CO5580743A2 - Piperidinas y piperazinas 3,4-disustituidas, 3,5- disustituidas y 3,4,5-sustituidas - Google Patents
Piperidinas y piperazinas 3,4-disustituidas, 3,5- disustituidas y 3,4,5-sustituidasInfo
- Publication number
- CO5580743A2 CO5580743A2 CO04048699A CO04048699A CO5580743A2 CO 5580743 A2 CO5580743 A2 CO 5580743A2 CO 04048699 A CO04048699 A CO 04048699A CO 04048699 A CO04048699 A CO 04048699A CO 5580743 A2 CO5580743 A2 CO 5580743A2
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- aryl
- alkoxy
- heteroaryl
- optionally substituted
- Prior art date
Links
- 150000003053 piperidines Chemical class 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical group C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 abstract 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005046 dihydronaphthyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- 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
-
- 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
-
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Psychology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
1.- Un compuesto de la fórmula I: o una sal farmacéuticamente aceptable o uno de sus ésteres, en donde Z es CH o N;en donde R1 y R3 son, de modo independiente:(I) alquilo C1-C10, opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados, de modo independiente, del grupo integrado por alquilo C1-C3, -F, -Cl, -Br, -I, -OH, -SH, -C=N, -CF3, alcoxi C1-C3, -O-fenilo, -NR1-aR1-b, en donde R1-a y R1-b son, de modo independiente -H o alquilo C1-C6, -OC=O NR1-aR1-b, -S(=O)0-2 R1-a, -NR1-aC=O NR1-aR1-b, -C=O NR1-aR1-b, y -S(=O)2 NR1-aR1-b, -(CH2)0-3-(C3-C8) cicloalquilo, en donde el cicloalquilo puede estar opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados del grupo integrado por alquilo C1-C3, -F, -Cl, -Br, -I, -OH, -SH, -C=N, -CF3, alcoxi C1-C6, -O- fenilo, -CO-OH, -CO-O- (alquilo C1-C4), -NR1-aR1-b; alcoxi C1-C3-(R1-arilo), alcoxi C1-C3 - (R1-heteroarilo),(II) - (CH2)n1- (R1-arilo), en donde n1 es cero o uno y, en donde R1-arilo es fenilo, 1-naftilo, 2 -naftilo e indanilo, indenilo, dihidronaftilo, tetralinilo opcionalmente sustituido con uno, dos, tres o cuatro de los siguientes sustituyentes seleccionados, de modo independiente, en el anillo arilo:(1) alquilo C1-C6 opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados, de modo independiente, del grupo integrado por alquilo C1-C3, -F, -Cl, -Br, -I, -OH, -SH, -S(alquilo C1-6), -S(aril-alquilo C1-6), S(heteroaril-alquilo C1-6), -S=O(alquilo C1-6), -S=O(arilalquilo C1-6), -S=O(heteroaril-alquilo C1-6), -SO2(alquilo C1-6), -SO2(aril-alquilo C1-6), -SO2 (heteroaril-alquilo C1-6), -NR1-aR1-b, -C=N, -CF3, alcoxi C1-C3, alcoxi C1-C3-(R1-arilo), alcoxi C1-C3 - (R1-heteroarilo), (2) alquenilo C2-C6 con uno o dos enlaces dobles, opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados, de modo independiente, del grupo integrado por -F, -Cl, -Br, -I, -OH, -SH, -S(alquilo C1-6), -S(aril-alquilo C1-6), -S(heteroaril-alquilo C1-6), -S=O (alquilo C1-6), S=O(aril-alquilo C1-6), -S=O(heteroaril-alquilo C1-6), SO2(alquilo C1-6), -SO2(aril-alquilo C1-6), -SO2(heteroaril-alquilo C1-6), -C=N, -CF3, alcoxi C1-C3, -NR1-aR1-b, alcoxi C1-C3-(R1-arilo), alcoxi C1-C3 - (R1-heteroarilo), ...
