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1. 发明授权

US07674938B2 Amino alcohol derivatives, pharmaceutical compositions containing the same, and use thereof 失效
标题翻译：氨基醇衍生物，含有它们的药物组合物及其用途
公开(公告)号：US07674938B2
公开(公告)日：2010-03-09
申请号：US11936680
申请日：2007-11-07
申请人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
IPC分类号： C07C217/14 , C07C217/20 , C07D307/79 , A61K31/195 , A61P1/16 , A61P3/04
CPC分类号： C07D307/79 , A61K31/195 , C07C217/18 , C07C217/20 , C07C323/62 , C07C2601/04
摘要： The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3, R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is —C(O)—R10, -A1-C(O)—R10, —O-A2-C(O)—R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物或其药学上可接受的盐，其中R 1和R 2各自为氢或低级烷基; R3，R4，R5和R6各自为氢，卤素，低级烷基或低级烷氧基; R 7和R 8各自为氢，卤素，低级烷基，卤代低级烷基，低级烷氧基，环烷基，芳基，杂芳基，氰基，羟基，低级酰基，羧基等; R9是-C（O）-R10，-A1-C（O）-R10，-O-A2-C（O）-R10或四唑-5-基，其表现出有效和选择性的3-肾上腺素受体刺激活动。本发明还提供含有所述化合物的药物组合物及其用途。

2. 发明申请

US20080249177A1 AMINO ALCOHOL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME, AND USE THEREOF 失效
标题翻译：氨基醇衍生物，含有它们的药物组合物及其用途
公开(公告)号：US20080249177A1
公开(公告)日：2008-10-09
申请号：US11936680
申请日：2007-11-07
申请人： Junichi KOBAYASHI , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi KOBAYASHI , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
IPC分类号： A61K31/192 , C07C229/00 , A61P3/00
CPC分类号： C07D307/79 , A61K31/195 , C07C217/18 , C07C217/20 , C07C323/62 , C07C2601/04
摘要： The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3, R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is —C(O)—R10, -A1-C(O)—R10, —O-A2-C(O)—R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物或其药学上可接受的盐，其中R 1和R 2各自为氢或低级烷基; R 3，R 4，R 5和R 6各自为氢，卤素，低级烷基或低级烷氧基 ; R 7和R 8各自为氢，卤素，低级烷基，卤代低级烷基，低级烷氧基，环烷基，芳基，杂芳基，氰基，羟基，低级酰基，羧基等; R 9是-C（O）-R 10，-A 1 -C（O）-R 10 O > - O 2 -C（O）-R 10或四唑-5-基，其显示出有效和选择性的β3肾上腺素受体刺激活性。本发明还提供含有所述化合物的药物组合物及其用途。

3. 发明授权

US07423185B2 Amino alcohol derivatives, pharmaceutical compositions containing the same, and use thereof 失效
标题翻译：氨基醇衍生物，含有它们的药物组合物及其用途
公开(公告)号：US07423185B2
公开(公告)日：2008-09-09
申请号：US10545380
申请日：2004-01-30
申请人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
IPC分类号： C07C217/14 , C07C217/20 , C07D307/79 , A61K31/195 , A61P1/00 , A61P1/16 , A61P3/04
CPC分类号： C07D307/79 , A61K31/195 , C07C217/18 , C07C217/20 , C07C323/62 , C07C2601/04
摘要： The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3, R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is —C(O)—R10, -A1-C(O)—R10, —O-A2-C(O)—R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物或其药学上可接受的盐，其中R 1和R 2各自为氢或低级烷基; R 3，R 4，R 5和R 6各自为氢，卤素，低级烷基或低级烷氧基 ; R 7和R 8各自为氢，卤素，低级烷基，卤代低级烷基，低级烷氧基，环烷基，芳基，杂芳基，氰基，羟基，低级酰基，羧基等; R 9是-C（O）-R 10，-A 1 -C（O）-R 10 O > - O 2 -C（O）-R 10或四唑-5-基，其显示出有效和选择性的β3肾上腺素受体刺激活性。本发明还提供含有所述化合物的药物组合物及其用途。

