ES2332470T3 - Derivados de tiofeno sustituidos como antagonistas del receptor de glucagon, preparacion y usos terapeuticos. - Google Patents
Derivados de tiofeno sustituidos como antagonistas del receptor de glucagon, preparacion y usos terapeuticos. Download PDFInfo
- Publication number
- ES2332470T3 ES2332470T3 ES06720513T ES06720513T ES2332470T3 ES 2332470 T3 ES2332470 T3 ES 2332470T3 ES 06720513 T ES06720513 T ES 06720513T ES 06720513 T ES06720513 T ES 06720513T ES 2332470 T3 ES2332470 T3 ES 2332470T3
- Authority
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- Spain
- Prior art keywords
- thiophene
- acid
- biphenyl
- carbonyl
- dimethyl
- 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.)
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- 229940122904 Glucagon receptor antagonist Drugs 0.000 title abstract description 4
- 238000002360 preparation method Methods 0.000 title description 199
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical class C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 title description 5
- 230000001225 therapeutic effect Effects 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 403
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 144
- 150000003839 salts Chemical class 0.000 claims abstract description 81
- 206010012601 diabetes mellitus Diseases 0.000 claims abstract description 27
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 19
- 239000002253 acid Substances 0.000 claims description 811
- -1 -nitro Chemical group 0.000 claims description 710
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 233
- 229910052739 hydrogen Inorganic materials 0.000 claims description 115
- 239000001257 hydrogen Substances 0.000 claims description 115
- 229910052736 halogen Inorganic materials 0.000 claims description 109
- 150000002367 halogens Chemical class 0.000 claims description 71
- 229910052799 carbon Inorganic materials 0.000 claims description 48
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 47
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 47
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 32
- 125000001424 substituent group Chemical group 0.000 claims description 32
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 30
- 238000011282 treatment Methods 0.000 claims description 30
- 125000001475 halogen functional group Chemical group 0.000 claims description 29
- 125000004429 atom Chemical group 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 25
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- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 6
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
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- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
- ZOIZUVVGWNGIIT-UHFFFAOYSA-N 3-[[5-[1-[3,5-dimethyl-4-(4-propan-2-ylphenyl)phenyl]sulfanyl-2-methylpropyl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C=1C=C(C(=O)NCCC(O)=O)SC=1C(C(C)C)SC(C=C1C)=CC(C)=C1C1=CC=C(C(C)C)C=C1 ZOIZUVVGWNGIIT-UHFFFAOYSA-N 0.000 claims 2
- PUPHPJVLDGGHTL-UHFFFAOYSA-N 3-[[5-[1-[3,5-dimethyl-4-[4-(trifluoromethyl)phenyl]phenoxy]butan-2-yl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C=1C=C(C(=O)NCCC(O)=O)SC=1C(CC)COC(C=C1C)=CC(C)=C1C1=CC=C(C(F)(F)F)C=C1 PUPHPJVLDGGHTL-UHFFFAOYSA-N 0.000 claims 2
- SJACMFJFHKBAPA-UHFFFAOYSA-N 3-[[5-[1-[4-(4-tert-butylphenyl)-3,5-dimethylphenoxy]-2-methylpropyl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C=1C=C(C(=O)NCCC(O)=O)SC=1C(C(C)C)OC(C=C1C)=CC(C)=C1C1=CC=C(C(C)(C)C)C=C1 SJACMFJFHKBAPA-UHFFFAOYSA-N 0.000 claims 2