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33270801P | 2001-11-19 | 2001-11-19 | |
| US38316702P | 2002-05-24 | 2002-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5580743A2 true CO5580743A2 (es) | 2005-11-30 |
Family
ID=26988352
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO04048699A CO5580743A2 (es) | 2001-11-19 | 2004-05-26 | Piperidinas y piperazinas 3,4-disustituidas, 3,5- disustituidas y 3,4,5-sustituidas |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7338965B2 (es) |
| EP (1) | EP1448200A2 (es) |
| JP (1) | JP2005514362A (es) |
| KR (1) | KR20050044533A (es) |
| AP (1) | AP2004003052A0 (es) |
| AU (1) | AU2002360403A1 (es) |
| BR (1) | BR0214295A (es) |
| CA (1) | CA2467749A1 (es) |
| CO (1) | CO5580743A2 (es) |
| EA (1) | EA200400699A1 (es) |
| GE (1) | GEP20074045B (es) |
| HR (1) | HRP20040550A2 (es) |
| IL (1) | IL162079A0 (es) |
| IS (1) | IS7271A (es) |
| MX (1) | MXPA04004772A (es) |
| NO (1) | NO20042580L (es) |
| NZ (1) | NZ533158A (es) |
| OA (1) | OA12812A (es) |
| RS (1) | RS54204A (es) |
| TN (1) | TNSN04088A1 (es) |
| WO (1) | WO2003043987A2 (es) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7521481B2 (en) | 2003-02-27 | 2009-04-21 | Mclaurin Joanne | Methods of preventing, treating and diagnosing disorders of protein aggregation |
| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| AU2006235344B2 (en) | 2005-04-08 | 2012-07-26 | Comentis, Inc. | Compounds which inhibit beta-secretase activity and methods of use thereof |
| EP1816122A3 (en) * | 2006-01-19 | 2007-09-19 | Speedel Experimenta AG | 3,4,5-substituted piperidines as therapeutic compounds |
| EP3231442B1 (en) | 2006-06-23 | 2019-12-25 | ADC Therapeutics SA | Polynucleotides and polypeptide sequences involved in cancer |
| KR100679869B1 (ko) * | 2006-10-27 | 2007-02-07 | 한국기계연구원 | Dpf시스템용 플라즈마 반응기와 이를 이용한 입자상물질의 저감 장치 |
| JP2010504330A (ja) | 2006-09-21 | 2010-02-12 | メルク エンド カムパニー インコーポレーテッド | アルツハイマー病治療のためのピペリジンおよびピロリジンベータ−セクレターゼ阻害剤 |
| KR100838645B1 (ko) * | 2006-09-28 | 2008-06-16 | 한국화학연구원 | 베타-세크리테아제 활성을 억제하는 피페리딘 화합물 |
| EP2089383B1 (en) | 2006-11-09 | 2015-09-16 | Probiodrug AG | 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases |
| US9126987B2 (en) | 2006-11-30 | 2015-09-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| EP2481408A3 (en) | 2007-03-01 | 2013-01-09 | Probiodrug AG | New use of glutaminyl cyclase inhibitors |
| WO2008128985A1 (en) | 2007-04-18 | 2008-10-30 | Probiodrug Ag | Thiourea derivatives as glutaminyl cyclase inhibitors |
| KR100894713B1 (ko) * | 2007-10-08 | 2009-04-24 | 한국화학연구원 | 베타-세크리테아제의 활성을 저해하는 아릴피페라진이 치환된 피페리딘 유도체 또는 이의 약제학적으로 허용 가능한 염 및 이를 유효성분으로 함유하는 신경퇴행성 질환의 예방 또는 치료용 조성물 |
| WO2010060186A1 (en) | 2008-11-03 | 2010-06-03 | Alethia Biotherapeutics Inc. | Antibodies that specifically block the biological activity of a tumor antigen |
| CA2772488C (en) | 2009-09-11 | 2018-04-17 | Probiodrug Ag | Heterocyclic derivatives as inhibitors of glutaminyl cyclase |
| JP6026284B2 (ja) | 2010-03-03 | 2016-11-16 | プロビオドルグ エージー | グルタミニルシクラーゼの阻害剤 |
| NZ602312A (en) | 2010-03-10 | 2014-02-28 | Probiodrug Ag | Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5) |
| JP5945532B2 (ja) | 2010-04-21 | 2016-07-05 | プロビオドルグ エージー | グルタミニルシクラーゼの阻害剤としてのベンゾイミダゾール誘導体 |
| EP2686313B1 (en) | 2011-03-16 | 2016-02-03 | Probiodrug AG | Benzimidazole derivatives as inhibitors of glutaminyl cyclase |
| PL3173427T3 (pl) | 2011-03-31 | 2019-11-29 | Adc Therapeutics Sa | Przeciwciała przeciwko antygenowi związanemu z nerkami 1 i ich fragmenty wiążące antygen |
| AU2013209234B2 (en) | 2012-01-09 | 2017-11-09 | Adc Therapeutics Sa | Method for treating breast cancer |
| ES2812698T3 (es) | 2017-09-29 | 2021-03-18 | Probiodrug Ag | Inhibidores de glutaminil ciclasa |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3992441A (en) * | 1972-12-26 | 1976-11-16 | Pfizer Inc. | Sulfamylbenzoic acids |
