PE20040935A1 - Analogos de 2-quinazolina sustituida-4-ilamina como moduladores de los receptores de capsaicina - Google Patents
Analogos de 2-quinazolina sustituida-4-ilamina como moduladores de los receptores de capsaicinaInfo
- Publication number
- PE20040935A1 PE20040935A1 PE2004000034A PE2004000034A PE20040935A1 PE 20040935 A1 PE20040935 A1 PE 20040935A1 PE 2004000034 A PE2004000034 A PE 2004000034A PE 2004000034 A PE2004000034 A PE 2004000034A PE 20040935 A1 PE20040935 A1 PE 20040935A1
- Authority
- PE
- Peru
- Prior art keywords
- quinazoline
- trifluoromethyl
- alkyl
- ilamine
- modulators
- Prior art date
Links
- 102000011040 TRPV Cation Channels Human genes 0.000 title abstract 2
- 108010062740 TRPV Cation Channels Proteins 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- -1 2-METHOXY-ETHYL Chemical class 0.000 abstract 1
- ODGIMMLDVSWADK-UHFFFAOYSA-N 4-trifluoromethylaniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1 ODGIMMLDVSWADK-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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Abstract
SE REFIERE A ANALOGOS DE 2-QUINAZOLINA SUSTITUIDA-4-ILAMINA DE FORMULA I, O UNA FORMA FARMACEUTICAMENTE ACEPTABLE DE ESTOS, DONDE X, V, W, Y y Z SON N o CR1, CON LA CONDICION DE QUE AL MENOS UNO DE V y X SEA N; R1 ES H, HALOGENO, HIDROXIDO, CIANO, ENTRE OTROS; R ES OR7 o N(R3)(R4); R7 ES H, ALQUILO C1-C8, ALQUENILO C2-C8, ALQUINILO C2-C8, ALCANOIL C2-C8, ENTRE OTROS; R3 Y R4 SON H, ALQUILO C1-C8, ALQUENILO C2-C8, ALQUINILO C2-C8, ENTRE OTROS; O R3 Y R4 JUNTOS FORMAN UN ANILLO HETEROCICLICO DE 4-10 MIEMBROS; R5 o R6 SON H, ALQUILO C1-C8, O CADA UNO JUNTO CON R3, R4 o R7 FORMAN UN ANILLO HETEROCICLICO DE 4-10 MIEMBROS; n ES 1, 2 o 3; Ar1 Y Ar2 SON GRUPOS ARILOS DE 6-10 MIEMBROS o GRUPOS HETEROCICLICOS DE 5-10 MIEMBROS. SON COMPUESTOS PREFERIDOS: [2-ISOPROPOXIMETIL-7-(3-TRIFLUOROMETIL-PIRIDINA-2-IL)-QUINAZOLINA-4-IL]-(4-TRIFLUOROMETIL-FENIL)-AMINA; 2-[4-(4-TRIFLUOROMETIL-FENILAMINA)-7-(3-TRIFLUOROMETIL-PIRIDINA-2-IL)-QUINAZOLINA-2-IL]-ETANOL; [2-(2-METOXI-ETIL)-7-(3-TRIFLUOROMETIL-PIRIDINA-2-IL)-QUINAZOLINA-4-IL]-(4-TRIFLUOROMETIL-FENIL)-AMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON MODULADORES DEL RECEPTOR DE CAPSAICINA REDUCIENDO LA CONDUCTANCIA DEL CALCIO DE DICHO RECEPTOR
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43313902P | 2002-12-13 | 2002-12-13 |
Publications (1)
Publication Number | Publication Date |
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PE20040935A1 true PE20040935A1 (es) | 2005-01-01 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PE2004000034A PE20040935A1 (es) | 2002-12-13 | 2004-01-05 | Analogos de 2-quinazolina sustituida-4-ilamina como moduladores de los receptores de capsaicina |
Country Status (13)
Country | Link |
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US (2) | US20040156869A1 (es) |
EP (2) | EP1569925A1 (es) |
JP (2) | JP2006515846A (es) |
KR (1) | KR20050084292A (es) |
CN (1) | CN1726205A (es) |
AR (1) | AR042461A1 (es) |
AU (2) | AU2003300898A1 (es) |
BR (1) | BR0317168A (es) |
CA (2) | CA2509233A1 (es) |
MX (1) | MXPA05006123A (es) |
PE (1) | PE20040935A1 (es) |
TW (1) | TW200418480A (es) |
