WO1999001423A8 - Antagonistes/agonistes inverses du glucagon - Google Patents
Antagonistes/agonistes inverses du glucagonInfo
- Publication number
- WO1999001423A8 WO1999001423A8 PCT/DK1998/000287 DK9800287W WO9901423A8 WO 1999001423 A8 WO1999001423 A8 WO 1999001423A8 DK 9800287 W DK9800287 W DK 9800287W WO 9901423 A8 WO9901423 A8 WO 9901423A8
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inverse agonists
- glucagon antagonists
- glucagon
- compounds
- antagonists
- 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.)
- Ceased
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
-
- 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
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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- 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
-
- 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
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- A—HUMAN NECESSITIES
- 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
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- A—HUMAN NECESSITIES
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/72—Hydrazones
- C07C251/86—Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to carbon atoms of six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
- C07C311/49—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom to nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/28—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/45—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms doubly-bound to the carbon skeleton
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- 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
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D309/06—Radicals substituted by oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU79083/98A AU749271B2 (en) | 1997-07-01 | 1998-06-30 | Glucagon antagonists/inverse agonists |
| BR9810378-4A BR9810378A (pt) | 1997-07-01 | 1998-06-30 | Composto,uso do mesmo, composição farmacêutica, e, processos de tratar a diabete do tipo i ou do tipo ii, de tratar a hiperglicemia, e de diminuir a glicose do sangue em um mamìfero |
| JP50616099A JP2003514508A (ja) | 1997-07-01 | 1998-06-30 | グルカゴン拮抗剤/逆作用剤 |
| CA002294046A CA2294046A1 (fr) | 1997-07-01 | 1998-06-30 | Antagonistes/agonistes inverses du glucagon |
| HU0002373A HUP0002373A3 (en) | 1997-07-01 | 1998-07-01 | Glucagon antagonists/inverse agonists |
| IL13337798A IL133377A0 (en) | 1997-07-01 | 1998-07-01 | Glucagon antagonists/inverse agonists |
| EP98929244A EP0994848A1 (fr) | 1997-07-01 | 1998-07-01 | Antagonistes/agonistes inverses du glucagon |
| NO996550A NO996550L (no) | 1997-07-01 | 1999-12-29 | Glukagonantagonister/inversagonister |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88678597A | 1997-07-01 | 1997-07-01 | |
| US08/886,785 | 1997-07-01 | ||
| US3251698A | 1998-02-27 | 1998-02-27 | |
| US09/032,516 | 1998-02-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO1999001423A1 WO1999001423A1 (fr) | 1999-01-14 |
