AR069666A1 - Derivados de imidazo[1, 2 - a]piridina e imidazo[1, 2 -b]piridazina, una composicion farmaceutica que los contiene y su uso en la preparacion de un medicamento para el tratamiento de enfermedades mediadas por las celulas b. - Google Patents
Derivados de imidazo[1, 2 - a]piridina e imidazo[1, 2 -b]piridazina, una composicion farmaceutica que los contiene y su uso en la preparacion de un medicamento para el tratamiento de enfermedades mediadas por las celulas b.Info
- Publication number
- AR069666A1 AR069666A1 ARP080105399A ARP080105399A AR069666A1 AR 069666 A1 AR069666 A1 AR 069666A1 AR P080105399 A ARP080105399 A AR P080105399A AR P080105399 A ARP080105399 A AR P080105399A AR 069666 A1 AR069666 A1 AR 069666A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- heterocycloalkyl
- heteroaryl
- lower alkyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Los derivados de imidazo[1,2-a]piridina e imidazo[1,2-b]piridazina inhiben la Btk y son utiles para el tratamiento de enfermedades autoinmunes e inflamatorias, provocadas por la activacion aberrante de las células B, p.ej. la artritis. Reivindicacion 1: Un compuesto de la formula (1) en la que Z es carbono o nitrogeno, R* es H, -R1, -R1-R2-R3, -R1-R3 o -R2-R3; en los que: R1 es arilo, heteroarilo, cicloalquilo o heterocicloalquilo, y está opcionalmente sustituido por alquilo inferior, hidroxi, alcoxi inferior, halogeno, nitro, amino, ciano o halo-alquilo inferior; R2 es -C(=O), -C(=O)O, -C(=O)NH, -S(=O)2, O, NR3 o alquilo inferior; R3 es H o R4; R4 es alquilo inferior, alcoxi inferior, arilo, arilalquilo, alquilarilo, heteroarilo, alquil-heteroarilo, heteroaril-alquilo, cicloalquilo, alquil-cicloalquilo, cicloalquil-alquilo, heterocicloalquilo, alquil-heterocicloalquilo o heterocicloalquil-alquilo, y está opcionalmente sustituido por alquilo inferior, hidroxi, alcoxi inferior, halogeno, nitro, amino, ciano, alquilo inferior-sulfonilo, heterocicloalquilo o halo-alquilo inferior; R** es un grupo de la formula (2) o (3); Q es pirrolilo, cicloalquilo o cicloalquenilo; X es H, halogeno, alquilo inferior, hidroxi, hidroxi-alquilo inferior o alcoxi inferior; Y es H, -R5-R6, -R6 o -R5-R6-R7; R5 es -NHC(=O) , -NHC(=O)NR5', -(CH2)nC(=O)NR5', -NH o -(CH2)n-C(=O); en el que n es el numero 0, 1 o 2; y R5' es H, alquilo inferior, alcoxi inferior o hidroxi-alquilo inferior; R6 es alquilo inferior, alquenilo inferior, alquinilo inferior, arilo, arilalquilo, alquilarilo, heteroarilo, alquil-heteroarilo, heteroaril-alquilo, cicloalquilo, alquil-cicloalquilo, cicloalquil-alquilo, heterocicloalquilo, alquil-heterocicloalquilo o heterocicloalquil-alquilo y está opcionalmente sustituido por uno o más sustituyentes elegidos entre el grupo formado por alquilo inferior, hidroxi, halo-alquilo inferior, alcoxi inferior, halo-alcoxi inferior, halogeno, nitro, amino, amido, amido-alquilo inferior, ciano y trialquilsilanilo; y R7 es arilo, heteroarilo, cicloalquilo o heterocicloalquilo, opcionalmente sustituidos por uno o más sustituyentes elegidos entre el grupo formado por alquilo inferior, hidroxi, halo-alquilo