RU98118906A - AMIDIC DERIVATIVES OR THEIR SALTS - Google Patents
AMIDIC DERIVATIVES OR THEIR SALTSInfo
- Publication number
- RU98118906A RU98118906A RU98118906/04A RU98118906A RU98118906A RU 98118906 A RU98118906 A RU 98118906A RU 98118906/04 A RU98118906/04 A RU 98118906/04A RU 98118906 A RU98118906 A RU 98118906A RU 98118906 A RU98118906 A RU 98118906A
- Authority
- RU
- Russia
- Prior art keywords
- amino
- phenylethyl
- hydroxy
- ethyl
- acetanilide
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims 5
- 239000011780 sodium chloride Substances 0.000 title claims 5
- 150000001408 amides Chemical class 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- -1 hydroxy-2-phenylethyl Chemical group 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000008177 pharmaceutical agent Substances 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- BXGZQNFJRKTVCG-NRFANRHFSA-N 2-(6-aminopyridin-2-yl)-N-[4-[2-[[(2R)-2-hydroxy-2-phenylethyl]amino]ethyl]phenyl]acetamide Chemical compound NC1=CC=CC(CC(=O)NC=2C=CC(CCNC[C@H](O)C=3C=CC=CC=3)=CC=2)=N1 BXGZQNFJRKTVCG-NRFANRHFSA-N 0.000 claims 1
- NNUMYESNXIYWKR-DEOSSOPVSA-N 2-[1-[(3,4-dichlorophenyl)methyl]tetrazol-5-yl]-N-[4-[2-[[(2R)-2-hydroxy-2-phenylethyl]amino]ethyl]phenyl]acetamide Chemical compound C([C@H](O)C=1C=CC=CC=1)NCCC(C=C1)=CC=C1NC(=O)CC1=NN=NN1CC1=CC=C(Cl)C(Cl)=C1 NNUMYESNXIYWKR-DEOSSOPVSA-N 0.000 claims 1
- ZAGAMAQKESDRCH-SANMLTNESA-N 2-[1-[(4-chlorophenyl)methyl]imidazol-2-yl]-N-[4-[2-[[(2R)-2-hydroxy-2-phenylethyl]amino]ethyl]phenyl]acetamide Chemical compound C([C@H](O)C=1C=CC=CC=1)NCCC(C=C1)=CC=C1NC(=O)CC1=NC=CN1CC1=CC=C(Cl)C=C1 ZAGAMAQKESDRCH-SANMLTNESA-N 0.000 claims 1
- FZERHIULMFGESH-UHFFFAOYSA-N Acetanilide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims 1
- 206010012601 Diabetes mellitus Diseases 0.000 claims 1
- XWWXOJXRVHMBPD-QFIPXVFZSA-N N-[4-[2-[[(2R)-2-hydroxy-2-phenylethyl]amino]ethyl]phenyl]-2-pyridin-2-ylacetamide Chemical compound C([C@H](O)C=1C=CC=CC=1)NCCC(C=C1)=CC=C1NC(=O)CC1=CC=CC=N1 XWWXOJXRVHMBPD-QFIPXVFZSA-N 0.000 claims 1
- 229960001413 acetanilide Drugs 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
Claims (4)
где кольцо В представляет гетероарильную группу; Х представляет связь или низшую алкиленовую группу; R представляет атом водорода, атом галогена, низшую алкильную группу, амино группу, арил-(низшую) алкильную группу или галогенарил (низшую) алкильную группу, или его соль.1. The amide derivative represented by the following formula:
where ring B represents a heteroaryl group; X represents a bond or a lower alkylene group; R represents a hydrogen atom, a halogen atom, a lower alkyl group, an amino group, an aryl- (lower) alkyl group or a halogenaryl (lower) alkyl group, or a salt thereof.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JPHEI-9-285778 | 1997-10-17 | ||
JP28577897 | 1997-10-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU98118906A true RU98118906A (en) | 2000-06-27 |
RU2186763C2 RU2186763C2 (en) | 2002-08-10 |
Family
ID=17695954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU98118906/04A RU2186763C2 (en) | 1997-10-17 | 1998-10-16 | Amide derivatives or their salts |
