TN2013000529A1 - Trpm8 antagonists and their use in treatments - Google Patents
Trpm8 antagonists and their use in treatmentsInfo
- Publication number
- TN2013000529A1 TN2013000529A1 TNP2013000529A TN2013000529A TN2013000529A1 TN 2013000529 A1 TN2013000529 A1 TN 2013000529A1 TN P2013000529 A TNP2013000529 A TN P2013000529A TN 2013000529 A TN2013000529 A TN 2013000529A TN 2013000529 A1 TN2013000529 A1 TN 2013000529A1
- Authority
- TN
- Tunisia
- Prior art keywords
- compounds
- treatments
- trpm8
- useful
- disorders
- Prior art date
Links
- 101150111302 Trpm8 gene Proteins 0.000 title abstract 3
- 239000005557 antagonist Substances 0.000 title abstract 2
- 238000011282 treatment Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 208000035475 disorder Diseases 0.000 abstract 3
- 102000003610 TRPM8 Human genes 0.000 abstract 2
- 208000019695 Migraine disease Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- 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
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- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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- 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
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- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161500843P | 2011-06-24 | 2011-06-24 | |
| PCT/US2012/043566 WO2012177893A2 (fr) | 2011-06-24 | 2012-06-21 | Antagonistes de trpm8 et leur utilisation dans des traitements |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2013000529A1 true TN2013000529A1 (en) | 2015-03-30 |
Family
ID=46384521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2013000529A TN2013000529A1 (en) | 2011-06-24 | 2013-12-23 | Trpm8 antagonists and their use in treatments |
Country Status (23)
| Country | Link |
|---|---|
| US (3) | US8710043B2 (fr) |
| EP (1) | EP2723717A2 (fr) |
| JP (1) | JP2014527511A (fr) |
| KR (1) | KR20140045507A (fr) |
| CN (1) | CN103906733A (fr) |
| AP (1) | AP2013007331A0 (fr) |
| AR (1) | AR086750A1 (fr) |
| AU (1) | AU2012272895B2 (fr) |
| BR (1) | BR112013033316A2 (fr) |
| CA (1) | CA2839699A1 (fr) |
| CL (1) | CL2013003715A1 (fr) |
| CO (1) | CO6852073A2 (fr) |
| CR (1) | CR20140037A (fr) |
| EA (1) | EA201490152A1 (fr) |
| MA (1) | MA35271B1 (fr) |
| MX (1) | MX2013015274A (fr) |
| MY (1) | MY157429A (fr) |
| PE (1) | PE20140868A1 (fr) |
| PH (1) | PH12013502611A1 (fr) |
| TN (1) | TN2013000529A1 (fr) |
| TW (2) | TW201429948A (fr) |
| UY (1) | UY34160A (fr) |
| WO (1) | WO2012177893A2 (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
| SG11201702483QA (en) | 2014-09-29 | 2017-04-27 | Scripps Research Inst | Sphingosine-1-phospate receptor modulators for treatment of cardiopulmonary disorders |
| US9765026B2 (en) * | 2015-08-28 | 2017-09-19 | Scinopharm Taiwan, Ltd. | Forms of apremilast and the process of making the same |
| CN113384577A (zh) * | 2016-06-13 | 2021-09-14 | 田边三菱制药株式会社 | 用于治疗或预防血管舒缩症状的组合物 |
| JP2020524717A (ja) * | 2017-06-22 | 2020-08-20 | キュラデブ・ファーマ・リミテッドCuradev Pharma Limited | ヒトstingの小分子調節因子 |
| JP7296954B2 (ja) | 2017-06-22 | 2023-06-23 | キュラデブ・ファーマ・リミテッド | ヒトstingの小分子調節因子 |
| AR113963A1 (es) | 2017-12-19 | 2020-07-01 | Mitsubishi Tanabe Pharma Corp | Composiciones y métodos para el tratamiento o la prevención de los síntomas vasomotores |
| US11279668B2 (en) * | 2018-03-21 | 2022-03-22 | Piramal Pharma Limited | Asymmetric synthesis of alpha-(diarylmethyl) alkyl amines |
| EP3781547A4 (fr) * | 2018-04-18 | 2022-04-13 | Piramal Pharma Limited | Synthèse asymétrique améliorée d'amines chirales alpha-ramifiées |
| CN110981795B (zh) * | 2019-12-18 | 2021-02-12 | 武汉世纪久海检测技术有限公司 | 一种利用2-氰基异烟酸甲酯制备2-氨酰基异烟酸的方法 |
| MX2022015579A (es) * | 2020-06-17 | 2023-01-24 | Merck Sharp & Dohme Llc | 2-oxo-oxazolidin-5-carboxamidas como inhibidores de nav1.8. |