WO (2) | WO2004055004A1 (es) |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2400339T3 (es) | 2002-07-15 | 2013-04-09 | Symphony Evolution, Inc. | Compuestos, composiciones farmacéuticas de los mismos y su uso en el tratamiento del cáncer |
US20040156869A1 (en) * | 2002-12-13 | 2004-08-12 | Neurogen Corporation | 2-substituted quinazolin-4-ylamine analogues |
US20040142958A1 (en) * | 2002-12-13 | 2004-07-22 | Neurogen Corporation | Combination therapy for the treatment of pain |
CN1820007A (zh) * | 2003-07-10 | 2006-08-16 | 神经能质公司 | 经芳基取代的苯并[d]异噻唑-3-基胺类似物 |
TW200510373A (en) * | 2003-07-14 | 2005-03-16 | Neurogen Corp | Substituted quinolin-4-ylamine analogues |
US7329664B2 (en) | 2003-07-16 | 2008-02-12 | Neurogen Corporation | Substituted (7-pyridyl-4-phenylamino-quinazolin-2-yl)-methanol analogues |
US20070105865A1 (en) * | 2003-09-09 | 2007-05-10 | Neurogen Corporation | Substituted bicyclic quinazolin-4-ylamine derivatives |
PT2210607E (pt) | 2003-09-26 | 2012-01-31 | Exelixis Inc | N-[3-fluoro-4-({6-(metiloxi)-7-[(3-morfolina-4-ilpropil)oxi]quinolina-4-il}oxi)fenil]-n'-(4-fluorofenil)ciclopropano-1,1-dicarboxamida para o tratamento do cancro |
WO2005070929A1 (en) * | 2004-01-23 | 2005-08-04 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
CA2555867A1 (en) * | 2004-03-04 | 2005-09-22 | Neurogen Corporation | Arylalkylamino-substituted quinazoline analogues |
EP1732560A4 (en) * | 2004-04-08 | 2010-08-18 | Neurogen Corp | SUBSTITUTED CINNOLINE-4-YLAMINE |
JP2008508190A (ja) * | 2004-07-19 | 2008-03-21 | ノボ ノルディスク アクティーゼルスカブ | 肥満または肥満に関連する疾患および障害の治療におけるカプサイシン受容体の活性の阻害 |
TW200621251A (en) * | 2004-10-12 | 2006-07-01 | Neurogen Corp | Substituted biaryl quinolin-4-ylamine analogues |
US20060128710A1 (en) * | 2004-12-09 | 2006-06-15 | Chih-Hung Lee | Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof |
GB0428475D0 (en) * | 2004-12-30 | 2005-02-02 | 4 Aza Bioscience Nv | Pyrido(3,2-D)pyrimidine derivatives and pharmaceutical compositions useful as medicines for the treatment of autoimmune disorders |
CA2594998A1 (en) * | 2005-01-25 | 2006-08-03 | Neurogen Corporation | Substituted pyridazinyl-and pyrimidinyl-quinolin-4-ylamine analogues |
KR20060087386A (ko) | 2005-01-28 | 2006-08-02 | 주식회사 대웅제약 | 신규 벤조이미다졸 유도체 및 이를 함유하는 약제학적조성물 |
AU2006261607A1 (en) * | 2005-06-24 | 2006-12-28 | Gilead Sciences, Inc. | Pyrido(3,2-d)pyrimidines and pharmaceutical compositions useful for treating hepatitis C. |
CN101243081A (zh) * | 2005-07-21 | 2008-08-13 | 霍夫曼-拉罗奇有限公司 | 作为PTP1B抑制剂的吡啶并[2,3-d]嘧啶-2,4-二胺化合物 |
US8217042B2 (en) | 2005-11-11 | 2012-07-10 | Zentaris Gmbh | Pyridopyrazines and their use as modulators of kinases |
EP1790342A1 (de) | 2005-11-11 | 2007-05-30 | Zentaris GmbH | Pyridopyrazin-Derivate und deren Verwendung als Modulatoren der Signaltransduktionswege |
CN101360746B (zh) * | 2005-11-22 | 2013-12-11 | 库多斯药物有限公司 | 作为mTOR抑制剂的吡啶并-、吡唑并-和嘧啶并-嘧啶衍生物 |
JP2009521480A (ja) | 2005-12-21 | 2009-06-04 | アボット・ラボラトリーズ | 抗ウイルス化合物 |
ES2378473T3 (es) * | 2005-12-21 | 2012-04-12 | Abbott Laboratories | Compuestos antivirales |
EP2345652A1 (en) | 2005-12-21 | 2011-07-20 | Abbott Laboratories | Antiviral compounds |
