JP4064818B2 - 6−置換ピリド−ピリミジン類 - Google Patents
6−置換ピリド−ピリミジン類 Download PDFInfo
- Publication number
- JP4064818B2 JP4064818B2 JP2002564525A JP2002564525A JP4064818B2 JP 4064818 B2 JP4064818 B2 JP 4064818B2 JP 2002564525 A JP2002564525 A JP 2002564525A JP 2002564525 A JP2002564525 A JP 2002564525A JP 4064818 B2 JP4064818 B2 JP 4064818B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- mmol
- cycloalkyl
- hydrogen
- amino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 0 *C[C@@]1C(*N=C)C1 Chemical compound *C[C@@]1C(*N=C)C1 0.000 description 15
- HGWUUOXXAIISDB-UHFFFAOYSA-N C1C2C1CNC2 Chemical compound C1C2C1CNC2 HGWUUOXXAIISDB-UHFFFAOYSA-N 0.000 description 1
- QDNQZUXNEDSKMF-SOFGYWHQSA-N CC(C(C)(C)O)/C(/C)=N/O Chemical compound CC(C(C)(C)O)/C(/C)=N/O QDNQZUXNEDSKMF-SOFGYWHQSA-N 0.000 description 1
- NCWUOPZDKPNSFG-UHFFFAOYSA-N CC(C(Cc1c(C)cccc1)C(N1C)=O)c2c1nc(NC1(CO)CCCCC1)nc2 Chemical compound CC(C(Cc1c(C)cccc1)C(N1C)=O)c2c1nc(NC1(CO)CCCCC1)nc2 NCWUOPZDKPNSFG-UHFFFAOYSA-N 0.000 description 1
- LGODECIUDNPHQO-UHFFFAOYSA-N CC(C)N(c1c(C=C2Oc(ccc(F)c3)c3F)cnc(S(Cc3ccccc3)(=O)=O)n1)C2=O Chemical compound CC(C)N(c1c(C=C2Oc(ccc(F)c3)c3F)cnc(S(Cc3ccccc3)(=O)=O)n1)C2=O LGODECIUDNPHQO-UHFFFAOYSA-N 0.000 description 1
- LYLPRVUTJGLNPP-UHFFFAOYSA-N CC(CC(C)(C)O)N Chemical compound CC(CC(C)(C)O)N LYLPRVUTJGLNPP-UHFFFAOYSA-N 0.000 description 1
- AMSPAHRCHHWSSW-UHFFFAOYSA-N CC(CC=C1OC(C(N2C)=O)=Cc3c2nc(NC2CCSCC2)nc3)C=C1F Chemical compound CC(CC=C1OC(C(N2C)=O)=Cc3c2nc(NC2CCSCC2)nc3)C=C1F AMSPAHRCHHWSSW-UHFFFAOYSA-N 0.000 description 1
- GOSYXFHOYFGVOW-UHFFFAOYSA-N CCC(CCNC(Oc1ccccc1)=O)Nc1nc(N(C)C(C(Oc(ccc(F)c2)c2F)=C2)=O)c2cn1 Chemical compound CCC(CCNC(Oc1ccccc1)=O)Nc1nc(N(C)C(C(Oc(ccc(F)c2)c2F)=C2)=O)c2cn1 GOSYXFHOYFGVOW-UHFFFAOYSA-N 0.000 description 1
- DDBHIMLKZVWPPV-UHFFFAOYSA-N CCNC(N=C(CCC=C1)SC)=C1C(OCC)=O Chemical compound CCNC(N=C(CCC=C1)SC)=C1C(OCC)=O DDBHIMLKZVWPPV-UHFFFAOYSA-N 0.000 description 1
- QCDOUHFYODXAQJ-UHFFFAOYSA-N CCNc1nc(SC)ncc1CO Chemical compound CCNc1nc(SC)ncc1CO QCDOUHFYODXAQJ-UHFFFAOYSA-N 0.000 description 1
- CPDLXBDVVJCDEQ-UHFFFAOYSA-N CCOC(N(CC1)CCC1Nc1nc(N(C)C(C(Oc(ccc(F)c2)c2F)=C2)=O)c2cn1)=O Chemical compound CCOC(N(CC1)CCC1Nc1nc(N(C)C(C(Oc(ccc(F)c2)c2F)=C2)=O)c2cn1)=O CPDLXBDVVJCDEQ-UHFFFAOYSA-N 0.000 description 1
- IIOKOTJPNBSEHP-UHFFFAOYSA-N CN(CC(OC)=O)c(ccc(F)c1)c1F Chemical compound CN(CC(OC)=O)c(ccc(F)c1)c1F IIOKOTJPNBSEHP-UHFFFAOYSA-N 0.000 description 1
