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1. 发明专利

JP2009504932A Auxiliary visor with hat 审中-公开
公开(公告)号：JP2009504932A
公开(公告)日：2009-02-05
申请号：JP2008526863
申请日：2006-05-15
申请人：キム,スン−ギュKIM, Sung−Gyu
发明人：キム，スン−ギュ
IPC分类号： A42B1/18
CPC分类号： A42B1/064
摘要：ここに開示したのは補助バイザー付き帽子である。前記帽子には、十分な弾性を有し、ユーザーの頭に着用されるヘアバンドと、太陽光を遮断するように前記ヘアバンドの前部に結合されたフロントバイザーと、前記前記フロントバイザーの上部又は底面にヒンジ結合され、それに対して着脱手段によって固定された少なくとも１つの補助バイザーと、が含まれる。前記補助バイザーは、紫外線からユーザーの顔側面を保護できるように選択的に展開し、美観の観点から、前記フロントバイザーと重なり合うように折りたたまれるように構成されている。
【選択図】図１

2. 发明专利

GB0804661D0 Cap having auxiliary visor 未知
公开(公告)号：GB0804661D0
公开(公告)日：2008-04-16
申请号：GB0804661
申请日：2006-05-15
申请人： KIM SUNG GYU
摘要： Disclosed is a cap having an auxiliary visor. The cap includes a hair band having enough elasticity to be worn on a user's head, a front visor coupled to the front of the hair band so as to block sunlight, and at least one auxiliary visor hinge-coupled to the top or bottom surface of the front visor and fixed thereto by an attachment/detachment means. The auxiliary visor is adapted to selectively unfold so as to shield the side of the user's face from UV rays, as well as fold so as to overlap the front visor for an aesthetic appearance.

3. 发明专利

GB2444202A Cap having auxiliary visor 未知
公开(公告)号：GB2444202A
公开(公告)日：2008-05-28
申请号：GB0804661
申请日：2006-05-15
申请人： KIM SUNG-GYU
发明人： KIM SUNG-GYU
IPC分类号： A42B1/18
摘要： Disclosed is a cap having an auxiliary visor. The cap includes a hair band having enough elasticity to be worn on a user's head, a front visor coupled to the front of the hair band so as to block sunlight, and at least one auxiliary visor hinge-coupled to the top or bottom surface of the front visor and fixed thereto by an attachment/detachment means. The auxiliary visor is adapted to selectively unfold so as to shield the side of the user's face from UV rays, as well as fold so as to overlap the front visor for an aesthetic appearance.

4. 发明申请

WO2008087560A9 THIAZOLIDINE DERIVATIVES AND METHODS FOR THE PREPARATION THEREOF 审中-公开
公开(公告)号：WO2008087560A9
公开(公告)日：2008-07-24
申请号：PCT/IB2008/000773
申请日：2008-01-16
申请人： KAINOS MEDICINE, INC., , KOREAN RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , YUNGJIN PHARM. Co Ltd., , KIM, Sung Soo , AHN, Jin Hee , CHEON, Hyae Gyeong , RHEE, Sang Dal , KANG, Nam Sook , KIM, Ki Young , KANG, Seung Kyu , JUNG, Won Hoon , KIM, Sung Gyu , KIM, Sun Young , KWEON, Jae Hong , SOHN, Sang Kwon , SHIN, Min Ki , HA, Ni Na
发明人： KIM, Sung Soo , AHN, Jin Hee , CHEON, Hyae Gyeong , RHEE, Sang Dal , KANG, Nam Sook , KIM, Ki Young , KANG, Seung Kyu , JUNG, Won Hoon , KIM, Sung Gyu , KIM, Sun Young , KWEON, Jae Hong , SOHN, Sang Kwon , SHIN, Min Ki , HA, Ni Na
IPC分类号： C07D277/22 , C07D277/24 , C07D277/04 , A61P3/04 , A61P3/10 , A61P19/10
摘要： The present invention relates to novel 2-carbonyl-3-acyl-1,3-thiazolidines having a β-amino group on the acyl chain, in free, prodrug form or pharmaceutically acceptable salt thereof, including their enantiomers, diastereomers and racemates, as efficient inhibitors against DPP-IV. The invention further relates to the pharmaceutical compositions comprising the disclosed compounds. The present invention also relates to methods for preparing the disclosed compounds and for treating DPP-IV-mediated diseases.