| IL299180A (en) | 2020-06-17 | 2023-02-01 | Merck Sharp & Dohme Llc | 2-oxoimidazolidine-4-carboxamides as nav1.8 inhibitors |
| EP4167993A4 (fr) * | 2020-06-17 | 2024-07-24 | Merck Sharp & Dohme LLC | 2-oxoimidazolidine-3-carboxamides utiles en tant qu'inhibiteurs de nav1.8 |
| CN117561244A (zh) * | 2021-06-08 | 2024-02-13 | 杭州格博生物医药有限公司 | 异吲哚啉酮类化合物及其用途 |
| CN115108980B (zh) * | 2022-06-22 | 2023-06-16 | 济南大学 | 一种2-甲基喹啉类化合物的4号位酰基化衍生物的制备方法 |
| CN120025283A (zh) * | 2023-11-28 | 2025-05-23 | 成都地奥制药集团有限公司 | 酰胺类化合物及其用途 |
| CN119118901B (zh) * | 2024-09-09 | 2025-09-30 | 中国人民解放军北部战区总医院 | 一种氧吲哚类衍生物及其制备方法与在trpa1抑制剂方向的应用 |
Family Cites Families (178)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2483250A (en) * | 1949-09-27 | Tt a it tt | ||
| DE2417763A1 (de) | 1974-04-11 | 1975-10-30 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE2428673A1 (de) | 1974-06-14 | 1976-01-02 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| US5081131A (en) | 1986-01-13 | 1992-01-14 | American Cyanamid Company | Omega-((hetero)alkyl)benz(cd)-indol-2-amines |
| US5223499A (en) | 1989-05-30 | 1993-06-29 | Merck & Co., Inc. | 6-amino substituted imidazo[4,5-bipyridines as angiotensin II antagonists |
| ZA913730B (en) | 1990-05-30 | 1992-02-26 | Ici Plc | Anti-tumor compounds |
| US5380721A (en) | 1990-09-10 | 1995-01-10 | Sterling Winthrop Inc. | Aryl-fused and hetaryl-fused-2,4-diazepine and 2,4-diazocine antiarrhythmic agents |
| WO1992012973A1 (fr) | 1991-01-23 | 1992-08-06 | Nippon Kayaku Kabushiki Kaisha | Derive de chromane |
| ES2036926B1 (es) | 1991-08-08 | 1994-01-16 | Uriach & Cia Sa J | "procedimiento para la obtencion de derivados de la (2-alquil-3-piridil)metilpiperazina". |
| JP2600644B2 (ja) | 1991-08-16 | 1997-04-16 | 藤沢薬品工業株式会社 | チアゾリルベンゾフラン誘導体 |
| DE4135474A1 (de) | 1991-10-28 | 1993-04-29 | Bayer Ag | 2-aminomethyl-chromane |
| DE4138819A1 (de) | 1991-11-26 | 1993-05-27 | Basf Ag | Hydroxypyridoncarbonsaeureamide, deren herstellung und verwendung |
| GB9127041D0 (en) | 1991-12-20 | 1992-02-19 | Fujisawa Pharmaceutical Co | New use |
| FR2692895A1 (fr) | 1992-06-26 | 1993-12-31 | Adir | Nouveaux 1-oxo 2,4,5,6-tétrahydro 2,3,7-triazaphénalènes leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent. |
| DE4304455A1 (de) | 1993-02-15 | 1994-08-18 | Bayer Ag | Heterocyclisch substituierte Phenyl-cyclohexan-carbonsäurederivate |
| JPH07179488A (ja) | 1993-11-12 | 1995-07-18 | Tanabe Seiyaku Co Ltd | グルコサミン誘導体、その製法及びその合成中間体 |
| CN1183770A (zh) | 1994-12-23 | 1998-06-03 | 卡尔·托马博士公司 | 哌嗪衍生物,含该化合物的药物,其用途以及制法 |
| AU707084B2 (en) | 1995-03-14 | 1999-07-01 | Edward G. Shaskan | Compositions comprising nicotynylalanine and an inhibitor of glycine conjugation or vitamin B6 |
| US5891872A (en) | 1995-04-07 | 1999-04-06 | Schering Corporation | Tricyclic compounds |
| IL117940A (en) | 1995-04-19 | 2003-06-24 | Kumiai Chemical Industry Co | Benzylsulfide derivatives, process for their production and insecticide compositions containing them |
| DE19518681A1 (de) | 1995-05-22 | 1996-11-28 | Bayer Ag | Verfahren zur Herstellung von 5,6-Dihydro-1,3-oxazinen |
| DE19523087A1 (de) | 1995-06-26 | 1997-01-02 | Bayer Ag | 1,3-Oxa(thia)zin-Derivate |
| IL118631A (en) | 1995-06-27 | 2002-05-23 | Tanabe Seiyaku Co | History of pyridazinone and processes for their preparation |
| GB9518552D0 (en) | 1995-09-11 | 1995-11-08 | Fujisawa Pharmaceutical Co | New heterocyclic compounds |
| EP0858457A1 (fr) | 1995-10-20 | 1998-08-19 | Dr. Karl Thomae GmbH | Heterocycles a 5 chainons, medicaments contenant ces composes, utilisation et procede de production correspondants |
| GB9525828D0 (en) | 1995-12-18 | 1996-02-21 | Bayer Ag | Use of hetarylacetic acid derivatives |
