AR064921A1 - Pirazol-amidas sustituidas antagonistas de receptores alfa 7 nicotinicos de acetilcolina,composiciones farmaceuticas que las contienen y usos para el tratamiento de enfermedades neurologicas,psiquiatricas e inflamatorias. - Google Patents
Pirazol-amidas sustituidas antagonistas de receptores alfa 7 nicotinicos de acetilcolina,composiciones farmaceuticas que las contienen y usos para el tratamiento de enfermedades neurologicas,psiquiatricas e inflamatorias.Info
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- AR064921A1 AR064921A1 ARP080100189A ARP080100189A AR064921A1 AR 064921 A1 AR064921 A1 AR 064921A1 AR P080100189 A ARP080100189 A AR P080100189A AR P080100189 A ARP080100189 A AR P080100189A AR 064921 A1 AR064921 A1 AR 064921A1
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- 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
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61P25/00—Drugs for disorders of the nervous system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
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- 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
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- 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
- C07D231/14—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 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
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
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- 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
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- 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
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- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
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- 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
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- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
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- Organic Chemistry (AREA)
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- General Chemical & Material Sciences (AREA)
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- Neurology (AREA)
- Neurosurgery (AREA)
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- Toxicology (AREA)
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- Hospice & Palliative Care (AREA)
- Gynecology & Obstetrics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicacion 1: Un compuesto de la formula (1), en donde T es un alcano C3-5-alfa,omega-diilo o alqueno-alfa,omega-diilo, que opcionalmente porta un grupo oxo y se sustituye opcionalmente con uno o más halogenos; grupos hidroxi; grupos alquilo C1- 5, alcoxi, fluoralquilo, hidroxialquilo, alquilideno, fluoralquilideno, grupos cicloalcano C3-6-1,1-diilo, oxacicloalcano-1,1-diilo; grupos cicloalcano C3-6-1,2-diilo, oxacicloalcano-1,2-diilo, en donde los enlaces del radical 1,2-diilo forman un anillo fusionado con la cadena T; y con la condicion de que cuando T porta un grupo oxo, éste no es parte de un enlace amida; Z es CH2, N, O, S, S(=O), o S(=O)2; q y q' son, independientemente uno del otro, numero enteros de 1 a 4; p es 0, 1 , o 2; R', independientemente uno del otro para p = 2, se selecciona del grupo compuesto por mono- o di-[alquilo C1-6 