- NEZROUPXRYUIIU-UHFFFAOYSA-N CN(c(ccc(F)c1)c1F)C(C(N1C)=O)=Cc(cn2)c1nc2SC Chemical compound CN(c(ccc(F)c1)c1F)C(C(N1C)=O)=Cc(cn2)c1nc2SC NEZROUPXRYUIIU-UHFFFAOYSA-N 0.000 description 1
- DCLXKEBXLZKEDV-UHFFFAOYSA-N CN(c1c(C=C2Oc(cccc3)c3F)cnc(NC3CCNCC3)n1)C2=O Chemical compound CN(c1c(C=C2Oc(cccc3)c3F)cnc(NC3CCNCC3)n1)C2=O DCLXKEBXLZKEDV-UHFFFAOYSA-N 0.000 description 1
- WDSKEDIRSQIXKA-UHFFFAOYSA-N CN(c1c(C=C2Oc3ccccc3F)cnc(NC(CC3)CCS3=O)n1)C2=O Chemical compound CN(c1c(C=C2Oc3ccccc3F)cnc(NC(CC3)CCS3=O)n1)C2=O WDSKEDIRSQIXKA-UHFFFAOYSA-N 0.000 description 1
- MXCUGZFASBUTCR-UHFFFAOYSA-N CN(c1cc(Cl)ncc1C=C1Oc(ccc(F)c2)c2F)C1=O Chemical compound CN(c1cc(Cl)ncc1C=C1Oc(ccc(F)c2)c2F)C1=O MXCUGZFASBUTCR-UHFFFAOYSA-N 0.000 description 1
- RPGDVPAENGWKAO-UHFFFAOYSA-N CNc(c(F)c1)ccc1F Chemical compound CNc(c(F)c1)ccc1F RPGDVPAENGWKAO-UHFFFAOYSA-N 0.000 description 1
- NXNGLEYSIAXGCL-UHFFFAOYSA-N CNc1nc(SC)ncc1CO Chemical compound CNc1nc(SC)ncc1CO NXNGLEYSIAXGCL-UHFFFAOYSA-N 0.000 description 1
- BBSNGCRLDDIQNF-UHFFFAOYSA-N COC(CN(C(OCc1ccccc1)=O)c(ccc(F)c1)c1F)=O Chemical compound COC(CN(C(OCc1ccccc1)=O)c(ccc(F)c1)c1F)=O BBSNGCRLDDIQNF-UHFFFAOYSA-N 0.000 description 1
- MCUICEQLBVRIIY-UHFFFAOYSA-N COC(COc(cccc1)c1F)=O Chemical compound COC(COc(cccc1)c1F)=O MCUICEQLBVRIIY-UHFFFAOYSA-N 0.000 description 1
- YGXKYXWOJHKSJY-UHFFFAOYSA-N CSc1nc(N(C2CC2)C(C(Oc2ccccc2F)=C2)=O)c2cn1 Chemical compound CSc1nc(N(C2CC2)C(C(Oc2ccccc2F)=C2)=O)c2cn1 YGXKYXWOJHKSJY-UHFFFAOYSA-N 0.000 description 1
- FSMNTIWDSABENX-UHFFFAOYSA-N Cc(cc1)ccc1OC(C(N(C)C1N2)=O)=CC1=CN=C2SC Chemical compound Cc(cc1)ccc1OC(C(N(C)C1N2)=O)=CC1=CN=C2SC FSMNTIWDSABENX-UHFFFAOYSA-N 0.000 description 1
- RNWTXRSVYQJWPO-UHFFFAOYSA-N Cc1ccccc1CC(C(N1C)=O)=Cc(cn2)c1nc2S(C)(=O)=O Chemical compound Cc1ccccc1CC(C(N1C)=O)=Cc(cn2)c1nc2S(C)(=O)=O RNWTXRSVYQJWPO-UHFFFAOYSA-N 0.000 description 1
- JSAYKGNHIVNWPQ-UHFFFAOYSA-N O=C(Nc(ccc(F)c1)c1F)OCc1ccccc1 Chemical compound O=C(Nc(ccc(F)c1)c1F)OCc1ccccc1 JSAYKGNHIVNWPQ-UHFFFAOYSA-N 0.000 description 1
- JSOCKEAVBQVLQD-UHFFFAOYSA-N O=C1Nc2nc(SCc3ccccc3)ncc2C=C1Oc(ccc(F)c1)c1F Chemical compound O=C1Nc2nc(SCc3ccccc3)ncc2C=C1Oc(ccc(F)c1)c1F JSOCKEAVBQVLQD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
-
- 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
-
- 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
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26837501P | 2001-02-12 | 2001-02-12 | |
| US33465401P | 2001-11-30 | 2001-11-30 | |