Country Status (21)
Country | Link |
---|---|
US (1) | US6346532B1 (en) |
EP (1) | EP1028111B1 (en) |
JP (1) | JP3193706B2 (en) |
KR (1) | KR100506568B1 (en) |
CN (1) | CN1136193C (en) |
AR (1) | AR017340A1 (en) |
AT (1) | ATE266639T1 (en) |
AU (1) | AU9462198A (en) |
BR (1) | BR9804500B1 (en) |
CA (1) | CA2305802C (en) |
DE (1) | DE69823858T2 (en) |
DK (1) | DK1028111T3 (en) |
ES (1) | ES2221204T3 (en) |
HU (1) | HU227560B1 (en) |
ID (1) | ID23989A (en) |
NO (2) | NO316673B1 (en) |
PL (1) | PL196510B1 (en) |
PT (1) | PT1028111E (en) |
RU (1) | RU2186763C2 (en) |
TW (1) | TW557295B (en) |
WO (1) | WO1999020607A1 (en) |
Families Citing this family (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2356197A (en) | 1999-10-12 | 2001-05-16 | Merck & Co Inc | Amide derivatives as beta 3 agonists |
US6525202B2 (en) * | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
US6498170B2 (en) | 2000-07-17 | 2002-12-24 | Wyeth | Cyclamine sulfonamides as β-3 adrenergic receptor agonists |
US6537994B2 (en) | 2000-07-17 | 2003-03-25 | Wyeth | Heterocyclic β3 adrenergic receptor agonists |
US6410734B1 (en) | 2000-07-17 | 2002-06-25 | Wyeth | 2-substituted thiazolidinones as beta-3 adrenergic receptor agonists |
US6451814B1 (en) | 2000-07-17 | 2002-09-17 | Wyeth | Heterocyclic β-3 adrenergic receptor agonists |
US6465501B2 (en) | 2000-07-17 | 2002-10-15 | Wyeth | Azolidines as β3 adrenergic receptor agonists |
UA82048C2 (en) | 2000-11-10 | 2008-03-11 | Эли Лилли Энд Компани | Peroxisome proliferator activated receptor alpha agonists |
US7342117B2 (en) * | 2001-10-30 | 2008-03-11 | Astellas Pharma Inc. | α-form or β-form crystal of acetanilide derivative |
WO2003042160A1 (en) | 2001-11-13 | 2003-05-22 | Theravance, Inc. | Aryl aniline beta-2 adrenergic receptor agonists |
TWI249515B (en) * | 2001-11-13 | 2006-02-21 | Theravance Inc | Aryl aniline beta2 adrenergic receptor agonists |
AU2002364291B2 (en) * | 2001-12-20 | 2007-08-02 | Merck Serono Sa | Triazoles as oxytocin antagonists |
CA2503570C (en) | 2002-11-07 | 2011-04-19 | Yamanouchi Pharmaceutical Co., Ltd. | Remedy for overactive bladder comprising acetic acid anilide derivative as the active ingredient |
EP1424079A1 (en) * | 2002-11-27 | 2004-06-02 | Boehringer Ingelheim International GmbH | Combination of a beta-3-receptor agonist and of a reuptake inhibitor of serotonin and/or norepinephrine |
DE102004001413A1 (en) * | 2004-01-09 | 2005-08-18 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 3-hydroxymethyl-4-hydroxy-phenyl derivatives for the treatment of chronic obstructive pulmonary disease |
WO2006014704A1 (en) * | 2004-07-21 | 2006-02-09 | Theravance, Inc. | DIARYL ETHER β2 ADRENERGIC RECEPTOR AGONISTS |
CN101595088B (en) | 2007-01-31 | 2013-06-19 | 东丽株式会社 | Benzylamine derivative or pharmaceutically acceptable acid addition salt thereof, and use thereof for medical purposes |
US20100240697A1 (en) | 2007-11-02 | 2010-09-23 | Astellas Pharma Inc. | Pharmaceutical composition for treating overactive bladder |
EP2223690A4 (en) | 2007-12-21 | 2011-02-23 | Astellas Pharma Inc | Pharmaceutical composition for ameliorating lower urinary tract symptom |
