MX2009005174A - Derivados de 5-sulfanilmetil-[1,2,4]triazol[1,5-a]pirimidin-7-ol como antagonistas de cxcr2. - Google Patents
Derivados de 5-sulfanilmetil-[1,2,4]triazol[1,5-a]pirimidin-7-ol como antagonistas de cxcr2.Info
- Publication number
- MX2009005174A MX2009005174A MX2009005174A MX2009005174A MX2009005174A MX 2009005174 A MX2009005174 A MX 2009005174A MX 2009005174 A MX2009005174 A MX 2009005174A MX 2009005174 A MX2009005174 A MX 2009005174A MX 2009005174 A MX2009005174 A MX 2009005174A
- Authority
- MX
- Mexico
- Prior art keywords
- sulfanylmethyl
- triazol
- pyrimidin
- derivatives
- cxcr2 antagonists
- Prior art date
Links
- 229940124803 CXCR2 antagonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 102000002791 Interleukin-8B Receptors Human genes 0.000 abstract 1
- 108010018951 Interleukin-8B Receptors Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
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
- 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
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
-
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- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Gastroenterology & Hepatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Biotechnology (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
Abstract
La presente invención se refiere a compuestos de fórmula (I) y el uso de éstos compuestos como productos farmacéuticos, por ejemplo en prevenir o tratar una condición o enfermedad mediada por el receptor CXCR2.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06124679 | 2006-11-23 | ||
| PCT/EP2007/010098 WO2008061741A1 (en) | 2006-11-23 | 2007-11-21 | 5-sulfanylmethyl-[1,2,4] triazol[1, 5-a] pyrimidin-7-ol derivatives as cxcr2 antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2009005174A true MX2009005174A (es) | 2009-05-25 |
Family
ID=37891509
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2009005174A MX2009005174A (es) | 2006-11-23 | 2007-11-21 | Derivados de 5-sulfanilmetil-[1,2,4]triazol[1,5-a]pirimidin-7-ol como antagonistas de cxcr2. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20100069407A1 (es) |
| EP (1) | EP2094696B1 (es) |
| JP (1) | JP2010510268A (es) |
| KR (1) | KR20090080998A (es) |
| CN (1) | CN101541794A (es) |
| AT (1) | ATE484505T1 (es) |
| AU (1) | AU2007323336A1 (es) |
| BR (1) | BRPI0718947A2 (es) |
| CA (1) | CA2670202A1 (es) |
| DE (1) | DE602007009865D1 (es) |
| MX (1) | MX2009005174A (es) |
| RU (1) | RU2009123525A (es) |
| WO (1) | WO2008061741A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2358716B1 (en) * | 2008-11-12 | 2016-01-06 | Merck Sharp & Dohme Corp. | Inhibitors of fatty acid binding protein (fabp) |
| WO2011043994A1 (en) | 2009-10-08 | 2011-04-14 | Schering Corporation | Inhibitors of fatty acid binding protein (fabp) |
| JP2015507007A (ja) * | 2012-02-14 | 2015-03-05 | ジーアールエル | 抗ウイルス性の特性を有する小分子 |
| WO2018073248A1 (en) | 2016-10-17 | 2018-04-26 | Icm (Institut Du Cerveau Et De La Moelle Épinière) | Prognosis of demyelinating diseases patients and treatment thereof |
| TW201922291A (zh) | 2017-11-16 | 2019-06-16 | 瑞士商諾華公司 | 組合療法 |
| AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
| KR20210106437A (ko) | 2018-12-20 | 2021-08-30 | 노파르티스 아게 | 3-(1-옥소이소인돌린-2-일)피페리딘-2,6-디온 유도체를 포함하는 투약 요법 및 약학적 조합물 |
| CN113490528B (zh) | 2019-02-15 | 2024-12-03 | 诺华股份有限公司 | 3-(1-氧代-5-(哌啶-4-基)异吲哚啉-2-基)哌啶-2,6-二酮衍生物及其用途 |
| EP3924055B1 (en) | 2019-02-15 | 2024-04-03 | Novartis AG | Substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| JP7535532B2 (ja) | 2019-02-26 | 2024-08-16 | バイエル・アクチエンゲゼルシヤフト | 有害生物防除剤としての縮合二環式複素環式誘導体 |
| MX2022007759A (es) | 2019-12-20 | 2022-07-19 | Novartis Ag | Combinacion del anticuerpo anti tim-3 mbg453 y anticuerpo anti tgf-beta nis793, con o sin decitabina o el anticuerpo anti pd-1 spartalizumab, para el tratamiento de mielofibrosis y sindrome mielodisplasico. |
| CN115916199A (zh) | 2020-06-23 | 2023-04-04 | 诺华股份有限公司 | 包含3-(1-氧代异吲哚啉-2-基)哌啶-2,6-二酮衍生物的给药方案 |
| US20230271940A1 (en) | 2020-08-03 | 2023-08-31 | Novartis Ag | Heteroaryl substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3682543D1 (de) * | 1985-06-11 | 1992-01-02 | Agfa Gevaert Nv | Diffusionsuebertragungsumkehrverfahren. |
| DE3534651A1 (de) * | 1985-09-28 | 1987-04-09 | Bayer Ag | Triazolo-pyrimidine |
| GB0401334D0 (en) * | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
| WO2005113534A2 (en) * | 2004-05-12 | 2005-12-01 | Schering Corporation | Cxcr1 and cxcr2 chemokine antagonists |
| EP1676834A1 (en) * | 2004-12-30 | 2006-07-05 | Sanofi-Aventis Deutschland GmbH | Fused bicyclic carboxamide derivates for use as CXCR2 inhibitors in the treatment of inflammation |
-
2007
- 2007-11-21 DE DE602007009865T patent/DE602007009865D1/de active Active
- 2007-11-21 WO PCT/EP2007/010098 patent/WO2008061741A1/en not_active Ceased
- 2007-11-21 KR KR1020097010517A patent/KR20090080998A/ko not_active Withdrawn
- 2007-11-21 AT AT07819889T patent/ATE484505T1/de not_active IP Right Cessation
- 2007-11-21 MX MX2009005174A patent/MX2009005174A/es not_active Application Discontinuation
- 2007-11-21 CA CA002670202A patent/CA2670202A1/en not_active Abandoned
- 2007-11-21 BR BRPI0718947-8A patent/BRPI0718947A2/pt not_active Application Discontinuation
- 2007-11-21 CN CNA2007800432499A patent/CN101541794A/zh active Pending
- 2007-11-21 RU RU2009123525/04A patent/RU2009123525A/ru not_active Application Discontinuation
- 2007-11-21 JP JP2009537541A patent/JP2010510268A/ja active Pending
- 2007-11-21 EP EP07819889A patent/EP2094696B1/en not_active Not-in-force
- 2007-11-21 AU AU2007323336A patent/AU2007323336A1/en not_active Abandoned
- 2007-11-21 US US12/514,734 patent/US20100069407A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20100069407A1 (en) | 2010-03-18 |
| EP2094696A1 (en) | 2009-09-02 |
| ATE484505T1 (de) | 2010-10-15 |
| DE602007009865D1 (de) | 2010-11-25 |
| RU2009123525A (ru) | 2010-12-27 |
| CN101541794A (zh) | 2009-09-23 |
| JP2010510268A (ja) | 2010-04-02 |
| BRPI0718947A2 (pt) | 2013-12-17 |
| EP2094696B1 (en) | 2010-10-13 |
| WO2008061741A1 (en) | 2008-05-29 |
| KR20090080998A (ko) | 2009-07-27 |
| AU2007323336A1 (en) | 2008-05-29 |
| CA2670202A1 (en) | 2008-05-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |