UY31063A1 - Derivados de n-[6-amino-5-aril-piridin -2-il]-carboxamida, composiciones conteniéndolos, procedimientos de preparación, itermedios utilizados en la preparación y aplicaciones. - Google Patents
Derivados de n-[6-amino-5-aril-piridin -2-il]-carboxamida, composiciones conteniéndolos, procedimientos de preparación, itermedios utilizados en la preparación y aplicaciones.Info
- Publication number
- UY31063A1 UY31063A1 UY31063A UY31063A UY31063A1 UY 31063 A1 UY31063 A1 UY 31063A1 UY 31063 A UY31063 A UY 31063A UY 31063 A UY31063 A UY 31063A UY 31063 A1 UY31063 A1 UY 31063A1
- Authority
- UY
- Uruguay
- Prior art keywords
- preparation
- compositions containing
- piridin
- aril
- carboxamide
- Prior art date
Links
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
- C07D401/12—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
-
- 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
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La presente invención se refiere a compuestos de la fórmula (I): y sus sales y solvatos farmacéuticamente aceptables, a procedimientos para la preparación de, intermedios usados en la preparación de, y composiciones que contienen tales compuestos y los usos de tales compuestos para el tratamiento del dolor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US91574507P | 2007-05-03 | 2007-05-03 | |
US95753607P | 2007-08-23 | 2007-08-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY31063A1 true UY31063A1 (es) | 2009-01-05 |
Family
ID=39855225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY31063A UY31063A1 (es) | 2007-05-03 | 2008-04-30 | Derivados de n-[6-amino-5-aril-piridin -2-il]-carboxamida, composiciones conteniéndolos, procedimientos de preparación, itermedios utilizados en la preparación y aplicaciones. |
Country Status (33)
Country | Link |
---|---|
US (1) | US8134007B2 (es) |
EP (1) | EP2183241B1 (es) |
JP (1) | JP4657384B2 (es) |
KR (1) | KR20100007956A (es) |
CN (1) | CN101675040A (es) |
AP (1) | AP2516A (es) |
AR (1) | AR070636A1 (es) |
AU (1) | AU2008247102B2 (es) |
BR (1) | BRPI0810202A2 (es) |
CA (1) | CA2684105C (es) |
CL (1) | CL2008001268A1 (es) |
CO (1) | CO6251367A2 (es) |
CR (1) | CR11061A (es) |
CU (1) | CU23846B1 (es) |
DO (1) | DOP2009000254A (es) |
EA (1) | EA015952B1 (es) |
EC (1) | ECSP099710A (es) |
ES (1) | ES2398606T3 (es) |
GE (1) | GEP20125379B (es) |
GT (1) | GT200900280A (es) |
IL (1) | IL201569A0 (es) |
MA (1) | MA31419B1 (es) |
MX (1) | MX2009011816A (es) |
NI (1) | NI200900192A (es) |
NZ (1) | NZ581614A (es) |
PA (1) | PA8779201A1 (es) |
PE (1) | PE20090730A1 (es) |
SV (1) | SV2009003400A (es) |
TN (1) | TN2009000450A1 (es) |
TW (1) | TWI375675B (es) |
UY (1) | UY31063A1 (es) |
WO (1) | WO2008135826A2 (es) |
ZA (1) | ZA200907609B (es) |
Families Citing this family (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT2767537T (pt) | 2008-08-06 | 2017-07-17 | Medivation Technologies Inc | Inibidores de di-hidropiridoftalazinona de poli(adp-ribose)polimerase (parp) |