lineal, ramificado o cíclico]aminocarbonilo; alquilo C1-6 lineal, ramificado o cíclico, alcoxi, acilo; Q es un grupo de la formula (2)- (3); Rö es alquilo C1-3; j es 0 o 1; R es un anillo aromático o heteroaromático de 5 a 10 miembros; m es 0, 1, 2 o 3; Y representa, independientemente uno del otro cuando m es superior a 1 halogeno; hidroxi; mercapto; ciano; nitro; amino; alquilo C1- 6 lineal, ramificado o cíclico, trihaloalquilo, di- o trihaloalcoxi, alcoxi, o alquilcarbonilo; cicloalquilo C3-6-alcoxi C1-6; cicloalquilo C3-6-alquilo C1-6; alquilcarbonilamino C1-6 lineal, ramificado o cíclico; mono- o di-alquilaminocarbonilo C1- 6 lineal, ramificado o cíclico; carbamoilo; alquilsulfonilamino C1-6 lineal, ramificado o cíclico; alquilsulfonilo C1-6 lineal, ramificado o cíclico; mono- o di-alquilsulfamoilo C1-6 lineal, ramificado o cíclico; alcoxi C1-6-alquilo C1-6 lineal, ramificado o cíclico; o cuando m=2, dos sustituyentes Y junto con los átomos del grupo R al que están unidos, pueden formar un anillo; sales, isomeros, diastomeros, mezclas racémicas y composiciones isotopicas de los mismos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US88062907P | 2007-01-16 | 2007-01-16 |
Publications (1)
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AR064921A1 true AR064921A1 (es) | 2009-05-06 |
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ARP080100189A AR064921A1 (es) | 2007-01-16 | 2008-01-16 | Pirazol-amidas sustituidas antagonistas de receptores alfa 7 nicotinicos de acetilcolina,composiciones farmaceuticas que las contienen y usos para el tratamiento de enfermedades neurologicas,psiquiatricas e inflamatorias. |
Country Status (25)
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US (1) | US8163729B2 (es) |
EP (1) | EP2118067B1 (es) |
JP (1) | JP2010515770A (es) |
KR (1) | KR20090116707A (es) |
CN (1) | CN101679287B (es) |
AR (1) | AR064921A1 (es) |
AU (1) | AU2008206759B2 (es) |
BR (1) | BRPI0806665A2 (es) |
CA (1) | CA2675676A1 (es) |
CL (1) | CL2008000119A1 (es) |
CO (1) | CO6351782A2 (es) |
CR (1) | CR10930A (es) |
EA (1) | EA016948B1 (es) |
EC (1) | ECSP099490A (es) |
HK (1) | HK1142335A1 (es) |
IL (1) | IL199889A0 (es) |
MX (1) | MX2009007615A (es) |
NZ (1) | NZ578411A (es) |
PA (1) | PA8766201A1 (es) |
SA (1) | SA08290018B1 (es) |
SV (1) | SV2009003334A (es) |
TW (1) | TW200901974A (es) |
UA (1) | UA98317C2 (es) |
WO (1) | WO2008087529A1 (es) |
ZA (1) | ZA200904943B (es) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CL2008000119A1 (es) | 2007-01-16 | 2008-05-16 | Wyeth Corp | Compuestos derivados de pirazol, antagonistas del receptor nicotinico de acetilcolina; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como demencia senil, alzheimer y esquizofrenia. |
WO2009091832A1 (en) * | 2008-01-14 | 2009-07-23 | Wyeth | Synthesis of pyrazoles |
US20090181952A1 (en) * | 2008-01-14 | 2009-07-16 | Wyeth | Compounds useful as alpha7 nicotinic acetylcholine receptor agonists |
US20090181953A1 (en) * | 2008-01-14 | 2009-07-16 | Wyeth | Compound forms and uses thereof |
TW201004941A (en) * | 2008-07-16 | 2010-02-01 | Wyeth Corp | Alpha7 nicotinic acetylcholine receptor inhibitors |
MX2011001887A (es) | 2008-08-22 | 2011-04-04 | Baxter Int | Derivados de bencil carbonato polimericos. |