| WO1999001423A8 true WO1999001423A8 (fr) | 1999-05-14 |
Family
ID=26708528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/DK1998/000287 Ceased WO1999001423A1 (fr) | 1997-07-01 | 1998-06-30 | Antagonistes/agonistes inverses du glucagon |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0994848A1 (fr) |
| JP (1) | JP2003514508A (fr) |
| KR (1) | KR20010020590A (fr) |
| CN (1) | CN1267281A (fr) |
| AU (1) | AU749271B2 (fr) |
| BR (1) | BR9810378A (fr) |
| HU (1) | HUP0002373A3 (fr) |
| IL (1) | IL133377A0 (fr) |
| NO (1) | NO996550L (fr) |
| PL (1) | PL337781A1 (fr) |
| WO (1) | WO1999001423A1 (fr) |
Families Citing this family (132)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6613942B1 (en) * | 1997-07-01 | 2003-09-02 | Novo Nordisk A/S | Glucagon antagonists/inverse agonists |
| JP2002534512A (ja) * | 1999-01-15 | 2002-10-15 | ノボ ノルディスク アクティーゼルスカブ | 非ペプチドglp−1アゴニスト |
| US6927214B1 (en) | 1999-01-15 | 2005-08-09 | Novo Nordisk A/S | Non-peptide GLP-1 agonists |
| KR20020014797A (ko) * | 1999-05-17 | 2002-02-25 | 한센 핀 베네드, 안네 제헤르, 웨이콥 마리안느 | 글루카곤 길항제/역 아고니스트 |
| US6503949B1 (en) | 1999-05-17 | 2003-01-07 | Noro Nordisk A/S | Glucagon antagonists/inverse agonists |
| AUPQ262499A0 (en) | 1999-09-02 | 1999-09-23 | University Of Queensland, The | Novel iron chelators |
| ES2275654T5 (es) | 2000-01-21 | 2012-06-07 | Novartis Ag | Combinaciones que contienen inhibidores de la dipeptidilpeptidasa-IV y agentes antidiabéticos |
| WO2001055107A2 (fr) * | 2000-01-28 | 2001-08-02 | Melacure Therapeutics Ab | Nouveaux amines et amides aromatiques agissant sur les recepteurs de la melanocortine |
| US6562807B2 (en) | 2000-06-23 | 2003-05-13 | Novo Nordisk A/S | Glucagon antagonists/inverse agonists |
| HUP0301501A2 (hu) * | 2000-06-23 | 2003-08-28 | Novo Nordisk A/S | Glükagon antaagonista/inverz agonista vegyületek, ezeket tartalmazó gyógyászati készítmények, valamint a vegyületek alkalmazása gyógyászati készítmények előállítására |
| WO2002040446A1 (fr) * | 2000-11-17 | 2002-05-23 | Novo Nordisk A/S | Antagonistes/agonistes inverses du glucagon |
| US6706744B2 (en) | 2000-11-17 | 2004-03-16 | Novo Nordisk A/S | Glucagon antagonists/inverse agonists |
| WO2002040445A1 (fr) * | 2000-11-17 | 2002-05-23 | Novo Nordisk A/S | Agonistes de glucagon/antagonistes inverses |
| US6821960B2 (en) | 2000-11-17 | 2004-11-23 | Noyo Nordisk Pharmaceuticals, Inc. | Glucagon antagonists/inverse agonists |
| WO2002040444A1 (fr) * | 2000-11-17 | 2002-05-23 | Novo Nordisk A/S | Antagonistes/agonistes inverses de glucagon |
| UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| WO2003031432A1 (fr) | 2001-10-12 | 2003-04-17 | Novo Nordisk A/S | Nouvelles piperidines substituees |
| US6881746B2 (en) | 2001-12-03 | 2005-04-19 | Novo Nordick A/S | Glucagon antagonists/inverse agonists |
| US6762318B2 (en) | 2001-12-03 | 2004-07-13 | Novo Nordisk A/S | Glucagon antagonists |
| IL162620A0 (en) | 2001-12-21 | 2005-11-20 | Novo Nordisk As | Amide derivatives as gk activators |