CA2747419C (en) | 2009-01-12 | 2014-07-08 | Icagen, Inc. | Sulfonamide derivatives |
CN101638352B (zh) * | 2009-08-14 | 2011-08-31 | 大连理工大学 | 一种芳基取代的氮杂环化合物的制备方法 |
WO2011077313A1 (en) | 2009-12-22 | 2011-06-30 | Pfizer Inc. | Piperidinecarboxamides as mpges - 1 inhibitors |
TW201139406A (en) * | 2010-01-14 | 2011-11-16 | Glaxo Group Ltd | Voltage-gated sodium channel blockers |
CN101768036B (zh) * | 2010-01-23 | 2013-05-08 | 大连理工大学 | 一种在醇溶剂中制备芳基取代的氮杂芳环化合物的方法 |
CN102869258A (zh) | 2010-02-03 | 2013-01-09 | 生物马林药物股份有限公司 | 用于pten基因缺失相关疾病的治疗的聚(adp-核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂 |
RU2561732C2 (ru) | 2010-02-08 | 2015-09-10 | Байомарин Фармасьютикал Инк. | Способы синтеза производных дигидропиридофталазинона |
WO2011104649A1 (en) | 2010-02-25 | 2011-09-01 | Pfizer Limited | Peptide analogues |
CA2803118C (en) | 2010-07-09 | 2015-11-03 | Pfizer Limited | Sulfonamide derivatives as nav 1.7 inhibitors |
ES2533065T3 (es) | 2010-07-09 | 2015-04-07 | Pfizer Limited | Bencenosulfonamidas útiles como inhibidores de los canales de sodio |
ES2526981T3 (es) | 2010-07-12 | 2015-01-19 | Pfizer Limited | N-sulfonilbenzamidas como inhibidores de canales de sodio dependientes de voltaje |
CA2801032A1 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | N-sulfonylbenzamide derivatives useful as voltage gated sodium channel inhibitors |
WO2012007877A2 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Chemical compounds |
CA2804877A1 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Sulfonamide derivatives as nav1.7 inhibitors for the treatment of pain |
US9096500B2 (en) | 2010-07-12 | 2015-08-04 | Pfizer Limited | Acyl sulfonamide compounds |
WO2012007836A1 (en) | 2010-07-16 | 2012-01-19 | Purdue Pharma .Lp. | Pyridine compounds as sodium channel blockers |
WO2012053186A1 (en) * | 2010-10-18 | 2012-04-26 | Raqualia Pharma Inc. | Arylamide derivatives as ttx-s blockers |
PL2630146T3 (pl) | 2010-10-21 | 2020-11-02 | Medivation Technologies Llc | Krystaliczna sól tosylanowa (8S,9R)-5-fluoro-8-(4-fluorofenylo)-9-(1-metylo-1H-1,2,4-triazol-5-ilo)-8,9-dihydro-2H-pirydo[4,3,2-de]ftalazyno-3(7H)-onu |
WO2012095781A1 (en) | 2011-01-13 | 2012-07-19 | Pfizer Limited | Indazole derivatives as sodium channel inhibitors |
WO2012120398A1 (en) | 2011-03-04 | 2012-09-13 | Pfizer Limited | Aryl substituted carboxamide derivatives as trpm8 modulators |
JP5595616B2 (ja) | 2011-04-05 | 2014-09-24 | ファイザー・リミテッド | トロポミオシン関連キナーゼ阻害薬としてのピロロ[2,3−d]ピリミジン誘導体 |
JP5898767B2 (ja) | 2011-07-13 | 2016-04-06 | ファイザー・リミテッドPfizer Limited | エンケファリン類似体 |
WO2013054185A1 (en) | 2011-10-13 | 2013-04-18 | Pfizer, Inc. | Pyrimidine and pyridine derivatives useful in therapy |
SG11201401032YA (en) | 2011-10-26 | 2014-07-30 | Pfizer Ltd | (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators |
CA2853231C (en) | 2011-10-28 | 2020-08-04 | Inhibitaxin Limited | Pyridazine derivatives with autotaxin activity for use in therapy |
WO2013088315A1 (en) | 2011-12-15 | 2013-06-20 | Pfizer Limited | Sulfonamide derivatives |
WO2013093688A1 (en) | 2011-12-19 | 2013-06-27 | Pfizer Limited | Sulfonamide derivatives and use thereof as vgsc inhibitors |
WO2013102826A1 (en) | 2012-01-04 | 2013-07-11 | Pfizer Limited | N-aminosulfonyl benzamides |
CA2861439C (en) | 2012-02-03 | 2016-07-12 | Pfizer Inc. | Benzimidazole and imidazopyridine derivatives as sodium channel modulators |
US9206127B2 (en) | 2012-03-16 | 2015-12-08 | Purdue Pharm, L.P. | Substituted pyridines as sodium channel blockers |
RU2632899C2 (ru) * | 2012-04-25 | 2017-10-11 | Раквалиа Фарма Инк. | Амидопроизводные как блокаторы ttx-s |
EP2912036A1 (en) | 2012-10-04 | 2015-09-02 | Pfizer Limited | Pyrrolo[3,2-c]pyridine tropomyosin-related kinase inhibitors |
CA2885253A1 (en) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Pyrrolo[2,3-d]pyrimidine tropomyosin-related kinase inhibitors |
US20150250785A1 (en) | 2012-10-04 | 2015-09-10 | Pfizer Limited | Tropomyosin-Related Kinase Inhibitors |
JP6225356B2 (ja) * | 2012-10-31 | 2017-11-08 | ラクオリア創薬株式会社 | Ttx−s遮断薬としてのピラゾロピリジン誘導体 |
EP2935257B1 (en) | 2012-12-20 | 2018-02-07 | Purdue Pharma LP | Cyclic sulfonamides as sodium channel blockers |
TWI631105B (zh) | 2013-01-31 | 2018-08-01 | 維泰克斯製藥公司 | 作爲鈉通道調節劑之喹啉及喹噁啉醯胺 |
CN108164457B (zh) | 2013-01-31 | 2021-07-09 | 沃泰克斯药物股份有限公司 | 作为钠通道调节剂的吡啶酮酰胺 |
AP2015008716A0 (en) | 2013-03-08 | 2015-09-30 | Amgen Inc | Perfluorinated cyclopropyl fused 1,3-oxazin-2-amine compounds as beta-secretase inhibitors and methods of use |
UA119147C2 (uk) | 2013-07-19 | 2019-05-10 | Вертекс Фармасьютікалз Інкорпорейтед | Сульфонаміди як модулятори натрієвих каналів |
BR112016008257A2 (pt) | 2013-10-15 | 2017-09-26 | Janssen Pharmaceutica Nv | moduladores de roryt de álcool quinolínico secundário |
EP3066084A1 (en) * | 2013-11-07 | 2016-09-14 | Medivation Technologies, Inc. | Triazole intermediates useful in the synthesis of protected n-alkyltriazolecarbaldehydes |
LT3080134T (lt) | 2013-12-13 | 2018-11-12 | Vertex Pharmaceuticals Incorporated | Piridono amidų provaistai, naudotini kaip natrio kanalų moduliatoriai |
US10730866B2 (en) | 2014-04-07 | 2020-08-04 | Purdue Pharma L.P. | Indole derivatives and use thereof |
EP3193603A4 (en) * | 2014-09-10 | 2018-02-28 | Epizyme, Inc. | Isoxazole carboxamide compounds |
CN106674264A (zh) * | 2016-12-20 | 2017-05-17 | 苏州汉德创宏生化科技有限公司 | (2,2,2‑三氟乙氧基)苯硼酸类化合物的合成方法 |
KR102714561B1 (ko) | 2017-05-16 | 2024-10-10 | 버텍스 파마슈티칼스 인코포레이티드 | 나트륨 채널의 조절제로서의 중수소화 피리돈 아미드 및 이의 프로드럭 |
EP3651752B1 (en) | 2017-07-11 | 2024-11-20 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
MX2020001793A (es) * | 2017-08-17 | 2020-07-22 | Ikena Oncology Inc | Inhibidores del receptor de hidrocarburos de arilo (ahr) y usos de los mismos. |