CA2754180A1 (en) * | 2009-03-09 | 2010-09-16 | The Regents Of The University Of California | Substituted heterocycles and their use as allosteric modulators of nicotinic and gabaa receptors |
US20120157464A1 (en) * | 2009-07-23 | 2012-06-21 | Novartis Ag | Use of azabicycloalkyl derivatives or pyrrolidine-2-one derivatives for the treatment or prevention of ataxia |
TWI558398B (zh) | 2009-09-22 | 2016-11-21 | 諾華公司 | 菸鹼乙醯膽鹼受體α7活化劑之用途 |
MX355782B (es) * | 2010-11-03 | 2018-04-30 | Dow Agrosciences Llc | Composiciones pesticidas y procesos relacionados a las mismas. |
WO2012068553A2 (en) * | 2010-11-18 | 2012-05-24 | Dignity Health | Methods of diagnosing and treating neurodegenerative diseases |
EP2905279A4 (en) * | 2012-10-02 | 2016-04-20 | Sumitomo Dainippon Pharma Co Ltd | imidazole |
CN105254564A (zh) * | 2015-10-31 | 2016-01-20 | 丁玉琴 | 一种2-甲基-3,4-二硝基-5-(甲氧苯基)吡唑的合成方法 |
CN105646358B (zh) * | 2016-03-01 | 2018-03-09 | 苏州艾缇克药物化学有限公司 | 一种3‑氨基‑5‑(4‑甲氧苯基)吡唑的合成方法 |
CN112457255B (zh) * | 2017-11-08 | 2022-08-19 | 北京嘉林药业股份有限公司 | 化合物及其治疗癌症的用途 |
TWI805699B (zh) | 2018-03-01 | 2023-06-21 | 日商日本煙草產業股份有限公司 | 甲基內醯胺環化合物及其用途 |
WO2019194207A1 (ja) | 2018-04-04 | 2019-10-10 | 日本たばこ産業株式会社 | ヘテロアリールで置換されたピラゾール化合物及びその医薬用途 |
GB202006382D0 (en) | 2020-04-30 | 2020-06-17 | Spermatech As | Use |
CN113925606B (zh) * | 2021-10-25 | 2023-07-07 | 四川大学华西医院 | 一种神经调控导航定位方法、装置和神经调控治疗系统 |
Family Cites Families (100)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU167263B (es) * | 1973-02-12 | 1975-09-27 | ||
DE2527677A1 (de) * | 1975-06-21 | 1977-01-20 | Bayer Ag | Verfahren zur herstellung von 2,4- dioxo-1,2,3,4-tetrahydro-s-triazino- eckige klammer auf 1,2-a eckige klammer zu -benzimidazolen |
US4665183A (en) | 1985-12-20 | 1987-05-12 | American Home Products Corp. | Process for preparing 6,7,8,9-tetrahydro-10-methylpyrido[1,2-a]indol-9-amines and derivatives thereof useful for the treatment of cognitive impairments |
US4624954A (en) | 1985-12-20 | 1986-11-25 | American Home Products Corporation | 6,7,8,9-tetrahydro-10-methylpyrido[1,2-a]indol-9-amines and derivatives thereof, useful for the treatment of cognitive impairments |
US5219857A (en) | 1986-10-16 | 1993-06-15 | American Cyanamid Company | Method of treating cognitive and related neural behavioral problems |
US4904658A (en) * | 1988-04-15 | 1990-02-27 | American Cyanamid Company | Substituted-6H,8H-pyrimido-[1,2,3-cd]purine-8,10-(9H)-diones and substituted-6H,10H-pyrimido[1,2-cd]purin-10-ones |
US5260331A (en) | 1989-01-02 | 1993-11-09 | John Wyeth & Brother Limited | Composition for treating depression with (S- or O-heteroaryl)alkyl amines |
US5422355A (en) * | 1989-06-02 | 1995-06-06 | John Wyeth & Brother, Limited | Composition for treating depression with (N-heteroaryl)alkylamines |
FR2655988B1 (fr) | 1989-12-20 | 1994-05-20 | Adir Cie | Nouveaux derives de la napht-1-yl piperazine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
IE911774A1 (en) | 1990-06-11 | 1991-12-18 | Akzo Nv | Pyridinylpiperazine derivatives |
AU645681B2 (en) * | 1991-05-02 | 1994-01-20 | John Wyeth & Brother Limited | Piperazine derivatives |
GB9125615D0 (en) * | 1991-12-02 | 1992-01-29 | Wyeth John & Brother Ltd | Amines |
CA2126976A1 (en) | 1991-12-31 | 1993-07-08 | Hisashi Takasugi | Oxadiazole derivatives having acetylcholinesterase-inhibitory and muscarinic agonist activity |
JPH0616638A (ja) | 1992-03-30 | 1994-01-25 | Yoshitomi Pharmaceut Ind Ltd | ピリジン化合物およびその医薬用途 |