| US4248876A (en) | 1977-01-08 | 1981-02-03 | John Wyeth & Brother Ltd. | Piperidine derivatives |
| US5142056A (en) | 1989-05-23 | 1992-08-25 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| GB8430581D0 (en) * | 1984-12-04 | 1985-01-09 | Ferrosan As | Treatment |
| 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 |
| GB8714789D0 (en) * | 1987-06-24 | 1987-07-29 | Lundbeck & Co As H | Heterocyclic compounds |
| IE63906B1 (en) * | 1987-11-13 | 1995-06-14 | Novo Nordisk As | Azabicyclic compounds and their preparation and use |
| US4997836A (en) * | 1988-11-11 | 1991-03-05 | Takeda Chemical Industries, Ltd. | Trisubstituted piperazine compounds, their production and use |
| US5708004A (en) | 1990-11-19 | 1998-01-13 | Monsanto Company | Retroviral protease inhibitors |
| ES2123065T3 (es) | 1992-08-25 | 1999-01-01 | Searle & Co | Hidroxietilamino-sulfonamidas utiles como inhibidores de proteasas retroviricas. |
| US5475138A (en) | 1994-07-07 | 1995-12-12 | Pharm-Eco Laboratories Incorporated | Method preparing amino acid-derived diaminopropanols |
| IL123293A (en) * | 1995-09-07 | 2003-06-24 | Hoffmann La Roche | Piperidine derivatives, their preparation and pharmaceutical compositions containing them |
| JP2001510474A (ja) | 1997-02-04 | 2001-07-31 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | カテプシンdのナノモルの非ペプチド阻害剤 |
| AU9740998A (en) * | 1997-09-08 | 1999-03-29 | F. Hoffmann-La Roche Ag | Piperidine derivatives against malaria |
| EP1034174B1 (en) * | 1997-11-05 | 2003-08-13 | Neurosearch A/S | Azaring-ether derivatives and their use as nicotinic ach receptor modulators |
| HUP0101320A3 (en) * | 1998-01-21 | 2002-11-28 | Kyowa Hakko Kogyo Kk | Benzo- and pyridobenzoxepine and -benzazepine derivatives and use thereof |
| GB9810671D0 (en) * | 1998-05-18 | 1998-07-15 | Pfizer Ltd | Anti-pruritic agents |
| BR9912013A (pt) * | 1998-07-10 | 2001-04-10 | Astrazeneca Ab | Composto, composição farmacêutica, método de tratar uma condição de doença, e, processo para preparar um composto |
| US6274735B1 (en) | 1998-08-10 | 2001-08-14 | Hoffmann-La Roche Inc. | Process and intermediates for preparation of substituted piperidines |
| EP1119553A1 (en) * | 1998-10-07 | 2001-08-01 | Georgetown University | Monomeric and dimeric heterocycles, and therapeutic uses thereof |
| GB9904786D0 (en) | 1999-03-02 | 1999-04-28 | Merck Sharp & Dohme | Therapeutic agents |
| WO2002066469A2 (en) * | 2001-02-16 | 2002-08-29 | Aventis Pharmaceuticals Inc. | Novel heterocyclic amide derivatives and their use as dopamine d3 receptor ligands |
| AU2002306848A1 (en) | 2001-03-23 | 2002-10-08 | Elan Pharmaceuticals, Inc. | Methods of treating alzheimer's disease with piperidin derivates |
| AU2002256418A1 (en) * | 2001-04-27 | 2002-11-11 | Vertex Pharmaceuticals Incorporated | Inhibitors of bace |
-
2002
- 2002-11-19 MX MXPA04004772A patent/MXPA04004772A/es not_active Application Discontinuation
- 2002-11-19 HR HR20040550A patent/HRP20040550A2/xx not_active Application Discontinuation
- 2002-11-19 AU AU2002360403A patent/AU2002360403A1/en not_active Abandoned
- 2002-11-19 JP JP2003545624A patent/JP2005514362A/ja active Pending
- 2002-11-19 GE GE5634A patent/GEP20074045B/en unknown
- 2002-11-19 EA EA200400699A patent/EA200400699A1/ru unknown
- 2002-11-19 NZ NZ533158A patent/NZ533158A/en unknown
- 2002-11-19 BR BR0214295-3A patent/BR0214295A/pt not_active IP Right Cessation
- 2002-11-19 KR KR1020047007631A patent/KR20050044533A/ko not_active Withdrawn
- 2002-11-19 US US10/299,746 patent/US7338965B2/en not_active Expired - Fee Related
- 2002-11-19 IL IL16207902A patent/IL162079A0/xx unknown
- 2002-11-19 OA OA1200400289A patent/OA12812A/en unknown
- 2002-11-19 CA CA002467749A patent/CA2467749A1/en not_active Abandoned