- LGJNFYPXUZNCQR-UHFFFAOYSA-N 3-[[5-[1-[4-(4-tert-butylphenyl)-3,5-dimethylphenoxy]butan-2-yl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C=1C=C(C(=O)NCCC(O)=O)SC=1C(CC)COC(C=C1C)=CC(C)=C1C1=CC=C(C(C)(C)C)C=C1 LGJNFYPXUZNCQR-UHFFFAOYSA-N 0.000 claims 2
- WESNADSNJTYRQU-UHFFFAOYSA-N 3-[[5-[1-[3,5-dimethyl-4-(4-propan-2-ylphenyl)phenoxy]-2-methylpropyl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C=1C=C(C(=O)NCCC(O)=O)SC=1C(C(C)C)OC(C=C1C)=CC(C)=C1C1=CC=C(C(C)C)C=C1 WESNADSNJTYRQU-UHFFFAOYSA-N 0.000 claims 1
- JEBLXYMEFUOKFB-UHFFFAOYSA-N 3-[[5-[1-[4-(4-tert-butylphenyl)-3,5-dimethylphenyl]sulfanylethyl]thiophene-2-carbonyl]amino]propanoic acid Chemical class C=1C=C(C(=O)NCCC(O)=O)SC=1C(C)SC(C=C1C)=CC(C)=C1C1=CC=C(C(C)(C)C)C=C1 JEBLXYMEFUOKFB-UHFFFAOYSA-N 0.000 claims 1
- GTYRZJKWBQUPAY-UHFFFAOYSA-N 3-[[5-[3,3-dimethyl-1-[5-methyl-4-phenyl-1-(trifluoromethyl)cyclohexa-2,4-dien-1-yl]oxybutyl]thiophene-2-carbonyl]amino]propanoic acid Chemical compound C1C(C)=C(C=2C=CC=CC=2)C=CC1(C(F)(F)F)OC(CC(C)(C)C)C1=CC=C(C(=O)NCCC(O)=O)S1 GTYRZJKWBQUPAY-UHFFFAOYSA-N 0.000 claims 1
- HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 claims 1
- 206010052428 Wound Diseases 0.000 claims 1
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- 125000005018 aryl alkenyl group Chemical group 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000037390 scarring Effects 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 255
- 229960004666 glucagon Drugs 0.000 abstract description 52
- 102000051325 Glucagon Human genes 0.000 abstract description 50
- 108060003199 Glucagon Proteins 0.000 abstract description 50
- MASNOZXLGMXCHN-ZLPAWPGGSA-N glucagon Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O)C(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC=1NC=NC=1)[C@@H](C)O)[C@@H](C)O)C1=CC=CC=C1 MASNOZXLGMXCHN-ZLPAWPGGSA-N 0.000 abstract description 50
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 289
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 90
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- ARYHTUPFQTUBBG-UHFFFAOYSA-N thiophen-2-ylboronic acid Chemical compound OB(O)C1=CC=CS1 ARYHTUPFQTUBBG-UHFFFAOYSA-N 0.000 description 1
- 229960004605 timolol Drugs 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229960002277 tolazamide Drugs 0.000 description 1
- OUDSBRTVNLOZBN-UHFFFAOYSA-N tolazamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)NN1CCCCCC1 OUDSBRTVNLOZBN-UHFFFAOYSA-N 0.000 description 1
- 229960004394 topiramate Drugs 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 229960001130 urapidil Drugs 0.000 description 1
- 239000000777 urocortin Substances 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 229960001729 voglibose Drugs 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 208000016261 weight loss Diseases 0.000 description 1
- 229940071104 xylenesulfonate Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65249205P | 2005-02-11 | 2005-02-11 | |
| US652492P | 2005-02-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2332470T3 true ES2332470T3 (es) | 2010-02-05 |
Family
ID=36694345
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES06720513T Active ES2332470T3 (es) | 2005-02-11 | 2006-02-09 | Derivados de tiofeno sustituidos como antagonistas del receptor de glucagon, preparacion y usos terapeuticos. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8084489B2 (enExample) |
