RS51156B - Inhibitori renina - Google Patents
Inhibitori reninaInfo
- Publication number
- RS51156B RS51156B YUP-771/01A YUP77101A RS51156B RS 51156 B RS51156 B RS 51156B YU P77101 A YUP77101 A YU P77101A RS 51156 B RS51156 B RS 51156B
- Authority
- RS
- Serbia
- Prior art keywords
- methoxynaphthalen
- methoxybenzyl
- alkoxy
- imidazol
- cyano
- Prior art date
Links
- 239000002461 renin inhibitor Substances 0.000 title 1
- 229940086526 renin-inhibitors Drugs 0.000 title 1
- -1 4-methoxynaphthalen-2-yl Chemical group 0.000 abstract 6
- 125000002927 2-methoxybenzyl group Chemical group [H]C1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 abstract 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 150000003053 piperidines Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/42—Oxygen atoms attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pyridine Compounds (AREA)
Abstract
Derivati piperidina formule (I)naznačeni time stoR1 je naftil proizvoljno supstituisan sa jednom do tri C1-C5-alkoksi grupe;R2 je fenil ili benzil, proizvoljno supstituisan sa supstituentima nezavisno izabranim od jedne do tri halogene, jedne do tri cijano, C1-C3-alkoksi i nitro grupe;R3 je H-[CH(OR4)]2-CH2-O-CH2-, iliR3a-(CH2)k-[CH(OR4)]1,-CH2-O-; gde R3a je hidroksi ili C1-C3-alkoksi, R4 je vodonik ili C1-C3-alkil; k je 1 ili 2, a1 je 1 ili 2; iliR3a je metilamino, k je 1, a 1 je 1, pod uslovom da R1 je 4-metoksinaftalen-2-il, R2 je 2-metoksibenzil; iliR3a je metoksietoksi, k je 1, a 1 je 1, pod uslovom da R1 je 4-metoksinaftalen-2-il, R2 je 2-metoksibenzil ili fenil supstituisan u položaju 2 sa cijano; iliR3a je 1,2,4—triazo1- 1- i1 ili imidazol-l-il, k je 1, a 1 je 1, pod uslovom da R1 je 4-metoksinaftalen-2-il, R2 je fenil supstituisan u položaju 2 sa nitro; ili R3 je hidroksimetil ili imidazol-l-ilmetil, pod uslovom da R1 je 4- metoksinaftalen-2-il, R2 je 2-metoksibenzil; i njihove farmaceutski prihvatljive soli.Prijava sadrži još 25 patentna zahteva.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99108199 | 1999-04-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| YU77101A YU77101A (sh) | 2004-09-03 |
| RS51156B true RS51156B (sr) | 2010-10-31 |
Family
ID=8238050
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| YUP-771/01A RS51156B (sr) | 1999-04-27 | 2000-04-19 | Inhibitori renina |
Country Status (35)
| Country | Link |
|---|---|
| US (2) | US6376672B1 (sr) |
| EP (1) | EP1175400B1 (sr) |
| JP (1) | JP3808706B2 (sr) |
| KR (1) | KR100443684B1 (sr) |
| CN (1) | CN1147471C (sr) |
| AR (2) | AR018719A1 (sr) |
| AT (1) | ATE512949T1 (sr) |
| AU (1) | AU763718B2 (sr) |
| BR (1) | BR0010080B1 (sr) |
| CA (1) | CA2370888C (sr) |
| CO (1) | CO5170513A1 (sr) |
| CZ (1) | CZ302012B6 (sr) |
| DK (1) | DK1175400T3 (sr) |
| EG (1) | EG23979A (sr) |
| ES (1) | ES2366668T3 (sr) |
| GC (1) | GC0000251A (sr) |
| HK (1) | HK1045999B (sr) |
| HR (1) | HRP20010762A2 (sr) |
| HU (1) | HU227764B1 (sr) |
| IL (2) | IL146002A0 (sr) |
| JO (1) | JO2256B1 (sr) |
| MA (1) | MA26787A1 (sr) |
| MX (1) | MXPA01010934A (sr) |
| MY (1) | MY127894A (sr) |
| NO (1) | NO320803B1 (sr) |
| NZ (1) | NZ514981A (sr) |
| PE (1) | PE20010069A1 (sr) |
| PL (1) | PL199895B1 (sr) |
| PT (1) | PT1175400E (sr) |
| RS (1) | RS51156B (sr) |
| RU (1) | RU2213731C2 (sr) |
| TR (1) | TR200103095T2 (sr) |
| TW (1) | TWI224593B (sr) |
| WO (1) | WO2000064873A1 (sr) |
| ZA (1) | ZA200108735B (sr) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
