AU2002234134A1 - 3-substituted oxindole beta 3 agonists - Google Patents
3-substituted oxindole beta 3 agonistsInfo
- Publication number
- AU2002234134A1 AU2002234134A1 AU2002234134A AU3413402A AU2002234134A1 AU 2002234134 A1 AU2002234134 A1 AU 2002234134A1 AU 2002234134 A AU2002234134 A AU 2002234134A AU 3413402 A AU3413402 A AU 3413402A AU 2002234134 A1 AU2002234134 A1 AU 2002234134A1
- Authority
- AU
- Australia
- Prior art keywords
- beta
- agonists
- substituted oxindole
- sub
- oxindole
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/96—Spiro-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
The present invention relates to a beta<SUB>3 </SUB>adrenergic receptor agonist of formula I: or a pharmaceutical salt thereof; which is useful for treating Type II diabetes and/or obesity.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24730400P | 2000-11-10 | 2000-11-10 | |
US60/247,304 | 2000-11-10 | ||
US30679301P | 2001-07-20 | 2001-07-20 | |
US60/306,793 | 2001-07-20 | ||
PCT/US2001/050666 WO2002038544A2 (en) | 2000-11-10 | 2001-10-26 | 3-substituted oxindole beta 3 agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2002234134A1 true AU2002234134A1 (en) | 2002-05-21 |
Family
ID=26938590
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002234134A Abandoned AU2002234134A1 (en) | 2000-11-10 | 2001-10-26 | 3-substituted oxindole beta 3 agonists |
AU2432002A Pending AU2432002A (en) | 2000-11-10 | 2001-11-02 | 3-substituted oxindole beta 3 agonists |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2432002A Pending AU2432002A (en) | 2000-11-10 | 2001-11-02 | 3-substituted oxindole beta 3 agonists |
Country Status (10)
Country | Link |
---|---|
US (2) | US6825220B2 (en) |
EP (1) | EP1341759B1 (en) |
JP (1) | JP2004513164A (en) |
AT (1) | ATE329901T1 (en) |
AU (2) | AU2002234134A1 (en) |
CA (1) | CA2421594A1 (en) |
DE (1) | DE60120748T2 (en) |
ES (1) | ES2265447T3 (en) |
IL (1) | IL154928A0 (en) |
WO (2) | WO2002038544A2 (en) |
Families Citing this family (60)
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PL368109A1 (en) * | 2001-04-19 | 2005-03-21 | 2-iminopyrrolidine derivates | |
ES2272749T3 (en) | 2001-08-14 | 2007-05-01 | Eli Lilly And Company | DERIVATIVES OF INDOL AS BETA-3 ADRENERGIC AGONISTS FOR THE TREATMENT OF TYPE 2 DIABETES. |
DE60211199T2 (en) * | 2001-08-14 | 2007-02-01 | Eli Lilly And Co., Indianapolis | 3-SUBSTITUTED OXINDOL BETA-3 AGONISTS |
TWI249515B (en) | 2001-11-13 | 2006-02-21 | Theravance Inc | Aryl aniline beta2 adrenergic receptor agonists |
WO2003042160A1 (en) | 2001-11-13 | 2003-05-22 | Theravance, Inc. | Aryl aniline beta-2 adrenergic receptor agonists |
DE60204718T2 (en) | 2001-11-20 | 2006-05-18 | Eli Lilly And Co., Indianapolis | 3-SUBSTITUTED OXINDOL BETA 3 AGONISTS |
AU2002353844A1 (en) | 2001-11-20 | 2003-06-10 | Eli Lilly And Company | Beta 3 adrenergic agonists |
US7009060B2 (en) | 2002-01-11 | 2006-03-07 | Eli Lilly And Company | 2-oxo-benzimidazolyl substituted ethanolamine derivatives and their use as β3 agonists |
EA008861B1 (en) | 2002-09-19 | 2007-08-31 | Эли Лилли Энд Компани | Diaryl ethers as opioid antagonists |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
TW200526547A (en) * | 2003-09-22 | 2005-08-16 | Theravance Inc | Amino-substituted ethylamino β2 adrenergic receptor agonists |
EP1699783B1 (en) | 2003-12-22 | 2012-07-25 | Eli Lilly And Company | Opioid receptor antagonists |
TW200531692A (en) * | 2004-01-12 | 2005-10-01 | Theravance Inc | Aryl aniline derivatives as β2 adrenergic receptor agonists |
US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
WO2006014704A1 (en) | 2004-07-21 | 2006-02-09 | Theravance, Inc. | DIARYL ETHER β2 ADRENERGIC RECEPTOR AGONISTS |