| US5977090A (en) | 1996-09-27 | 1999-11-02 | Guilford Pharmaceuticals Inc. | Pharmaceutical compositions and methods of treating compulsive disorders using NAALADase inhibitors |
| US6268384B1 (en) | 1997-08-29 | 2001-07-31 | Vertex Pharmaceuticals Incorporated | Compounds possessing neuronal activity |
| US6075029A (en) | 1998-01-02 | 2000-06-13 | Cell Therapeutics, Inc. | Xanthine modulators of metabolism of cellular P-450 |
| AU742423B2 (en) | 1998-01-21 | 2002-01-03 | Msd K.K. | Substituted 5-(2,2-difluoro-1,3-benzodioxol-5-yl) cyclopentenopyridine derivative |
| WO1999062486A1 (fr) | 1998-06-03 | 1999-12-09 | Gpi Nil Holdings Inc. | Compositions pour la croissance des cheveux a base de n-oxydes de ketones, de thioesters, d'amides ou d'esters heterocycliques, et utilisation de ces compositions |
| US5910595A (en) | 1998-06-26 | 1999-06-08 | Salsbury Chemicals, Inc. | Process for preparing oximidazoles |
| US6617351B1 (en) | 1998-07-31 | 2003-09-09 | Eli Lilly And Company | Amide, carbamate, and urea derivatives |
| US6166028A (en) | 1998-12-09 | 2000-12-26 | American Home Products Corporation | Diaminopuridine-containing thiourea inhibitors of herpes viruses |
| WO2000035889A1 (fr) | 1998-12-11 | 2000-06-22 | Sankyo Company, Limited | Benzylamines substituees |
| EP1058549A4 (fr) | 1998-12-23 | 2003-11-12 | Bristol Myers Squibb Pharma Co | INHIBITEURS DU FACTEUR Xa OU DE LA THROMBINE |
| US6200993B1 (en) | 1999-05-05 | 2001-03-13 | Merck Frosst Canada & Co. | Heterosubstituted pyridine derivatives as PDE4 inhibitors |
| CZ290178B6 (cs) | 1999-07-22 | 2002-06-12 | Sankyo Company Limited | Deriváty cyklobutenu |
| GB9919588D0 (en) | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| WO2001016271A1 (fr) | 1999-09-01 | 2001-03-08 | Unilever Plc | Composition et procede de blanchiment d'un substrat |
| BR0013592A (pt) | 1999-09-01 | 2002-05-07 | Unilever Nv | Embalagem comercial para alvejar manchas de tecido em um licor de lavagem aquoso, e, uso da mesma |
| BR0013593A (pt) | 1999-09-01 | 2002-05-07 | Unilever Nv | Método para alvejar manchas de tecido |
| US7291641B2 (en) | 1999-10-11 | 2007-11-06 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derivatives of heterocycles with 5 members, their preparation and their use as medicaments |
| CA2325358C (fr) | 1999-11-10 | 2005-08-02 | Pfizer Products Inc. | Amides de l'acide 7-¬(4'-trifluoromethylbiphenyl-2-carbonyl)amino|-quinoleine-3-carboxylique et methodes pour inhiber la secretion d'apolipoproteine b |
| IL139450A0 (en) | 1999-11-10 | 2001-11-25 | Pfizer Prod Inc | Methods of administering apo b-secretion/mtp inhibitors |
| NZ519238A (en) | 1999-11-10 | 2003-11-28 | Takeda Chemical Industries Ltd | 5-membered N-heterocyclic compounds with hypolglycemic and hypolipidemic activity |
| TW574193B (en) | 1999-12-03 | 2004-02-01 | Astrazeneca Ab | Novel phenalkyloxy-phenyl derivatives, pharmaceutical composition containing the same and their uses |
| NZ518886A (en) | 1999-12-28 | 2004-02-27 | Pfizer Prod Inc | Non-peptidyl inhibitors of VLA-4 dependent cell binding useful in treating inflammatory, autoimmune, and respiratory diseases |
| WO2001055106A2 (fr) | 2000-01-28 | 2001-08-02 | Melacure Therapeutics Ab | Nouveaux agonistes et antagonistes de recepteurs des melanocortines |
| WO2001058869A2 (fr) | 2000-02-11 | 2001-08-16 | Bristol-Myers Squibb Company | Modulateurs de recepteurs aux cannabinoides, leurs procedes de preparation et utilisations de modulateurs de recepteurs aux cannabinoides pour le traitement de maladies respiratoires et non respiratoires |
| US20020019527A1 (en) | 2000-04-27 | 2002-02-14 | Wei-Bo Wang | Substituted phenyl farnesyltransferase inhibitors |
| CA2407093A1 (fr) | 2000-04-27 | 2001-11-01 | Gary T. Wang | Inhibiteurs de phenyle farnesyltransferase substitues |
