ZA200802369B - Triazolopyridine derivatives as inhibitors of lipases and phospholipases - Google Patents
Triazolopyridine derivatives as inhibitors of lipases and phospholipasesInfo
- Publication number
- ZA200802369B ZA200802369B ZA200802369A ZA200802369A ZA200802369B ZA 200802369 B ZA200802369 B ZA 200802369B ZA 200802369 A ZA200802369 A ZA 200802369A ZA 200802369 A ZA200802369 A ZA 200802369A ZA 200802369 B ZA200802369 B ZA 200802369B
- Authority
- ZA
- South Africa
- Prior art keywords
- phospholipases
- lipases
- inhibitors
- triazolopyridine derivatives
- triazolopyridine
- Prior art date
Links
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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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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- 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
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- A61P9/12—Antihypertensives
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Virology (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Psychology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005049954A DE102005049954A1 (de) | 2005-10-19 | 2005-10-19 | Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200802369B true ZA200802369B (en) | 2009-01-28 |
Family
ID=37487398
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200802369A ZA200802369B (en) | 2005-10-19 | 2008-03-13 | Triazolopyridine derivatives as inhibitors of lipases and phospholipases |
Country Status (26)
Country | Link |
---|---|
US (2) | US7718669B2 (xx) |
EP (1) | EP1940838B1 (xx) |
JP (1) | JP2009512649A (xx) |
KR (1) | KR20080057299A (xx) |
CN (1) | CN101291932A (xx) |
AR (1) | AR058095A1 (xx) |
AU (1) | AU2006303551A1 (xx) |
BR (1) | BRPI0617712A2 (xx) |
CA (1) | CA2625442A1 (xx) |
CR (1) | CR9851A (xx) |
DE (1) | DE102005049954A1 (xx) |
DO (1) | DOP2006000227A (xx) |
EC (1) | ECSP088376A (xx) |
HN (1) | HN2006035237A (xx) |
IL (1) | IL190715A0 (xx) |
MA (1) | MA29857B1 (xx) |
MY (1) | MY140514A (xx) |
NO (1) | NO20082159L (xx) |
NZ (1) | NZ567574A (xx) |
PE (1) | PE20070820A1 (xx) |
RU (1) | RU2008119435A (xx) |
TN (1) | TNSN08178A1 (xx) |
TW (1) | TW200800987A (xx) |
UY (1) | UY29878A1 (xx) |
WO (1) | WO2007045392A1 (xx) |
ZA (1) | ZA200802369B (xx) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005049954A1 (de) * | 2005-10-19 | 2007-05-31 | Sanofi-Aventis Deutschland Gmbh | Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen |
EP3205644A1 (en) | 2005-12-29 | 2017-08-16 | Celtaxsys Inc. | Diamine derivatives as inhibitors of leukotriene a4 hydrolase |
FR2915198B1 (fr) * | 2007-04-18 | 2009-12-18 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique. |
FR2915197B1 (fr) | 2007-04-18 | 2009-06-12 | Sanofi Aventis Sa | Derives de triazolopyridine-carboxamides, leur preparation et leur application therapeutique. |
FR2915199B1 (fr) * | 2007-04-18 | 2010-01-22 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyrimidine-carboxamides, leur preparation et leur application en therapeutique. |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
US8957219B2 (en) | 2008-10-17 | 2015-02-17 | Shionogi & Co., Ltd. | Acetic acid amide derivative having inhibitory activity on endothelial lipase |
AU2009330821B2 (en) * | 2008-12-24 | 2015-06-11 | Bial - Portela & Ca, S.A. | Pharmaceutical compounds |
RU2012127701A (ru) | 2009-12-15 | 2014-01-27 | Шионоги энд Ко. Лтд. | Производное оксадиазола, обладающее ингибирующей активностью в отношении эндотелиальной липазы |
AU2011261375B2 (en) | 2010-06-04 | 2016-09-22 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
US9333202B2 (en) | 2012-05-01 | 2016-05-10 | The Trustees Of Columbia University In The City Of New York | Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease |
RU2686101C2 (ru) | 2013-03-12 | 2019-04-24 | Селтакссис, Инк. | Способы ингибирования лейкотриен- а4-гидролазы |
EP2970309A4 (en) | 2013-03-14 | 2016-11-09 | Celtaxsys Inc | INHIBITORS OF LEUCOTRIENE A4 HYDROLASE |
MX2015011677A (es) | 2013-03-14 | 2016-07-08 | Celtaxsys Inc | Inhibidores de leucotrieno a4 hidrolasa. |
US9944644B2 (en) | 2013-03-14 | 2018-04-17 | The Trustees Of Columbia University In The City Of New York | Octahydropyrrolopyrroles their preparation and use |
US9938291B2 (en) | 2013-03-14 | 2018-04-10 | The Trustess Of Columbia University In The City Of New York | N-alkyl-2-phenoxyethanamines, their preparation and use |
DK2968304T3 (en) | 2013-03-14 | 2019-01-28 | Univ Columbia | 4-PHENYLPIPERIDINES, THEIR PREPARATION AND USE. |