ATE253909T1 (de) | 1992-07-24 | 2003-11-15 | Univ California | Arzneimittel die den durch ampa rezeptoren vermittelten synaptischen response erhöhen |
TW336932B (en) | 1992-12-17 | 1998-07-21 | Pfizer | Amino-substituted pyrazoles |
TW370529B (en) | 1992-12-17 | 1999-09-21 | Pfizer | Pyrazolopyrimidines |
KR0170567B1 (ko) | 1992-12-17 | 1999-02-18 | 알렌 제이. 스피겔 | 부신피질자극호르몬-유리 인자 길항물질 활성을 갖는 피라졸 및 피라졸로피리미딘 |
DK0674641T3 (da) | 1992-12-17 | 1999-09-27 | Pfizer | Pyrrolopyrimidiner som CRF-antagonister |
EP0959074A3 (en) | 1992-12-17 | 2000-06-07 | Pfizer Inc. | Substituted pyrazoles as CRF antagonists |
GB9302622D0 (en) | 1993-02-10 | 1993-03-24 | Wellcome Found | Heteroaromatic compounds |
KR100327270B1 (ko) | 1994-01-14 | 2002-08-01 | 닛뽕쇼지가부시끼가이샤 | 디아자시클로알킨알킬술폰아미드유도체 |
JP3319651B2 (ja) * | 1994-04-26 | 2002-09-03 | 富士写真フイルム株式会社 | 感光性転写シート |
US5650409A (en) | 1995-06-02 | 1997-07-22 | Cortex Pharmaceuticals, Inc. | Benzoyl piperidines/pyrrolidines for enhancing synaptic response |
GB9514901D0 (en) | 1995-07-20 | 1995-09-20 | American Home Prod | Piperazine derivatives |
US6288091B1 (en) * | 1995-12-29 | 2001-09-11 | Boehringer Ingelheim Ltd. | Antiherpes virus compounds and methods for their preparation and use |
SE9600683D0 (sv) | 1996-02-23 | 1996-02-23 | Astra Ab | Azabicyclic esters of carbamic acids useful in therapy |
US5736543A (en) | 1996-04-03 | 1998-04-07 | The Regents Of The University Of California | Benzoxazines for enhancing synaptic response |
PL329803A1 (en) | 1996-05-11 | 1999-04-12 | Smithkline Beecham Plc | Derivatives of tetrahydroisoquinoline as modulators od dopamine d receptors |
GB9708694D0 (en) | 1997-04-30 | 1997-06-18 | Smithkline Beecham Plc | Compounds |
GB9708805D0 (en) | 1997-05-01 | 1997-06-25 | Smithkline Beecham Plc | Compounds |
US6329368B1 (en) | 1997-05-09 | 2001-12-11 | The Regents Of The University Of California | Endocrine modulation with positive modulators of AMPA type glutamate receptors |
KR100247563B1 (ko) | 1997-07-16 | 2000-04-01 | 박영구 | 키랄3,4-에폭시부티르산및이의염의제조방법 |
EP1007523B9 (en) * | 1997-07-25 | 2004-09-08 | H. Lundbeck A/S | Indole and 2,3-dihydroindole derivatives, their preparation and use |
US6632823B1 (en) | 1997-12-22 | 2003-10-14 | Merck & Co., Inc. | Substituted pyridine compounds useful as modulators of acetylcholine receptors |
ZA991301B (en) | 1998-02-18 | 1999-09-13 | Neurosearch As | Glutamate receptor modulators. |
JP2002509918A (ja) | 1998-03-31 | 2002-04-02 | アケイディア ファーマスーティカルズ インコーポレイテッド | ムスカリン性レセプタに活性を有する化合物 |
US6124278A (en) | 1998-04-03 | 2000-09-26 | The Regents Of The University Of California | Acylbenzoxazines for enhancing synaptic response |
DE69913520T2 (de) | 1998-06-01 | 2004-11-25 | Ortho-Mcneil Pharmaceutical, Inc. | Tetrahydronaphtalene verbindungen und deren verwendung zur behandlung von neurodegenerativen krankheiten |
US6605623B1 (en) * | 1998-12-18 | 2003-08-12 | Bristol-Myers Squibb Pharma Co. | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
US6313126B1 (en) | 1999-01-07 | 2001-11-06 | American Home Products Corp | Arylpiperazinyl-cyclohexyl indole derivatives for the treatment of depression |
SE9900100D0 (sv) | 1999-01-15 | 1999-01-15 | Astra Ab | New compounds |