| US6835686B2 (en) * | 2001-07-05 | 2004-12-28 | Millennium Specialty Chemicals | Catalyst system and process for rearrangement of epoxides to allylic alcohols |
| EP1519920A1 (en) * | 2002-06-27 | 2005-04-06 | Actelion Pharmaceuticals Ltd. | Novel tetrahydropyridine derivatives as renin inhibitors |
| US20040214832A1 (en) * | 2003-04-10 | 2004-10-28 | Cuiman Cai | Piperazine derivative renin inhibitors |
| KR20060007041A (ko) * | 2003-04-29 | 2006-01-23 | 액테리온 파마슈티칼 리미티드 | 신규의 3,4-이치환된 1,2,3,6-테트라하이드로피리딘 유도체 |
| TW200513461A (en) | 2003-10-01 | 2005-04-16 | Speedel Experimenta Ag | Organische verbindungen |
| AR045950A1 (es) * | 2003-10-09 | 2005-11-16 | Speedel Experimenta Ag | Compuestos derivados de piperazina, composiciones farmaceuticas que los contienen y su uso en la fabricacion de medicamentos. |
| WO2005037317A2 (en) * | 2003-10-17 | 2005-04-28 | Cornell Research Foundation, Inc. | Mast cell-derived renin |
| DE602004022704D1 (de) * | 2003-11-26 | 2009-10-01 | Novartis Ag | 4-phenylpiperidinderivate als renininhibitoren |
| TW200613274A (en) * | 2004-07-09 | 2006-05-01 | Speedel Experimenta Ag | Organic compounds |
| PT1799199E (pt) | 2004-10-08 | 2012-07-03 | Novartis Ag | Uso de inibidores da renina para a prevenção ou tratamento da disfunção diastólica ou insuficiência cardíaca diastólica |
| GB0428526D0 (en) * | 2004-12-30 | 2005-02-09 | Novartis Ag | Organic compounds |
| GB0500784D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| EP1897879A3 (en) * | 2005-03-31 | 2008-06-11 | Speedel Experimenta AG | 2,4,5-substituted piperidines as renin inhibitors |
| CN101230060A (zh) * | 2005-03-31 | 2008-07-30 | 斯皮德尔实验股份公司 | 取代的哌啶 |
| WO2006103275A1 (en) * | 2005-03-31 | 2006-10-05 | Speedel Experimenta Ag | 3,4,5-substituted piperidines as renin inhibitors |
| TW200716622A (en) * | 2005-03-31 | 2007-05-01 | Speedel Experimenta Ag | Substituted piperidines |
| TW200722424A (en) * | 2005-03-31 | 2007-06-16 | Speedel Experimenta Ag | Substituted piperidines |
| EP1707202A1 (de) * | 2005-03-31 | 2006-10-04 | Speedel Experimenta AG | Organische Verbindungen |
| KR100963455B1 (ko) | 2005-05-27 | 2010-06-18 | 액테리온 파마슈티칼 리미티드 | 신규한 피페리딘 카르복실산 아미드 유도체 |
| GB0514203D0 (en) * | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
| JP2009512715A (ja) * | 2005-10-21 | 2009-03-26 | ノバルティス アクチエンゲゼルシャフト | レニン阻害剤と抗異脂肪血症剤および／または抗肥満症剤の組み合わせ |
| CN101356156B (zh) * | 2005-11-14 | 2012-12-05 | 生命医药公司 | 天冬氨酸蛋白酶抑制剂 |
| KR20080086921A (ko) * | 2005-12-30 | 2008-09-26 | 노파르티스 아게 | 레닌 억제제로서의 ３,５-치환된 피페리딘 화합물 |
| EP1816122A3 (en) * | 2006-01-19 | 2007-09-19 | Speedel Experimenta AG | 3,4,5-substituted piperidines as therapeutic compounds |
| TW200804359A (en) | 2006-01-19 | 2008-01-16 | Speedel Experimenta Ag | Substituted 4-phenylpiperidines |
| TW200821303A (en) * | 2006-08-08 | 2008-05-16 | Speedel Experimenta Ag | Organic compounds |
| WO2008021552A2 (en) * | 2006-08-18 | 2008-02-21 | Duke University | Biased ligands and methods of identifying same |
| EP1908761A1 (en) * | 2006-10-04 | 2008-04-09 | Speedel Experimenta AG | Organic compounds |
| EP1911758A1 (en) * | 2006-10-04 | 2008-04-16 | Speedel Experimenta AG | Phenyl piperidine derivatives for use as renin inhibitors |
| KR101238479B1 (ko) | 2007-06-25 | 2013-03-04 | 노파르티스 아게 | 레닌 억제제로 사용하기 위한 ｎ５-(２-에톡시에틸)-ｎ３-(２-피리디닐)-３,５-피페리딘디카르복스아미드 유도체 |
| CA2699889A1 (en) * | 2007-11-02 | 2009-05-07 | Novartis Ag | 4,4-disubstituted piperdines |
| US10517839B2 (en) | 2008-06-09 | 2019-12-31 | Cornell University | Mast cell inhibition in diseases of the retina and vitreous |