JP7506379B2 (ja) * | 2018-02-05 | 2024-06-26 | ユニヴェルスィテ・ドゥ・ストラスブール | 疼痛を治療するための化合物および組成物 |
CN111918650A (zh) | 2018-02-12 | 2020-11-10 | 沃泰克斯药物股份有限公司 | 治疗疼痛的方法 |
CN109053434A (zh) * | 2018-07-18 | 2018-12-21 | 上海华堇生物技术有限责任公司 | 一种2,4-二甲氧基苯甲酰氯的新制备方法 |
CN108794328A (zh) * | 2018-08-03 | 2018-11-13 | 上海华堇生物技术有限责任公司 | 3,4-二甲氧基苯甲酰氯的制备方法 |
WO2020146682A1 (en) | 2019-01-10 | 2020-07-16 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
US20220110923A1 (en) | 2019-01-10 | 2022-04-14 | Vertex Pharmaceuticals Incorporated | Esters and carbamates as modulators of sodium channels |
WO2020176763A1 (en) | 2019-02-27 | 2020-09-03 | Vertex Pharmaceuticals Incorporated | Dosage form comprising prodrug of na 1.8 sodium channel inhibitor |
WO2020219867A1 (en) | 2019-04-25 | 2020-10-29 | Vertex Pharmaceuticals Incorporated | Pyridone amide co-crystal compositions for the treatment of pain |
EP4010328A1 (en) * | 2019-08-06 | 2022-06-15 | Domain Therapeutics | 5-heteroaryl-pyridin-2-amine confounds as neuropeptide ff receptor antagonists |
UY38979A (es) | 2019-12-06 | 2021-07-30 | Vertex Pharma | Tetrahidrofuranos sustituidos como moduladores de canales de sodio |
CN113248455A (zh) * | 2021-05-25 | 2021-08-13 | 湖北科技学院 | 一种3,5-二取代异噁唑类衍生物及其合成方法 |
EP4347583A1 (en) | 2021-06-04 | 2024-04-10 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofuran analogs as modulators of sodium channels |
KR20240031300A (ko) | 2021-06-04 | 2024-03-07 | 버텍스 파마슈티칼스 인코포레이티드 | 나트륨 채널 조절제로서의 n-(하이드록시알킬 (헤테로)아릴) 테트라하이드로푸란 카르복스아미드 |
EP4346818A1 (en) | 2021-06-04 | 2024-04-10 | Vertex Pharmaceuticals Incorporated | Solid dosage forms and dosing regimens comprising (2r,3s,4s,5r)-4-[[3-(3,4-difluoro-2-methoxy-phenyl)-4,5-dimethyl-5-(trifluoromethyl) tetrahydrofuran-2-carbonyl]amino]pyridine-2-carboxamide |
JP2024520648A (ja) | 2021-06-04 | 2024-05-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | ナトリウムチャネルの調節因子としての置換テトラヒドロフラン-2-カルボキサミド |
EP4347033A1 (en) | 2021-06-04 | 2024-04-10 | Vertex Pharmaceuticals Incorporated | Hydroxy and (halo)alkoxy substituted tetrahydrofurans as modulators of sodium channels |
CN117794919A (zh) | 2021-06-04 | 2024-03-29 | 沃泰克斯药物股份有限公司 | N-(羟烷基(杂)芳基)四氢呋喃甲酰胺类似物作为钠通道调节剂 |
CN115703719B (zh) * | 2021-08-03 | 2024-04-30 | 联化科技股份有限公司 | 一种溴化肟类化合物的制备方法 |
WO2023205465A1 (en) | 2022-04-22 | 2023-10-26 | Vertex Pharmaceuticals Incorporated | Heteroaryl compounds for the treatment of pain |
WO2023205468A1 (en) | 2022-04-22 | 2023-10-26 | Vertex Pharmaceuticals Incorporated | Heteroaryl compounds for the treatment of pain |
AU2023256603A1 (en) | 2022-04-22 | 2024-11-07 | Vertex Pharmaceuticals Incorporated | Heteroaryl compounds for the treatment of pain |
TW202408501A (zh) | 2022-04-22 | 2024-03-01 | 美商維泰克斯製藥公司 | 用於治療疼痛之雜芳基化合物 |
WO2024123815A1 (en) | 2022-12-06 | 2024-06-13 | Vertex Pharmaceuticals Incorporated | Process for the synthesis of substituted tetrahydrofuran modulators of sodium channels |