| PCT/EP2002/001106 WO2002064594A2 (en) | 2001-02-12 | 2002-02-04 | 6-substituted pyrido-pyrimidines |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004525896A JP2004525896A (ja) | 2004-08-26 |
| JP2004525896A5 JP2004525896A5 (https=) | 2005-06-09 |
| JP4064818B2 true JP4064818B2 (ja) | 2008-03-19 |
Family
ID=26953040
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002564525A Expired - Lifetime JP4064818B2 (ja) | 2001-02-12 | 2002-02-04 | 6−置換ピリド−ピリミジン類 |
Country Status (31)
| Country | Link |
|---|---|
| US (3) | US6696566B2 (https=) |
| EP (1) | EP1361880B1 (https=) |
| JP (1) | JP4064818B2 (https=) |
| KR (1) | KR100639772B1 (https=) |
| CN (1) | CN100376571C (https=) |
| AR (1) | AR035854A1 (https=) |
| AT (1) | ATE305303T1 (https=) |
| AU (1) | AU2002256615B2 (https=) |
| BR (1) | BRPI0207172B8 (https=) |
| CA (1) | CA2434834C (https=) |
| CZ (1) | CZ20032416A3 (https=) |
| DE (1) | DE60206363T2 (https=) |
| DK (1) | DK1361880T3 (https=) |
| ES (1) | ES2249574T3 (https=) |
| HR (1) | HRP20030624B1 (https=) |
| HU (1) | HU229604B1 (https=) |
| IL (2) | IL156872A0 (https=) |
| JO (1) | JO2410B1 (https=) |
| MA (1) | MA26993A1 (https=) |
| MX (1) | MXPA03007166A (https=) |
| MY (1) | MY131518A (https=) |
| NO (1) | NO326133B1 (https=) |
| NZ (1) | NZ526961A (https=) |
| PA (1) | PA8539201A1 (https=) |
| PE (1) | PE20020976A1 (https=) |
| PL (1) | PL366918A1 (https=) |
| RU (1) | RU2269527C2 (https=) |
| SK (1) | SK11322003A3 (https=) |
| WO (1) | WO2002064594A2 (https=) |
| YU (1) | YU63703A (https=) |
| ZA (1) | ZA200305938B (https=) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7053070B2 (en) * | 2000-01-25 | 2006-05-30 | Warner-Lambert Company | Pyrido[2,3-d]pyrimidine-2,7-diamine kinase inhibitors |
| DE60206363T2 (de) | 2001-02-12 | 2006-07-06 | F. Hoffmann-La Roche Ag | 6-substituierte pyridopyrimidine |
| MXPA04005939A (es) | 2002-01-22 | 2005-01-25 | Warner Lambert Co | 2-(piridin-2-ilamino)-pirido[2,3-d]pirimidin-7-onas. |
| JP2006503802A (ja) | 2002-04-03 | 2006-02-02 | エフ.ホフマン−ラ ロシュ アーゲー | イミダゾ縮合化合物 |
| AU2003251661A1 (en) | 2002-08-06 | 2004-02-25 | F. Hoffmann-La Roche Ag | 6-alkoxy-pyrido-pyrimidines as p-38 map kinase inhibitors |
| AU2003300076C1 (en) | 2002-12-30 | 2010-03-04 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
| DK1603570T5 (da) * | 2003-02-26 | 2013-12-09 | Sugen Inc | Aminoheteroarylforbindelser som proteinkinaseinhibitorer |