inferior, alcoxi inferior, halo-alcoxi inferior, halogeno, nitro, amino, oxo, ciano y trialquilsilanilo, o está opcionalmente conectado a un anillo arilo, heteroarilo, cicloalquilo o heterocicloalquilo, de modo que los dos anillos formen un sistema de anillos fusionados bicíclico espirocíclico, opcionalmente sustituido por uno o más sustituyentes elegidos entre el grupo formado por alquilo inferior, hidroxi, halo-alquilo inferior, alcoxi inferior, halo-alcoxi inferior, halogeno, nitro, amino, oxo, ciano y trialquilsilanilo; con la condicion de que si Z es carbono, R* es C(=O)CH3 y R** es un grupo I** en el que X es H, entonces Y no sea CF3 ni H; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1376207P | 2007-12-14 | 2007-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR069666A1 true AR069666A1 (es) | 2010-02-10 |
Family
ID=40428199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080105399A AR069666A1 (es) | 2007-12-14 | 2008-12-12 | Derivados de imidazo[1, 2 - a]piridina e imidazo[1, 2 -b]piridazina, una composicion farmaceutica que los contiene y su uso en la preparacion de un medicamento para el tratamiento de enfermedades mediadas por las celulas b. |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP2229390B1 (es) |
JP (2) | JP5643105B2 (es) |
CN (1) | CN101952283B (es) |
AR (1) | AR069666A1 (es) |
CA (1) | CA2708361C (es) |
CL (1) | CL2008003698A1 (es) |
ES (1) | ES2462642T3 (es) |
PE (1) | PE20091085A1 (es) |
TW (1) | TW200930720A (es) |
WO (1) | WO2009077334A1 (es) |
Families Citing this family (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009077334A1 (en) * | 2007-12-14 | 2009-06-25 | F. Hoffmann-La Roche Ag | Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives |
AU2009215191A1 (en) | 2008-02-13 | 2009-08-20 | Gilead Connecticut, Inc. | 6-aryl-imidaz0[l, 2-a] pyrazine derivatives, method of making, and method of use thereof |
EP2247595B1 (en) | 2008-02-25 | 2011-07-20 | F. Hoffmann-La Roche AG | Pyrrolopyrazine kinase inhibitors |
CN102066366B (zh) | 2008-06-24 | 2014-04-16 | 霍夫曼-拉罗奇有限公司 | 新型取代的吡啶-2-酮和哒嗪-3-酮 |
CN102066370B (zh) * | 2008-07-15 | 2014-05-14 | 霍夫曼-拉罗奇有限公司 | 苯基-咪唑并吡啶类和哒嗪类 |
ES2461494T3 (es) | 2008-07-18 | 2014-05-20 | F. Hoffmann-La Roche Ag | Nuevas fenilimidazopirazinas |
CN102307581B (zh) | 2008-12-08 | 2016-08-17 | 吉利德康涅狄格股份有限公司 | 咪唑并哌嗪syk抑制剂 |
RS55055B1 (sr) | 2008-12-08 | 2016-12-30 | Gilead Connecticut Inc | Imidazopirazin syk inhibitori |
US8450321B2 (en) | 2008-12-08 | 2013-05-28 | Gilead Connecticut, Inc. | 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor |
US8299077B2 (en) | 2009-03-02 | 2012-10-30 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
EP2493889B1 (en) | 2009-10-30 | 2017-09-06 | Janssen Pharmaceutica, N.V. | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
ES2530449T3 (es) * | 2010-03-11 | 2015-03-02 | Gilead Connecticut Inc | Inhibidores de Syk de imidazopiridinas |
AR082590A1 (es) | 2010-08-12 | 2012-12-19 | Hoffmann La Roche | Inhibidores de la tirosina-quinasa de bruton |