ES2395386T3 (es) | 2005-12-21 | 2013-02-12 | Abbott Laboratories | Compuestos antivirales |
WO2007081978A2 (en) * | 2006-01-11 | 2007-07-19 | Angion Biomedica Corporation | Modulators of hepatocyte growth factor / c-met activity |
US8338435B2 (en) | 2006-07-20 | 2012-12-25 | Gilead Sciences, Inc. | Substituted pyrido(3,2-D) pyrimidines and pharmaceutical compositions for treating viral infections |
WO2008057300A2 (en) * | 2006-10-27 | 2008-05-15 | Redpoint Bio Corporation | Trpvi antagonists and uses thereof |
WO2008133753A2 (en) | 2006-12-20 | 2008-11-06 | Abbott Laboratories | Anti-viral compounds |
TW200840584A (en) | 2006-12-26 | 2008-10-16 | Gilead Sciences Inc | Pyrido(3,2-d)pyrimidines useful for treating viral infections |
US20090209536A1 (en) * | 2007-06-17 | 2009-08-20 | Kalypsys, Inc. | Aminoquinazoline cannabinoid receptor modulators for treatment of disease |
KR101252334B1 (ko) | 2008-04-18 | 2013-04-08 | 주식회사 대웅제약 | 신규 벤조옥사진 벤즈이미다졸 유도체, 이를 포함하는 약학 조성물 및 이의 용도 |
JPWO2009130900A1 (ja) * | 2008-04-24 | 2011-08-11 | 日本曹達株式会社 | オキシム誘導体、中間体化合物および植物病害防除剤 |
WO2010006115A1 (en) * | 2008-07-11 | 2010-01-14 | Myriad Pharmaceuticals, Inc. | Pharmaceutical compounds as cytotoxic agents and the use thereof |
WO2010029996A1 (ja) * | 2008-09-11 | 2010-03-18 | 協和発酵キリン株式会社 | 医薬組成物 |
US8703962B2 (en) * | 2008-10-24 | 2014-04-22 | Purdue Pharma L.P. | Monocyclic compounds and their use as TRPV1 ligands |
US8759362B2 (en) * | 2008-10-24 | 2014-06-24 | Purdue Pharma L.P. | Bicycloheteroaryl compounds and their use as TRPV1 ligands |
US8546388B2 (en) * | 2008-10-24 | 2013-10-01 | Purdue Pharma L.P. | Heterocyclic TRPV1 receptor ligands |
EA038195B1 (ru) | 2009-01-16 | 2021-07-22 | Экселиксис, Инк. | Малатная соль n-(4-{[6,7-бис-(метилокси)хинолин-4-ил]окси}фенил)-n'-(4-фторфенил)циклопропан-1,1-дикарбоксамида и ее применение для лечения рака почек и печени |
KR20110124787A (ko) | 2009-02-27 | 2011-11-17 | 암비트 바이오사이언시즈 코포레이션 | Jak 키나아제 조절 퀴나졸린 유도체 및 이의 사용 방법 |
UA108618C2 (uk) | 2009-08-07 | 2015-05-25 | Застосування c-met-модуляторів в комбінації з темозоломідом та/або променевою терапією для лікування раку | |
AR079814A1 (es) * | 2009-12-31 | 2012-02-22 | Otsuka Pharma Co Ltd | Compuestos heterociclicos, composiciones farmaceuticas que los contienen y sus usos |
JP5933554B2 (ja) * | 2010-09-01 | 2016-06-15 | アムビト ビオスシエンセス コルポラチオン | 光学活性のあるピラゾリルアミノキナゾリン及びその医薬組成物及び使用方法 |
EP2611789A1 (en) | 2010-09-01 | 2013-07-10 | Ambit Biosciences Corporation | Quinazoline compounds and methods of use thereof |
US9238643B2 (en) | 2010-09-06 | 2016-01-19 | Guangzhou Institutes Of Biomedicine And Health, Chinese Academy Of Sciences | Amide compounds |
MX352926B (es) | 2010-09-27 | 2017-12-14 | Exelixis Inc | Inhibidores dobles de met y factor de crecimiento endotelial vascular (vegf) para el tratamiento de cancer de prostata resistente a la castracion y metastasis osteoblasticas en los huesos. |
KR101293384B1 (ko) | 2010-10-13 | 2013-08-05 | 주식회사 대웅제약 | 신규 피리딜 벤조옥사진 유도체, 이를 포함하는 약학 조성물 및 이의 용도 |
EP2654751B1 (en) | 2010-12-22 | 2016-11-23 | Purdue Pharma L.P. | Phosphorus-substituted quinoxaline-type piperidine compounds and uses thereof |
