KR101235497B1 - 신규 화합물 - Google Patents
신규 화합물 Download PDFInfo
- Publication number
- KR101235497B1 KR101235497B1 KR1020077021881A KR20077021881A KR101235497B1 KR 101235497 B1 KR101235497 B1 KR 101235497B1 KR 1020077021881 A KR1020077021881 A KR 1020077021881A KR 20077021881 A KR20077021881 A KR 20077021881A KR 101235497 B1 KR101235497 B1 KR 101235497B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- heteroaryl
- aryl
- cycloalkyl
- hydrogen
- 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 - Fee Related
Links
- 0 C*C1=C(C)NC(*)=C(C(C)=O)C(NC)=[Mn]1 Chemical compound C*C1=C(C)NC(*)=C(C(C)=O)C(NC)=[Mn]1 0.000 description 21
- CNPGOONUQONHKI-ALCCZGGFSA-N CBc1nc(N(C(C=C2)=O)c(c(F)ccc3)c3F)c2c(C(C)C/C=C\C(C)=C)n1 Chemical compound CBc1nc(N(C(C=C2)=O)c(c(F)ccc3)c3F)c2c(C(C)C/C=C\C(C)=C)n1 CNPGOONUQONHKI-ALCCZGGFSA-N 0.000 description 1
- JWZHMQJLLRSVNF-CLFYSBASSA-N CC(/C=C\C(C1(C(C(C)=CC2)=CC2C(O)OC)N2C1)=C(N)N=C2[n]1c(CN)ccc1)=O Chemical compound CC(/C=C\C(C1(C(C(C)=CC2)=CC2C(O)OC)N2C1)=C(N)N=C2[n]1c(CN)ccc1)=O JWZHMQJLLRSVNF-CLFYSBASSA-N 0.000 description 1
- JMFBSQBNMSUETN-UHFFFAOYSA-N CC(CC1)CCN1C(CC1)CCN1c1nc(-c2cc(C(O)=O)ccc2C)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 Chemical compound CC(CC1)CCN1C(CC1)CCN1c1nc(-c2cc(C(O)=O)ccc2C)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 JMFBSQBNMSUETN-UHFFFAOYSA-N 0.000 description 1
- MVCUQTSFJJCIDJ-YRNVUSSQSA-N CCC(CC)Nc1nc(/C=C/CC)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 Chemical compound CCC(CC)Nc1nc(/C=C/CC)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 MVCUQTSFJJCIDJ-YRNVUSSQSA-N 0.000 description 1
- MNGMBGKHQRYLNJ-UHFFFAOYSA-N CCCCCc1ccc(C)c(-c2c(C=CC(N3c(c(F)ccc4)c4F)=O)c3nc(N(CC3)CCC3C3CCC(C)CC3)n2)c1 Chemical compound CCCCCc1ccc(C)c(-c2c(C=CC(N3c(c(F)ccc4)c4F)=O)c3nc(N(CC3)CCC3C3CCC(C)CC3)n2)c1 MNGMBGKHQRYLNJ-UHFFFAOYSA-N 0.000 description 1
- HJJOSJPGSQFZKI-UHFFFAOYSA-N CCCCNC(NC)NCCC(C)(CCO)C=C Chemical compound CCCCNC(NC)NCCC(C)(CCO)C=C HJJOSJPGSQFZKI-UHFFFAOYSA-N 0.000 description 1
- KKTBUCVHSCATGB-UHFFFAOYSA-N CNC1CCCC1 Chemical compound CNC1CCCC1 KKTBUCVHSCATGB-UHFFFAOYSA-N 0.000 description 1
- XTSVTLOWTXKOLD-UHFFFAOYSA-N Cc(c(-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(NCc2ncc[nH]2)n1)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(NCc2ncc[nH]2)n1)c1)ccc1C(NC1CC1)=O XTSVTLOWTXKOLD-UHFFFAOYSA-N 0.000 description 1
- DYWSZXDQVJZGBA-UHFFFAOYSA-N Cc(ccc(C(O)=O)c1)c1-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(SC)n1 Chemical compound Cc(ccc(C(O)=O)c1)c1-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(SC)n1 DYWSZXDQVJZGBA-UHFFFAOYSA-N 0.000 description 1
- FFXSYKVMQNWPCD-UHFFFAOYSA-N Cc1cc(C(Nc(cc2-c3c(C=CC(N4c(c(F)ccc5)c5F)=O)c4nc(SC)n3)ccc2C#N)=O)ccc1F Chemical compound Cc1cc(C(Nc(cc2-c3c(C=CC(N4c(c(F)ccc5)c5F)=O)c4nc(SC)n3)ccc2C#N)=O)ccc1F FFXSYKVMQNWPCD-UHFFFAOYSA-N 0.000 description 1
- JXDCMNODVYNKQS-UHFFFAOYSA-N ICCNC1CC1 Chemical compound ICCNC1CC1 JXDCMNODVYNKQS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
-
- 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
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
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- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Transplantation (AREA)
- Endocrinology (AREA)
- Ophthalmology & Optometry (AREA)
- Emergency Medicine (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66531505P | 2005-03-25 | 2005-03-25 | |