DE102008014523A1 (en) * | 2008-03-15 | 2009-09-17 | Robert Bosch Gmbh | heater |
CA2724077C (en) * | 2008-05-14 | 2016-04-26 | Astellas Pharma Inc. | Amide compound |
TWI478712B (en) * | 2008-09-30 | 2015-04-01 | Astellas Pharma Inc | Pharmaceutical composition for modified release |
WO2010147830A2 (en) | 2009-06-15 | 2010-12-23 | Auspex Pharmaceuticals, Inc. | Aminothiazole modulators of beta-3-adrenoreceptor |
US20120070465A1 (en) | 2010-03-29 | 2012-03-22 | Astellas Pharma Inc. | Pharmaceutical composition for modified release |
US8877214B2 (en) * | 2010-03-29 | 2014-11-04 | Astellas Pharma Inc. | Pharmaceutical composition for modified release |
US9655885B2 (en) | 2011-05-18 | 2017-05-23 | Dr. Reddy's Laboratories Ltd. | Amorphous mirabegron and processes for crystal forms of mirabegron |
IN2013CN09704A (en) * | 2011-05-18 | 2015-07-03 | Reddys Lab Ltd Dr | |
JPWO2013147134A1 (en) | 2012-03-30 | 2015-12-14 | アステラス製薬株式会社 | Mirabegron-containing pharmaceutical composition |
CN103387500A (en) * | 2012-05-11 | 2013-11-13 | 上海医药工业研究院 | Preparation methods for mirabegron and intermediate thereof |
CN104602693A (en) | 2012-08-31 | 2015-05-06 | 安斯泰来制药株式会社 | Orally administered medical composition |
US9784726B2 (en) | 2013-01-08 | 2017-10-10 | Atrogi Ab | Screening method, a kit, a method of treatment and a compound for use in a method of treatment |
CN103193730A (en) * | 2013-04-17 | 2013-07-10 | 苏州永健生物医药有限公司 | Synthesis method of mirabegron |
CN103232368B (en) * | 2013-04-18 | 2015-08-12 | 苏州永健生物医药有限公司 | A kind of synthetic method of (R)-4-nitrophenethyl-(2-hydroxyl-2-styroyl)-t-butyl carbamate |
WO2015040605A1 (en) | 2013-09-23 | 2015-03-26 | Ranbaxy Laboratories Limited | Crystalline form of mirabegron |
WO2015040573A1 (en) | 2013-09-23 | 2015-03-26 | Ranbaxy Laboratories Limited | Mirabegron dimethyl sulphoxide solvate and its use for the treatment of overactive bladder |
WO2015044965A1 (en) | 2013-09-30 | 2015-04-02 | Megafine Pharma (P) Ltd. | A process for preparation of mirabegron and alpha crystalline form thereof |
ITMI20131653A1 (en) * | 2013-10-07 | 2015-04-08 | Dipharma Francis Srl | CRYSTALLINE FORMS OF AN ADRENERGIC AGONIST |
CN104876889B (en) * | 2014-02-27 | 2017-02-22 | 人福医药集团股份公司 | A synthesis method of a compound |
WO2015162536A1 (en) * | 2014-04-22 | 2015-10-29 | Calyx Chemicals And Pharmaceuticals Ltd. | Novel process for preparation of mirabegron and it's intermediate |
CN103896872A (en) * | 2014-04-29 | 2014-07-02 | 黑龙江大学 | Method for synthesizing mirabegron |
JP6759185B2 (en) | 2014-08-06 | 2020-09-23 | インテルキム、ソシエダッド アノニマ | Method for synthesizing mirabegron and its derivatives |
WO2016024284A2 (en) | 2014-08-07 | 2016-02-18 | Wanbury Ltd. | A process for the preparation of mirabegron and its intermediates |
CN105481705A (en) * | 2014-08-23 | 2016-04-13 | 南京海纳医药科技有限公司 | Preparation and application of (R)-2-[[2-(4-aminophenyl)ethyl]amino]-1-phenylethyl alcohol |
CA2962664A1 (en) * | 2014-10-01 | 2016-04-07 | Apotex Inc. | Solid forms of mirabegron |
CN104496841B (en) * | 2014-11-26 | 2017-01-25 | 南京工业大学 | Method for synthesizing mirabegron intermediate |