| AU2003239609B2 (en) | 2002-02-01 | 2008-10-23 | Dainippon Sumitomo Pharma Co., Ltd. | 2-Furancarboxylic acid hydrazides and pharmaceutical compositions containing the same |
| AUPS120902A0 (en) * | 2002-03-19 | 2002-04-18 | Unisearch Limited | Iron chelators as anti-proliferative agents against tumour cells |
| JPWO2003097031A1 (ja) * | 2002-05-22 | 2005-09-15 | 株式会社三和化学研究所 | メチリデンヒドラジド化合物を有効成分とする、肥満の予防又は改善剤 |
| MXPA05000130A (es) | 2002-06-27 | 2005-02-17 | Novo Nordisk As | Derivados de aril-carbonilo como agentes terapeuticos. |
| US7196106B2 (en) | 2002-11-05 | 2007-03-27 | Merck & Co., Inc | Cyanothiophene derivatives, compositions containing such compounds and methods of use |
| US7078419B2 (en) | 2003-03-10 | 2006-07-18 | Boehringer Ingelheim Pharmaceuticals, Inc. | Cytokine inhibitors |
| EP1615698B1 (fr) | 2003-04-11 | 2010-09-29 | High Point Pharmaceuticals, LLC | Nouvelles amides substitues et leur utilisation pharmaceutique |
| JP2005060385A (ja) * | 2003-07-31 | 2005-03-10 | Dainippon Pharmaceut Co Ltd | 2−フランカルボン酸ヒドラジド化合物からなる医薬 |
| RU2381233C2 (ru) | 2003-09-30 | 2010-02-10 | Ново Нордиск А/С | Агонисты рецептора меланокортина |
| EP2298337B1 (fr) | 2003-12-09 | 2017-02-22 | Novo Nordisk A/S | Régulation des préférences alimentaires en utilisant des agonistes du GLP-1 |
| CN102516240A (zh) | 2004-01-06 | 2012-06-27 | 诺和诺德公司 | 杂芳基脲及其作为葡糖激酶活化剂的用途 |
| WO2005120492A1 (fr) | 2004-06-11 | 2005-12-22 | Novo Nordisk A/S | Remede contre l'obesite induite par les medicaments au moyen d'agonistes glp-1 |
| DE102004030987A1 (de) * | 2004-06-26 | 2006-01-12 | Merck Patent Gmbh | Ortho-substituierte (3-Hydroxyphenyl)-essigsäure-benzyliden-hydrazide |
| WO2006028970A1 (fr) | 2004-09-02 | 2006-03-16 | Cengent Therapeutics, Inc. | Derives d'inhibiteurs de thiazole et de thiadiazole de tyrosine phosphatases |
| US8263551B2 (en) | 2004-11-22 | 2012-09-11 | Novo Nordisk A/S | Soluble, stable insulin-containing formulations with a protamine salt |
| AU2005311269B2 (en) | 2004-12-03 | 2011-11-10 | Transtech Pharma, Inc. | Heteroaromatic glucokinase activators |
| NZ560481A (en) | 2005-01-10 | 2010-02-26 | Cortendo Invest Ab | Methods and compositions for treating diabetes, metabolic syndrome and other conditions |
| ES2435522T3 (es) | 2005-02-02 | 2013-12-20 | Novo Nordisk A/S | Derivados de insulina |
| JP4933455B2 (ja) | 2005-02-02 | 2012-05-16 | ノヴォ ノルディスク アー/エス | 新規のインスリン誘導体 |
| WO2006102067A1 (fr) | 2005-03-21 | 2006-09-28 | Merck & Co., Inc. | Derives d'aryle et d'heteroaryle substitues |
| EP1868985A4 (fr) | 2005-03-30 | 2010-05-05 | Merck Sharp & Dohme | Composes antagonistes du recepteur du glucagon, compositions renfermant de tels composes et methodes d'utilisation |
| WO2007003581A1 (fr) | 2005-06-30 | 2007-01-11 | Novo Nordisk A/S | Acides phénoxyacétiques en tant qu'activateurs de rapp-delta |
| AU2006264966B2 (en) | 2005-07-04 | 2013-02-21 | High Point Pharmaceuticals, Llc | Histamine H3 receptor antagonists |