4. 发明申请

US20060128807A1 Amino alcohol derivatives, pharmaceutical compositions containing the same, and use thereof 失效
标题翻译：氨基醇衍生物，含有它们的药物组合物及其用途
公开(公告)号：US20060128807A1
公开(公告)日：2006-06-15
申请号：US10545380
申请日：2004-01-30
申请人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi Kobayashi , Tetsuya Nakamura , Ritsu Suzuki , Hideyuki Muranaka , Tomonaga Ozawa , Yuichiro Kai , Takehiro Ishikawa , Tatsuhiro Kondo , Tetsuro Tamai , Satoshi Akahane
IPC分类号： A61K31/195 , C07C229/22
CPC分类号： C07D307/79 , A61K31/195 , C07C217/18 , C07C217/20 , C07C323/62 , C07C2601/04
摘要： The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3, R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is —C(O)—R10, -A1-C(O)—R10, —O-A2-C(O)—R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物或其药学上可接受的盐，其中R 1和R 2各自为氢或低级烷基; R 3，R 4，R 5和R 6各自为氢，卤素，低级烷基或低级烷氧基 ; R 7和R 8各自为氢，卤素，低级烷基，卤代低级烷基，低级烷氧基，环烷基，芳基，杂芳基，氰基，羟基，低级酰基，羧基等; R 9是-C（O）-R 10，-A 1 -C（O）-R 10 O > - O 2 -C（O）-R 10或四唑-5-基，其显示出有效和选择性的β3肾上腺素受体刺激活性。本发明还提供含有所述化合物的药物组合物及其用途。

5. 发明授权

US07417169B2 Amino alcohol derivatives, medicinal composition containing the same, and use of these 失效
标题翻译：氨基醇衍生物，含有该组合物的药用组合物及其用途
公开(公告)号：US07417169B2
公开(公告)日：2008-08-26
申请号：US10576753
申请日：2004-10-05
申请人： Junichi Kobayashi , Tetsuya Nakamura , Hideyuki Muranaka , Takehiro Ishikawa , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi Kobayashi , Tetsuya Nakamura , Hideyuki Muranaka , Takehiro Ishikawa , Tetsuro Tamai , Satoshi Akahane
IPC分类号： C07C211/00 , C07C311/00 , A61K31/18 , A61K31/135
CPC分类号： C07D235/24 , C07C233/43 , C07C311/21
摘要： The present invention provides compounds represented by general formula (I): a prodrug thereof, or pharmaceutical acceptable salts thereof, wherein R1 is hydrogen or lower alkyl; each of R2 and R3 is independently hydrogen or lower alkyl; each of R4, R5 and R6 is independently hydrogen, halogen, lower alkyl or lower alkoxy; R7 is hydrogen or lower alkyl; R8 is hydrogen, halogen, lower alkyl, lower alkoxy, etc; R9 is —COR10, -A1-COR10, —O-A2-COR10, etc; Ar is optionally substituted phenyl or heteroaryl; and A is a bond, —OCH2—, etc, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物：其前药或其药学上可接受的盐，其中R 1是氢或低级烷基; R2和R3各自独立地为氢或低级烷基; R 4，R 5和R 6各自独立地是氢，卤素，低级烷基或低级烷氧基; R 7是氢或低级烷基; R 8是氢，卤素，低级烷基，低级烷氧基等; R 9是-COR 10，-A 1 -OR 10，-OA 2， SUP> -COR 10等; Ar是任选取代的苯基或杂芳基; 并且A是表现出有效和选择性的β3肾上腺素受体刺激活性的键-OCH 2 - 2等。本发明还提供含有所述化合物的药物组合物及其用途。