EP3253741A1 (en) | 2015-02-02 | 2017-12-13 | Lupin Limited | Process for preparation of polymorphic form of mirabegron |
JP2018090490A (en) | 2015-03-31 | 2018-06-14 | アステラス製薬株式会社 | Mirabegron-containing pharmaceutical composition |
CN105111165B (en) * | 2015-09-14 | 2017-10-31 | 保定博洋生物科技有限公司 | A kind of preparation method of Mirabegron |
EP3353156B1 (en) * | 2015-09-23 | 2021-11-03 | The General Hospital Corporation | Tead transcription factor autopalmitoylation inhibitors |
FR3043555B1 (en) * | 2015-11-17 | 2019-10-25 | Centre National De La Recherche Scientifique (Cnrs) | MIRABEGRON FOR THE TREATMENT OF RETINAL DISEASES |
EP3184516A1 (en) | 2015-12-23 | 2017-06-28 | Enantia, S.L. | Crystalline inclusion complexes of mirabegron with beta-cyclodextrin |
HU231124B1 (en) * | 2016-02-10 | 2020-12-28 | Egis Gyógyszergyár Zrt. | Method for producing morphologically homogenous mirabegron and mirabegron monohydrochloride |
WO2017186598A1 (en) | 2016-04-25 | 2017-11-02 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
EP3448367A1 (en) | 2016-04-25 | 2019-03-06 | Synthon BV | Tablets comprising mirabegron and solifenacin |
GB201612165D0 (en) * | 2016-07-13 | 2016-08-24 | Atrogi Ab | Combinations for the treatment of type 2 diabetes |
US9988402B2 (en) | 2016-08-19 | 2018-06-05 | Purdue Research Foundation | Amine-boranes bearing borane-intolerant functionalities |
EP3335700A1 (en) | 2016-12-13 | 2018-06-20 | Stada Arzneimittel Ag | Solid pharmaceutical oral dosage form comprising an extended release of the active ingredient comprising mirabegron |
SI3360866T1 (en) | 2017-02-14 | 2019-04-30 | Alfred E. Tiefenbacher (Gmbh & Co. Kg) | Mirabegron prodrugs |
KR101868438B1 (en) | 2017-04-13 | 2018-06-20 | (주) 성운파마코피아 | Method for preparing amide derivatives |
KR102398639B1 (en) | 2017-06-20 | 2022-05-17 | (주) 성운파마코피아 | Salts of amide derivatives and method for preparing the same |
WO2019013583A2 (en) | 2017-07-14 | 2019-01-17 | 주식회사 대웅제약 | Pharmaceutical preparation and preparation method therefor |
KR101937713B1 (en) | 2017-07-14 | 2019-01-14 | 주식회사 대웅제약 | Pharmaceutical formulation and preparation method for the same |
GB201714736D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
GB201714740D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
GB201714745D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
GB201714734D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
EP3694492A1 (en) | 2017-10-12 | 2020-08-19 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
EP3292864A1 (en) | 2017-10-12 | 2018-03-14 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
US10478399B2 (en) | 2017-10-12 | 2019-11-19 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
KR101928987B1 (en) * | 2018-08-28 | 2018-12-13 | (주) 성운파마코피아 | A New and Highly Pure Crystalline monohydrate of mirabegron, Method for Preparing or Use Thereof |
CN109776373B (en) * | 2019-01-29 | 2020-04-21 | 广东东阳光药业有限公司 | Amide-substituted pyrrolidine amide derivatives and uses thereof |
CN109734712B (en) * | 2019-01-30 | 2020-10-20 | 广东东阳光药业有限公司 | Aryl or heteroaryl substituted pyrrolidine amide derivatives and uses thereof |