JP6184328B2 (ja) | 2011-02-18 | 2017-08-23 | アサナ・バイオサイエンシズ,リミテッド・ライアビリティ・カンパニー | アミノインダン化合物および疼痛治療におけるその使用 |
WO2013003586A1 (en) * | 2011-06-29 | 2013-01-03 | Otsuka Pharmaceutical Co., Ltd. | Quinazolines as therapeutic compounds and related methods of use |
JP6121658B2 (ja) * | 2011-06-29 | 2017-04-26 | 大塚製薬株式会社 | 治療用化合物、及び関連する使用の方法 |
TWI603957B (zh) | 2012-08-15 | 2017-11-01 | 阿沙納生物科學有限責任公司 | 胺基氫茚化合物用於治療膀胱過動症及間質性膀胱炎之用途 |
WO2017031427A1 (en) * | 2015-08-19 | 2017-02-23 | 3-V Biosciences, Inc. | COMPOUNDS AND METHODS FOR INHIBITING mTOR |
WO2017147146A1 (en) * | 2016-02-23 | 2017-08-31 | Concentric Analgesics, Inc. | Prodrugs of phenolic trpv1 agonists |
PL3464318T3 (pl) | 2016-06-02 | 2021-11-08 | Abbvie Inc. | Agonista receptora glukokortykoidowego i jego immunokoniugaty |
US10239875B2 (en) | 2017-06-16 | 2019-03-26 | King Saud University | Naphthyridinyl hydrazine derivatives as potent peripheral analgesic agents |
US11427531B2 (en) * | 2017-10-09 | 2022-08-30 | Ramot At Tel-Aviv University Ltd. | Modulators of potassium ion and TRPV1 channels and uses thereof |
CA3082356A1 (en) | 2017-12-01 | 2019-06-06 | Abbvie Inc. | Glucocorticoid receptor agonist and immunoconjugates thereof |
KR20210108979A (ko) * | 2018-12-21 | 2021-09-03 | 소렌토 쎄라퓨틱스, 인코포레이티드 | 부적응 통증을 치료하기 위한 레시니페라톡신의 신경 주위 투여 |
CN113614081A (zh) | 2019-01-22 | 2021-11-05 | 索伦托药业有限公司 | 通过施用树脂毒素治疗骨关节炎疼痛的方法 |
WO2021257857A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Naphthyridinone compounds as jak2 v617f inhibitors |
US11753413B2 (en) | 2020-06-19 | 2023-09-12 | Incyte Corporation | Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors |
WO2022006456A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic pyridone compounds as jak2 v617f inhibitors |
TW202216713A (zh) | 2020-07-02 | 2022-05-01 | 美商英塞特公司 | 作為jak2 v617f抑制劑之三環脲化合物 |
US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
TW202237119A (zh) | 2020-12-10 | 2022-10-01 | 美商住友製藥腫瘤公司 | Alk﹘5抑制劑和彼之用途 |
CN116546986A (zh) * | 2020-12-10 | 2023-08-04 | 住友制药肿瘤公司 | Alk-5抑制剂及其用途 |
US11919908B2 (en) | 2020-12-21 | 2024-03-05 | Incyte Corporation | Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors |
WO2022182839A1 (en) | 2021-02-25 | 2022-09-01 | Incyte Corporation | Spirocyclic lactams as jak2 v617f inhibitors |
WO2023078252A1 (en) | 2021-11-02 | 2023-05-11 | Flare Therapeutics Inc. | Pparg inverse agonists and uses thereof |
WO2023141522A2 (en) * | 2022-01-21 | 2023-07-27 | Slap Pharmaceuticals Llc | Multicyclic compounds |
US20230235248A1 (en) * | 2022-01-24 | 2023-07-27 | Inter-Med, Inc. | Dental material compositions for cleansing and removal of anionic contaminants from substrates & their methods of use |
DE102022104759A1 (de) | 2022-02-28 | 2023-08-31 | SCi Kontor GmbH | Co-Kristall-Screening Verfahren, insbesondere zur Herstellung von Co-Kristallen |
CR20240447A (es) | 2022-03-17 | 2025-01-29 | Incyte Corp | Compuestos de urea tricíclica como inhibidores de v617f de jak2. |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3501696A1 (de) * | 1985-01-19 | 1986-07-24 | Bayer Ag, 5090 Leverkusen | Pyridopyrimidine, mehrere verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