| US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
| US6417367B1 (en) | 2000-08-11 | 2002-07-09 | Pfizer Inc. | Methods of making quinoline amides |
| US20030050211A1 (en) | 2000-12-14 | 2003-03-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Enzymatic detergent compositions |
| WO2002051396A1 (fr) | 2000-12-26 | 2002-07-04 | Sankyo Company, Limited | Compositions pharmaceutiques contenant des derives de cyclobutene |
| US20040106635A1 (en) | 2001-03-29 | 2004-06-03 | Iwao Takamuro | Spiroisoquinoline compound, a method for preparing the same and an intermediate thereof |
| DE10121003A1 (de) | 2001-04-28 | 2002-12-19 | Aventis Pharma Gmbh | Anthranilsäureamide, Verfahren zur Herstellung, ihrer Verwendung als Medikament sowie sie enthaltende pharmazeutische Zubereitungen |
| MY130373A (en) | 2001-10-29 | 2007-06-29 | Malesci Sas | Linear basic compounds having nk-2 antagonist activity and formulations thereof |
| ES2303558T3 (es) | 2001-11-27 | 2008-08-16 | F. Hoffmann-La Roche Ag | Derivados de benzotiazol. |
| US20050038035A1 (en) | 2001-11-28 | 2005-02-17 | Hisashi Takasugi | Heterocyclic amide compounds as apolipoprotein b inhibitors |
| TWI261053B (en) | 2001-12-06 | 2006-09-01 | Novartis Ag | Amidoacetonitrile compounds, their preparation, compositions and use as pesticides |
| SE0104248D0 (sv) | 2001-12-14 | 2001-12-14 | Astrazeneca Ab | Method of treatment |
| KR100659428B1 (ko) | 2002-02-04 | 2006-12-19 | 에프. 호프만-라 로슈 아게 | Npy 길항제로서의 퀴놀린 유도체 |
| AU2003240757B2 (en) | 2002-03-28 | 2008-07-03 | Merck Serono Sa | Thiazolidine carboxamide derivatives as modulators of the prostaglandin F receptor |
| JP4570878B2 (ja) | 2002-04-11 | 2010-10-27 | メルク・シャープ・エンド・ドーム・コーポレイション | 選択的糖質コルチコイド受容体モジュレーターとしての1H−ベンゾ[f]インダゾール−5−イル誘導体 |
| FR2838739B1 (fr) | 2002-04-19 | 2004-05-28 | Sanofi Synthelabo | Derives de n-[phenyl(piperidin-2-yl)methyl)benzamide, leur preparation et leur application en therapeutique |
| KR20040104643A (ko) | 2002-04-26 | 2004-12-10 | 이시하라 산교 가부시끼가이샤 | 피리딘계 화합물 또는 이의 염 및 이들을 함유하는 제초제 |
| US7375093B2 (en) | 2002-07-05 | 2008-05-20 | Intrexon Corporation | Ketone ligands for modulating the expression of exogenous genes via an ecdysone receptor complex |
| FR2842805A1 (fr) | 2002-07-29 | 2004-01-30 | Sanofi Synthelabo | Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide,leur preparation et leur application et therapeutique |
| GB0221697D0 (en) | 2002-09-18 | 2002-10-30 | Unilever Plc | Novel compouds and their uses |
| CA2499497A1 (fr) | 2002-09-27 | 2004-04-08 | Merck & Co., Inc. | Pyrimidines substituees |
| WO2004039795A2 (fr) | 2002-10-29 | 2004-05-13 | Fujisawa Pharmaceutical Co., Ltd. | Composes amide |
| US7618959B2 (en) | 2002-11-05 | 2009-11-17 | Smithklinebeecham Corp | Antibacterial agents |
| WO2004058755A2 (fr) | 2002-12-24 | 2004-07-15 | Biofocus Plc | Bibliotheques de composes |
| US7601868B2 (en) | 2003-02-12 | 2009-10-13 | Takeda Pharmaceutical Company Limited | Amine derivative |
| EP1625115A1 (fr) | 2003-05-09 | 2006-02-15 | Pharmacia & Upjohn Company LLC | Derives pyrimidiques substitues |
| WO2005005392A1 (fr) | 2003-07-07 | 2005-01-20 | Ionix Pharmaceuticals Limited | Composes azacycliques convenant comme inhibiteurs des canaux specifiques des neurones sensoriels |
| EP1776362A1 (fr) | 2003-07-18 | 2007-04-25 | Virochem Pharma Inc. | Composes spiro et procedes pour moduler une activite de recepteur de chimiokime |
| US7094791B2 (en) | 2003-07-31 | 2006-08-22 | Avalon Pharmaceuticals, Inc. | Derivatives of 3-hydroxy-pyrrole-2,4-dicarboxylic acid and uses thereof |
| WO2005021545A1 (fr) | 2003-09-03 | 2005-03-10 | Galapagos Nv | Derives d'imidazo[1,5-a]pyridine ou d'imidazo[1,5-a]piperidine et leur utilisation dans la preparation d'un medicament dirige contre les troubles lies au recepteur 5-ht2a |