5. 发明申请

WO1997003076A1 HETEROCYCLE-FUSED THIAZOLE DERIVATIVES 审中-公开
标题翻译：杂交 - 热熔化的噻唑衍生物
公开(公告)号：WO1997003076A1
公开(公告)日：1997-01-30
申请号：PCT/KR1996000082
申请日：1996-06-01
申请人： YUNGJIN PHARMACEUTICAL CO., LTD. , YOO, Han, Yong , CHUNG, Kae, Jong , CHAI, Jun, Pyo , CHANG, Man, Sik , KIM, Sung, Gyu , CHOI, Wahn, Soo , KIM, Young, Hun , CHUN, Jae, Kwang , CHUNG, Young, Kuk , KIM, Young, Heui , PAEK, Jang, Hoon , SEO, Kwi, Hyon , KANG, Dae, Pil
发明人： YUNGJIN PHARMACEUTICAL CO., LTD.
IPC分类号： C07D513/04
CPC分类号： C07D513/04 , C07D513/14
摘要： A thiazole compound represented by general formula (I), wherein R is hydrogen atom, a hydroxy group, a straight or branched C1-C6 lower alkyl group, a C1-C4 lower alkoxy group, phenyl group, a phenyl group having one to three substituents selected from a group consisting of a C1-C4 lower alkyl group, a C1-C4 lower alkoxy group, fluorine, chlorine, bromine and an amino group, a C1-C5 alkylphenyl group, a phenyl group having one to three substituents selected from a group consisting of a C1-C4 lower alkyl group, a C1-C4 lower alkoxy group, fluorine, chlorine, bromine and an amino group, a substituted or unsubstituted guanidino group, or an amino group having a general formula: NR3R4 in which R3 and R4, identical to or different from each other, represent independently a hydrogen atom, a C1-C6 lower alkyl group, a C3-C6 cycloalkyl group, a substituted or unsubstituted pyridyl group, a phenyl group having one to three substituents selected from a group consisting of a C1-C4 lower alkyl group, a C1-C4 lower alkoxy group, a halogen atom, an amino group, a cyano group and a nitro group, a piperidine group or C1-C4 alkylpiperidine group; R1 and R2, identical to or different from each other, are independently a hydrogen atom, a hydroxy group, a C1-C6 lower alkyl group, phenyl group, a phenyl group having one substituent selected from a group consisting of a C1-C4 lower alkyl group, a C1-C4 lower alkoxy group, a halogen atom, a nitro and a cyano group, a C1-C5 alkylphenyl group, or a pyridine group; R5, R6, R7 and R8, identical to or different from each other, are independently a hydrogen atom, a hydroxy group, a C1-C4 lower alkyl group, a C1-C4 lower alkoxy group, phenyl group, or a phenyl group substituted with a C1-C4 alkyl group, a C1-C4 alkoxy group or a halogen atom, or a C1-C3 alkylphenyl group; Het is a 3-, 4- or 5-membered unsaturated monocyclic group, or 6- to 12-membered unsaturated fused cyclic group, said monocyclic and fused cyclic group being comprised of one or more hetero atoms selected from oxygen, oxidative nitrogen and oxidative sulfur atom are disclosed. These compounds show excellent anti-ulcer activity.
摘要翻译：由通式（I）表示的噻唑化合物，其中R是氢原子，羟基，直链或支链C 1 -C 6低级烷基，C 1 -C 4低级烷氧基，苯基，具有1至3个选自C1-C4低级烷基，C1-C4低级烷氧基，氟，氯，溴和氨基的取代基，C1-C5烷基苯基，具有1〜3个选自由C1-C4低级烷基，C1-C4低级烷氧基，氟，氯，溴和氨基组成的基团，取代或未取代的胍基，或具有通式NR 3 R 4的氨基，其中R 3 和R 4彼此相同或不同，分别独立地表示氢原子，C1-C6低级烷基，C3-C6环烷基，取代或未取代的吡啶基，具有1〜3个选自由C1-C4低级烷基组成的组 C1-C4低级烷氧基，卤素原子，氨基，氰基和硝基，哌啶基或C1-C4烷基哌啶基; R1和R2彼此相同或不同，独立地为氢原子，羟基，C1-C6低级烷基，苯基，具有一个取代基的苯基，所述取代基选自C1-C4低级烷基，C1-C4低级烷氧基，卤素原子，硝基和氰基，C1-C5烷基苯基或吡啶基; R5，R6，R7和R8彼此相同或不同，独立地为氢原子，羟基，C1-C4低级烷基，C1-C4低级烷氧基，苯基或苯基取代 C1-C4烷基，C1-C4烷氧基或卤原子，或C1-C3烷基苯基; Het是3-，4-或5-元不饱和单环基团，或6至12元不饱和稠合环基团，所述单环和稠环基团由一个或多个选自氧，氧化氮和氧化氮的杂原子组成硫原子。这些化合物显示出优异的抗溃疡活性。