KR20200117091A (en) | 2019-04-02 | 2020-10-14 | 제이투에이치바이오텍 (주) | Prodrug compound of mirabegron and its medical use for treating or alleviating overactive bladder diseases |
KR20210012082A (en) | 2019-07-23 | 2021-02-03 | 콜마파마(주) | A pharmaceutical composition comprising mirabegron and tamsulosin |
CN110590699B (en) * | 2019-09-29 | 2022-11-15 | 广东先强药业有限公司 | Refining method of mirabegron |
EP3722285B1 (en) | 2020-04-08 | 2022-03-30 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Process for preparing mirabegron enacarbil |
KR102333167B1 (en) | 2021-05-26 | 2021-12-01 | 유니셀랩 주식회사 | An efficient and mass-producible Mirabegron amorphous manufacturing method |
GB202205895D0 (en) | 2022-04-22 | 2022-06-08 | Atrogi Ab | New medical uses |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2965655D1 (en) * | 1978-06-28 | 1983-07-21 | Beecham Group Plc | Secondary amines, their preparation, pharmaceutical compositions containing them and their use |
US5223614A (en) * | 1987-12-19 | 1993-06-29 | Boehringer Ingelheim Gmbh | New quaternary ammonium compounds, their preparation and use |
DE3743265A1 (en) * | 1987-12-19 | 1989-06-29 | Boehringer Ingelheim Kg | NEW AMMONIUM COMPOUNDS, THEIR MANUFACTURE AND USE |
WO1993019861A1 (en) | 1992-03-27 | 1993-10-14 | Kawasaki Steel Corporation | Method of detecting roll clearance setting error for universal rolling machines and method of rolling h-beam having favorable flange size by utilizing said method |
US5451677A (en) * | 1993-02-09 | 1995-09-19 | Merck & Co., Inc. | Substituted phenyl sulfonamides as selective β 3 agonists for the treatment of diabetes and obesity |
US5614544A (en) | 1993-09-14 | 1997-03-25 | Takeda Chemical Industries, Ltd. | Oxazolidinedione derivatives and their use |
JP3722855B2 (en) * | 1993-09-14 | 2005-11-30 | 武田薬品工業株式会社 | 2,4-oxazolidinedione derivative and pharmaceutical comprising the same |
IL113410A (en) * | 1994-04-26 | 1999-11-30 | Merck & Co Inc | Substituted sulfonamides having an asymmetric center and pharmaceutical compositions containing them |
US5541197A (en) * | 1994-04-26 | 1996-07-30 | Merck & Co., Inc. | Substituted sulfonamides as selective β3 agonists for the treatment of diabetes and obesity |
WO1998032742A1 (en) | 1997-01-23 | 1998-07-30 | Yamanouchi Pharmaceutical Co., Ltd. | Novel amide derivatives and medicinal compositions thereof |
JPH10218861A (en) * | 1997-02-04 | 1998-08-18 | Yamanouchi Pharmaceut Co Ltd | New phenethanol derivative or its salt |
-
1998
- 1998-10-15 BR BRPI9804500-8A patent/BR9804500B1/en not_active IP Right Cessation
- 1998-10-15 US US09/529,096 patent/US6346532B1/en not_active Expired - Lifetime
- 1998-10-15 AR ARP980105127A patent/AR017340A1/en active IP Right Grant
- 1998-10-15 DE DE69823858T patent/DE69823858T2/en not_active Expired - Lifetime
- 1998-10-15 CA CA002305802A patent/CA2305802C/en not_active Expired - Lifetime
- 1998-10-15 PT PT98947894T patent/PT1028111E/en unknown
- 1998-10-15 DK DK98947894T patent/DK1028111T3/en active
- 1998-10-15 AT AT98947894T patent/ATE266639T1/en active
- 1998-10-15 JP JP2000516949A patent/JP3193706B2/en not_active Expired - Lifetime