| GB0320983D0 (en) | 2003-09-08 | 2003-10-08 | Biofocus Plc | Compound libraries |
| WO2005023810A1 (fr) | 2003-09-10 | 2005-03-17 | Virochem Pharma Inc. | Composes de spirohydantoine et procedes de modulation de l'activite des recepteurs de chimiokine |
| AR046276A1 (es) * | 2003-10-07 | 2005-11-30 | Renovis Inc | Derivados de amida como ligandos de canales ionicos y composiciones farmaceuticas y metodos que los utilizan. |
| US20050176767A1 (en) | 2003-10-30 | 2005-08-11 | Laval Chan Chun Kong | Pyridine carboxamide and methods for inhibiting HIV integrase |
| EP1716137A1 (fr) | 2004-02-04 | 2006-11-02 | Pfizer Products Incorporated | Composes de quinoline substitues |
| GB0403578D0 (en) | 2004-02-18 | 2004-03-24 | Biofocus Discovery Ltd | Compounds which interact with the G-protein coupled receptor family |
| JP2007526324A (ja) | 2004-03-02 | 2007-09-13 | スミスクライン・ビーチャム・コーポレイション | Akt活性のある阻害剤 |
| MXPA06011414A (es) | 2004-03-31 | 2007-04-20 | Johnson & Johnson | Compuestos heterociclicos sin imidazol como ligandos del receptor de h3 histamina. |
| DE102004022897A1 (de) | 2004-05-10 | 2005-12-08 | Bayer Cropscience Ag | Azinyl-imidazoazine |
| US7550499B2 (en) | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| EP1758571A1 (fr) | 2004-05-29 | 2007-03-07 | 7TM Pharma A/S | Ligands du recepteur crth2 utilises a des fins therapeutiques |
| DE102004039876A1 (de) | 2004-06-23 | 2006-01-26 | Lanxess Deutschland Gmbh | Herstellung von fluorierten 1,3-Benzodioxanen |
| DE102004031323A1 (de) | 2004-06-29 | 2006-01-19 | Bayer Cropscience Ag | Substituierte Pyridazincarboxamide und Derivate hiervon |
| CN101035783A (zh) * | 2004-08-30 | 2007-09-12 | 神经医药品有限公司 | 作为钙通道阻断剂的脲衍生物 |
| AR050926A1 (es) | 2004-09-03 | 2006-12-06 | Astrazeneca Ab | Derivados de benzamida como inhibidores de la histonadesacetilasa(hdac) |
| KR100677149B1 (ko) | 2004-11-12 | 2007-02-02 | 삼성전자주식회사 | 잉크 조성물 |
| JPWO2006057448A1 (ja) | 2004-11-26 | 2008-06-05 | 武田薬品工業株式会社 | アリールアルカン酸誘導体 |
| US20080306055A1 (en) | 2004-12-21 | 2008-12-11 | Astrazeneca Ab | Heterocyclic Mchr1 Antagonists And Their Use In Therapy |
| US20060173183A1 (en) | 2004-12-31 | 2006-08-03 | Alantos Pharmaceuticals, Inc., | Multicyclic bis-amide MMP inhibitors |
| CA2593718A1 (fr) | 2004-12-31 | 2007-05-31 | Gpc Biotech Ag | Composes de naphtyridine utilises comme inhibiteurs de rock |
| WO2006080884A1 (fr) | 2005-01-27 | 2006-08-03 | Astrazeneca Ab | Nouveaux composes biaromatiques, inhibiteurs du recepteur p2x7 |
| WO2006094246A2 (fr) | 2005-03-03 | 2006-09-08 | Sirtris Pharmaceuticals, Inc. | Modulateurs de sirtuine a base de n-arylmethyl benzamide |
| US20070155738A1 (en) | 2005-05-20 | 2007-07-05 | Alantos Pharmaceuticals, Inc. | Heterobicyclic metalloprotease inhibitors |
| BRPI0613535A2 (pt) | 2005-06-02 | 2011-01-18 | Bayer Cropscience Ag | derivados de heteroarila substituìda por fenilalquila |
| JP5340729B2 (ja) | 2005-06-13 | 2013-11-13 | メルク シャープ エンド ドーム リミテッド | 治療剤 |
| CA2613517A1 (fr) | 2005-06-27 | 2007-01-04 | Exelixis, Inc. | Modulateurs des lxr a base de pyrazoles |
| CA2609319C (fr) | 2005-07-15 | 2014-02-04 | Nissan Chemical Industries, Ltd. | Composes thiophenes et activateurs du recepteur thrombopoietine |
| CN100494167C (zh) | 2005-08-02 | 2009-06-03 | 天津大学 | 抗乙肝病毒的叔胺氧化物及制备方法和制备药物的应用 |
| WO2007017093A1 (fr) | 2005-08-04 | 2007-02-15 | Bayer Healthcare Ag | Derives amides d'acide 2-benzyloxy-benzoique substitue |
| EP1764098A1 (fr) | 2005-09-17 | 2007-03-21 | Speedel Experimenta AG | Dérivés de diaminoalcols et leur utilization pour le traitement de la malaria, de la maladie d'Alzheimer et du SIDA |
| EP1948172A1 (fr) | 2005-11-10 | 2008-07-30 | Bayer HealthCare AG | Diaryle-urees servant a traiter une neuropathie diabetique |
