AR039665A1 - Fenilacetamidas sustituidas y su uso como activadores de glucoquinasa - Google Patents
Fenilacetamidas sustituidas y su uso como activadores de glucoquinasaInfo
- Publication number
- AR039665A1 AR039665A1 ARP030101426A ARP030101426A AR039665A1 AR 039665 A1 AR039665 A1 AR 039665A1 AR P030101426 A ARP030101426 A AR P030101426A AR P030101426 A ARP030101426 A AR P030101426A AR 039665 A1 AR039665 A1 AR 039665A1
- Authority
- AR
- Argentina
- Prior art keywords
- chain
- lower alkyl
- substituted
- atom
- perfluoro
- Prior art date
Links
- 239000012190 activator Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000004432 carbon atom Chemical group C* 0.000 abstract 8
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- -1 amino, hydroxyamino Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- 101500021084 Locusta migratoria 5 kDa peptide Proteins 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 229960003328 benzoyl peroxide Drugs 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/50—Y being a hydrogen or an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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
- C07D241/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
-
- 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
- C07D307/16—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Furan Compounds (AREA)
- Pyrane Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1) en donde R1 y R2 son independientemente H, halo, amino, hidroxiamino, ciano, nitro, alquilo inferior, -OR5 o un resto de fórmula (2), perfluoro-alquilo inferior, tioalquilo inferior, perfluoro-tioalquilo inferior, sulfonil alquilo inferior, perfluoro-sulfonilalquilo inferior, sulfinil alquilo inferior, o sulfonamido; R3 es una cadena de alquilo no ramificada de 4-5 átomos de C o una cadena de heteroalquilo no ramificada de 3-4 átomos de C más un átomo de O ó de S, en donde la cadena, en combinación con el átomo de C que está unida, forma un anillo de 5 o 6 miembros, y cuando la cadena no contiene heteroátomos, un C miembro de la cadena está sustituido con una fracción seleccionada del grupo consistente en hidroxi, oxo, hidroxiimino, metoxiimino, halo, metoxilo, y acetoxilo, o un C miembro de la cadena está disustituido con un hidroxilo y un alquilo inferior o está disustituido con halógeno cuando la cadena contiene un heteroátomo O, la cadena no está sustituida, y cuando la cadena contiene un heteroátomo S, la cadena no está sustituida o el heteroátomo S miembro de la cadena está sustituido por un grupo oxo; R4 un resto de fórmula (3), o un anillo heteroaromático de 5 o 6 miembros no sustituido o mono-sustituido unido por un átomo de C del anillo al grupo amina mostrado, cuyo anillo heteroaromático de 5 o 6 miembros contiene de 1 a 3 heteroátomos seleccionados de S, O, o N, siendo un heteroátomo N que es adyacente a dicho átomo de C enlazante del anillo; dicho anillo heteroaromático mono-sustituido estando mono-sustituido en una posición diferente al átomo de C del anillo adyacente a dicho átomo de C enlazante con un sustituyente seleccionado del grupo consistente en alquilo inferior, halo, nitro, ciano, perfluoro-alquilo inferior, amidooxina, o un resto seleccionado del grupo de fórmulas (4), n es 0, 1, 2, 3 o 4; R5 es H, alquilo inferior, o perfluoro-alquilo inferior; R6 es alquilo inferior; y R7 es H o alquilo inferior; * denota un átomo de C que es asimétrico en todos o la mayoría de los compuestos de fórmula (1); o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37616102P | 2002-04-26 | 2002-04-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR039665A1 true AR039665A1 (es) | 2005-03-02 |
Family
ID=29420328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030101426A AR039665A1 (es) | 2002-04-26 | 2003-04-24 | Fenilacetamidas sustituidas y su uso como activadores de glucoquinasa |
Country Status (34)
| Country | Link |
|---|---|
| US (2) | US7105671B2 (es) |
| EP (1) | EP1501815B1 (es) |
| JP (1) | JP4091600B2 (es) |
| KR (1) | KR100669587B1 (es) |
| CN (1) | CN1329386C (es) |
| AR (1) | AR039665A1 (es) |
| AT (1) | ATE346056T1 (es) |
| AU (1) | AU2003232204B8 (es) |
| BR (1) | BR0309546A (es) |
| CA (1) | CA2482346C (es) |
| DE (1) | DE60309856T2 (es) |
| DK (1) | DK1501815T3 (es) |
| EA (1) | EA011297B1 (es) |
| EC (1) | ECSP045382A (es) |
| ES (1) | ES2276097T3 (es) |
| GT (1) | GT200300096A (es) |
| HR (1) | HRP20040953A2 (es) |
| IL (1) | IL164780A (es) |
| MA (1) | MA27113A1 (es) |
| MX (1) | MXPA04010605A (es) |
| MY (1) | MY135222A (es) |
| NO (1) | NO20044534L (es) |
| NZ (1) | NZ535706A (es) |
| PA (1) | PA8572301A1 (es) |
| PE (1) | PE20040451A1 (es) |
| PL (1) | PL373701A1 (es) |
| PT (1) | PT1501815E (es) |
| RS (1) | RS93604A (es) |
| TN (1) | TNSN04211A1 (es) |
| TW (1) | TWI281917B (es) |
| UA (1) | UA80427C2 (es) |
| UY (1) | UY27787A1 (es) |
| WO (1) | WO2003095438A1 (es) |
| ZA (1) | ZA200407986B (es) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04115996U (ja) * | 1991-03-28 | 1992-10-15 | 東洋運搬機株式会社 | ボートリフタ |
| SE0102299D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| RU2005113713A (ru) * | 2002-10-03 | 2006-01-20 | Новартис АГ (CH) | Замещенные (тиазол-2-ил)амиды или сульфонамиды в качестве активаторов глюкокиназы, которые могут применяться при лечении диабета типа 2 |
| GB0226931D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| PL378117A1 (pl) | 2003-02-11 | 2006-03-06 | Prosidion Limited | Tricyklopodstawione związki amidowe |
| AU2005214132B9 (en) | 2004-02-18 | 2009-06-25 | Astrazeneca Ab | Benzamide derivatives and their use as glucokinae activating agents |
| CA2560689C (en) | 2004-04-02 | 2011-03-01 | Novartis Ag | Sulfonamide-thiazolpyridine derivatives as glucokinase activators useful in the treatment of type 2 diabetes |
| JP2007530631A (ja) | 2004-04-02 | 2007-11-01 | ノバルティス アクチエンゲゼルシャフト | チアゾロピリジン誘導体、それを含む医薬組成物およびグルコキナーゼ介在性状態の処置法 |
| CA2563192A1 (en) * | 2004-04-21 | 2005-11-03 | Prosidion Limited | Tri(cyclo) substituted amide compounds |
| UA90264C2 (ru) * | 2004-04-21 | 2010-04-26 | Прозидион Лтд. | Три(цикло)замещенные амиды, фармацевтическая композиция, способы лечения и профилактики, способ получения соединения |
| TW200600086A (en) | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| US7745491B2 (en) | 2004-08-12 | 2010-06-29 | Prosidion Limited | Substituted phenylacetamides and their use as glucokinase activators |