6. 发明申请

US20070078184A1 Amino alcohol derivatives, medicinal composition containing the same, and use of these 失效
标题翻译：氨基醇衍生物，含有该组合物的药用组合物及其用途
公开(公告)号：US20070078184A1
公开(公告)日：2007-04-05
申请号：US10576753
申请日：2004-10-05
申请人： Junichi Kobayashi , Tetsuya Nakamura , Hideyuki Muranaka , Takehiro Ishikawa , Tetsuro Tamai , Satoshi Akahane
发明人： Junichi Kobayashi , Tetsuya Nakamura , Hideyuki Muranaka , Takehiro Ishikawa , Tetsuro Tamai , Satoshi Akahane
IPC分类号： A61K31/195 , C07C309/50
CPC分类号： C07D235/24 , C07C233/43 , C07C311/21
摘要： The present invention provides compounds represented by general formula (I): a prodrug thereof, or pharmaceutical acceptable salts thereof, wherein R1 is hydrogen or lower alkyl; each of R2 and R3 is independently hydrogen or lower alkyl; each of R4, R5 and R6 is independently hydrogen, halogen, lower alkyl or lower alkoxy; R7 is hydrogen or lower alkyl; R8 is hydrogen, halogen, lower alkyl, lower alkoxy, etc; R9 is —COR10, -A1-COR10, —O-A2-COR10, etc; Ar is optionally substituted phenyl or heteroaryl; and A is a bond, —OCH2—, etc, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.
摘要翻译：本发明提供由通式（I）表示的化合物：其前药或其药学上可接受的盐，其中R 1是氢或低级烷基; R2和R3各自独立地为氢或低级烷基; R 4，R 5和R 6各自独立地是氢，卤素，低级烷基或低级烷氧基; R 7是氢或低级烷基; R 8是氢，卤素，低级烷基，低级烷氧基等; R 9是-COR 10，-A 1 -OR 10，-OA 2， SUP> -COR 10等; Ar是任选取代的苯基或杂芳基; 并且A是表现出有效和选择性的β3肾上腺素受体刺激活性的键-OCH 2 - 2等。本发明还提供含有所述化合物的药物组合物及其用途。

7. 发明授权

US06353025B1 Phenylaminoalkylcarboxylic acid derivatives and pharmaceutical compositions comprising the same 失效
标题翻译：苯基氨基烷基羧酸衍生物和包含它们的药物组合物
公开(公告)号：US06353025B1
公开(公告)日：2002-03-05
申请号：US09581851
申请日：2000-06-19
申请人： Tetsuro Tamai , Nobuyuki Tanaka , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
发明人： Tetsuro Tamai , Nobuyuki Tanaka , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
IPC分类号： A01N3712
CPC分类号： C07D295/185 , C07C229/18 , C07C237/06
摘要： The present invention provides novel phenylaminoalkyl-carboxylic acid derivatives represented by the general formula: (wherein R1 represents a hydroxy group, a lower alkoxy group, an aralkoxy group, an amino group, an alicyclic amino group or a mono or di(lower alkyl)amino group which may have a hydroxy group or a lower alkoxy group as a substituent; R2 represents a hydrogen atom or a lower alkyl group; R3 represents a hydrogen atom or a halogen atom; R4 and R5 are the same or different and each represents a hydrogen atom, a halogen atom or a lower alkyl group; A represents a lower alkylene group; the carbon atom marked with (R) represents a carbon atom in (R) configuration; and the carbon atom marked with (S) represents a carbon atom in (S) configuration) and pharmaceutically acceptable salts thereof, which have excellent &bgr;3-adrenoceptor stimulating effects and are useful as agents for the prevention or treatment of obesity, hyperglycemia, the diseases caused by intestinal hypermotility, pollakiuria, urinary incontinence, depression, or the diseases caused by biliary calculi or hypermotility of biliary tract.
摘要翻译：本发明提供由通式（其中R1表示羟基，低级烷氧基，芳烷氧基，氨基，脂环族氨基或单或二（低级烷基））表示的新型苯基氨基烷基 - 羧酸衍生物，可以具有羟基或低级烷氧基作为取代基的氨基; R2表示氢原子或低级烷基; R3表示氢原子或卤素原子; R4和R5相同或不同，表示氢原子，卤素原子或低级烷基; A表示低级亚烷基;（R）表示的碳原子表示（R）构型的碳原子，（S）表示的碳原子表示碳原子（S）构型）及其药学上可接受的盐，其具有优异的β3肾上腺素能受体刺激作用，并且可用作预防或治疗肥胖症，高血糖症，由肠道超嗜热引起的疾病遗尿，尿频，尿失禁，抑郁症或由胆汁结石或胆汁运动障碍引起的疾病。