| PL1948176T3 (pl) | 2005-11-10 | 2011-05-31 | Bayer Schering Pharma Ag | Diarylomoczniki do leczenia nadciśnienia płucnego |
| US7888376B2 (en) | 2005-11-23 | 2011-02-15 | Bristol-Myers Squibb Company | Heterocyclic CETP inhibitors |
| DE102005059479A1 (de) | 2005-12-13 | 2007-06-14 | Merck Patent Gmbh | Hydroxychinolinderivate |
| EP1962829A1 (fr) | 2005-12-15 | 2008-09-03 | Bayer HealthCare AG | Urees de diaryle pour le traitement des infections virales |
| WO2007068381A1 (fr) | 2005-12-15 | 2007-06-21 | Bayer Healthcare Ag | Diaryle-urees pour le traitement de maladies inflammatoires de la peau, l'oeil et/ou l'oreille |
| TWI412322B (zh) | 2005-12-30 | 2013-10-21 | Du Pont | 控制無脊椎害蟲之異唑啉 |
| WO2007086799A1 (fr) | 2006-01-27 | 2007-08-02 | Astrazeneca Ab | Quinoléines substituées par un amide |
| EP1987037A2 (fr) | 2006-02-23 | 2008-11-05 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique fusionné |
| DE102006012251A1 (de) | 2006-03-15 | 2007-11-08 | Grünenthal GmbH | Substituierte 4-Amino-chinazolin-Derivate und ihre Verwendung zur Herstellung von Arzneimitteln |
| PL2010493T3 (pl) * | 2006-04-12 | 2016-08-31 | Merck Sharp & Dohme | Pirydyloamidy jako antagoniści kanałów wapniowych typu t |
| JP2009538317A (ja) | 2006-05-26 | 2009-11-05 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 癌治療のための置換ジアリールウレアを用いた薬物の組み合わせ |
| GB0611152D0 (en) | 2006-06-06 | 2006-07-19 | Ucb Sa | Therapeutic agents |
| WO2008003746A1 (fr) | 2006-07-06 | 2008-01-10 | Bayer Cropscience Sa | Nouveaux dérivés de n-(4-pyridin-2-ylbutyle) carboxamide, procédé de préparation et utilisation comme fongicides |
| RU2009106461A (ru) | 2006-07-25 | 2010-08-27 | Энвиво Фармасьютикалз, Инк. (Us) | Хинолиновые производные |
| WO2008022938A1 (fr) * | 2006-08-21 | 2008-02-28 | F. Hoffmann-La Roche Ag | Amides di-aromatiques substitués en tant qu'inhibiteurs de la glyt1 |
| US7834023B2 (en) | 2006-09-20 | 2010-11-16 | Portola Pharmaceuticals, Inc. | Substituted dihydroquinazolines as platelet ADP receptor inhibitors |
| WO2008056687A1 (fr) | 2006-11-09 | 2008-05-15 | Daiichi Sankyo Company, Limited | Nouveau dérivé de spiropipéridine |
| WO2008063670A1 (fr) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Inhibiteurs de métalloprotéases hétérobicycliques |
| WO2008063667A1 (fr) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Inhibiteurs de métalloprotéase hétérotricyclique |
| WO2008073825A1 (fr) | 2006-12-08 | 2008-06-19 | Exelixis, Inc. | Modulateurs lxr et fxr |
| CN101641351A (zh) | 2006-12-21 | 2010-02-03 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| WO2008112156A1 (fr) | 2007-03-08 | 2008-09-18 | Altiris Therapeutics | Modulateurs des récepteurs des chimiokines |
| AU2008239754A1 (en) | 2007-04-11 | 2008-10-23 | Merck Sharp & Dohme Corp. | CGRP receptor antagonists with tertiary amide, sulfonamide, carbamate and urea end groups |
| WO2008153849A1 (fr) | 2007-06-05 | 2008-12-18 | Merck & Co., Inc. | Antagonistes des récepteurs cgrp à base de carboxamide hétérocyclique |
| US20100261723A1 (en) | 2007-07-09 | 2010-10-14 | Astrazeneca Ab | Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases |
| WO2009023179A2 (fr) | 2007-08-10 | 2009-02-19 | Genelabs Technologies, Inc. | Entités chimiques bicycliques azotées pour traiter les infections virales |
| JP2010535855A (ja) | 2007-08-10 | 2010-11-25 | クリスタルゲノミクス、インク. | ピリジン誘導体およびその使用方法 |
| US20090082358A1 (en) | 2007-09-20 | 2009-03-26 | Nobuko Nishimura | Vanilloid receptor ligands and their use in treatments |
| US8476297B2 (en) | 2007-12-04 | 2013-07-02 | Amgen Inc. | TRP-M8 receptor ligands and their use in treatments |
| JPWO2009072621A1 (ja) | 2007-12-07 | 2011-04-28 | 日産化学工業株式会社 | 置換ジヒドロアゾール化合物及び有害生物防除剤 |
| CN102036981B (zh) * | 2008-03-18 | 2015-04-08 | 默沙东公司 | 取代的4-羟基嘧啶-5-甲酰胺 |