US7566785B2 (en) * | 2004-09-10 | 2009-07-28 | Theravance, Inc. | Amidine substituted aryl aniline compounds |
MY144968A (en) | 2005-04-11 | 2011-11-30 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their uses as therapeutic agents |
MY145694A (en) | 2005-04-11 | 2012-03-30 | Xenon Pharmaceuticals Inc | Spiroheterocyclic compounds and their uses as therapeutic agents |
MX2009001043A (en) | 2006-08-08 | 2009-02-06 | Sanofi Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use. |
WO2008046083A2 (en) * | 2006-10-12 | 2008-04-17 | Xenon Pharmaceuticals Inc. | Use of oxindole compounds as therapeutic agents |
EP2073806B1 (en) | 2006-10-12 | 2012-02-15 | Xenon Pharmaceuticals Inc. | Use of spiro-oxindole compounds as therapeutic agents |
EP1947103A1 (en) | 2007-01-22 | 2008-07-23 | 4Sc Ag | Aryloxypropanolamines, methods of preparation thereof and use of aryloxypropanolamines as medicaments |
WO2008151257A2 (en) | 2007-06-04 | 2008-12-11 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
EP2025674A1 (en) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs |
WO2009149279A2 (en) | 2008-06-04 | 2009-12-10 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
AR072707A1 (en) | 2008-07-09 | 2010-09-15 | Sanofi Aventis | HETEROCICLIC COMPOUNDS, PROCESSES FOR THEIR PREPARATION, DRUGS THAT UNDERSTAND THESE COMPOUNDS AND THE USE OF THEM |
WO2010009319A2 (en) | 2008-07-16 | 2010-01-21 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
CA2741029A1 (en) | 2008-10-17 | 2010-04-22 | Xenon Pharmaceuticals Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
WO2010045197A1 (en) | 2008-10-17 | 2010-04-22 | Xenon Pharmaceuticals, Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
WO2010047982A1 (en) | 2008-10-22 | 2010-04-29 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
WO2010051206A1 (en) | 2008-10-31 | 2010-05-06 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
AR077252A1 (en) | 2009-06-29 | 2011-08-10 | Xenon Pharmaceuticals Inc | ESPIROOXINDOL COMPOUND ENANTIOMERS AND THEIR USES AS THERAPEUTIC AGENTS |
ES2443016T3 (en) | 2009-08-26 | 2014-02-17 | Sanofi | New crystalline hydrates of heteroaromatic fluoroglycosides, pharmaceutical products comprising these compounds, and their use |
RU2544852C2 (en) | 2009-10-14 | 2015-03-20 | Ксенон Фармасьютикалз Инк. | Method for synthesis of spiro-oxyindole compounds |
AU2011218830B2 (en) | 2010-02-25 | 2014-07-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
BR112012021086A2 (en) | 2010-02-26 | 2016-05-17 | Xenon Pharmaceuticals Inc | pharmaceutical compositions of spiro-oxindole compound for topical administration and their use as therapeutic agents |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
CN103476258B (en) | 2011-02-25 | 2017-04-26 | 默沙东公司 | Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents |
EP2683705B1 (en) | 2011-03-08 | 2015-04-22 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
EP2683700B1 (en) | 2011-03-08 | 2015-02-18 | Sanofi | Tetra-substituted oxathiazine derivatives, method for their preparation, their usage as medicament and medicament containing same and its use |
WO2012120055A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
WO2012120052A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
EP2880028B1 (en) | 2012-08-02 | 2020-09-30 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
WO2014055286A1 (en) | 2012-10-02 | 2014-04-10 | Eli Lilly And Company | Methods for improving chicken production |
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EP2970119B1 (en) | 2013-03-14 | 2021-11-03 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