8. 发明授权

US6136852A 3,4-disubstituted phenylethanolaminotetralincarboxylic acid derivatives 有权
标题翻译： 3,4-二取代苯乙醇氨基四氢萘羧酸衍生物
公开(公告)号：US6136852A
公开(公告)日：2000-10-24
申请号：US155345
申请日：1999-03-08
申请人： Makio Kitazawa , Kosuke Okazaki , Tetsuro Tamai , Masaru Saito , Nobuyuki Tanaka , Hiroaki Kobayashi , Ken Kikuchi , Hideyuki Muranaka
发明人： Makio Kitazawa , Kosuke Okazaki , Tetsuro Tamai , Masaru Saito , Nobuyuki Tanaka , Hiroaki Kobayashi , Ken Kikuchi , Hideyuki Muranaka
IPC分类号： C07C217/74 , C07C229/46 , C07C229/50 , A61K31/215 , A61K31/19 , C07C62/06 , C07C69/76
CPC分类号： C07C229/50 , C07C217/74 , C07C2102/10 , Y02P20/55
摘要： The present invention relates to 3,4-disubstituted phenylethanolaminotetralincarboxylic acid derivatives represented by the general formula: ##STR1## [wherein Q represents a vinylene group or a group represented by the general formula:-A-(CH.sub.2).sub.m --(wherein A represents an oxygen atom or a methylene group; and m is an integer of from 1 to 6); R represents a hydrogen atom or a lower alkyl group; n is an integer of 1 or 2; the carbon atom marked with * represents a carbon atom in R configuration, S configuration or a mixture thereof; and the carbon atom marked with (S) represents a carbon atom in S configuration] and pharmaceutically acceptable salts thereof, which have a selective .beta..sub.2 -adrenergic receptor stimulating effect with relieved burdens on the heart such as tachycardia and are useful as an agent for the prevention of threatened abortion and premature labor, a bronchodilator and an agent for pain remission and promoting stone removal in urolithiasis.
摘要翻译： PCT No.PCT / JP97 / 01008 Sec。 371日期1999年3月8日 102（e）1999年3月8日PCT 1997年3月26日PCT公布。公开号WO97 / 35835 日期：1997年10月2日本发明涉及由以下通式表示的3,4-二取代苯乙醇氨基四氢萘羧酸衍生物：[其中Q表示亚乙烯基或由通式-A-（CH 2）m - 表示的基团 A表示氧原子或亚甲基; m表示1〜6的整数）; R表示氢原子或低级烷基; n为1或2的整数; 标有*的碳原子表示R构型，S构型或其混合物中的碳原子; 标记有（S）的碳原子表示S构型的碳原子及其药学上可接受的盐，其具有选择性β2-肾上腺素能受体刺激作用，并且在心脏上缓解负担，例如心动过速，并且可用作防止威胁堕胎和早产，支气管扩张剂和止痛剂，促进尿石症中的除石。