| CA2520785A1 (en) * | 2003-04-16 | 2004-10-28 | F. Hoffmann-La Roche Ag | Substituted 7-aza-quinazoline compounds |
| RU2348632C2 (ru) * | 2003-11-13 | 2009-03-10 | Ф.Хоффманн-Ля Рош Аг | Гидроксиалкилзамещенные пиридо-7-пиримидин-7-оны |
| WO2006056863A1 (en) * | 2004-11-23 | 2006-06-01 | Ranbaxy Laboratories Limited | Pyrido’2, 3-d!pyrimidines as anti-inflammatory agents |
| US20060142312A1 (en) * | 2004-12-23 | 2006-06-29 | Pfizer Inc | C6-aryl and heteroaryl substituted pyrido[2,3-D] pyrimidin-7-ones |
| WO2006082492A1 (en) * | 2005-02-02 | 2006-08-10 | Ranbaxy Laboratories Limited | Azabicyclo derivatives as anti-inflammatory agents |
| MX2007013595A (es) * | 2005-05-04 | 2008-01-24 | Renovis Inc | Compuestos heterociclicos fusionados y composiciones y usos de estos. |
| ES2336603T3 (es) * | 2005-07-21 | 2010-04-14 | F. Hoffmann-La Roche Ag | Compuestos de pirido(2,3-d)pirimidina-2,4-diamina como inhibidores de ptp1b. |
| WO2007021795A2 (en) * | 2005-08-09 | 2007-02-22 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| WO2007022946A1 (de) | 2005-08-21 | 2007-03-01 | Abbott Gmbh & Co. Kg | Heterocyclische verbindungen und ihre verwendung als bindungspartner für 5-ht5-rezeptoren |
| JO2783B1 (en) * | 2005-09-30 | 2014-03-15 | نوفارتيس ايه جي | Compounds 2-Amino-7, 8-dihydro-6H-Bayredo (3,4-D) Pyrimidine-5-Ones |
| AU2007268749B2 (en) * | 2006-05-26 | 2012-07-26 | Taisho Pharmaceutical Co., Ltd. | Novel heterocyclic compound or salt thereof and intermediate thereof |
| WO2008150260A1 (en) * | 2007-06-06 | 2008-12-11 | Gpc Biotech, Inc. | 8-oxy-2-aminopyrido (2, 3-d) pyrimidin-7-one derivatives as kinase inhibitors and anticancer agents |
| WO2008078249A1 (en) * | 2006-12-21 | 2008-07-03 | Ranbaxy Laboratories Limited | Anti-inflammatory agents |
| WO2008136948A1 (en) | 2007-05-07 | 2008-11-13 | Amgen Inc. | Pyrazolo-pyridinone and pyrazolo-pyrazinone compounds as p38 modulators, process for their preparation, and their pharmaceutical use |
| WO2008151992A2 (en) | 2007-06-15 | 2008-12-18 | F. Hoffmann-La Roche Ag | A novel process for the preparation of 3-amino-pentan-1,5-diol |
| US8367671B2 (en) | 2008-03-21 | 2013-02-05 | Amgen Inc. | Pyrazolo[3.4-B]pyrazine compounds as p38 modulators and methods of use as anti-inflamatory agents |
| EP2112150B1 (en) | 2008-04-22 | 2013-10-16 | Forma Therapeutics, Inc. | Improved raf inhibitors |
| CA2734037A1 (en) * | 2008-10-22 | 2010-04-29 | F. Hoffmann-La Roche Ag | Pyrimidinyl pyridone inhibitors of jnk |