| GB0418058D0 (en) * | 2004-08-12 | 2004-09-15 | Prosidion Ltd | Fluorination process |
| GB0418046D0 (en) * | 2004-08-12 | 2004-09-15 | Prosidion Ltd | Eantioselective process |
| KR20110084339A (ko) | 2005-07-09 | 2011-07-21 | 아스트라제네카 아베 | 당뇨병 치료에 있어 ｇｌｋ 활성화제로서 사용하기 위한 헤테로아릴 벤즈아미드 유도체 |
| TWI359149B (en) | 2005-07-11 | 2012-03-01 | Mitsubishi Tanabe Pharma Corp | An oxime derivative and preparations thereof |
| JPWO2007026761A1 (ja) | 2005-08-31 | 2009-03-12 | アステラス製薬株式会社 | チアゾール誘導体 |
| JP2007063225A (ja) | 2005-09-01 | 2007-03-15 | Takeda Chem Ind Ltd | イミダゾピリジン化合物 |
| JP2009509988A (ja) | 2005-09-29 | 2009-03-12 | サノフィ−アベンティス | フェニル−及びピリジニル−１，２，４−オキサジアゾロン誘導体、その製造方法、及び医薬品としてのその使用 |
| GT200600428A (es) | 2005-09-30 | 2007-05-21 | Compuestos organicos | |
| GT200600429A (es) | 2005-09-30 | 2007-04-30 | Compuestos organicos | |
| CA2625668A1 (en) | 2005-10-24 | 2007-05-03 | Peter John Harrington | Preparation of cyclic, ketalized ketones by favorskii rearrangement and the use thereof for the preparation of glucokinase activator 70 |
| US20080293741A1 (en) * | 2005-11-03 | 2008-11-27 | Matthew Colin Thor Fyfe | Tricyclo Substituted Amides as Glucokinase Modulators |
| US8034822B2 (en) | 2006-03-08 | 2011-10-11 | Takeda San Diego, Inc. | Glucokinase activators |
| WO2007115968A2 (en) * | 2006-04-12 | 2007-10-18 | F. Hoffmann-La Roche Ag | Process for the preparation of a glucokinase activator |
| WO2007115967A1 (en) * | 2006-04-12 | 2007-10-18 | F. Hoffmann-La Roche Ag | Crystalline isopropanol solvate of glucokinase activator |
| PE20110235A1 (es) | 2006-05-04 | 2011-04-14 | Boehringer Ingelheim Int | Combinaciones farmaceuticas que comprenden linagliptina y metmorfina |
| JP5386350B2 (ja) | 2006-05-31 | 2014-01-15 | タケダ カリフォルニア インコーポレイテッド | グルコキナーゼ活性剤としての、インダゾールおよびイソインドール誘導体 |
| EP2431367A3 (en) | 2006-06-27 | 2012-07-04 | Takeda Pharmaceutical Company Limited | Fused cyclic compounds as GPR40 receptor modulators |
| US7888504B2 (en) | 2006-07-06 | 2011-02-15 | Bristol-Myers Squibb Company | Glucokinase activators and methods of using same |
| US7910747B2 (en) | 2006-07-06 | 2011-03-22 | Bristol-Myers Squibb Company | Phosphonate and phosphinate pyrazolylamide glucokinase activators |
| EP2261216A3 (en) | 2006-07-24 | 2011-12-14 | F. Hoffmann-La Roche AG | Pyrazoles as glucokinase activators |
| TW200819457A (en) | 2006-08-30 | 2008-05-01 | Actelion Pharmaceuticals Ltd | Spiro antibiotic derivatives |
| CL2007003061A1 (es) | 2006-10-26 | 2008-08-01 | Astrazeneca Ab | Compuestos derivados de 3,5-dioxi-benzamida; proceso de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar una enfermedad mediada a traves de glk, tal como la diabetes tipo 2. |
| US7902248B2 (en) * | 2006-12-14 | 2011-03-08 | Hoffmann-La Roche Inc. | Oxime glucokinase activators |
| US8163779B2 (en) | 2006-12-20 | 2012-04-24 | Takeda San Diego, Inc. | Glucokinase activators |
| WO2008074694A1 (en) * | 2006-12-20 | 2008-06-26 | F. Hoffmann-La Roche Ag | Crystallization of glucokinase activators |
| TW200831081A (en) * | 2006-12-25 | 2008-08-01 | Kyorin Seiyaku Kk | Glucokinase activator |
| WO2008080824A1 (en) * | 2006-12-29 | 2008-07-10 | F. Hoffmann-La Roche Ag | Aromatic sulfonated ketals |
