车门
    • US08556332B2
    • 2013-10-15
    • US13606532
    • 2012-09-07
    • Atsushi NakashimaHitoshi Ohki
    • Atsushi NakashimaHitoshi Ohki
    • B60R5/04
    • B60J5/0416B60R13/0243B60R21/04B60R21/0428
    • A vehicle door includes a door main body having a hollow portion, a work hole, a door hole seal that covers the work hole, a door trim, a protruding member provided so as to protrude from the door trim toward the vehicle interior side surface, and a harness routed through the door hole seal to the door trim side. The door hole seal is provided with a general surface, a bulging portion facing the protruding member and bulging from the general surface toward the inside of the hollow portion, and a harness pull-out hole through which the harness is passed. The bulging portion has an inclined surface.
    • 车门包括具有中空部分的门主体,工作孔,覆盖工作孔的门孔密封件,门装饰件,设置成从门饰件朝向车辆内侧表面突出的突出构件, 以及通过门孔密封件通向门饰边的线束。 门孔密封件设置有一般表面,与突出构件相对的凸出部分,并且从一般表面朝向中空部分的内侧突出,以及线束拉出孔,线束穿过该孔。 凸出部分具有倾斜表面。
    • 8. 发明授权
    • Cis-substituted fluoromethylpyrrolidine derivative
    • 顺式取代的氟甲基吡咯烷衍生物
    • US06656952B2
    • 2003-12-02
    • US09446696
    • 1999-12-23
    • Makoto TakemuraHisashi TakahashiHitoshi OhkiKenichi KimuraRie MiyauchiToshiyuki Takeda
    • Makoto TakemuraHisashi TakahashiHitoshi OhkiKenichi KimuraRie MiyauchiToshiyuki Takeda
    • A61K3147
    • C07D401/04
    • An antibacterial drug having potent antibacterial activities upon various bacteria including resistant strains and high safety is disclosed, which comprises as an active ingredient, quinolone derivatives represented by the following formula (I), its salts or hydrates thereof: wherein R1 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, R2 represents a halogenomethoxyl group or an alkoxyl group, R3 represents an alkyl group, an alkenyl group, a halogenoalkyl group, a cyclic alkyl group, a heteroaryl group, an alkoxyl group or an alkylamino group, and R4 represents a hydrogen atom, a phenyl group, an acetoxymethyl group, a pivaloyloxymethyl group, an ethoxycarbonyl group, a choline group, a dimethylaminoethyl group, a 5-indanyl group, a phthalidinyl group, a 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl group, 3-acetoxy-2-oxobutyl group, an alkyl group, an alkoxylmethyl group or a phenylalkyl group. These substituents may further have additional substituents.
    • 本发明公开了一种对各种细菌(包括耐药菌株)和高度安全性具有有效抗菌活性的抗菌药物,其包含作为活性成分的由下式(I)表示的喹诺酮衍生物,其盐或水合物:其中R 1表示 氢原子或碳原子数1〜6的烷基,R 2表示卤代甲氧基或烷氧基,R 3表示烷基,链烯基,卤代烷基,环状烷基,杂芳基 基团,烷氧基或烷基氨基,R 4表示氢原子,苯基,乙酰氧基甲基,新戊酰氧基甲基,乙氧基羰基,胆碱基,二甲基氨基乙基,5-二氢化茚基, 5-烷基-2-氧代-1,3-二氧杂环戊烯-4-基甲基,3-乙酰氧基-2-氧代丁基,烷基,烷氧基甲基或苯基烷基。 这些取代基还可以具有另外的取代基。