CL2008001104A1 - Compuestos derivados de [1,2,3]triazolo[4,5-b]piridin-carboxamidas y [1,2,3]triazolo[4,5-d]pirimidin-carboxamidas, inhibidores de mgl y faah; procedimiento de preparacion; composicion farmaceutica; y su uso en el tratamiento de delolores agudos o cronicos, vertigos, vomitos, nauseas, sindrome metaloico, dispipidemia, entre otros. - Google Patents
Compuestos derivados de [1,2,3]triazolo[4,5-b]piridin-carboxamidas y [1,2,3]triazolo[4,5-d]pirimidin-carboxamidas, inhibidores de mgl y faah; procedimiento de preparacion; composicion farmaceutica; y su uso en el tratamiento de delolores agudos o cronicos, vertigos, vomitos, nauseas, sindrome metaloico, dispipidemia, entre otros.Info
- Publication number
- CL2008001104A1 CL2008001104A1 CL2008001104A CL2008001104A CL2008001104A1 CL 2008001104 A1 CL2008001104 A1 CL 2008001104A1 CL 2008001104 A CL2008001104 A CL 2008001104A CL 2008001104 A CL2008001104 A CL 2008001104A CL 2008001104 A1 CL2008001104 A1 CL 2008001104A1
- Authority
- CL
- Chile
- Prior art keywords
- carboxamides
- triazolo
- nausea
- vomiting
- acute
- Prior art date
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- 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
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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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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Abstract
Compuestos derivados de triazolopiridin-carboxamidas y triazolopirimidin-carboxamidas; procedimiento de preparación; composición farmacéutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de dolores agudos o crónicos, vértigos, vómitos, nauseas, síndrome metabólico, dislipidemia, epilepsia, cáncer, enfermedad infecciosa y viral.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0702809A FR2915199B1 (fr) | 2007-04-18 | 2007-04-18 | Derives de triazolopyridine-carboxamides et triazolopyrimidine-carboxamides, leur preparation et leur application en therapeutique. |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2008001104A1 true CL2008001104A1 (es) | 2009-01-16 |
Family
ID=38776272
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2008001104A CL2008001104A1 (es) | 2007-04-18 | 2008-04-17 | Compuestos derivados de [1,2,3]triazolo[4,5-b]piridin-carboxamidas y [1,2,3]triazolo[4,5-d]pirimidin-carboxamidas, inhibidores de mgl y faah; procedimiento de preparacion; composicion farmaceutica; y su uso en el tratamiento de delolores agudos o cronicos, vertigos, vomitos, nauseas, sindrome metaloico, dispipidemia, entre otros. |
Country Status (17)
Country | Link |
---|---|
US (1) | US8080547B2 (es) |
EP (1) | EP2146990A1 (es) |
JP (1) | JP2010524904A (es) |
KR (1) | KR20090130057A (es) |
CN (1) | CN101668758A (es) |
AR (1) | AR066107A1 (es) |
AU (1) | AU2008257320A1 (es) |
BR (1) | BRPI0810440A2 (es) |
CA (1) | CA2683929A1 (es) |
CL (1) | CL2008001104A1 (es) |
FR (1) | FR2915199B1 (es) |
IL (1) | IL201450A0 (es) |
MX (1) | MX2009011212A (es) |
RU (1) | RU2009142431A (es) |
TW (1) | TW200901993A (es) |
UY (1) | UY31032A1 (es) |
WO (1) | WO2008145839A1 (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2915198B1 (fr) * | 2007-04-18 | 2009-12-18 | Sanofi Aventis | Derives de triazolopyridine-carboxamides et triazolopyridine -carboxamides, leur preparation et leur application en therapeutique. |
CN102333568B (zh) | 2008-12-24 | 2016-01-20 | 比亚尔-珀特拉和Ca股份公司 | 药物化合物 |
AU2010238745A1 (en) * | 2009-04-22 | 2011-11-10 | Janssen Pharmaceutica Nv | Heteroaromatic and aromatic piperazinyl azetidinyl amides as monoacylglycerol lipase inhibitor |
US8435977B2 (en) | 2009-04-22 | 2013-05-07 | Janssen Pharmaceutica, Nv | Heteroaromatic and aromatic piperazinyl azetidinyl amides as monoacylglycerol lipase inhibitors |
KR20120005517A (ko) * | 2009-04-22 | 2012-01-16 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파제 억제제로서의 헤테로방향족 및 방향족 피페라지닐 아제티디닐 아미드 |
EP2421848A1 (en) * | 2009-04-22 | 2012-02-29 | Janssen Pharmaceutica N.V. | Azetidinyl diamides as monoacylglycerol lipase inhibitors |
JP5738766B2 (ja) * | 2009-09-09 | 2015-06-24 | 大日本住友製薬株式会社 | 8−オキソジヒドロプリン誘導体 |