AU2012277912B2 (en) | 2011-06-27 | 2017-03-23 | Janssen Pharmaceutica Nv | 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline derivatives |
AU2012282229B2 (en) | 2011-07-08 | 2015-05-07 | Novartis Ag | Novel pyrrolo pyrimidine derivatives |
MX343561B (es) * | 2011-11-01 | 2016-11-09 | Hoffmann La Roche | Compuestos de imidazolpiridazina. |
CA2852964A1 (en) * | 2011-11-03 | 2013-05-10 | F. Hoffmann-La Roche Ag | Bicyclic piperazine compounds |
CA2860547A1 (en) | 2012-01-10 | 2013-07-18 | Johannes Cornelius Hermann | Pyridazine amide compounds and their use as syk inhibitors |
US9365566B2 (en) | 2012-03-27 | 2016-06-14 | Takeda Pharmaceutical Company Limited | Cinnoline derivatives |
EP2863909B1 (en) | 2012-06-26 | 2020-11-04 | Janssen Pharmaceutica N.V. | Combinations comprising 4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline compounds as pde 2 inhibitors and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
MX362197B (es) | 2012-07-09 | 2019-01-08 | Janssen Pharmaceutica Nv | Derivados de imidazo[1,2-b]piridazina e imidazo[1,2-a]pirazina como inhibidores de la fosfodiesterasa 10; y el uso de los mismos en el tratamiento de trastornos neurológicos, psiquiátricos y metabólicos. |
JO3377B1 (ar) | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
MX367918B (es) | 2013-04-25 | 2019-09-11 | Beigene Ltd | Compuestos heterociclicos fusionados como inhibidores de proteina quinasa. |
PL3027171T3 (pl) | 2013-07-30 | 2020-08-24 | Gilead Connecticut, Inc. | Formulacja inhibitorów syk |
PL3027618T3 (pl) | 2013-07-30 | 2021-04-19 | Kronos Bio, Inc. | Polimorf inhibitorów syk |
CN103360399B (zh) * | 2013-08-02 | 2016-03-02 | 北京大学 | 6-芳基取代-咪唑-[1,2-b]哒嗪类衍生物,其制备方法及用途 |
CN112457403B (zh) | 2013-09-13 | 2022-11-29 | 广州百济神州生物制药有限公司 | 抗pd1抗体及其作为治疗剂与诊断剂的用途 |
CN105764516A (zh) | 2013-12-04 | 2016-07-13 | 吉利德科学公司 | 治疗癌症的方法 |
UY35898A (es) | 2013-12-23 | 2015-07-31 | Gilead Sciences Inc | ?compuestos inhibidores de syk y composiciones que los comprenden?. |
US9290505B2 (en) | 2013-12-23 | 2016-03-22 | Gilead Sciences, Inc. | Substituted imidazo[1,2-a]pyrazines as Syk inhibitors |
WO2015157955A1 (en) * | 2014-04-17 | 2015-10-22 | Abbvie Inc. | Heterocyclic btk inhibit ors |
KR102130600B1 (ko) | 2014-07-03 | 2020-07-08 | 베이진 엘티디 | Pd-l1 항체와 이를 이용한 치료 및 진단 |
KR20170029580A (ko) | 2014-07-14 | 2017-03-15 | 길리애드 사이언시즈, 인코포레이티드 | 암을 치료하기 위한 조합물 |
EP3124479A1 (en) * | 2015-07-29 | 2017-02-01 | Solvay SA | Method for the manufacture of fluorinated cyclic carbonates |
CN105418615B (zh) * | 2015-12-09 | 2018-02-02 | 北京工业大学 | 苯甲酰胺衍生物及制备和应用 |
CN109071496B (zh) | 2016-03-31 | 2021-07-30 | 武田药品有限公司 | 异喹啉基三唑酮复合物 |
CN109475536B (zh) | 2016-07-05 | 2022-05-27 | 百济神州有限公司 | 用于治疗癌症的PD-l拮抗剂和RAF抑制剂的组合 |
KR20230162137A (ko) | 2016-08-16 | 2023-11-28 | 베이진 스위찰랜드 게엠베하 | (s)-7-(1-아크릴로일피페리딘-4-일)-2-(4-페녹시페닐)-4,5,6,7-테트라-하이드로피라졸로 [1,5-a] 피리미딘-3-카르복스아미드의 제조 및 그 용도 |
CN118252927A (zh) | 2016-08-19 | 2024-06-28 | 百济神州有限公司 | 使用包含btk抑制剂的组合产品治疗癌症 |
KR20190058550A (ko) | 2016-09-19 | 2019-05-29 | 메이 파마, 아이엔씨. | 병용 요법 |
CN110461847B (zh) | 2017-01-25 | 2022-06-07 | 百济神州有限公司 | (S)-7-(1-(丁-2-炔酰基)哌啶-4-基)-2-(4-苯氧基苯基)-4,5,6,7-四氢吡唑并[1,5-a]嘧啶-3-甲酰胺的结晶形式、其制备及用途 |