DE68917485T2 (de) * | 1988-01-23 | 1995-02-09 | Kyowa Hakko Kogyo Kk | Pyridazinon-Derivate und diese enthaltende pharmazeutische Zubereitungen. |
GB8910722D0 (en) | 1989-05-10 | 1989-06-28 | Smithkline Beckman Intercredit | Compounds |
GB8928281D0 (en) | 1989-12-14 | 1990-02-21 | Smith Kline French Lab | Compounds |
DE4131029A1 (de) * | 1991-09-18 | 1993-07-29 | Basf Ag | Substituierte pyrido (2,3-d) pyrimidine als antidots |
AU661533B2 (en) * | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
GB9323290D0 (en) * | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
TW263498B (es) * | 1993-11-10 | 1995-11-21 | Takeda Pharm Industry Co Ltd | |
US6395733B1 (en) | 1995-06-07 | 2002-05-28 | Pfizer Inc | Heterocyclic ring-fused pyrimidine derivatives |
AR004010A1 (es) | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
GB9603097D0 (en) * | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline compounds |
GB9603095D0 (en) * | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
PL331154A1 (en) * | 1996-07-13 | 1999-06-21 | Glaxo Group Ltd | Bicyclic heteroaromatic compounds as inhibitors of proteinous tyrosine kinase |
HRP970371A2 (en) * | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
US6391874B1 (en) * | 1996-07-13 | 2002-05-21 | Smithkline Beecham Corporation | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
US6225318B1 (en) * | 1996-10-17 | 2001-05-01 | Pfizer Inc | 4-aminoquinazolone derivatives |
WO1998023613A1 (en) * | 1996-11-27 | 1998-06-04 | Pfizer Inc. | Fused bicyclic pyrimidine derivatives |
CO4940469A1 (es) * | 1997-03-05 | 2000-07-24 | Sugen Inc | Composicion oral de estabilidad mejorada que comprende un derivado de indolinona y una mezcla de gliceridos o esteres de polietilenglicol |
US5939421A (en) | 1997-07-01 | 1999-08-17 | Signal Pharmaceuticals, Inc. | Quinazoline analogs and related compounds and methods for treating inflammatory conditions |
US6251912B1 (en) * | 1997-08-01 | 2001-06-26 | American Cyanamid Company | Substituted quinazoline derivatives |
RS49779B (sr) * | 1998-01-12 | 2008-06-05 | Glaxo Group Limited, | Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze |
GB2345486A (en) * | 1999-01-11 | 2000-07-12 | Glaxo Group Ltd | Heteroaromatic protein tyrosine kinase inhibitors |
BR0014116A (pt) | 1999-09-21 | 2002-05-21 | Astrazeneca Ab | Uso de um composto, composto, métodos para preparação de um composto, e para inibir aurora 2 quinase em um animal de sangue quente, e, composição farmacêutica |
EP1229025A4 (en) | 1999-10-01 | 2003-04-09 | Japan Energy Corp | NEW QUINAZOLINE DERIVATIVES |
JP2004525071A (ja) * | 2000-07-20 | 2004-08-19 | ニューロジェン コーポレイション | カプサイシン受容体リガンド |
ES2266258T3 (es) | 2000-09-15 | 2007-03-01 | Vertex Pharmaceuticals Incorporated | Compuestos de pirazol utiles como inhibidores de proteina cinasas. |
US7582657B2 (en) * | 2001-12-10 | 2009-09-01 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
EP1461311A2 (en) | 2001-12-26 | 2004-09-29 | Bayer HealthCare AG | Urea derivatives as vr1-antagonists |
TW200406390A (en) | 2002-01-17 | 2004-05-01 | Neurogen Corp | Substituted quinazolin-4-ylamine analogues |
WO2003097586A1 (en) | 2002-05-17 | 2003-11-27 | Janssen Pharmaceutica N.V. | Aminotetralin-derived urea modulators of vanilloid vr1 receptor |