| KR101446973B1 (ko) | 2005-07-14 | 2014-10-07 | 트랜스테크 파르마 엘엘씨 | 우레아 글루코키나제 활성제 |
| ES2426345T3 (es) | 2005-07-20 | 2013-10-22 | Eli Lilly And Company | Compuesto unidos en posición 1-amino |
| PT1931350E (pt) | 2005-09-14 | 2014-02-12 | Takeda Pharmaceutical | Administração de inibidores de dipeptidil peptidase |
| TW200745031A (en) | 2005-10-13 | 2007-12-16 | Merck & Co Inc | Acyl indoles, compositions containing such compounds and methods of use |
| EP1801098A1 (fr) | 2005-12-16 | 2007-06-27 | Merck Sante | Dérivés de 2-Adamantylurea comme inhibiteurs de 11B-HSD1 |
| EA201101084A1 (ru) | 2005-12-22 | 2012-04-30 | ХАЙ ПОЙНТ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи | Феноксиуксусные кислоты в качестве активаторов ppar дельта |
| AU2007229850A1 (en) | 2006-03-23 | 2007-10-04 | Merck & Co., Inc. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
| MX2008011123A (es) | 2006-03-28 | 2008-09-30 | High Point Pharmaceuticals Llc | Benzotiazoles que tienen actividad de receptor h3 de histamina. |
| WO2007136577A2 (fr) | 2006-05-16 | 2007-11-29 | Merck & Co., Inc. | Composés antagonistes du récepteur du glucagon, compositions contenant ces composés, et procédés d'utilisation |
| CN102295606A (zh) | 2006-05-29 | 2011-12-28 | 高点制药有限责任公司 | 合成3-(1,3-苯并间二氧杂环戊烯-5-基)-6-(4-环丙基哌嗪-1-基)-哒嗪的方法及其适用的中间体 |
| AU2007303219A1 (en) | 2006-10-02 | 2008-04-10 | Cortendo Ab (Publ) | Ketoconazole enantiomer in humans |
| TW200821284A (en) | 2006-10-03 | 2008-05-16 | Merck & Co Inc | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
| EP2086951B1 (fr) | 2006-11-15 | 2011-12-21 | High Point Pharmaceuticals, LLC | Nouvelles 2-(2-hydroxyphényl) benzothiadiazines utilisées pour traiter l'obésité et le diabète |
| US7786139B2 (en) | 2006-11-21 | 2010-08-31 | Omeros Corporation | PDE10 inhibitors and related compositions and methods |
| EP1935420A1 (fr) | 2006-12-21 | 2008-06-25 | Merck Sante | Dérivés du 2-adamantyl-butyramide en tant qu'inhibiteurs selectifs de la 11beta-HSD1 |
| JP5226008B2 (ja) | 2007-01-11 | 2013-07-03 | ノボ・ノルデイスク・エー/エス | ウレアグルコキナーゼアクチベーター |
| CA2677230A1 (fr) | 2007-02-02 | 2008-08-14 | Redpoint Bio Corporation | Utilisation d'un inhibiteur de trpm5 pour reguler une secretion d'insuline et de glp-1 |
| EP2110374A1 (fr) | 2008-04-18 | 2009-10-21 | Merck Sante | Dérivés de benzofurane, benzothiophène, benzothiazol en tant que modulateurs FXR |
| FR2932482B1 (fr) * | 2008-06-13 | 2010-10-08 | Sanofi Aventis | Nouveaux derives de (phenyl-3,6-dihydro-2h-pyridinyl)- (piperazinyl ponte)-1-alcanone et leur utilisation comme inhibiteurs de p75 |
| FR2932481B1 (fr) | 2008-06-13 | 2010-10-08 | Sanofi Aventis | Derives de 4-{2-°4-phenyl-3,6-dihydro-2h-pyridin-1-yl!-2- oxo-alkyl}-1-piperazin-2-one, leur preparation et leur application en therapeutique. |
| US20100035932A1 (en) * | 2008-08-07 | 2010-02-11 | Schepetkin Igor A | Novel formyl peptide receptor like 1 agonists that induce macrophage tumor necrosis factor alpha and computational structure-activity relationship analysis of thereof |