EP2968265A4 (en) | 2013-03-14 | 2016-12-28 | Celtaxsys Inc | INHIBITORS OF THE LEUKOTRIEN A4 HYDROLASE |
US9637450B2 (en) | 2013-03-14 | 2017-05-02 | The Trustees Of Columbia University In The City Of New York | Octahydrocyclopentapyrroles, their preparation and use |
WO2015061272A1 (en) * | 2013-10-22 | 2015-04-30 | Bristol-Myers Squibb Company | Isotopically labeled triazolopyridine 11-beta hydroxysteroid dehydrogenase type i inhibitors |
DK3137168T3 (da) | 2014-04-30 | 2022-03-21 | Univ Columbia | Substituerede 4-phenylpiperidiner, deres fremstilling og anvendelse |
JOP20180094A1 (ar) | 2017-10-18 | 2019-04-18 | Hk Inno N Corp | مركب حلقي غير متجانس كمثبط بروتين كيناز |
EP3801559A4 (en) | 2018-05-31 | 2022-03-02 | Celltaxis, LLC | METHOD FOR REDUCING LUNG EXACERBATIONS IN PATIENTS SUFFERING FROM RESPIRATORY DISEASE |
CN117126134A (zh) * | 2022-05-20 | 2023-11-28 | 中国科学院上海药物研究所 | 新型四氢异喹啉类化合物、其制备方法、包含此类化合物的药物组合物及其用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0100624D0 (en) * | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical compounds VII |
DE10247680B4 (de) * | 2002-10-12 | 2005-09-01 | Aventis Pharma Deutschland Gmbh | Neue bicyclische Inhibitoren der Hormon Sensitiven Lipase |
DE102004005172A1 (de) * | 2004-02-02 | 2005-08-18 | Aventis Pharma Deutschland Gmbh | Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase |
DE102005049954A1 (de) * | 2005-10-19 | 2007-05-31 | Sanofi-Aventis Deutschland Gmbh | Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen |
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2005
- 2005-10-19 DE DE102005049954A patent/DE102005049954A1/de not_active Withdrawn
-
2006
- 2006-10-12 CA CA002625442A patent/CA2625442A1/en not_active Abandoned
- 2006-10-12 CN CNA200680039028XA patent/CN101291932A/zh active Pending
- 2006-10-12 RU RU2008119435/04A patent/RU2008119435A/ru not_active Application Discontinuation
- 2006-10-12 BR BRPI0617712-3A patent/BRPI0617712A2/pt not_active IP Right Cessation
- 2006-10-12 MY MYPI20081120A patent/MY140514A/en unknown
- 2006-10-12 WO PCT/EP2006/009856 patent/WO2007045392A1/de active Application Filing
- 2006-10-12 EP EP06806215A patent/EP1940838B1/de active Active
- 2006-10-12 KR KR1020087009354A patent/KR20080057299A/ko not_active Application Discontinuation
- 2006-10-12 AU AU2006303551A patent/AU2006303551A1/en not_active Abandoned
- 2006-10-12 JP JP2008535941A patent/JP2009512649A/ja not_active Abandoned
- 2006-10-12 NZ NZ567574A patent/NZ567574A/en not_active IP Right Cessation
- 2006-10-17 PE PE2006001256A patent/PE20070820A1/es not_active Application Discontinuation
- 2006-10-17 AR ARP060104518A patent/AR058095A1/es not_active Application Discontinuation
- 2006-10-17 TW TW095138144A patent/TW200800987A/zh unknown
- 2006-10-17 DO DO2006000227A patent/DOP2006000227A/es unknown
- 2006-10-18 HN HN2006035237A patent/HN2006035237A/es unknown
- 2006-10-19 UY UY29878A patent/UY29878A1/es not_active Application Discontinuation
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2008
- 2008-03-13 ZA ZA200802369A patent/ZA200802369B/xx unknown
- 2008-03-28 CR CR9851A patent/CR9851A/es not_active Application Discontinuation
- 2008-04-08 IL IL190715A patent/IL190715A0/en unknown
- 2008-04-08 MA MA30824A patent/MA29857B1/fr unknown
- 2008-04-09 US US12/099,922 patent/US7718669B2/en not_active Expired - Fee Related
- 2008-04-17 EC EC2008008376A patent/ECSP088376A/es unknown
- 2008-04-18 TN TNP2008000178A patent/TNSN08178A1/en unknown
- 2008-05-08 NO NO20082159A patent/NO20082159L/no not_active Application Discontinuation
-
2010
- 2010-03-25 US US12/731,225 patent/US20100190801A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
DE102005049954A1 (de) | 2007-05-31 |
DOP2006000227A (es) | 2007-05-15 |
NO20082159L (no) | 2008-05-08 |
ECSP088376A (es) | 2008-05-30 |
RU2008119435A (ru) | 2009-11-27 |
MY140514A (en) | 2009-12-31 |
CA2625442A1 (en) | 2007-04-26 |
MA29857B1 (fr) | 2008-10-03 |
NZ567574A (en) | 2010-03-26 |
JP2009512649A (ja) | 2009-03-26 |
TW200800987A (en) | 2008-01-01 |
US7718669B2 (en) | 2010-05-18 |
CR9851A (es) | 2008-07-29 |
CN101291932A (zh) | 2008-10-22 |
US20090030011A1 (en) | 2009-01-29 |
UY29878A1 (es) | 2007-05-31 |
EP1940838B1 (de) | 2012-08-22 |
BRPI0617712A2 (pt) | 2011-08-02 |
IL190715A0 (en) | 2008-11-03 |
WO2007045392A1 (de) | 2007-04-26 |
TNSN08178A1 (en) | 2009-10-30 |
HN2006035237A (es) | 2010-03-11 |
EP1940838A1 (de) | 2008-07-09 |
AU2006303551A1 (en) | 2007-04-26 |
AR058095A1 (es) | 2008-01-23 |
KR20080057299A (ko) | 2008-06-24 |
US20100190801A1 (en) | 2010-07-29 |
PE20070820A1 (es) | 2007-09-04 |
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