JP2005531574A (ja) | 2002-05-22 | 2005-10-20 | アムジエン・インコーポレーテツド | 痛みの治療にバニロイド受容体リガンドとして使用するためのアミノ−ピリジン、−ピリジンおよびピリダジン誘導体 |
AU2003273856A1 (en) | 2002-09-24 | 2004-04-19 | Bayer Healthcare Ag | Vr1 antagonists for the treatment of urological disorders |
US20040156869A1 (en) * | 2002-12-13 | 2004-08-12 | Neurogen Corporation | 2-substituted quinazolin-4-ylamine analogues |
US20060100245A1 (en) * | 2002-12-19 | 2006-05-11 | Neurogen Corporation | Substituted biphenyl-4-carboxylic acid arylamide analogues |
TW200510373A (en) * | 2003-07-14 | 2005-03-16 | Neurogen Corp | Substituted quinolin-4-ylamine analogues |
US7329664B2 (en) * | 2003-07-16 | 2008-02-12 | Neurogen Corporation | Substituted (7-pyridyl-4-phenylamino-quinazolin-2-yl)-methanol analogues |
US20070105865A1 (en) * | 2003-09-09 | 2007-05-10 | Neurogen Corporation | Substituted bicyclic quinazolin-4-ylamine derivatives |
AU2004285052A1 (en) * | 2003-10-31 | 2005-05-12 | Neurogen Corporation | 4-amino (AZA) quinoline derivatives as capsaicin receptor agonists |
TW200621251A (en) * | 2004-10-12 | 2006-07-01 | Neurogen Corp | Substituted biaryl quinolin-4-ylamine analogues |
AU2006204752A1 (en) * | 2005-01-14 | 2006-07-20 | Neurogen Corporation | Heteroaryl substituted quinolin-4-ylamine analogues |
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2003
- 2003-12-12 US US10/735,607 patent/US20040156869A1/en not_active Abandoned
- 2003-12-12 JP JP2004560827A patent/JP2006515846A/ja not_active Withdrawn
- 2003-12-12 EP EP03813410A patent/EP1569925A1/en not_active Withdrawn
- 2003-12-12 WO PCT/US2003/039607 patent/WO2004055004A1/en active Application Filing
- 2003-12-12 AU AU2003300898A patent/AU2003300898A1/en not_active Abandoned
- 2003-12-12 CA CA002509233A patent/CA2509233A1/en not_active Abandoned
- 2003-12-12 BR BR0317168-0A patent/BR0317168A/pt not_active Application Discontinuation
- 2003-12-12 MX MXPA05006123A patent/MXPA05006123A/es not_active Application Discontinuation
- 2003-12-12 US US10/539,031 patent/US7432275B2/en not_active Expired - Fee Related
- 2003-12-12 TW TW092135120A patent/TW200418480A/zh unknown
- 2003-12-12 KR KR1020057010845A patent/KR20050084292A/ko not_active Withdrawn
- 2003-12-12 JP JP2004560828A patent/JP2006515847A/ja not_active Withdrawn
- 2003-12-12 CA CA002509239A patent/CA2509239A1/en not_active Abandoned
- 2003-12-12 AU AU2003296984A patent/AU2003296984A1/en not_active Abandoned
- 2003-12-12 EP EP03813411A patent/EP1569926A1/en not_active Withdrawn
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- 2003-12-12 CN CNA2003801058156A patent/CN1726205A/zh active Pending
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AU2003296984A1 (en) | 2004-07-09 |
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US20040156869A1 (en) | 2004-08-12 |
EP1569926A1 (en) | 2005-09-07 |
BR0317168A (pt) | 2005-11-01 |
MXPA05006123A (es) | 2005-09-30 |
AU2003300898A1 (en) | 2004-07-09 |
US7432275B2 (en) | 2008-10-07 |
AR042461A1 (es) | 2005-06-22 |
JP2006515847A (ja) | 2006-06-08 |
JP2006515846A (ja) | 2006-06-08 |
CN1726205A (zh) | 2006-01-25 |
WO2004055003A1 (en) | 2004-07-01 |
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