| JO2870B1 (en) | 2008-11-13 | 2015-03-15 | ميرك شارب اند دوهم كورب | Amino Tetra Hydro Pirans as Inhibitors of Peptide Dipeptide IV for the Treatment or Prevention of Diabetes |
| WO2010056717A1 (fr) | 2008-11-17 | 2010-05-20 | Merck Sharp & Dohme Corp. | Amines bicycliques substituées pour le traitement du diabète |
| AU2009316802B2 (en) | 2008-11-21 | 2015-02-26 | Vtv Therapeutics Llc | Adamantyl benzamide compounds |
| WO2011011506A1 (fr) | 2009-07-23 | 2011-01-27 | Schering Corporation | Composés oxazépine spirocyclique en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| WO2011011508A1 (fr) | 2009-07-23 | 2011-01-27 | Schering Corporation | Composés doxazépine benzofusionnés en tant quinhibiteurs de la coenzyme-stéaroyle a delta-9 désaturase |
| EP2464228B1 (fr) | 2009-08-13 | 2017-12-06 | Merck Sharp & Dohme Corp. | Composés cyclopropyle substitués, compositions contenant de tels composés et procédés de traitement |
| JP5734981B2 (ja) | 2009-09-02 | 2015-06-17 | メルク・シャープ・エンド・ドーム・コーポレイション | 糖尿病の治療又は予防のためのジペプチジルペプチダーゼiv阻害剤としてのアミノテトラヒドロピラン |
| WO2011041293A1 (fr) | 2009-09-30 | 2011-04-07 | Takeda Pharmaceutical Company Limited | Dérivés pyrazolo [1, 5a] pyrimidines comme inhibiteurs de kinase 1 régulatrice de signal d'apoptose |
| JP2013510834A (ja) | 2009-11-16 | 2013-03-28 | メリテク | [1,5]‐ジアゾシン誘導体 |
| FR2953839A1 (fr) | 2009-12-14 | 2011-06-17 | Sanofi Aventis | Nouveaux derives d'(heterocycle-piperidine condensee)-(piperazinyl)-1alcanone ou d'(heterocycle-pyrrolidine condensee)-(piperazinyl)-1alcanone et leur utilisation comme inhibiteurs de p75 |
| FR2953836B1 (fr) | 2009-12-14 | 2012-03-16 | Sanofi Aventis | Nouveaux derives (heterocycle-tetrahydro-pyridine)-(piperazinyl)-1-alcanone et (heterocycle-dihydro-pyrrolidine)-(piperazinyl)-1-alcanone et leur utilisation comme inhibiteurs de p75 |
| WO2011079778A1 (fr) | 2009-12-30 | 2011-07-07 | China Shanghai Fochon Pharmaceutical Co Ltd | Dérivés de 3-(3-aminopipéridin-1-yl)-5-oxo-1,2,4-triazine à titre d'inhibiteurs de dipeptidyl peptidase iv (dpp-iv) |
| WO2011097079A1 (fr) | 2010-02-03 | 2011-08-11 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinase 1 régulant le signal d'apoptose |
| WO2011103256A1 (fr) | 2010-02-22 | 2011-08-25 | Merck Sharp & Dohme Corp. | Aminotétrahydrothiopyranes substitués et dérivés de ceux-ci utilisés en tant qu'inhibiteurs de la dipeptidylpeptidase-iv dans le cadre du traitement du diabète |
| WO2011104378A1 (fr) | 2010-02-26 | 2011-09-01 | Novo Nordisk A/S | Peptides de traitement de l'obésité |
| BR112012021231A2 (pt) | 2010-02-26 | 2015-09-08 | Basf Plant Science Co Gmbh | método para acentuar o rendimento em plantas, planta, construto, uso de um construto, método para a produção de uma planta transgênica, partes coletáveis de uma planta, produtos derivados de uma planta, uso de um ácido nucleíco e método para a produção de um produto |
| KR20130018410A (ko) | 2010-03-26 | 2013-02-21 | 노보 노르디스크 에이/에스 | 새로운 글루카곤 유사체 |