| EP (1) | EP1856090B1 (enExample) |
| JP (1) | JP4988604B2 (enExample) |
| KR (1) | KR20070104409A (enExample) |
| CN (1) | CN101115735B (enExample) |
| AT (1) | ATE445609T1 (enExample) |
| AU (1) | AU2006213894B2 (enExample) |
| BR (1) | BRPI0607015A2 (enExample) |
| CA (1) | CA2597073C (enExample) |
| CR (1) | CR9304A (enExample) |
| CY (1) | CY1109624T1 (enExample) |
| DE (1) | DE602006009773D1 (enExample) |
| DK (1) | DK1856090T3 (enExample) |
| EA (1) | EA200701705A1 (enExample) |
| ES (1) | ES2332470T3 (enExample) |
| IL (1) | IL184932A0 (enExample) |
| MA (1) | MA29432B1 (enExample) |
| MX (1) | MX2007009661A (enExample) |
| NO (1) | NO20074567L (enExample) |
| PL (1) | PL1856090T3 (enExample) |
| PT (1) | PT1856090E (enExample) |
| SI (1) | SI1856090T1 (enExample) |
| TN (1) | TNSN07313A1 (enExample) |
| WO (1) | WO2006086488A2 (enExample) |
| ZA (1) | ZA200706354B (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI1758853T1 (sl) * | 2004-06-14 | 2010-05-31 | Lilly Co Eli | Antagonisti glukagonskega receptorja priprava inuporaba v terapiji |
| ES2494294T3 (es) | 2007-02-09 | 2014-09-15 | Metabasis Therapeutics, Inc. | Antagonistas del receptor de glucagón |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| ES2714207T3 (es) | 2008-08-13 | 2019-05-27 | Metabasis Therapeutics Inc | Antagonistas de glucagón |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2011157827A1 (de) | 2010-06-18 | 2011-12-22 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| BR112013016033A2 (pt) | 2010-12-23 | 2018-06-05 | Pfizer | moduladores do receptor de glucagon |
| ES2597972T3 (es) | 2011-02-08 | 2017-01-24 | Pfizer Inc | Modulador del receptor de glucagón |
| US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8927577B2 (en) | 2011-07-22 | 2015-01-06 | Pfizer Inc. | Quinolinyl glucagon receptor modulators |
| 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 |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| TW201427658A (zh) | 2012-12-10 | 2014-07-16 | Merck Sharp & Dohme | 藉由投予升糖素受體拮抗劑及膽固醇吸收抑制劑治療糖尿病之方法 |
| WO2015066252A1 (en) | 2013-11-04 | 2015-05-07 | Merck Sharp & Dohme Corp. | Glucagon receptor antagonist compounds, compositions thereof, and methods of use |
| JP2017519000A (ja) | 2014-06-12 | 2017-07-13 | リガンド・ファーマシューティカルズ・インコーポレイテッド | グルカゴンアンタゴニスト |
| EP3350200A4 (en) | 2015-09-18 | 2019-03-27 | Wake Forest University Health Services | ANGIOTENSIN (1 7) ANALOGUE AND ASSOCIATED PROCEDURES |
| EP3821917A1 (en) | 2015-10-05 | 2021-05-19 | Hettwer Holding ApS | Compositions and methods for treatment of bone defects |
| CA2914601A1 (en) * | 2015-12-11 | 2017-06-11 | Wake Forest University Health Sciences | Angiotensin-(1-7) analogs and methods relating thereto |
| SG11201901355SA (en) | 2016-08-30 | 2019-03-28 | Regeneron Pharma | Methods of treating severe insulin resistance by interfering with glucagon receptor signaling |
| EP3529278A1 (en) | 2016-10-20 | 2019-08-28 | Regeneron Pharmaceuticals, Inc. | Methods of lowering blood glucose levels |
| US12139546B2 (en) | 2017-08-22 | 2024-11-12 | Regeneron Pharmaceuticals, Inc. | Methods of treating urea cycle disorders by interfering with glucagon receptor signaling |
| TW202003453A (zh) | 2018-02-13 | 2020-01-16 | 美商利根德製藥公司 | 升糖素受體拮抗劑 |