Family Cites Families (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0527736T3 (da) * | 1990-05-18 | 1997-10-20 | Hoechst Ag | Isoxazol-4-carboxylsyreamider og hydroxyalkyliden-cyanoacetamider, lægemidler indeholdende disse forbindelser og anvendelsen af disse lægemidler. |
AU5704594A (en) | 1992-12-18 | 1994-07-19 | Wellcome Foundation Limited, The | Pyrimidine, pyridine, pteridinone and indazole derivatives as enzyme inhibitors |
WO1996018616A1 (en) | 1994-12-12 | 1996-06-20 | Merck & Co., Inc. | Substituted 2-aminopyridines as inhibitors of nitric oxide synthase |
WO1996018617A1 (en) | 1994-12-12 | 1996-06-20 | Merck & Co., Inc. | Substituted 2-acylamino-pyridines as inhibitors of nitric oxide synthase |
US6011051A (en) | 1996-07-31 | 2000-01-04 | Hoechst Aktiengesellschaft | Use of isoxazole and crotonamide derivatives for the modulation of apoptosis |
US6020357A (en) * | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
US6060491A (en) * | 1997-06-19 | 2000-05-09 | Dupont Pharmaceuticals | 6-membered aromatics as factor Xa inhibitors |
DE19857009A1 (de) | 1998-12-10 | 2000-06-15 | Aventis Pharma Gmbh | Zubereitung mit verbesserter therapeutischer Breite, enthaltend Nukleotidsyntheseinhibitoren |
US6458789B1 (en) | 1999-09-29 | 2002-10-01 | Lion Bioscience Ag | 2-aminopyridine derivatives and combinatorial libraries thereof |
GB0002666D0 (en) * | 2000-02-04 | 2000-03-29 | Univ London | Blockade of voltage dependent sodium channels |
AR029489A1 (es) | 2000-03-10 | 2003-07-02 | Euro Celtique Sa | Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento |
CA2411859A1 (en) * | 2000-06-05 | 2001-12-13 | Jae-Gul Lee | Novel oxazolidinone derivatives and a process for the preparation thereof |
US6849660B1 (en) | 2000-08-01 | 2005-02-01 | Isis Pharmaceuticals, Inc. | Antimicrobial biaryl compounds |
DE10132308A1 (de) | 2001-07-06 | 2003-01-30 | Aventis Behring Gmbh | Kombinationspräparat zur Therapie von immunologischen Erkrankungen |
AR036873A1 (es) | 2001-09-07 | 2004-10-13 | Euro Celtique Sa | Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento |
AR037233A1 (es) | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
JP2003086564A (ja) * | 2001-09-14 | 2003-03-20 | Mitsubishi Electric Corp | 遠心乾燥装置および半導体装置の製造方法ならびに半導体製造装置 |
CA2465207C (en) * | 2001-11-01 | 2011-01-04 | Icagen, Inc. | Pyrazole-amides and -sulfonamides |
US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
DK1474395T3 (da) | 2002-02-12 | 2008-02-11 | Smithkline Beecham Corp | Nicotinamidderivater, der er nyttige som p38-inhibitorer |
WO2004080999A1 (en) | 2003-03-14 | 2004-09-23 | Biolipox Ab | Pyrazole compounds useful in the treatment of inflammation |
CA2524352A1 (en) | 2003-05-09 | 2004-11-18 | Pharmacia & Upjohn Company Llc | Substituted pyrimidine derivatives |
AR044688A1 (es) | 2003-06-12 | 2005-09-21 | Euro Celtique Sa | Agentes terapeuticos utiles para el tratamiento del dolor |