| EP2488661B1 (en) | 2009-10-14 | 2014-12-24 | Oberbauer, Rainer | Acute kidney injury risk testing |
| WO2013045505A1 (en) | 2011-09-28 | 2013-04-04 | Novartis Ag | Biomarkers for raas combination therapy |
| EP2810644A1 (en) | 2013-06-06 | 2014-12-10 | Ferrer Internacional, S.A. | Oral formulation for the treatment of cardiovascular diseases |
| WO2018002673A1 (en) | 2016-07-01 | 2018-01-04 | N4 Pharma Uk Limited | Novel formulations of angiotensin ii receptor antagonists |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4868181A (en) * | 1986-08-04 | 1989-09-19 | E. I. Du Pont De Nemours And Company | 1,4-dihydropyridine derivatives with calcium agonist and alpha1 -antagonist activity |
| DK231088D0 (da) | 1988-04-28 | 1988-04-28 | Ferrosan As | Piperidinforbindelser, deres fremstilling og anvendelse |
| DE3640475A1 (de) | 1986-11-27 | 1988-06-09 | Hoechst Sa Lab | Arzneimittel auf basis von derivaten des 3,4-diphenylpiperidins, die verwendung der derivate als arzneimittel sowie neue 3,4-diphenylpiperidinderivate und verfahren zu ihrer herstellung |
| DK0594618T3 (da) | 1991-06-24 | 1996-08-26 | Optische Ind De Oude Delft Nv | Indretning til måling af en persons respiration |
| WO1997003911A1 (de) | 1995-07-24 | 1997-02-06 | Railfix N.V. | Elektro-permanentmagnetsystem zum manövrieren von einer magnetischen insbesondere ferromagnetischen last |
| JP3648251B2 (ja) | 1995-09-07 | 2005-05-18 | エフ．ホフマン−ラ ロシュ アーゲー | 心及び腎不全を治療するための新規４−（オキシアルコキシフェニル）−３−オキシ−ピペリジン |
| WO1999012532A2 (en) * | 1997-09-08 | 1999-03-18 | F.Hoffmann-La Roche Ag | Piperidine derivatives against malaria |
| US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
-
2000
- 2000-04-04 US US09/542,303 patent/US6376672B1/en not_active Expired - Fee Related
- 2000-04-19 NZ NZ514981A patent/NZ514981A/xx not_active IP Right Cessation
- 2000-04-19 DK DK00922651.5T patent/DK1175400T3/da active
- 2000-04-19 WO PCT/EP2000/003555 patent/WO2000064873A1/en active IP Right Grant
- 2000-04-19 AU AU42968/00A patent/AU763718B2/en not_active Ceased
- 2000-04-19 CA CA002370888A patent/CA2370888C/en not_active Expired - Fee Related
- 2000-04-19 JP JP2000613826A patent/JP3808706B2/ja not_active Expired - Fee Related
- 2000-04-19 BR BRPI0010080-3A patent/BR0010080B1/pt not_active IP Right Cessation
- 2000-04-19 PT PT00922651T patent/PT1175400E/pt unknown
- 2000-04-19 IL IL14600200A patent/IL146002A0/xx active IP Right Grant
- 2000-04-19 MX MXPA01010934A patent/MXPA01010934A/es active IP Right Grant
- 2000-04-19 TR TR2001/03095T patent/TR200103095T2/xx unknown
- 2000-04-19 TW TW089107377A patent/TWI224593B/zh not_active IP Right Cessation
- 2000-04-19 ES ES00922651T patent/ES2366668T3/es not_active Expired - Lifetime
- 2000-04-19 CZ CZ20013854A patent/CZ302012B6/cs not_active IP Right Cessation
- 2000-04-19 RS YUP-771/01A patent/RS51156B/sr unknown
- 2000-04-19 HU HU0203669A patent/HU227764B1/hu not_active IP Right Cessation
- 2000-04-19 HK HK02107639.0A patent/HK1045999B/zh not_active IP Right Cessation
- 2000-04-19 HR HR20010762A patent/HRP20010762A2/xx not_active Application Discontinuation
- 2000-04-19 KR KR10-2001-7013696A patent/KR100443684B1/ko not_active Expired - Fee Related
- 2000-04-19 AT AT00922651T patent/ATE512949T1/de active
- 2000-04-19 RU RU2001130163/04A patent/RU2213731C2/ru not_active IP Right Cessation
- 2000-04-19 PL PL353442A patent/PL199895B1/pl not_active IP Right Cessation
- 2000-04-19 CN CNB008068003A patent/CN1147471C/zh not_active Expired - Fee Related