AU3076700A (en) | 1999-01-26 | 2000-08-18 | Ono Pharmaceutical Co. Ltd. | 2h-phthalazin-1-one derivatives and drugs comprising these derivatives as the active ingredient |
US20010044445A1 (en) * | 1999-04-08 | 2001-11-22 | Bamaung Nwe Y. | Azole inhibitors of cytokine production |
US6387900B1 (en) | 1999-08-12 | 2002-05-14 | Pharmacia & Upjohn S.P.A. | 3(5)-ureido-pyrazole derivatives process for their preparation and their use as antitumor agents |
EP1237849A1 (en) | 1999-11-05 | 2002-09-11 | University College London | Activators of soluble guanylate cyclase |
SE9904176D0 (sv) | 1999-11-18 | 1999-11-18 | Astra Ab | New use |
CN1422262A (zh) * | 2000-02-07 | 2003-06-04 | 艾博特股份有限两合公司 | 2-苯并噻唑基脲衍生物及其作为蛋白激酶抑制剂的应用 |
ATE361297T1 (de) | 2000-03-31 | 2007-05-15 | Ortho Mcneil Pharm Inc | Phenyl-substituierte imidazopyridine |
ES2325477T3 (es) | 2000-03-31 | 2009-09-07 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indoles sustituidos por fenilo como antagonistas del receptor de histamina h3. |
CA2405089A1 (en) | 2000-04-10 | 2001-10-18 | Pfizer Products Inc. | Benzoamide piperidine containing compounds and related compounds |
US6448276B1 (en) | 2000-05-17 | 2002-09-10 | Inspire Pharmaceuticals, Inc. | Method for treating vaginal dryness with nicotinic acetylcholine receptor agonists |
WO2001098268A2 (en) | 2000-06-21 | 2001-12-27 | Bristol-Myers Squibb Pharma Company | Piperidine amides as modulators of chemokine receptor activity |
JP2002030073A (ja) | 2000-07-19 | 2002-01-29 | Ono Pharmaceut Co Ltd | 4−(3−(4−モルホリノブチリルアミノ)フェニル)−2h−フタラジン−1−オン・メタンスルホン酸塩・1水和物およびその製造方法。 |
US7211594B2 (en) * | 2000-07-31 | 2007-05-01 | Signal Pharmaceuticals, Llc | Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith |
US20020173507A1 (en) | 2000-08-15 | 2002-11-21 | Vincent Santora | Urea compounds and methods of uses |
IL145209A0 (en) | 2000-09-06 | 2002-06-30 | Pfizer Prod Inc | Pharmaceutical combinations for the treatment of stroke and traumatic brain injury |
JP2004509891A (ja) | 2000-09-22 | 2004-04-02 | スミスクライン ビーチャム パブリック リミテッド カンパニー | 抗糖尿病薬としてのピラゾロピリジンおよびピラゾロピリダジン |
US6469007B2 (en) * | 2000-11-28 | 2002-10-22 | Wyeth | Serotonergic agents |
UA73619C2 (en) | 2000-12-13 | 2005-08-15 | Pfizer Prod Inc | Stable pharmaceutical compositions of nmda receptor agonist (variants) and method of treatment |
KR100869061B1 (ko) * | 2000-12-13 | 2008-11-17 | 와이어쓰 | 베타 아밀로이드 생성의 헤테로고리 술폰아미드 저해제 |
DE60216753T2 (de) | 2001-02-16 | 2008-01-03 | Aventis Pharmaceuticals Inc. | Heterocyclische harnstoffderivate und deren verwendung als dopamine d3 receptor liganden |
DE60208157T2 (de) | 2001-02-16 | 2006-08-10 | Aventis Pharmaceuticals Inc. | Heterocyclische substituierte carbonyl derivate und ihre verwendung als dopamin d3 rezeptor liganden |
HUP0103986A2 (hu) | 2001-09-28 | 2003-06-28 | Richter Gedeon Vegyészeti Gyár Rt. | Új karbonsavamid szerkezetet tartalmazó piperidinil vegyületek, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények |
HUP0103987A3 (en) | 2001-09-28 | 2004-11-29 | Richter Gedeon Vegyeszet | Phenylpiperazinylalkyl carboxylic acid amid derivatives, process for their preparation, pharmaceutical compositions containing them and their intermediates |
KR100579813B1 (ko) | 2001-10-16 | 2006-05-12 | 주식회사 에스티씨나라 | 피페리딘 유도체, 이의 제조방법 및 이를 포함하는 치매치료용 약학적 조성물 |
WO2003070707A1 (fr) * | 2002-02-19 | 2003-08-28 | Ono Pharmaceutical Co., Ltd. | Composes condenses derives de la pyridazine et medicaments contenant lesdits composes comme ingredients actifs |