| WO2010071846A2 (en) | 2008-12-19 | 2010-06-24 | Afraxis, Inc. | Compounds for treating neuropsychiatric conditions |
| US8372970B2 (en) | 2009-10-09 | 2013-02-12 | Afraxis, Inc. | 8-ethyl-6-(aryl)pyrido[2,3-D]pyrimidin-7(8H)-ones for the treatment of CNS disorders |
| JP5797664B2 (ja) * | 2009-12-18 | 2015-10-21 | テンプル・ユニバーシティ−オブ・ザ・コモンウェルス・システム・オブ・ハイアー・エデュケイションTemple University−Of The Commonwealth System Of Higher Education | 置換ピリド[2,3−d]ピリミジン−7(8H)−オン及びそれらの治療用の使用 |
| CN105294682B (zh) | 2014-07-26 | 2017-07-07 | 广东东阳光药业有限公司 | Cdk类小分子抑制剂的化合物及其用途 |
| ES2866883T3 (es) | 2016-06-08 | 2021-10-20 | Support Venture Gmbh | Combinaciones farmacéuticas para el tratamiento del cáncer |
| PT3497103T (pt) | 2016-08-15 | 2021-06-17 | Pfizer | Inibidores de piridopirimidinona cdk2/4/6 |
| BR112019003006A2 (pt) * | 2016-08-17 | 2019-05-14 | Support-Venture Gmbh | uso de uma combinação farmacêutica e kit para prevenir ou tratar perda auditiva |
| WO2018132550A1 (en) * | 2017-01-11 | 2018-07-19 | The General Hospital Corporation | Voltage gated sodium channel imaging agents |
| BR112019020754A2 (pt) | 2017-04-04 | 2020-04-28 | Strekin Ag | métodos de prevenção ou tratamento de doenças oftalmológicas |
| CN111032655B (zh) * | 2017-08-31 | 2022-09-02 | 达纳-法伯癌症研究所股份有限公司 | Egfr和/或her2抑制剂和使用方法 |
| BR112020006677A2 (pt) | 2017-10-05 | 2020-10-06 | Fulcrum Therapeutics, Inc. | uso de inibidores p38 para reduzir a expressão de dux4 |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| US12312346B2 (en) | 2018-06-27 | 2025-05-27 | Tufts Medical Center, Inc. | Pyridopyrimidine compounds and methods of their use |
| KR20210031909A (ko) | 2018-07-13 | 2021-03-23 | 키나루스 아게 | 섬유증 질환을 예방 또는 치료하기 위한 ppar 효능제 및 p38 키나제 억제제의 조합물 |
| TW202112368A (zh) | 2019-06-13 | 2021-04-01 | 荷蘭商法西歐知識產權股份有限公司 | 用於治療有關dux4表現之疾病的抑制劑組合 |
| US20230263803A1 (en) | 2020-08-11 | 2023-08-24 | Kinarus Ag | Methods of preventing or treating covid-19 and related viral diseases or disorders |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4215216A (en) | 1979-04-18 | 1980-07-29 | American Home Products Corporation | 7,8-Dihydro-2,5,8-trisubstituted-7-oxo-pyrido[2,3-d]pyrimidine-6-carboxylic acid derivatives |
| US5037826A (en) | 1986-10-15 | 1991-08-06 | Schering Corporation | 1-substituted naphthyridine and pyridopyrazine derivatives |
| GB8702758D0 (en) * | 1987-02-06 | 1987-03-11 | Wellcome Found | Treatment of disease |
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