| EP2272841A1 (fr) | 2008-03-28 | 2011-01-12 | Banyu Pharmaceutical Co., Ltd. | Dérivé de diarylméthylamide à activité antagoniste sur un récepteur d'hormone concentrant la mélanine |
| CA2720530A1 (fr) | 2008-04-11 | 2009-10-15 | Merck Serono S.A. | Sulfonamides |
| DE102008019838A1 (de) | 2008-04-19 | 2009-12-10 | Boehringer Ingelheim International Gmbh | Neue Arylsulfonylglycin-Derivate, deren Herstellung und deren Verwendung als Arzneimittel |
| JP2011523958A (ja) | 2008-06-12 | 2011-08-25 | メルク・シャープ・エンド・ドーム・コーポレイション | Cgrp受容体アンタゴニストとしての分岐状3−及び6−置換キノリン |
| MX2010014441A (es) | 2008-06-25 | 2011-01-21 | Bayer Schering Pharma Ag | Diaril ureas para tratar la insuficiencia cardiaca. |
| WO2010021882A2 (fr) * | 2008-08-19 | 2010-02-25 | Janssen Pharmaceutica Nv | Antagonistes des récepteurs au froid activés par menthol |
| CN101343313B (zh) | 2008-09-03 | 2011-11-16 | 南京农业大学 | 一种葡萄糖二肽类化合物及其制备方法和用途 |
| TWI389913B (zh) | 2008-09-08 | 2013-03-21 | Lg Life Sciences Ltd | 并合雜環化合物 |
| EP2337563B1 (fr) | 2008-09-08 | 2014-04-09 | The Board of Trustees of The Leland Stanford Junior University | Modulateurs de l'activité de l'aldéhyde déshydrogénase et leurs procédés d'utilisation |
| WO2010046780A2 (fr) | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Composés antiviraux |
| TW201030001A (en) | 2008-11-14 | 2010-08-16 | Amgen Inc | Pyridine and pyrimidine derivatives as phosphodiesterase 10 inhibitors |
| UY32525A (es) | 2009-04-03 | 2010-10-29 | Astrazeneca Ab | Compuestos que tienen actividad agonista del receptor de glucocorticosteroides |
| MX2011011428A (es) * | 2009-05-01 | 2011-11-29 | Raqualia Pharma Inc | Derivados de acido sulfamoilbenzoico como antagonistas de trpm8. |
| KR101605061B1 (ko) | 2009-05-29 | 2016-03-21 | 라퀄리아 파마 인코포레이티드 | 칼슘 또는 나트륨 채널 차단제로서의 아릴 치환된 카복사미드 유도체 |
| US8481750B2 (en) | 2009-06-02 | 2013-07-09 | Boehringer Ingelheim International Gmbh | Derivatives of 6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-carboxylic acid amides |
| TW201103941A (en) * | 2009-06-10 | 2011-02-01 | Janssen Pharmaceutica Nv | Benzimidazole derivatives useful as TRPM8 channel modulators |
| EP3871671A3 (fr) | 2009-07-29 | 2022-03-09 | Olsen, Elise | Antagonistes du recepteur fp pour inhiber la pousse des cheveux |
| DE102009028929A1 (de) | 2009-08-27 | 2011-07-07 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Heterocyclisch-substituierte 2-Acetamido-5-Aryl-1,2,4-triazolone und deren Verwendung |
| UY32940A (es) | 2009-10-27 | 2011-05-31 | Bayer Cropscience Ag | Amidas sustituidas con halogenoalquilo como insecticidas y acaricidas |
| US8618302B2 (en) | 2010-01-06 | 2013-12-31 | Joseph P. Errico | Methods and compositions of targeted drug development |
| WO2011094890A1 (fr) | 2010-02-02 | 2011-08-11 | Argusina Inc. | Dérivés phénylalanines et leur utilisation comme modulateurs non peptidiques du récepteur de glp-1 |
| US20110212969A1 (en) | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| JPWO2011142359A1 (ja) | 2010-05-10 | 2013-07-22 | 日産化学工業株式会社 | スピロ化合物及びアディポネクチン受容体活性化薬 |
| EP2571855B1 (fr) | 2010-05-17 | 2014-12-24 | Merck Sharp & Dohme Corp. | Nouveaux inhibiteurs de prolylcarboxypeptidase |
| WO2011147765A1 (fr) | 2010-05-27 | 2011-12-01 | Bayer Cropscience Ag | Dérivés de l'acide pyridinylcarboxylique en tant que fongicides |
| JP2013540145A (ja) | 2010-10-21 | 2013-10-31 | ウニベルシテート デス ザールランデス | コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤 |
| ES2974690T3 (es) | 2010-11-05 | 2024-07-01 | Firmenich Incorporated | Compuestos útiles como moduladores de la TRPM8 |
| EP2649075B1 (fr) | 2010-12-08 | 2018-04-25 | The U.S.A. As Represented By The Secretary, Department Of Health And Human Services | Pyrazolopyrimidines substituées comme activateurs de la glucocerebrosidase |