US20130150346A1 (en) | 2010-01-08 | 2013-06-13 | Quest Ventures Ltd. | Use of FAAH Inhibitors for Treating Parkinson's Disease and Restless Legs Syndrome |
WO2011101644A1 (en) | 2010-02-18 | 2011-08-25 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Triazolo [4, 5 - b] pyridin derivatives |
US20130224151A1 (en) | 2010-03-31 | 2013-08-29 | United States Of America | Use of FAAH Inhibitors for Treating Abdominal, Visceral and Pelvic Pain |
NZ703111A (en) | 2010-05-17 | 2016-07-29 | Incozen Therapeutics Pvt Ltd | Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of protein kinases |
JP2013536852A (ja) | 2010-09-03 | 2013-09-26 | ヤンセン ファーマシューティカ エヌ.ベー. | モノアシルグリセロールリパーゼ阻害剤としてのジ−アゼチジニルジアミド |
CN103080103A (zh) | 2010-09-27 | 2013-05-01 | 詹森药业有限公司 | 作为单酰甘油脂肪酶抑制剂的氧代哌嗪-氮杂环丁烷酰胺和氧代二氮杂*-氮杂环丁烷酰胺 |
AU2011316975A1 (en) | 2010-10-22 | 2013-05-23 | Janssen Pharmaceutica Nv | Amino-pyrrolidine-azetidine diamides as monoacylglycerol lipase inhibitors |
US8513423B2 (en) | 2010-10-22 | 2013-08-20 | Janssen Pharmaceutica, Nv | Piperidin-4-yl-azetidine diamides as monoacylglycerol lipase inhibitors |
JP2014076947A (ja) * | 2011-02-03 | 2014-05-01 | Dainippon Sumitomo Pharma Co Ltd | 2−オキシ置換8−オキソジヒドロプリン誘導体 |
CA2850100A1 (en) * | 2011-09-30 | 2013-04-04 | Janssen Pharmaceutica Nv | Monoacylglycerol lipase inhibitors for the treatment of metabolic diseases and related disorders |
Family Cites Families (6)
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FR2816938B1 (fr) * | 2000-11-22 | 2003-01-03 | Sanofi Synthelabo | Derives de 3-aroylindole, leur procede de preparation et les compositions pharmaceutiques en contenant |
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 |
US7632837B2 (en) * | 2005-06-17 | 2009-12-15 | Bristol-Myers Squibb Company | Bicyclic heterocycles as cannabinoid-1 receptor modulators |
DE102005049954A1 (de) * | 2005-10-19 | 2007-05-31 | Sanofi-Aventis Deutschland Gmbh | Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen |
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2007
- 2007-04-18 FR FR0702809A patent/FR2915199B1/fr not_active Expired - Fee Related
-
2008
- 2008-04-16 AU AU2008257320A patent/AU2008257320A1/en not_active Abandoned
- 2008-04-16 JP JP2010503547A patent/JP2010524904A/ja active Pending
- 2008-04-16 WO PCT/FR2008/000532 patent/WO2008145839A1/fr active Application Filing
- 2008-04-16 RU RU2009142431/04A patent/RU2009142431A/ru not_active Application Discontinuation
- 2008-04-16 CA CA002683929A patent/CA2683929A1/fr not_active Abandoned
- 2008-04-16 CN CN200880012545A patent/CN101668758A/zh active Pending
- 2008-04-16 KR KR1020097021591A patent/KR20090130057A/ko not_active Application Discontinuation
- 2008-04-16 BR BRPI0810440-9A2A patent/BRPI0810440A2/pt not_active IP Right Cessation
- 2008-04-16 MX MX2009011212A patent/MX2009011212A/es not_active Application Discontinuation
- 2008-04-16 EP EP08787961A patent/EP2146990A1/fr not_active Withdrawn
- 2008-04-17 CL CL2008001104A patent/CL2008001104A1/es unknown
- 2008-04-17 TW TW097114018A patent/TW200901993A/zh unknown
- 2008-04-18 AR ARP080101601A patent/AR066107A1/es unknown
- 2008-04-18 UY UY31032A patent/UY31032A1/es not_active Application Discontinuation
-
2009
- 2009-10-06 US US12/573,959 patent/US8080547B2/en not_active Expired - Fee Related
- 2009-10-11 IL IL201450A patent/IL201450A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR2915199B1 (fr) | 2010-01-22 |
CN101668758A (zh) | 2010-03-10 |
EP2146990A1 (fr) | 2010-01-27 |
JP2010524904A (ja) | 2010-07-22 |
WO2008145839A8 (fr) | 2009-11-19 |
KR20090130057A (ko) | 2009-12-17 |
TW200901993A (en) | 2009-01-16 |
MX2009011212A (es) | 2009-11-02 |
FR2915199A1 (fr) | 2008-10-24 |
US20100041651A1 (en) | 2010-02-18 |
BRPI0810440A2 (pt) | 2014-10-14 |
IL201450A0 (en) | 2010-05-31 |
US8080547B2 (en) | 2011-12-20 |
CA2683929A1 (fr) | 2008-12-04 |
UY31032A1 (es) | 2008-11-28 |
AR066107A1 (es) | 2009-07-22 |
AU2008257320A1 (en) | 2008-12-04 |
WO2008145839A1 (fr) | 2008-12-04 |
RU2009142431A (ru) | 2011-05-27 |
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