EP2968439A2 (en) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Compositions useful for the treatment of gastrointestinal disorders |
JP2016514671A (en) | 2013-03-15 | 2016-05-23 | シナジー ファーマシューティカルズ インコーポレイテッド | Guanylate cyclase agonists and uses thereof |
CA2913737A1 (en) | 2013-06-05 | 2014-12-11 | Synergy Pharmaceuticals, Inc. | Ultra-pure agonists of guanylate cyclase c, method of making and using same |
US20160130226A1 (en) * | 2013-06-20 | 2016-05-12 | Boehringer Ingelheim International Gmbh | Spiro-substituted oxindole derivatives having ampk activity |
WO2015051496A1 (en) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
TW201636017A (en) | 2015-02-05 | 2016-10-16 | 梯瓦製藥國際有限責任公司 | Methods of treating postherpetic neuralgia with a topical formulation of a spiro-oxindole compound |
EP3551176A4 (en) | 2016-12-06 | 2020-06-24 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
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US11719050B2 (en) | 2021-06-16 | 2023-08-08 | Baker Hughes Oilfield Operations Llc | Cutting elements for earth-boring tools and related earth-boring tools and methods |
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AUPP796798A0 (en) | 1998-12-30 | 1999-01-28 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
JP2003055344A (en) | 1999-01-29 | 2003-02-26 | Dainippon Pharmaceut Co Ltd | 3,7-disubstituted indole derivative and medicinal composition including the same |
AU6050000A (en) | 1999-07-22 | 2001-02-13 | Eli Lilly And Company | Improved method of treating type ii diabetes and obesity |
AU1572701A (en) | 1999-11-15 | 2001-05-30 | Eli Lilly And Company | Treating wasting syndromes with aryloxy propanolamines |
WO2001036412A1 (en) | 1999-11-15 | 2001-05-25 | Eli Lilly And Company | Process for the preparation of aryloxy propanolamines |
US6420365B1 (en) | 2000-01-18 | 2002-07-16 | Neurogen Corporation | Imidazopyridines and related derivatives as selective modulators of bradykinin B2 receptors |
-
2001
- 2001-10-26 AT AT01985160T patent/ATE329901T1/en not_active IP Right Cessation
- 2001-10-26 AU AU2002234134A patent/AU2002234134A1/en not_active Abandoned
- 2001-10-26 IL IL15492801A patent/IL154928A0/en unknown
- 2001-10-26 JP JP2002541080A patent/JP2004513164A/en active Pending
- 2001-10-26 WO PCT/US2001/050666 patent/WO2002038544A2/en active IP Right Grant
- 2001-10-26 DE DE60120748T patent/DE60120748T2/en not_active Expired - Fee Related
- 2001-10-26 EP EP01985160A patent/EP1341759B1/en not_active Expired - Lifetime
- 2001-10-26 CA CA002421594A patent/CA2421594A1/en not_active Abandoned
- 2001-10-26 US US10/399,206 patent/US6825220B2/en not_active Expired - Fee Related
- 2001-10-26 ES ES01985160T patent/ES2265447T3/en not_active Expired - Lifetime
- 2001-11-02 AU AU2432002A patent/AU2432002A/en active Pending
- 2001-11-02 WO PCT/US2001/027793 patent/WO2002038543A2/en not_active Application Discontinuation
-
2004
- 2004-10-21 US US10/970,194 patent/US7122680B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
WO2002038544A2 (en) | 2002-05-16 |
US7122680B2 (en) | 2006-10-17 |
DE60120748T2 (en) | 2007-05-16 |
WO2002038543A2 (en) | 2002-05-16 |
JP2004513164A (en) | 2004-04-30 |
ATE329901T1 (en) | 2006-07-15 |
WO2002038543A3 (en) | 2002-07-04 |
EP1341759A2 (en) | 2003-09-10 |
EP1341759B1 (en) | 2006-06-14 |
AU2432002A (en) | 2002-05-21 |
WO2002038544A3 (en) | 2002-09-26 |
US6825220B2 (en) | 2004-11-30 |
DE60120748D1 (en) | 2006-07-27 |
IL154928A0 (en) | 2003-10-31 |
ES2265447T3 (en) | 2007-02-16 |
CA2421594A1 (en) | 2002-05-16 |
US20040097532A1 (en) | 2004-05-20 |
US20050054713A1 (en) | 2005-03-10 |
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