| WO2012082862A2 (fr) | 2010-12-14 | 2012-06-21 | Beth Israel Deaconess Medical Center | Inhibiteurs du récepteur des androgènes et leurs procédés d'utilisation |
| PT2652025T (pt) | 2010-12-15 | 2018-11-02 | Ppg Europe B V | Composição secante e a sua utilização |
| WO2012083190A1 (fr) | 2010-12-17 | 2012-06-21 | The Rockefeller University | Antagonistes de récepteurs olfactifs d'insecte |
| CN103635472B (zh) | 2011-02-28 | 2018-01-12 | 阵列生物制药公司 | 丝氨酸/苏氨酸激酶抑制剂 |
| WO2012120398A1 (fr) | 2011-03-04 | 2012-09-13 | Pfizer Limited | Dérivés de carboxamide substitués par aryle en tant que modulateurs de trpm8 |
| JP2014517074A (ja) | 2011-06-24 | 2014-07-17 | アムジエン・インコーポレーテツド | Trpm8アンタゴニストおよび治療におけるそれらの使用 |
-
2012
- 2012-06-21 EA EA201490152A patent/EA201490152A1/ru unknown
- 2012-06-21 WO PCT/US2012/043566 patent/WO2012177893A2/fr not_active Ceased
- 2012-06-21 PE PE2013002869A patent/PE20140868A1/es not_active Application Discontinuation
- 2012-06-21 AU AU2012272895A patent/AU2012272895B2/en not_active Ceased
- 2012-06-21 MX MX2013015274A patent/MX2013015274A/es not_active Application Discontinuation
- 2012-06-21 CN CN201280041145.5A patent/CN103906733A/zh active Pending
- 2012-06-21 PH PH1/2013/502611A patent/PH12013502611A1/en unknown
- 2012-06-21 US US13/529,860 patent/US8710043B2/en active Active
- 2012-06-21 MY MYPI2013004627A patent/MY157429A/en unknown
- 2012-06-21 KR KR1020147001927A patent/KR20140045507A/ko not_active Withdrawn
- 2012-06-21 EP EP12730134.9A patent/EP2723717A2/fr not_active Withdrawn
- 2012-06-21 BR BR112013033316A patent/BR112013033316A2/pt not_active IP Right Cessation
- 2012-06-21 AP AP2013007331A patent/AP2013007331A0/xx unknown
- 2012-06-21 JP JP2014517168A patent/JP2014527511A/ja active Pending
- 2012-06-21 CA CA2839699A patent/CA2839699A1/fr not_active Abandoned
- 2012-06-22 TW TW103114426A patent/TW201429948A/zh unknown
- 2012-06-22 TW TW101122538A patent/TWI448454B/zh not_active IP Right Cessation
- 2012-06-25 UY UY0001034160A patent/UY34160A/es not_active Application Discontinuation
- 2012-06-25 AR ARP120102273A patent/AR086750A1/es not_active Application Discontinuation
-
2013
- 2013-12-23 TN TNP2013000529A patent/TN2013000529A1/fr unknown
- 2013-12-24 CL CL2013003715A patent/CL2013003715A1/es unknown
-
2014
- 2014-01-10 CO CO14004185A patent/CO6852073A2/es active IP Right Grant
- 2014-01-20 MA MA36692A patent/MA35271B1/fr unknown
- 2014-01-24 CR CR20140037A patent/CR20140037A/es unknown
- 2014-02-24 US US14/187,677 patent/US9096527B2/en active Active
- 2014-02-24 US US14/187,732 patent/US20140171406A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CO6852073A2 (es) | 2014-01-30 |
| KR20140045507A (ko) | 2014-04-16 |
| CA2839699A1 (fr) | 2012-12-27 |
| US20130157996A1 (en) | 2013-06-20 |
| CN103906733A (zh) | 2014-07-02 |
| JP2014527511A (ja) | 2014-10-16 |
| PE20140868A1 (es) | 2014-07-18 |
| AP2013007331A0 (en) | 2013-12-31 |
| AR086750A1 (es) | 2014-01-22 |
| MY157429A (en) | 2016-06-15 |
| US9096527B2 (en) | 2015-08-04 |
| US20140171406A1 (en) | 2014-06-19 |
| CL2013003715A1 (es) | 2014-06-27 |
| PH12013502611A1 (en) | 2014-04-28 |
| UY34160A (es) | 2012-08-31 |
| AU2012272895A1 (en) | 2013-04-11 |
| CR20140037A (es) | 2014-03-13 |
| AU2012272895B2 (en) | 2015-01-22 |
| TWI448454B (zh) | 2014-08-11 |
| EA201490152A1 (ru) | 2014-05-30 |
| WO2012177893A3 (fr) | 2013-06-13 |
| US8710043B2 (en) | 2014-04-29 |
| MX2013015274A (es) | 2014-03-31 |
| MA35271B1 (fr) | 2014-07-03 |
| WO2012177893A2 (fr) | 2012-12-27 |
| TW201311643A (zh) | 2013-03-16 |
| EP2723717A2 (fr) | 2014-04-30 |
| BR112013033316A2 (pt) | 2017-01-31 |
| TW201429948A (zh) | 2014-08-01 |
| US20140171639A1 (en) | 2014-06-19 |
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