PL1664016T3 (pl) | 2003-09-22 | 2009-04-30 | Euro Celtique Sa | Środki terapeutyczne przydatne do leczenia bólu |
CA2555890A1 (en) | 2004-03-02 | 2005-09-15 | Neurogen Corporation | Heteroalkyl-substituted biphenyl-4-carboxylic acid arylamide analogues |
EP1802580A2 (en) * | 2004-07-23 | 2007-07-04 | Pfizer, Inc. | Pyridine derivatives |
US20060106011A1 (en) * | 2004-11-12 | 2006-05-18 | Bock Mark G | 2-(Bicyclo)alkylamino-derivatives as mediators of chronic pain and inflammation |
JP2008519814A (ja) | 2004-11-12 | 2008-06-12 | ガラパゴス・ナムローゼ・フェンノートシャップ | プロテインキナーゼ酵素の活性部位と結合する窒素複素環式芳香族化合物 |
US8211919B2 (en) | 2005-09-02 | 2012-07-03 | Astellas Pharma Inc. | Amide derivatives as rock inhibitors |
JO2722B1 (en) | 2005-09-09 | 2013-09-15 | سميث كلاين بيتشام كوربوريشن | New vehicles |
EP1764095A1 (en) | 2005-09-20 | 2007-03-21 | Revotar Biopharmaceuticals AG | Novel nitrocatechol derivatives having selectin ligand activity |
EP1764093A1 (en) | 2005-09-20 | 2007-03-21 | Revotar Biopharmaceuticals AG | Novel aromatic compounds and their use in medical applications |
ES2274712B1 (es) | 2005-10-06 | 2008-03-01 | Laboratorios Almirall S.A. | Nuevos derivados imidazopiridina. |
TW200732320A (en) | 2005-10-31 | 2007-09-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
TWI385169B (zh) * | 2005-10-31 | 2013-02-11 | Eisai R&D Man Co Ltd | 經雜環取代之吡啶衍生物及含有彼之抗真菌劑 |
EP1943234A1 (en) | 2005-10-31 | 2008-07-16 | Biolipox AB | Triazole compounds as lipoxygenase inhibitors |
NL2000284C2 (nl) | 2005-11-04 | 2007-09-28 | Pfizer Ltd | Pyrazine-derivaten. |
EP1945632B1 (en) | 2005-11-08 | 2013-09-18 | Vertex Pharmaceuticals Incorporated | Heterocyclic modulators of atp-binding cassette transporters |
WO2007058990A2 (en) | 2005-11-14 | 2007-05-24 | Kemia, Inc. | Therapy using cytokine inhibitors |
KR20080071562A (ko) | 2005-11-30 | 2008-08-04 | 아스텔라스세이야쿠 가부시키가이샤 | 2-아미노벤즈아미드 유도체 |
WO2007083239A1 (en) | 2006-01-23 | 2007-07-26 | Pfizer Limited | Pyridine derivatives as sodium channel modulators |
AU2007208240B2 (en) | 2006-01-25 | 2013-04-11 | Synta Pharmaceuticals Corp. | Substituted biaryl compounds for inflammation and immune-related uses |
EP1984338B8 (en) | 2006-01-31 | 2013-05-22 | Synta Pharmaceuticals Corp. | Pyridylphenyl compounds for inflammation and immune-related uses |
WO2007093901A1 (en) | 2006-02-17 | 2007-08-23 | Pfizer Limited | 3 -deazapurine derivatives as tlr7 modulators |
AU2007245059B2 (en) | 2006-03-31 | 2011-07-28 | Novartis Ag | New compounds |
PE20080906A1 (es) | 2006-08-17 | 2008-07-05 | Kemia Inc | Derivados heteroarilo como inhibidores de citocina |
EP2125778A1 (en) | 2006-12-22 | 2009-12-02 | Millennium Pharmaceuticals, Inc. | Certain pyrazoline derivatives with kinase inhibitory activity |
US7759344B2 (en) | 2007-01-09 | 2010-07-20 | Amgen Inc. | Bis-aryl amide derivatives and methods of use |
WO2008106692A1 (en) | 2007-03-01 | 2008-09-04 | Novartis Vaccines And Diagnostics, Inc. | Pim kinase inhibitors and methods of their use |