DE10211415A1 (de) | 2002-03-15 | 2003-09-25 | Bayer Ag | Bicyclische N-Biarylamide |
UA78999C2 (en) | 2002-06-04 | 2007-05-10 | Wyeth Corp | 1-(aminoalkyl)-3-sulfonylazaindoles as ligands of 5-hydroxytryptamine-6 |
UA77814C2 (en) | 2002-07-03 | 2007-01-15 | Lundbeck & Co As H | Spirocyclic piperidines as antagonists of mch1 and use thereof |
AU2003251828A1 (en) * | 2002-07-12 | 2004-02-02 | Janssen Pharmaceutica N.V. | Naphthol, quinoline and isoquinoline-derivatives as modulators of vanilloid vr1 receptor |
GB0216233D0 (en) | 2002-07-12 | 2002-08-21 | Glaxo Group Ltd | Compounds |
TW200401641A (en) | 2002-07-18 | 2004-02-01 | Wyeth Corp | 1-Heterocyclylalkyl-3-sulfonylindole or-indazole derivatives as 5-hydroxytryptamine-6 ligands |
WO2004013137A1 (en) | 2002-08-01 | 2004-02-12 | Pharmacia & Upjohn Company Llc | 1h-pyrazole and 1h-pyrrole-azabicyclic compounds with alfa-7 nachr activity |
AU2003269413A1 (en) | 2002-11-01 | 2004-05-25 | Pharmacia & Upjohn Company Llc | Nicotinic acetylcholine agonists in the treatment of glaucoma and retinal neuropathy |
US7157460B2 (en) * | 2003-02-20 | 2007-01-02 | Sugen Inc. | Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors |
US7186832B2 (en) * | 2003-02-20 | 2007-03-06 | Sugen Inc. | Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors |
TWI334868B (en) * | 2003-06-03 | 2010-12-21 | Nippon Kayaku Kk | [1,2,4] triazoro [1,5-a] pyrimidine-2-ylurea derivative and use thereof |
DE602004008474T2 (de) * | 2003-07-31 | 2008-05-15 | Wyeth | N-sulfonylheterocyclopyrrolylalkylamin-verbindungen als 5-hydroxytryptamin-6-liganden. |
EP1694686A1 (en) | 2003-12-19 | 2006-08-30 | Takeda San Diego, Inc. | Kinase inhibitors |
JP2007520525A (ja) | 2004-02-04 | 2007-07-26 | ノイロサーチ アクティーゼルスカブ | 二量体のアザ環式化合物及びその使用 |
WO2005084673A1 (en) * | 2004-03-02 | 2005-09-15 | Wyeth | Non-immunosuppressive immunophilin ligands as neuroprotective and/or neuroregenerative agents |
EP1720886A1 (en) * | 2004-03-02 | 2006-11-15 | Wyeth | Macrolides and methods for producing same |
ATE444962T1 (de) * | 2004-06-16 | 2009-10-15 | Wyeth Corp | Amino-5,5-diphenylimidazolon-derivate zur beta- sekretase-hemmung |
MXPA06014792A (es) | 2004-06-16 | 2007-02-16 | Wyeth Corp | Difenilimidazopirimidina y aminas imidazol como inhibidores de ??-secretasa. |
JP2008506744A (ja) * | 2004-07-20 | 2008-03-06 | シエナ ビオテク ソシエタ ペル アチオニ | α7ニコチン性アセチルコリン受容体の調節物質およびそれらの治療への使用 |
AU2005277203A1 (en) | 2004-08-20 | 2006-03-02 | Entremed, Inc. | Compositions and methods comprising proteinase activated receptor antagonists |
JP5475235B2 (ja) | 2005-01-21 | 2014-04-16 | アステックス・セラピューティクス・リミテッド | 医薬化合物 |
EP1853573A1 (en) | 2005-02-25 | 2007-11-14 | Rigel Pharmaceuticals, Inc. | Benzisothiazoles useful for treating or preventing hcv infection |
EP1949102A2 (en) * | 2005-11-15 | 2008-07-30 | Inverness Medical Switzerland GmbH | Assays |
BRPI0706610A2 (pt) * | 2006-01-18 | 2011-04-05 | Siena Biotech Spa | moduladores de receptores alfa 7 nicotìnico acetilcolina e usos terapêuticos destes |
CL2008000119A1 (es) | 2007-01-16 | 2008-05-16 | Wyeth Corp | Compuestos derivados de pirazol, antagonistas del receptor nicotinico de acetilcolina; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como demencia senil, alzheimer y esquizofrenia. |