| EP2571876B1 (fr) | 2010-05-21 | 2016-09-07 | Merck Sharp & Dohme Corp. | Composés hétérocycliques substitués à sept chaînons en tant qu'inhibiteurs de la dipeptidyl-peptidase iv pour le traitement du diabète |
| US8742110B2 (en) | 2010-08-18 | 2014-06-03 | Merck Sharp & Dohme Corp. | Spiroxazolidinone compounds |
| US8609672B2 (en) | 2010-08-27 | 2013-12-17 | University Of The Pacific | Piperazinylpyrimidine analogues as protein kinase inhibitors |
| NZ611529A (en) | 2010-12-23 | 2015-06-26 | Pfizer | Glucagon receptor modulators |
| KR101638671B1 (ko) | 2011-02-08 | 2016-07-11 | 화이자 인코포레이티드 | 글루카곤 수용체 조절자 |
| EP2691108A1 (fr) | 2011-03-28 | 2014-02-05 | Novo Nordisk A/S | Nouveaux analogues de glucagon |
| CA2831334A1 (fr) | 2011-04-08 | 2012-10-11 | Merck Sharp & Dohme Corp. | Composes a cyclopropyle substitue, compositions contenant de tels composes et methodes de traitement |
| CA2837517A1 (fr) | 2011-06-02 | 2012-12-06 | Intervet International B.V. | Derives d'imidazole |
| JP2014517036A (ja) | 2011-06-16 | 2014-07-17 | メルク・シャープ・アンド・ドーム・コーポレーション | 置換シクロプロピル化合物、そのような化合物を含有する組成物および治療方法 |
| RU2013157388A (ru) | 2011-07-22 | 2015-08-27 | Пфайзер Инк. | Хинолинильные модуляторы глюкагонового рецептора |
| WO2013041678A1 (fr) | 2011-09-23 | 2013-03-28 | Novo Nordisk A/S | Nouveaux analogues du glucagon |
| US9422266B2 (en) | 2011-09-30 | 2016-08-23 | Merck Sharp & Dohme Corp. | Substituted cyclopropyl compounds, compositions containing such compounds and methods of treatment |
| WO2013062838A1 (fr) | 2011-10-24 | 2013-05-02 | Merck Sharp & Dohme Corp. | Composés de pipéridinyle substitués utilisés comme agonistes du récepteur gpr119 |
| WO2013068328A1 (fr) | 2011-11-07 | 2013-05-16 | Intervet International B.V. | Composés d'acide bicyclo[2.2.2]octan-1-ylcarboxylique comme inhibiteurs de la dgat-1 |
| WO2013068439A1 (fr) | 2011-11-09 | 2013-05-16 | Intervet International B.V. | Composés 4-amino-5-oxo-7,8-dihydropyrimido[5, 4 -f] [1, 4] oxazépine comme inhibiteurs de dgat1 |
| US9029403B2 (en) | 2011-11-10 | 2015-05-12 | Memorial Sloan-Kettering Cancer Center | Treatment of ovarian cancer with benzylidenebenzohydrazides |
| WO2013074388A1 (fr) | 2011-11-15 | 2013-05-23 | Merck Sharp & Dohme Corp. | Composés de cyclopropyle substitués utiles à titre d'agonistes de gpr119 |
| EP2606894A1 (fr) | 2011-12-20 | 2013-06-26 | Sanofi | Nouvelle utilisation thérapeutique des antagonistes du récepteur p75 |
| EP2814485A4 (fr) | 2012-02-17 | 2015-08-26 | Merck Sharp & Dohme | Inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prévention du diabète |
| IN2014DN09640A (fr) | 2012-04-16 | 2015-07-31 | Kaneq Pharma Inc | |
| WO2014018350A1 (fr) | 2012-07-23 | 2014-01-30 | Merck Sharp & Dohme Corp. | Traitement du diabète par administration d'inhibiteurs de dipeptidyl peptidase-iv |
| WO2014093696A2 (fr) | 2012-12-12 | 2014-06-19 | Massachusetts Institute Of Technology | Dérivés d'insuline pour le traitement du diabète |