JP2010526051A (ja) | 2007-05-03 | 2010-07-29 | ファイザー・リミテッド | 疼痛を治療するためのnav1.8チャネルモジュレーターとしてのn−[6−アミノ−5−(フェニル)ピラジン−2−イル]−イソオキサゾール−4−カルボキサミド誘導体および関連化合物 |
-
2008
- 2008-04-21 GE GEAP200811541A patent/GEP20125379B/en unknown
- 2008-04-21 EA EA200970913A patent/EA015952B1/ru not_active IP Right Cessation
- 2008-04-21 NZ NZ581614A patent/NZ581614A/en not_active IP Right Cessation
- 2008-04-21 AP AP2009005009A patent/AP2516A/xx active
- 2008-04-21 WO PCT/IB2008/001050 patent/WO2008135826A2/en active Application Filing
- 2008-04-21 CA CA2684105A patent/CA2684105C/en not_active Expired - Fee Related
- 2008-04-21 ES ES08737559T patent/ES2398606T3/es active Active
- 2008-04-21 EP EP08737559A patent/EP2183241B1/en active Active
- 2008-04-21 CN CN200880014589A patent/CN101675040A/zh active Pending
- 2008-04-21 MX MX2009011816A patent/MX2009011816A/es active IP Right Grant
- 2008-04-21 AU AU2008247102A patent/AU2008247102B2/en not_active Ceased
- 2008-04-21 KR KR1020097025183A patent/KR20100007956A/ko active IP Right Grant
- 2008-04-21 BR BRPI0810202-3A2A patent/BRPI0810202A2/pt not_active IP Right Cessation
- 2008-04-21 JP JP2010504893A patent/JP4657384B2/ja not_active Expired - Fee Related
- 2008-04-30 UY UY31063A patent/UY31063A1/es not_active Application Discontinuation
- 2008-04-30 PE PE2008000775A patent/PE20090730A1/es not_active Application Discontinuation
- 2008-05-02 PA PA20088779201A patent/PA8779201A1/es unknown
- 2008-05-02 US US12/114,258 patent/US8134007B2/en active Active
- 2008-05-02 CL CL2008001268A patent/CL2008001268A1/es unknown
- 2008-05-02 TW TW097116408A patent/TWI375675B/zh not_active IP Right Cessation
- 2008-05-02 AR ARP080101868A patent/AR070636A1/es not_active Application Discontinuation
-
2009
- 2009-10-13 CR CR11061A patent/CR11061A/es not_active Application Discontinuation
- 2009-10-15 IL IL201569A patent/IL201569A0/en unknown
- 2009-10-26 CU CU2009000180A patent/CU23846B1/es not_active IP Right Cessation
- 2009-10-28 NI NI200900192A patent/NI200900192A/es unknown
- 2009-10-29 TN TNP2009000450A patent/TN2009000450A1/fr unknown
- 2009-10-29 ZA ZA2009/07609A patent/ZA200907609B/en unknown
- 2009-10-29 GT GT200900280A patent/GT200900280A/es unknown
- 2009-10-30 EC EC2009009710A patent/ECSP099710A/es unknown
- 2009-10-30 SV SV2009003400A patent/SV2009003400A/es unknown
- 2009-10-30 DO DO2009000254A patent/DOP2009000254A/es unknown
- 2009-11-03 MA MA32327A patent/MA31419B1/fr unknown
- 2009-11-03 CO CO09123852A patent/CO6251367A2/es not_active Application Discontinuation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY31063A1 (es) | Derivados de n-[6-amino-5-aril-piridin -2-il]-carboxamida, composiciones conteniéndolos, procedimientos de preparación, itermedios utilizados en la preparación y aplicaciones. | |
CO6400220A2 (es) | Derivados de sulfonamida | |
ECSP077185A (es) | Derivados de piridina | |