TWI778050B (zh) | 2017-04-21 | 2022-09-21 | 美商醫肯納腫瘤學公司 | 吲哚ahr抑制劑及其用途 |
AU2018290532A1 (en) | 2017-06-26 | 2019-11-21 | Beigene, Ltd. | Immunotherapy for hepatocellular carcinoma |
WO2019034009A1 (en) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY |
KR102399996B1 (ko) | 2017-08-25 | 2022-05-20 | 길리애드 사이언시즈, 인코포레이티드 | Syk 억제제의 다형체 |
WO2019108795A1 (en) | 2017-11-29 | 2019-06-06 | Beigene Switzerland Gmbh | Treatment of indolent or aggressive b-cell lymphomas using a combination comprising btk inhibitors |
EP3927708A1 (en) | 2019-02-22 | 2021-12-29 | Kronos Bio, Inc. | Solid forms of condensed pyrazines as syk inhibitors |
MX2022006308A (es) | 2019-11-26 | 2022-06-22 | Ikena Oncology Inc | Derivados de carbazol polimorfos y usos de los mismos. |
US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002501532A (ja) * | 1997-05-30 | 2002-01-15 | メルク エンド カンパニー インコーポレーテッド | 新規血管形成阻害薬 |
US7067520B2 (en) * | 2000-11-17 | 2006-06-27 | Ishihara Sangyo Kaisha, Ltd. | Preventive or therapeutic medicines for diabetes containing fused-heterocyclic compounds or their salts |
WO2004026867A2 (en) * | 2002-09-19 | 2004-04-01 | Schering Corporation | Imidazopyridines as cyclin dependent kinase inhibitors |
WO2006053121A2 (en) * | 2004-11-10 | 2006-05-18 | Cgi Pharmaceuticals, Inc. | Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity |
JP2008536817A (ja) * | 2005-03-24 | 2008-09-11 | グラクソ グループ リミテッド | 胃腸疾患の処置用医薬として有用なイミダゾ(1,2−a)ピリジン誘導体 |
CN101321760A (zh) | 2005-10-06 | 2008-12-10 | 先灵公司 | 作为蛋白激酶抑制剂的吡唑并嘧啶 |
WO2009077334A1 (en) * | 2007-12-14 | 2009-06-25 | F. Hoffmann-La Roche Ag | Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives |
-
2008
- 2008-12-04 WO PCT/EP2008/066758 patent/WO2009077334A1/en active Application Filing
- 2008-12-04 CN CN2008801206432A patent/CN101952283B/zh not_active Expired - Fee Related
- 2008-12-04 CA CA2708361A patent/CA2708361C/en not_active Expired - Fee Related
- 2008-12-04 ES ES08861971.3T patent/ES2462642T3/es active Active
- 2008-12-04 EP EP08861971.3A patent/EP2229390B1/en not_active Not-in-force
- 2008-12-04 JP JP2010537386A patent/JP5643105B2/ja not_active Expired - Fee Related
- 2008-12-11 PE PE2008002052A patent/PE20091085A1/es not_active Application Discontinuation
- 2008-12-11 TW TW097148307A patent/TW200930720A/zh unknown
- 2008-12-12 AR ARP080105399A patent/AR069666A1/es unknown
- 2008-12-12 CL CL2008003698A patent/CL2008003698A1/es unknown
-
2014
- 2014-06-04 JP JP2014116005A patent/JP5871992B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ES2462642T3 (es) | 2014-05-26 |
EP2229390A1 (en) | 2010-09-22 |
CN101952283A (zh) | 2011-01-19 |
TW200930720A (en) | 2009-07-16 |
JP5871992B2 (ja) | 2016-03-01 |
EP2229390B1 (en) | 2014-04-09 |
CA2708361C (en) | 2016-06-07 |
PE20091085A1 (es) | 2009-07-23 |
JP2014196316A (ja) | 2014-10-16 |
WO2009077334A1 (en) | 2009-06-25 |
JP2011506378A (ja) | 2011-03-03 |
CL2008003698A1 (es) | 2010-02-19 |
CN101952283B (zh) | 2013-04-17 |
JP5643105B2 (ja) | 2014-12-17 |
CA2708361A1 (en) | 2009-06-25 |
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