| AU2014255608B2 (en) | 2013-04-18 | 2018-01-25 | Novo Nordisk A/S | Stable, protracted GLP-1/glucagon receptor co-agonists for medical use |
| EP3065736B1 (fr) | 2013-11-04 | 2018-11-14 | Merck Sharp & Dohme Corp. | Composés antagonistes du récepteur du glucagon, compositions correspodantes et méthodes d'utilisation |
| EP3097101B1 (fr) | 2014-01-24 | 2020-12-23 | Merck Sharp & Dohme Corp. | Dérivés d'isoquinoline utilisés comme inhibiteurs de mgat2 |
| BR112016023839A8 (pt) | 2014-04-17 | 2023-04-11 | Merck Sharp & Dohme | Complexo de tanato de sitagliptina, composição farmacêutica, intermediário farmacêutico, forma de dosagem oral, e, uso de um complexo de tanato de sitagliptina |
| EP3151852A1 (fr) | 2014-06-04 | 2017-04-12 | Novo Nordisk A/S | Co-agonistes de récepteur du glucagon/glp-1 à usage médical |
| CA3093383A1 (fr) | 2014-10-24 | 2016-04-28 | Merck Sharp & Dohme Corp. | Co-agonistes des recepteurs du glucagon et du glp-1 |
| US10752588B2 (en) | 2014-12-19 | 2020-08-25 | The Broad Institute, Inc. | Dopamine D2 receptor ligands |
| WO2016100940A1 (fr) | 2014-12-19 | 2016-06-23 | The Broad Institute, Inc. | Ligands des récepteurs dopaminergiques d2 |
| CN104610157A (zh) * | 2015-02-13 | 2015-05-13 | 佛山市赛维斯医药科技有限公司 | 一类环丙基酰肼和卤代苯类结构的gpr119激动剂及其用途 |
| CN104557717A (zh) * | 2015-02-13 | 2015-04-29 | 佛山市赛维斯医药科技有限公司 | 酰肼类gpr119激动剂、制备方法及其用途 |
| CN104610151A (zh) * | 2015-02-13 | 2015-05-13 | 佛山市赛维斯医药科技有限公司 | 含酰肼和烷氧苯类结构的化合物、其制备方法及用途 |
| CN104672144A (zh) * | 2015-02-13 | 2015-06-03 | 佛山市赛维斯医药科技有限公司 | 一种环丙基酰肼和硝基苯类gpr119激动剂、制备方法及其用途 |
| CN104592120A (zh) * | 2015-02-13 | 2015-05-06 | 佛山市赛维斯医药科技有限公司 | 一种环丙基酰肼和甲氧苯类gpr119激动剂、制备方法及其用途 |
| CN104592121A (zh) * | 2015-02-13 | 2015-05-06 | 佛山市赛维斯医药科技有限公司 | 含酰肼和硝基苯类结构的化合物、其制备方法及用途 |
| CN104610150A (zh) * | 2015-02-13 | 2015-05-13 | 佛山市赛维斯医药科技有限公司 | 含酰肼和腈基苯类结构的化合物、其制备方法及用途 |
| CN104610156A (zh) * | 2015-02-13 | 2015-05-13 | 佛山市赛维斯医药科技有限公司 | 一种环丙基酰肼和腈基苯类gpr119激动剂、制备方法及其用途 |
| EP3359191A4 (fr) | 2015-10-05 | 2019-05-29 | Merck Sharp & Dohme Corp. | Conjugués anticorps-peptides ayant une activité agoniste au niveau des récepteurs au glucagon et au peptide-1 similaire au glucagon |
| CN107151220B (zh) * | 2015-10-19 | 2021-07-20 | 中国医学科学院药物研究所 | 含苄氧基苯基的酚类化合物、其制备方法及用途 |
| US10414775B2 (en) | 2016-08-15 | 2019-09-17 | Merck Sharp & Dohme Corp. | Compounds useful for altering the levels of bile acids for the treatment of diabetes and cardiometabolic disease |
| US10414774B2 (en) | 2016-08-15 | 2019-09-17 | Merck Sharp & Dohme Corp. | Compound useful for altering the levels of bile acids for the treatment of diabetes and cardiometabolc disease |
| CN111032680A (zh) | 2017-03-15 | 2020-04-17 | 诺和诺德股份有限公司 | 能够与黑皮质素4受体结合的双环化合物 |
| WO2019219714A1 (fr) | 2018-05-15 | 2019-11-21 | Novo Nordisk A/S | Composés capables de se lier au récepteur de la mélanocortine 4 |
| WO2020053414A1 (fr) | 2018-09-14 | 2020-03-19 | Novo Nordisk A/S | Composés bicycliques aptes à se lier aux agonistes du récepteur de la mélanocortine 4 |