ECSP088412A (es) | Derivados de pirazina como moduladores de canal de sodio en el tratamiento del dolor | |
ECSP099706A (es) | Nuevos derivados de n-(8-heteroariltetrahidronaftalen-2yl) y n-(5-heteroarilcroman-3-il) carboxamida para el tratamiento del dolor | |
UY30681A1 (es) | Compuestos de piridinamida que contienen carboxi, sales farmacéuticamente aceptables, procedimientos para la preparacion de los mismos, composiciones que los contienen y sus usos. | |
CL2008002768A1 (es) | Compuestos derivados de carboxiciclopropil-(bis-fenil-oxamidas); composicion farmaceutica que los contiene; procedimiento para la elaboracion de las composiciones y el uso de los compuestos en el tratamiento de diabetes y trastornos del sncentre otras enfermedades. | |
UY32158A (es) | Derivados heterociclicos y metodos de uso de los mismos | |
UY30498A1 (es) | Nueva clase de compuestos de benzimidazolilo, sus sales, composiciones farmacéuticas conteniéndolos y aplicaciones | |
UY31639A1 (es) | Derivados de amida espirocíclica de fórmula i, sales farmacéuticamente aceptables, composiciones farmacéuticas conteniéndolas, procesos de preparación y aplicaciones | |
UY31885A (es) | Derivados de las 1, 3, 5-triazina-2, 4-diaminas-6-sustituidas-n-sustituidas y sales farmacéuticamente aceptables de los mismos, composiciones y aplicaciones. | |
CO6690768A2 (es) | Derivados de triazina-oxadiazoles, útiles como inhibidores de los canales de sodio navi.7 | |
ECSP10010693A (es) | Compuestos pirazólicos 436 | |
UY32315A (es) | Compuestos de piperidina y usos de los mismo-596 | |
UY31906A (es) | Derivados de n-cicloalquil-3-fenilnicotinamida que inhiben pgds, sus composiciones, su uso para el tratamiento por ejemplo de afecciones alérgicas y respiratorias. | |
AR054786A1 (es) | (6-fluor-benzol(1,3) dioxolil)-morfolin-4-il-metanomas, moduladoras del receptor cb1 | |
SV2011003802A (es) | Derivados de triazol utiles para el tratamiento de enfermedades | |
UY29818A1 (es) | Nuevos compuestos de azetidina, composiciones farmaceuticas que los contienen, procesos de preparacion y sus usos terapeuticos | |
UY31141A1 (es) | Compuestos de piperidina y sus usos | |
CR11825A (es) | Derivados de urea heterociclicos para el tratamiento de infecciones bacterianas | |
UY31805A (es) | Agonistas m1, composiciones farmacéuticas de los mismos, procesos para su preparacion y sus usos para el tratamiento del dolor | |
AR077418A1 (es) | COMPUESTOS PIPERIDíNICOS, SU PROCEDIMIENTO DE PREPARACIoN, LAS COMPOSICIONES FARMACÉUTICAS QUE LOS CONTIENEN Y SU USO EN EL TRATAMIENTO DE LOS TRASTORNOS COGNITIVOS | |
AR105921A1 (es) | Compuestos terapéuticos para el dolor y síntesis de estos | |
UY31289A1 (es) | Nuevos derivados de la quinoliniloxipiperidina y pirrolidina, su preparacion, composiciones farmaceuticas que los contiene y sus usos en el tratamieno de enfermedades | |
DOP2007000086A (es) | Nuevos derivados de quinolinas |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20171005 |