| US60/665,315 | 2005-03-25 | ||
| PCT/US2006/010855 WO2006104915A2 (en) | 2005-03-25 | 2006-03-24 | 8-PHENYL-7,8-DIHYDROPYRIDO[2,3-d]PYRIMIDIN-7-ONES AND THEIR USE AS PHARMACEUTICALS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20070113255A KR20070113255A (ko) | 2007-11-28 |
| KR101235497B1 true KR101235497B1 (ko) | 2013-02-20 |
Family
ID=37053943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077021881A Expired - Fee Related KR101235497B1 (ko) | 2005-03-25 | 2006-03-24 | 신규 화합물 |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US7678801B2 (https=) |
| EP (3) | EP2436686A1 (https=) |
| JP (1) | JP5037487B2 (https=) |
| KR (1) | KR101235497B1 (https=) |
| CN (4) | CN101258148A (https=) |
| AR (1) | AR053346A1 (https=) |
| AU (1) | AU2006229993B2 (https=) |
| BR (1) | BRPI0609437A2 (https=) |
| CA (1) | CA2602553C (https=) |
| EA (1) | EA012875B1 (https=) |
| ES (2) | ES2398246T3 (https=) |
| IL (1) | IL185870A (https=) |
| MA (1) | MA29341B1 (https=) |
| MX (1) | MX2007011856A (https=) |
| MY (2) | MY145343A (https=) |
| NO (1) | NO20075275L (https=) |
| NZ (1) | NZ561237A (https=) |
| PE (2) | PE20100737A1 (https=) |
| SG (1) | SG166771A1 (https=) |
| TW (1) | TWI389690B (https=) |
| UA (1) | UA95444C2 (https=) |
| UY (1) | UY29440A1 (https=) |
| WO (1) | WO2006104915A2 (https=) |
| ZA (1) | ZA200707564B (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7235551B2 (en) * | 2000-03-02 | 2007-06-26 | Smithkline Beecham Corporation | 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases |
| CN100525768C (zh) * | 2000-10-23 | 2009-08-12 | 史密丝克莱恩比彻姆公司 | 新化合物 |
| KR20040103972A (ko) * | 2002-04-19 | 2004-12-09 | 스미스클라인 비참 코포레이션 | 신규 화합물 |
| MY145343A (en) * | 2005-03-25 | 2012-01-31 | Glaxo Group Ltd | Novel compounds |
| PE20061193A1 (es) * | 2005-03-25 | 2006-12-02 | Glaxo Group Ltd | DERIVADOS DE 3,4-DIHIDROPIRIMIDO[4,5-d]PIRIMIDIN-2-[1H]-0NA COMO INHIBIDORES DE QUINASA p38 |
| US7423042B2 (en) * | 2005-03-25 | 2008-09-09 | Glaxo Group Limited | Compounds |
| US20080096905A1 (en) * | 2005-03-25 | 2008-04-24 | Glaxo Group Limited | Process For Preparing Pyrido[2,3-D]Pyrimidin-7-One And 3,4-Dihydropyrimido{4,5-D}Pyrimidin-2(1H)-One Derivatives |
| US20090318424A1 (en) * | 2006-06-16 | 2009-12-24 | Mauro Corsi | Novel compounds |
| EP2034838A4 (en) * | 2006-06-16 | 2012-01-04 | Glaxo Group Ltd | NOVEL CONNECTIONS |
| GB0621830D0 (en) * | 2006-11-02 | 2006-12-13 | Chroma Therapeutics Ltd | Inhibitors of p38 mitogen-activated protein kinase |
| EP1992344A1 (en) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation |
| WO2012158197A2 (en) * | 2010-11-11 | 2012-11-22 | Lyndor Biosciences L.L.C. | Compounds useful as akt/pkb modulators and uses thereof |
| LT2748147T (lt) * | 2011-08-25 | 2017-10-25 | St. Jude Children`S Research Hospital | 2-alkil-1-okso-n-fenil-3-heteroaril-1,2,3,4-tetrahidroizochinolin-4-karboksamidai, skirti antimaliarinei terapijai |
| 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 |
| BR112020006677A2 (pt) | 2017-10-05 | 2020-10-06 | Fulcrum Therapeutics, Inc. | uso de inibidores p38 para reduzir a expressão de dux4 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US20030092712A1 (en) | 2000-12-20 | 2003-05-15 | Doherty James B. | (Halo-benzo carbonyl)heterocyclo fused phenyl p38 kinase inhibiting agents |
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