9. 发明授权

US06696489B1 2-Methylpropionic acid derivatives and medicinal compositions containing the same 失效
标题翻译： 2-甲基丙酸衍生物和含有它们的药物组合物
公开(公告)号：US06696489B1
公开(公告)日：2004-02-24
申请号：US09673308
申请日：2000-10-13
申请人： Tetsuro Tamai , Nobuyuki Tanaka , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
发明人： Tetsuro Tamai , Nobuyuki Tanaka , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
IPC分类号： A61K3124
CPC分类号： C07C217/60 , C07C229/18
摘要： The present invention provides novel 2-methylpropionic acid derivatives represented by the general formula: (wherein R1 represents a hydrogen atom, a lower alkyl group or an aralkyl group; R2 represents a hydrogen atom a lower alkyl group or a halogen atom; A represents an oxygen atom or an imino group; the carbon atom marked with (R) represents a carbon atom in R configuration; and the carbon atom marked with (S) represents a carbon atom in S configuration) and pharmaceutically acceptable salts thereof, which have excellent &bgr;3-adrenoceptor stimulating effects and are useful as agents for the prevention or treatment of obesity, hyperglycemia, the diseases caused by intestinal hypermotility, pollakiuria, urinary incontinence, depression, or the diseases caused by biliary calculi or hypermotility of the biliary tract.
摘要翻译：本发明提供由以下通式表示的新型2-甲基丙酸衍生物：其中R 1表示氢原子，低级烷基或芳烷基; R 2表示氢原子，低级烷基或卤素原子; A表示氧原子或亚氨基;由（R）标记的碳原子表示R构型的碳原子;标有（S）的碳原子表示S构型的碳原子）和药学上可接受的盐其具有优异的β3肾上腺素能受体刺激作用，并且可用作预防或治疗肥胖症，高血糖症，由肠蠕动过多引起的疾病，尿尿症，尿失禁，抑郁症或由胆汁结石或运动障碍引起的疾病胆道。

10. 发明授权

US06538152B1 Phenoxyacetic acid derivatives and medicinal compositions containing the same 失效
标题翻译：苯氧乙酸衍生物和含有它们的药物组合物
公开(公告)号：US06538152B1
公开(公告)日：2003-03-25
申请号：US09720976
申请日：2001-01-03
申请人： Nobuyuki Tanaka , Tetsuro Tamai , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
发明人： Nobuyuki Tanaka , Tetsuro Tamai , Harunobu Mukaiyama , Akihito Hirabayashi , Hideyuki Muranaka , Masaaki Sato , Masuo Akahane
IPC分类号： C07C22900
CPC分类号： C07C217/60 , C07C233/43 , C07C235/06 , C07C235/60 , C07C255/59
摘要： The present invention provides novel phenoxyacetic acid derivatives represented by the general formula: wherein R1 represents a hydroxy group, a lower alkoxy group, an aralkoxy group, an amino group, or a mono or di(lower alkyl)amino group; one of R2 and R3 is a hydrogen atom, a halogen atom, a lower alkyl group or a lower alkoxy group, while the other is a hydrogen atom; R4 represents a halogen atom, a lower alkyl group, a halo(lower alkyl) group, a hydroxy group, a lower alkoxy group, an aralkoxy group, a cyano group, a nitro group, an amino group, a mono or di(lower alkyl)amino group, a carbamoyl group, a mono or di(lower alkyl)carbamoyl group or a group represented by the general formula: —NHCOR5 (wherein R5 represents a hydrogen atom or a lower alkyl group); the carbon atom marked with (R) represents a carbon atom in R configuration; and the carbon atom marked with (S) represents a carbon atom in S configuration, and pharmaceutically acceptable salts thereof, which have excellent &bgr;3-adrenoceptor stimulating effects and are useful as agents for the prevention or treatment of obesity, hyperglycemia, the diseases caused by intestinal hypermotility, pollakiuria, urinary incontinence, depression, or the diseases caused by biliary calculi or hypermotility of biliary tract.
摘要翻译：本发明提供由通式表示的新型苯氧基乙酸衍生物：其中R1表示羟基，低级烷氧基，芳烷氧基，氨基或单或二（低级烷基）氨基; R2和R3中的一个是氢原子，卤素原子，低级烷基或低级烷氧基，而另一个是氢原子; R4表示卤原子，低级烷基，卤代（低级烷基），羟基，低级烷氧基，芳烷氧基，氰基，硝基，氨基，单或二（低级）烷基）氨基，氨基甲酰基，一或二（低级烷基）氨基甲酰基或由通式表示的基团：其中R5表示氢原子或低级烷基; 用（R）标记的碳原子表示R构型的碳原子; 标记有（S）的碳原子表示S构型的碳原子及其药学上可接受的盐，其具有优异的β3肾上腺素能受体刺激作用，并且可用作预防或治疗肥胖，高血糖，由高血糖引起的疾病肠蠕动过多，尿频尿失禁，抑郁症，胆汁结石或胆汁运动障碍引起的疾病。

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