| WO2020074958A1 (fr) | 2018-10-12 | 2020-04-16 | Strongbridge Dublin Limited | Lévokétoconazole pour le traitement de l'hyperplasie surrénale congénitale et de l'aldostéronisme primaire |
| WO2020205688A1 (fr) | 2019-04-04 | 2020-10-08 | Merck Sharp & Dohme Corp. | Inhibiteurs d'histone désacétylase -3 utiles pour le traitement du cancer, de l'inflammation, de maladies neurodégénératives et du diabète |
| CN110229056B (zh) * | 2019-06-21 | 2022-11-08 | 天津科技大学 | 一种新型姜黄素类似物及其制备方法和应用 |
| EP3842060A1 (fr) | 2019-12-23 | 2021-06-30 | Merck Sharp & Dohme Corp. | Co-agonistes lactames agrafés des récepteurs du glucagon et du glp-1 |
| EP3842449A1 (fr) | 2019-12-23 | 2021-06-30 | Merck Sharp & Dohme Corp. | Co-agonistes d'oléfine agrafés du glucagon et récepteurs glp-1 |
| EP3842061A1 (fr) | 2019-12-23 | 2021-06-30 | Merck Sharp & Dohme Corp. | Co-agonistes triazoles agrafés des récepteurs du glucagon et du glp-1 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3859281A (en) * | 1971-07-01 | 1975-01-07 | American Home Prod | 2,6-dichlorobenzylidenehydrazides |
| US3746703A (en) * | 1971-07-01 | 1973-07-17 | American Home Prod | 2,6-dichlorobenzylidenehydrazides |
| US3836580A (en) * | 1971-07-01 | 1974-09-17 | American Home Prod | 2,6-dichlorobenzylidenehydrazides |
| US4334015A (en) * | 1979-05-23 | 1982-06-08 | Minnesota Mining And Manufacturing Company | Imaging compositions |
| DE4033808A1 (de) * | 1990-04-11 | 1991-10-17 | Bayer Ag | Naphthalinderivate |
| JPH04121717A (ja) * | 1990-09-12 | 1992-04-22 | Fuji Photo Film Co Ltd | 新規な有機非線形光学材料及びそれを用いた光波長の変換方法 |
| JP3529491B2 (ja) * | 1995-05-16 | 2004-05-24 | 旭電化工業株式会社 | 感熱記録材料 |
| WO1997016442A1 (fr) * | 1995-10-31 | 1997-05-09 | Merck & Co., Inc. | Pyrroles de pyridyle substitues, compositions contenant de tels composes et mode d'utilisation |
-
1998
- 1998-06-30 AU AU79083/98A patent/AU749271B2/en not_active Ceased
- 1998-06-30 JP JP50616099A patent/JP2003514508A/ja active Pending
- 1998-06-30 BR BR9810378-4A patent/BR9810378A/pt not_active IP Right Cessation
- 1998-06-30 WO PCT/DK1998/000287 patent/WO1999001423A1/fr not_active Ceased
- 1998-07-01 IL IL13337798A patent/IL133377A0/xx unknown
- 1998-07-01 HU HU0002373A patent/HUP0002373A3/hu unknown
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- 1998-07-01 CN CN98808125A patent/CN1267281A/zh active Pending
- 1998-07-01 EP EP98929244A patent/EP0994848A1/fr not_active Withdrawn
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| AU749271B2 (en) | 2002-06-20 |
| JP2003514508A (ja) | 2003-04-15 |
| HUP0002373A3 (en) | 2000-11-28 |
| WO1999001423A1 (fr) | 1999-01-14 |
| IL133377A0 (en) | 2001-04-30 |
| KR20010020590A (ko) | 2001-03-15 |
| PL337781A1 (en) | 2000-09-11 |
| NO996550L (no) | 2000-02-29 |
| AU7908398A (en) | 1999-01-25 |
| HUP0002373A2 (hu) | 2000-10-28 |
| BR9810378A (pt) | 2000-08-29 |
| EP0994848A1 (fr) | 2000-04-26 |
| NO996550D0 (no) | 1999-12-29 |
| CN1267281A (zh) | 2000-09-20 |
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