6. 发明申请

WO1997003073A1 THIAZOLYL TRIAZOLOTHIAZOLE DERIVATIVES 审中-公开
标题翻译：三唑并噻唑衍生物
公开(公告)号：WO1997003073A1
公开(公告)日：1997-01-30
申请号：PCT/KR1996000079
申请日：1996-06-01
申请人： YUNGJIN PHARMACEUTICAL CO., LTD. , YOO, Han, Yong , CHUNG, Kae, Jong , CHAI, Jun, Pyo , CHANG, Man, Sik , KIM, Sung, Gyu , CHOI, Wahn, Soo , KANG, Dae, Pil , KIM, Young, Hun , KIM, Young, Heui , WOO, Tae, Wook , PAEK, Jang, Hoon , SEO, Kwi, Hyon
发明人： YUNGJIN PHARMACEUTICAL CO., LTD.
IPC分类号： C07D417/04
CPC分类号： C07D513/04
摘要： Novel thiazolyl triazolothiazole derivatives represented by general formula (I); wherein, R is hydrogen atom, a hydroxy group, a straight or branched C1 - C6 lower alkyl group, a C1 - C6 lower alkoxy group, a substituted or unsubstituted phenyl or pyridyl group, a substituted or unsubstituted guanidino group, or an amino group having a general formula : NR4R5 in which R4 and R5, identical to or different from each other, represent independently hydrogen atom, a C1 - C6 lower alkyl group, a C3 - C6 cycloalkyl group, a substituted or unsubstituted phenyl or pyridyl group, a C1 - C4 lower alkyl group, a C1 - C6 lower alkoxy group, or a C1 - C4 lower alkylphenyl group; R2 and R3, identical to or different from each other, are independently hydrogen atom, a C1 - C4 lower alkyl group, or a phenyl group which may be substituted; and X and Y, different from each other, are independently nitrogen atom or a group of a formula: CR6 in which R6 is hydrogen atom, a C1 - C6 lower alkyl group, or a phenyl group which may be substituted, and pharmaceutically acceptable salts thereof are disclosed. These compounds show excellent anti-ulcer activity.
摘要翻译：由通式（I）表示的新型噻唑基三唑并噻唑衍生物; 其中，R为氢原子，羟基，直链或支链C1-C6低级烷基，C1-C6低级烷氧基，取代或未取代的苯基或吡啶基，取代或未取代的胍基或氨基具有通式：其中R4和R5彼此相同或不同的NR4R5独立地表示氢原子，C1-C6低级烷基，C3-C6环烷基，取代或未取代的苯基或吡啶基， C1-C4低级烷基，C1-C6低级烷氧基或C1-C4低级烷基苯基; R2和R3彼此相同或不同，独立地为氢原子，C1-C4低级烷基或可被取代的苯基; 并且X和Y彼此不同，独立地为氮原子或式为CR 6的基团，其中R 6为氢原子，C 1 -C 6低级烷基或可被取代的苯基，以及药学上可接受的盐公开。这些化合物显示出优异的抗溃疡活性。