- 2000-04-19 EP EP00922651A patent/EP1175400B1/en not_active Expired - Lifetime
- 2000-04-23 JO JO200063A patent/JO2256B1/en active
- 2000-04-24 EG EG20000523A patent/EG23979A/xx active
- 2000-04-25 MY MYPI20001771A patent/MY127894A/en unknown
- 2000-04-25 GC GCP2000632 patent/GC0000251A/en active
- 2000-04-25 PE PE2000000386A patent/PE20010069A1/es not_active Application Discontinuation
- 2000-04-26 CO CO00029975A patent/CO5170513A1/es not_active Application Discontinuation
- 2000-04-26 AR ARP000101954A patent/AR018719A1/es active IP Right Grant
-
2001
- 2001-10-17 IL IL146002A patent/IL146002A/en not_active IP Right Cessation
- 2001-10-23 ZA ZA200108735A patent/ZA200108735B/xx unknown
- 2001-10-25 NO NO20015206A patent/NO320803B1/no not_active IP Right Cessation
- 2001-10-26 MA MA26386A patent/MA26787A1/fr unknown
- 2001-12-18 US US10/023,679 patent/US6673931B2/en not_active Expired - Fee Related
-
2009
- 2009-02-25 AR ARP090100634A patent/AR070473A2/es active IP Right Grant
Also Published As
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| Publication | Publication Date | Title |
|---|---|---|
| RS51156B (sr) | Inhibitori renina | |
| EA199800633A1 (ru) | Новые замещенные производные имидазола | |
| ES2184078T3 (es) | Uso de derivados de rapamicina en vasculopatias y xenotrasplantes. | |
| YU47444B (sh) | Oksidaciono sredstvo za keratinska vlakna koje sadrži derivat indolina i njegova primena | |
| ATE219765T1 (de) | Indolderivate als cgmp-pde inhibitoren | |
| TR199700419A2 (xx) | Yeni piridazinon t�revleri. | |
| SE9504661D0 (sv) | New compounds | |
| YU60198A (sh) | Supstituisani derivati indazola i njihova upotreba kao fosfodiesteraze (pde) tipa iv i inhibitora faktora nekroze tumora (tnf) | |
| YU56492A (sh) | Derivati hinuklidina | |
| IS7921A (is) | 2-oxó-1-pýrrólidín afleiða og lyfjafræðileg notkun hennar | |
| BR0008770A (pt) | Derivado de pirimidina, processo para a preparação de um derivado de pirimidina, processo para a produção de um efeito anti-câncer em um animal de sangue quente, uso de um derivado de pirimidina, e, composição farmacêutica | |
| GB2378443A (en) | Pyrazole derivatives and their use as gastrin and cholecystokin in receptor ligands | |
| RS51436B (sr) | Derivati triazolil tropana kao modulatori ccr5 | |
| RS50286B (sr) | Nove kompozicije lekova bazirane na solima tiotropijuma i solima salmeterola | |
| BR0007864A (pt) | Composto, e, uso de um composto | |
| AR018162A1 (es) | Pirroles substituidos, composicion farmaceutica y el uso de los mismos para la preparacion de dicha composicion farmaceutica | |
| YU48089B (sh) | Novi derivati tetrazola i postupak za njihovo pripremanje | |
| CO5150179A1 (es) | Derivados de n-etilpirimidin o (piridin)-2-(1,2-benzoisoxa- zol-3-il)-octahidro-2h-pirido[1,2-a]pirazina y sus composiciones farmaceuticas | |
| ES2176609T3 (es) | Derivados de hidratos de carbono. | |
| DK1109560T3 (da) | Som AICARFT-inhibitorer anvendelige forbindelser | |
| AR004691A1 (es) | Nuevos derivados de [3-alcoxi-fenoxi-)-etil]-dialquilamina, una composicion farmaceutica que los comprende, su uso como anestesicos locales y unprocedimiento para su preparacion | |
| AR002749A1 (es) | Derivados de estiril bencimidazol y composicion farmaceutica que los comprende. | |
| TR200100133T2 (tr) | FKBP İnhibitörleri | |
| RS50033B (sr) | Derivati etansulfonil-piperidina | |
| IS4794A (is) | Þéttaðar 2,3-bensódíasepín afleiður og notkun þeirra sem AMPA-viðtakahindrar |