- 1998-10-15 AU AU94621/98A patent/AU9462198A/en not_active Abandoned
- 1998-10-15 TW TW087117145A patent/TW557295B/en not_active IP Right Cessation
- 1998-10-15 EP EP98947894A patent/EP1028111B1/en not_active Expired - Lifetime
- 1998-10-15 WO PCT/JP1998/004671 patent/WO1999020607A1/en active IP Right Grant
- 1998-10-15 ES ES98947894T patent/ES2221204T3/en not_active Expired - Lifetime
- 1998-10-15 ID IDW20000418A patent/ID23989A/en unknown
- 1998-10-15 KR KR1019980043101A patent/KR100506568B1/en active IP Right Review Request
- 1998-10-16 HU HU9802417A patent/HU227560B1/en active Protection Beyond IP Right Term
- 1998-10-16 PL PL329233A patent/PL196510B1/en unknown
- 1998-10-16 CN CNB981213758A patent/CN1136193C/en not_active Expired - Lifetime
- 1998-10-16 RU RU98118906/04A patent/RU2186763C2/en active
-
2000
- 2000-04-14 NO NO20001983A patent/NO316673B1/en not_active IP Right Cessation
-
2013
- 2013-07-12 NO NO2013013C patent/NO2013013I1/en not_active Application Discontinuation
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU98118906A (en) | AMIDIC DERIVATIVES OR THEIR SALTS | |
JP2004532209A5 (en) | ||
EP1400518A4 (en) | Heterocyclic compound derivatives and medicines | |
EA201000300A1 (en) | METHOD FOR SYNTHESIS OF COMPOUNDS SUITABLE FOR THE TREATMENT OF HEPATITIS C | |
DE69118082D1 (en) | Imidazole derivatives, strong and selective angiotensin II receptor antagonists | |
DK1379520T3 (en) | N-substituted non-aryl heterocyclic NMDA / NR2B antagonists | |
RU97100151A (en) | DERIVATIVES OF PIPERAZINE AS ANTAGONISTS 5HT1A | |
CA2039056A1 (en) | 3,5-di-tertiarybutyl-4-hydroxyphenylmethylene derivatives of 2-substituted thiazolidinones, oxazolidinones, and imidazolidinones as antiinflammatory agents | |
PE20020917A1 (en) | DERIVATIVES OF IMIDAZOLE AS N-METHYL-D-ASPARTATE RECEPTOR BLOCKERS | |
RU2002100058A (en) | 1-Methylcarbapenem Crystal Derivatives | |
WO2001036425A3 (en) | Imidazole compounds used as phosphodiesterase vii inhibitors | |
EP0388909A3 (en) | Thiazole compounds, processes for the preparation thereof and pharmaceutical composition comprising the same | |
TR199801218T2 (en) | N-acyl-2-substituted-4-(Benzimidazolyl-or imidazopyridinyl-substituted residues)-piperidines as tachykinin antagonists. | |
ATA20991A (en) | NEW IMIDAZOLE DERIVATIVES, METHOD FOR THEIR PRODUCTION AND THEIR USE | |
EP0902018A3 (en) | 2-(Arylphenyl)amino-imidazoline derivatives | |
DE60016786D1 (en) | BICYCLIC VASOPRESSINE AGONIST | |
PE20010954A1 (en) | BENZHIMIDAZOLES, ITS PREPARATION AND ITS USE AS MEDICINES | |
IT1295405B1 (en) | USE OF AN ANGIOTENSIN II RECEPTORAL ANTAGONIST FOR DRUG PREPARATION TO INCREASE THE SURVIVAL RATE OF | |
JP2005513103A5 (en) | ||
DE69911557D1 (en) | Imidazoline derivatives, their preparation and pharmaceutical compositions containing them | |
EP0355827A3 (en) | Hydantoin derivatives | |
MXPA03009546A (en) | Novel insecticidal azoles. | |
DE69812010D1 (en) | 4-aminopyrrole (3,2-d) pyrimidines as antagonists of the neuropeptide Y receptor | |
RU2002111663A (en) | AMIDE COMPOUNDS | |
WO1999013871A3 (en) | Fused imidazole derivatives for improving oral bioavailability of pharmaceutical agents |