7. 发明申请

WO2008093940A1 QUINOLINE DERIVATIVES AS CASPASE-3 INHIBITOR, PREPARATION PROCESS FOR THE SAME AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME 审中-公开
标题翻译：喹啉衍生物作为CASPASE-3抑制剂，其制备方法和包含其的药物组合物
公开(公告)号：WO2008093940A1
公开(公告)日：2008-08-07
申请号：PCT/KR2008/000202
申请日：2008-01-11
申请人： YUNGJIN PHARMACEUTICAL CO., LTD. , HAN, Je Wook , KIM, Sung Gyu , SHIN, Min Ki , SOHN, Sang Kwon , JUNG, Yoon Sung , HA, Ni Na , KIM, Jong Hwan
发明人： HAN, Je Wook , KIM, Sung Gyu , SHIN, Min Ki , SOHN, Sang Kwon , JUNG, Yoon Sung , HA, Ni Na , KIM, Jong Hwan
IPC分类号： C07D401/04
CPC分类号： C07D215/54
摘要： Provided is a quinoline derivative represented by the following Formula (1) for use in treating a caspase- mediated disease by inhibition of caspase-3 activity. Further provided are a method for preparing the quinoline derivative or a pharmaceutically acceptable salt thereof and a pharmaceutical composition containing the same.
摘要翻译：本发明提供由下式（1）表示的喹啉衍生物，用于通过抑制胱天蛋白酶-3活性来治疗半胱天冬酶介导的疾病。还提供了制备喹啉衍生物或其药学上可接受的盐的方法和含有该喹啉衍生物的药物组合物。

8. 发明申请

WO2008087560A2 THIAZOLIDINE DERIVATIVES AND METHODS FOR THE PREPARATION THEREOF 审中-公开
标题翻译：噻唑烷衍生物及其制备方法
公开(公告)号：WO2008087560A2
公开(公告)日：2008-07-24
申请号：PCT/IB2008000773
申请日：2008-01-16
申请人： KAINOS MEDICINE INC , KOREAN RES INST OF CHEMICAL TE , YUNGJIN PHARM CO LTD , KIM SUNG SOO , AHN JIN HEE , CHEON HYAE GYEONG , RHEE SANG DAL , KANG NAM SOOK , KIM KI YOUNG , KANG SEUNG KYU , JUNG WON HOON , KIM SUNG GYU , KIM SUN YOUNG , KWEON JAE HONG , SOHN SANG KWON , SHIN MIN KI , HA NI NA
发明人： KIM SUNG SOO , AHN JIN HEE , CHEON HYAE GYEONG , RHEE SANG DAL , KANG NAM SOOK , KIM KI YOUNG , KANG SEUNG KYU , JUNG WON HOON , KIM SUNG GYU , KIM SUN YOUNG , KWEON JAE HONG , SOHN SANG KWON , SHIN MIN KI , HA NI NA
CPC分类号： C07D277/06 , C07D417/12 , Y02P20/55
摘要： The present invention relates to novel 2-carbonyl-3-acyl-1,3-thiazolidines having a ß-amino group on the acyl chain, in free, prodrug form or pharmaceutically acceptable salt thereof, including their enantiomers, diastereomers and racemates, as efficient inhibitors against DPP-IV. The invention further relates to the pharmaceutical compositions comprising the disclosed compounds. The present invention also relates to methods for preparing the disclosed compounds and for treating DPP-IV-mediated diseases.
摘要翻译：本发明涉及在酰基链上具有游离前药形式或其药学上可接受的盐中的β-氨基的新的2-羰基-3-酰基-1,3-噻唑烷，包括其对映异构体，非对映异构体和外消旋体，如有效的DPP-IV抑制剂。本发明还涉及包含所公开的化合物的药物组合物。本发明还涉及制备所公开化合物和用于治疗DPP-IV介导的疾病的方法。