- 2002-11-19 WO PCT/US2002/037037 patent/WO2003043987A2/en not_active Ceased
- 2002-11-19 EP EP02795653A patent/EP1448200A2/en not_active Withdrawn
- 2002-11-19 RS YU54204A patent/RS54204A/sr unknown
- 2002-11-19 AP APAP/P/2004/003052A patent/AP2004003052A0/en unknown
-
2004
- 2004-05-19 IS IS7271A patent/IS7271A/is unknown
- 2004-05-19 TN TNP2004000088A patent/TNSN04088A1/en unknown
- 2004-05-26 CO CO04048699A patent/CO5580743A2/es not_active Application Discontinuation
- 2004-06-18 NO NO20042580A patent/NO20042580L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20050044533A (ko) | 2005-05-12 |
| BR0214295A (pt) | 2004-11-09 |
| AU2002360403A1 (en) | 2003-06-10 |
| JP2005514362A (ja) | 2005-05-19 |
| OA12812A (en) | 2006-07-10 |
| AP2004003052A0 (en) | 2004-06-30 |
| US7338965B2 (en) | 2008-03-04 |
| CA2467749A1 (en) | 2003-05-30 |
| NZ533158A (en) | 2006-09-29 |
| MXPA04004772A (es) | 2005-06-06 |
| WO2003043987A3 (en) | 2003-07-10 |
| IL162079A0 (en) | 2005-11-20 |
| NO20042580L (no) | 2004-08-09 |
| EP1448200A2 (en) | 2004-08-25 |
| HRP20040550A2 (en) | 2006-11-30 |
| US20040034031A1 (en) | 2004-02-19 |
| GEP20074045B (en) | 2007-02-26 |
| WO2003043987A2 (en) | 2003-05-30 |
| TNSN04088A1 (en) | 2006-06-01 |
| IS7271A (is) | 2004-05-19 |
| EA200400699A1 (ru) | 2004-12-30 |
| RS54204A (sr) | 2006-12-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CO5580743A2 (es) | Piperidinas y piperazinas 3,4-disustituidas, 3,5- disustituidas y 3,4,5-sustituidas | |
| CO5550472A2 (es) | Piperazinas heterociclicas sustituidas para el tratamiento de la esquizofrenia | |
| PE20221277A1 (es) | Inhibidores de ras | |
| CO5640093A2 (es) | Derivados n-n` sustituidos de 1.3 diamino-2-hidroxipropano | |
| CO5640095A2 (es) | Hidroxietilaminas sustituidas | |
| KR100481124B1 (ko) | 폴리히드록시알카노에이트의 제조에 이용되는 미생물 | |
| ES2175919T3 (es) | Derivados del camptothecin con actividad antitumoral. | |
| KR870007116A (ko) | 인돌 유도체의 제조방법 | |
| HUP0300138A2 (en) | Cyclic amine derivatives as ccr5 antagonists, their production and use and pharmaceutical compositions containing them | |
| DK0610134T3 (da) | Indolderivater som 5-HT,1-lignende agonister | |
| CO5540299A2 (es) | Derivados de tiazol u oxazol que son utiles en el tratamiento de enfermedades cardiovasculares y relacionadas | |
| ATE202702T1 (de) | Verwendung von oestrogenagonisten und - antagonisten zur herstellung eines medikaments zur behandlung von atherosklerose, unabhängig von lipidsenkung | |
| ECSP077215A (es) | Derivados de n-(1h-indolil)-1h-indol-2-carboxamidas, su preparación y su aplicación en terapéutica | |
| HUP9904167A2 (hu) | 1,4-Diszubsztituált piperazin- és piperidinszármazékok, alkalmazásuk és az ezeket tartalmazó gyógyszerkészítmények | |
| JP2005504729A5 (es) | ||
| WO2004000762A3 (en) | Propionic acid derivatives and their use as hppars activators | |
| CO4930274A1 (es) | Tiazol bencenosulfonamidas como agonistas b3 para el trata- miento de la diabetes y la obesidad | |
| CO5690582A2 (es) | Derivados de n-tiazol-2-il-benzamida | |
| CY1108148T1 (el) | Αβερμεκτινης- και μονοσακχαριτη αβερμεκτινης παραγωγα υποκατεστημενα στην 4''- ή 4'- θεση που εχουν ζιζανιοκτονες ιδιοτητες | |
| KR860001074A (ko) | 생물학적으로 활성인 질소함유 헤테로시클릭 화합물의 제조방법 | |
| HUP0400772A2 (hu) | Eljárás piperazinszármazékok mezilátjainak előállítására és ezen vegyületek | |
| PT90912A (pt) | Processo para a preparacao de derivados de tiofenol | |
| AR039122A1 (es) | Derivados de ftalimido como inhibidores de monoamino oxidasa b | |
| ATE182589T1 (de) | Verfahren zur herstellung von benzyliden- derivaten | |
| AR018632A1 (es) | Compuestos derivados de acido 1,2,3,4-tetrahidroquinolin-2-carboxilico, su uso en la fabricacion de medicamentos, composicion farmaceutica que los contiene, proceso para su preparacion. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Application refused |