GB0723815D0 (en) | 2007-12-05 | 2008-01-16 | Glaxo Group Ltd | Compounds |
US20090181953A1 (en) * | 2008-01-14 | 2009-07-16 | Wyeth | Compound forms and uses thereof |
US20090181952A1 (en) | 2008-01-14 | 2009-07-16 | Wyeth | Compounds useful as alpha7 nicotinic acetylcholine receptor agonists |
WO2009091832A1 (en) | 2008-01-14 | 2009-07-23 | Wyeth | Synthesis of pyrazoles |
US20100016343A1 (en) * | 2008-07-16 | 2010-01-21 | Wyeth | Alpha7 nicotinic acetylcholine receptor inhibitors |
US20100016360A1 (en) * | 2008-07-16 | 2010-01-21 | Wyeth | Alpha7 nicotinic acetylcholine receptor inhibitors |
TW201004941A (en) * | 2008-07-16 | 2010-02-01 | Wyeth Corp | Alpha7 nicotinic acetylcholine receptor inhibitors |
US20100016598A1 (en) * | 2008-07-16 | 2010-01-21 | Wyeth | Alpha7 nicotinic acetylcholine receptor inhibitors |
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- 2008-01-15 CL CL200800119A patent/CL2008000119A1/es unknown
- 2008-01-15 TW TW097101453A patent/TW200901974A/zh unknown
- 2008-01-16 EA EA200900831A patent/EA016948B1/ru not_active IP Right Cessation
- 2008-01-16 KR KR1020097014828A patent/KR20090116707A/ko not_active Application Discontinuation
- 2008-01-16 ZA ZA200904943A patent/ZA200904943B/xx unknown
- 2008-01-16 WO PCT/IB2008/000090 patent/WO2008087529A1/en active Application Filing
- 2008-01-16 BR BRPI0806665-5A patent/BRPI0806665A2/pt not_active IP Right Cessation
- 2008-01-16 CN CN200880008464XA patent/CN101679287B/zh not_active Expired - Fee Related
- 2008-01-16 JP JP2009546013A patent/JP2010515770A/ja active Pending
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- 2008-01-16 MX MX2009007615A patent/MX2009007615A/es active IP Right Grant
- 2008-01-16 AR ARP080100189A patent/AR064921A1/es not_active Application Discontinuation
- 2008-01-16 NZ NZ578411A patent/NZ578411A/en not_active IP Right Cessation
- 2008-01-16 UA UAA200907422A patent/UA98317C2/ru unknown
- 2008-01-16 CA CA002675676A patent/CA2675676A1/en not_active Abandoned
- 2008-01-16 EP EP08702252.1A patent/EP2118067B1/en active Active
- 2008-01-16 SA SA08290018A patent/SA08290018B1/ar unknown
- 2008-01-16 AU AU2008206759A patent/AU2008206759B2/en not_active Ceased
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Also Published As
Publication number | Publication date |
---|---|
JP2010515770A (ja) | 2010-05-13 |
MX2009007615A (es) | 2009-07-27 |
SA08290018B1 (ar) | 2013-01-17 |
CO6351782A2 (es) | 2011-12-20 |
US20100029606A1 (en) | 2010-02-04 |
CR10930A (es) | 2013-02-12 |
HK1142335A1 (en) | 2010-12-03 |
EP2118067A1 (en) | 2009-11-18 |
BRPI0806665A2 (pt) | 2011-09-06 |
TW200901974A (en) | 2009-01-16 |
KR20090116707A (ko) | 2009-11-11 |
EA016948B1 (ru) | 2012-08-30 |
UA98317C2 (ru) | 2012-05-10 |
AU2008206759A1 (en) | 2008-07-24 |
EP2118067B1 (en) | 2013-05-08 |
AU2008206759B2 (en) | 2013-09-05 |
CA2675676A1 (en) | 2008-07-24 |
IL199889A0 (en) | 2010-04-15 |
CN101679287A (zh) | 2010-03-24 |
ECSP099490A (es) | 2009-09-29 |
EA200900831A1 (ru) | 2010-02-26 |
US8163729B2 (en) | 2012-04-24 |
CN101679287B (zh) | 2013-03-27 |
NZ578411A (en) | 2011-06-30 |
WO2008087529A1 (en) | 2008-07-24 |
ZA200904943B (en) | 2010-09-29 |
SV2009003334A (es) | 2010-08-09 |
PA8766201A1 (es) | 2008-11-19 |
CL2008000119A1 (es) | 2008-05-16 |
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