9. 发明申请

WO2003093240A1 QUINOLINE DERIVATIVES AS CASPASE-3 INHIBITOR, PREPARATION FOR PRODUCING THE SAME AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME 审中-公开
标题翻译：作为CASPASE-3抑制剂的喹啉衍生物，其制备方法和包含其的药物组合物
公开(公告)号：WO2003093240A1
公开(公告)日：2003-11-13
申请号：PCT/KR2003/000875
申请日：2003-04-30
申请人： YUNGJIN PHARMACEUTICAL CO., LTD. , KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , KIM, Sung-Gyu , JUNG, Yoon-Sung , KONG, Jae-Yang , PARK, Woo-Kyu
发明人： KIM, Sung-Gyu , JUNG, Yoon-Sung , KONG, Jae-Yang , PARK, Woo-Kyu
IPC分类号： C07D215/44
CPC分类号： C07D409/12 , C07D215/42 , C07D215/44 , C07D215/54 , C07D401/12 , C07D405/12
摘要： The present invention relates to new quinoline derivatives of formula (1) or their pharmaceutically acceptable salts with caspase-3 inhibitory activity and their preparation methods, wherein R 2 is H; halogen; C 1-6 alkyl; C 1-6 alkoxy; C 1-6 alkoxyalkyl; or C 3-6 cycloalkyl; R 1 is formula (a); -CN; or formula (b); R is H; C 6-14 aryl unsubstituted or substituted by halogen, C 1-6 alkyl, C 1-6 alkoxy or amino; 5 - 15 membered heterocyclic group unsubstituted or substituted by halogen, C 1-6 alkyl, C 1-6 alkoxy or amino; or -(CH 2 ) n -CHR 4 R 5 . The present invention relates to a pharmaceutical composition for treating caspase-associated diseases by inhibiting the activity of caspase-3 which comprises the compound of formula (1) or its pharmaceutically acceptable salt.
摘要翻译：本发明涉及式（1）的新喹啉衍生物或其与胱天蛋白酶-3抑制活性的药学上可接受的盐及其制备方法，其中R2为H; 卤素; C 1-6烷基; C 1-6烷氧基; C 1-6烷氧基烷基; 或C 3-6环烷基; R1是式（a）; -CN; 或式（b）; R为H; 未取代或被卤素，C 1-6烷基，C 1-6烷氧基或氨基取代的C 6-14芳基; 未取代或被卤素，C 1-6烷基，C 1-6烷氧基或氨基取代的5-15元杂环基; 或 - （CH 2）n -CHR 4 R 5。本发明涉及通过抑制胱天蛋白酶-3的活性来治疗半胱氨酸蛋白酶相关疾病的药物组合物，其包含式（1）化合物或其药学上可接受的盐。

10. 发明申请

WO2011010847A3 VISOR CAP HAVING VARIABLE VISORS 审中-公开
标题翻译： VISOR CAP具有可变视力
公开(公告)号：WO2011010847A3
公开(公告)日：2011-06-16
申请号：PCT/KR2010004706
申请日：2010-07-19
申请人： KIM SUNG GYU
发明人： KIM SUNG GYU
IPC分类号： A42B1/20 , A42B1/18 , A42B1/22
CPC分类号： A42B1/065 , A42B1/062
摘要： The present invention relates to a visor cap. It is an aim of the present invention to provide a visor cap which can widen a sun blocking area through variable visors and which enables a wearer to adjust the sun-blocking area while improving wearing comfort. To accomplish the aim, provided is a visor cap including a main body, a fixed visor, and a pair of variable visors hinged to both sides of an upper surface or a lower surface of the fixed visor, so as to vary the sun-blocking area, wherein each of the pair of variable visors includes: a first variable visor portion which is made of a textile material and one side of which is fixed at an edge of the fixed visor; and a second variable visor portion which is made of a synthetic resin material and which is coupled to the other side of the first variable visor portion. The visor cap of the present invention is advantageous in that it enables a wearer to adjust the sun-blocking area if needed, and is prevented from contacting the skin of the wearer, thus improving wearing comfort while expanding the sun-blocking area.
摘要翻译：本发明涉及遮阳帽。本发明的目的是提供一种可通过可变遮阳板加宽遮阳面积的面罩，并且能够使佩戴者在改善穿着舒适度的同时调节防晒面积。为了达到目的，提供了一种遮阳帽，其包括主体，固定遮阳板和铰接到固定遮阳板的上表面或下表面的两侧的一对可变遮阳板，以便改变遮阳所述一对可变面罩中的每一个包括：第一可变面罩部分，其由纺织材料制成，并且其一侧固定在所述固定遮阳板的边缘; 以及第二可变面罩部分，其由合成树脂材料制成并且联接到第一可变面罩部分的另一侧。本发明的遮阳帽的优点在于，如果需要，其能够使穿着者调节防晒面积，并且防止与穿着者的皮肤接触，从而在扩大防晒区域的同时提高穿着舒适性。

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