| CN118496197A (zh) | 2019-12-20 | 2024-08-16 | 拜耳公司 | 取代的噻吩甲酰胺、噻吩甲酸及其衍生物 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002365622A1 (en) * | 2001-12-03 | 2003-06-17 | Novo Nordisk A/S | Novel glucagon antagonists |
| AU2003233780A1 (en) * | 2002-06-27 | 2004-01-19 | Novo Nordisk A/S | Novel glucagon antagonists/inverse agonists |
| WO2005118542A1 (en) * | 2004-05-28 | 2005-12-15 | Eli Lilly And Company | Glucagon receptor antagonists, preparation and therapeutic uses |
| SI1758853T1 (sl) * | 2004-06-14 | 2010-05-31 | Lilly Co Eli | Antagonisti glukagonskega receptorja priprava inuporaba v terapiji |
-
2006
- 2006-02-09 MX MX2007009661A patent/MX2007009661A/es active IP Right Grant
- 2006-02-09 DE DE602006009773T patent/DE602006009773D1/de active Active
- 2006-02-09 SI SI200630534T patent/SI1856090T1/sl unknown
- 2006-02-09 AU AU2006213894A patent/AU2006213894B2/en not_active Ceased
- 2006-02-09 EP EP06720513A patent/EP1856090B1/en active Active
- 2006-02-09 AT AT06720513T patent/ATE445609T1/de active
- 2006-02-09 CA CA2597073A patent/CA2597073C/en not_active Expired - Fee Related
- 2006-02-09 PL PL06720513T patent/PL1856090T3/pl unknown
- 2006-02-09 ES ES06720513T patent/ES2332470T3/es active Active
- 2006-02-09 EA EA200701705A patent/EA200701705A1/ru unknown
- 2006-02-09 CN CN2006800046189A patent/CN101115735B/zh not_active Expired - Fee Related
- 2006-02-09 PT PT06720513T patent/PT1856090E/pt unknown
- 2006-02-09 BR BRPI0607015-9A patent/BRPI0607015A2/pt not_active IP Right Cessation
- 2006-02-09 DK DK06720513T patent/DK1856090T3/da active
- 2006-02-09 JP JP2007555195A patent/JP4988604B2/ja not_active Expired - Fee Related
- 2006-02-09 US US11/815,987 patent/US8084489B2/en not_active Expired - Fee Related
- 2006-02-09 WO PCT/US2006/004461 patent/WO2006086488A2/en not_active Ceased
- 2006-02-09 KR KR1020077018437A patent/KR20070104409A/ko not_active Ceased
-
2007
- 2007-07-30 IL IL184932A patent/IL184932A0/en unknown
- 2007-07-31 ZA ZA200706354A patent/ZA200706354B/xx unknown
- 2007-08-10 CR CR9304A patent/CR9304A/es not_active Application Discontinuation
- 2007-08-10 TN TNP2007000313A patent/TNSN07313A1/en unknown
- 2007-09-10 NO NO20074567A patent/NO20074567L/no not_active Application Discontinuation
- 2007-09-11 MA MA30221A patent/MA29432B1/fr unknown
-
2009
- 2009-11-12 CY CY20091101192T patent/CY1109624T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006086488A3 (en) | 2006-12-14 |
| EP1856090B1 (en) | 2009-10-14 |
| DK1856090T3 (da) | 2009-11-30 |
| JP2008530102A (ja) | 2008-08-07 |
| MA29432B1 (fr) | 2008-05-02 |
| EA200701705A1 (ru) | 2008-02-28 |
| NO20074567L (no) | 2007-11-08 |
| BRPI0607015A2 (pt) | 2009-12-01 |
| CN101115735B (zh) | 2013-01-09 |
| ATE445609T1 (de) | 2009-10-15 |
| MX2007009661A (es) | 2007-09-25 |
| WO2006086488A2 (en) | 2006-08-17 |
| KR20070104409A (ko) | 2007-10-25 |
| IL184932A0 (en) | 2007-12-03 |
| PL1856090T3 (pl) | 2010-02-26 |
| CR9304A (es) | 2008-03-31 |
| TNSN07313A1 (en) | 2008-12-31 |
| CY1109624T1 (el) | 2014-08-13 |
| CA2597073A1 (en) | 2006-08-17 |
| ZA200706354B (en) | 2008-11-26 |
| JP4988604B2 (ja) | 2012-08-01 |
| US20100137417A1 (en) | 2010-06-03 |
| CA2597073C (en) | 2014-11-25 |
| SI1856090T1 (sl) | 2010-02-26 |
| PT1856090E (pt) | 2009-11-18 |
| CN101115735A (zh) | 2008-01-30 |
| EP1856090A2 (en) | 2007-11-21 |
| US8084489B2 (en) | 2011-12-27 |
| AU2006213894A1 (en) | 2006-08-17 |
| DE602006009773D1 (de) | 2009-11-26 |
| AU2006213894B2 (en) | 2011-12-08 |
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