| WO2008080822A1 (en) * | 2006-12-29 | 2008-07-10 | F. Hoffmann-La Roche Ag | Epimerization methodologies for recovering stereo isomers in high yield and purity |
| EP2105435A4 (en) | 2007-01-10 | 2011-06-15 | Mitsubishi Tanabe Pharma Corp | Hydrazone derivative |
| EP2116533B1 (en) * | 2007-03-07 | 2013-07-10 | Kyorin Pharmaceutical Co., Ltd. | Glucokinase activator |
| WO2008116107A2 (en) | 2007-03-21 | 2008-09-25 | Takeda San Diego, Inc. | Piperazine derivatives as glucokinase activators |
| WO2009047798A2 (en) * | 2007-10-08 | 2009-04-16 | Advinus Therapeutics Private Limited | Acetamide derivatives as glucokinase activators, their process and medicinal applications |
| US8329707B2 (en) | 2008-01-18 | 2012-12-11 | Astellas Pharma Inc. | Substituted pyrazine compounds |
| US7741327B2 (en) * | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
| US8258134B2 (en) | 2008-04-16 | 2012-09-04 | Hoffmann-La Roche Inc. | Pyridazinone glucokinase activators |
| HUE025224T2 (en) | 2008-04-28 | 2016-02-29 | Kyorin Seiyaku Kk | Ciklopentilakrilsav amide derivatives |
| US20110021570A1 (en) | 2009-07-23 | 2011-01-27 | Nancy-Ellen Haynes | Pyridone glucokinase activators |
| US8222416B2 (en) | 2009-12-14 | 2012-07-17 | Hoffmann-La Roche Inc. | Azaindole glucokinase activators |
| EP3199623B1 (en) | 2010-03-31 | 2021-07-28 | The Scripps Research Institute | Reprogramming cells |
| US8178689B2 (en) | 2010-06-17 | 2012-05-15 | Hoffman-La Roche Inc. | Tricyclic compounds |
| EP2878339A1 (en) | 2013-12-02 | 2015-06-03 | Siena Biotech S.p.A. | SIP3 antagonists |
| AU2017317988B2 (en) | 2016-08-31 | 2020-12-24 | Jiangsu Hengrui Medicine Co., Ltd. | Oxopicolinamide derivative, preparation method therefor and pharmaceutical use thereof |
| GB201714777D0 (en) | 2017-09-14 | 2017-11-01 | Univ London Queen Mary | Agent |
| WO2019052932A1 (en) | 2017-09-18 | 2019-03-21 | Basf Se | SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE249241C (es) | 1910-05-01 | 1912-07-13 | ||
| US3431301A (en) * | 1966-03-24 | 1969-03-04 | Hoffmann La Roche | Process for producing methylhydrazine derivatives |
| US3776917A (en) * | 1972-06-05 | 1973-12-04 | Schering Corp | 2-amino-6-phenalkyl-aminopyridines and derivatives thereof |
| ES419319A1 (es) | 1973-10-04 | 1976-03-01 | Gallardo Antonio Sa | Un procedimiento para la obtencion de derivados de acidos 3-benzoilfenilalcanoicos. |
| GB8909574D0 (en) * | 1989-04-26 | 1989-06-14 | Ici Plc | Chemical process |
| US5169951A (en) * | 1990-04-23 | 1992-12-08 | Ciba-Geigy Corporation | Process for preparing nematicidal compositions |
| EP0566138B1 (en) | 1992-04-17 | 1998-11-18 | Hodogaya Chemical Co., Ltd. | Amino thiazole derivatives and their use as fungicides |
| US5556859A (en) * | 1994-12-22 | 1996-09-17 | Dowelanco | N-(4-pyrimidinyl)amide pesticides |
| GB9823871D0 (en) | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
| ES2226811T3 (es) * | 1999-03-29 | 2005-04-01 | F. Hoffmann-La Roche Ag | Activadores de glucoquinasa. |
| DE60111534T2 (de) * | 2000-07-20 | 2006-05-11 | F. Hoffmann-La Roche Ag | Alpha-acyl- und alpha-heteroatom-substituierte benzenacetamide verwendbar als glucokinase-aktivatoren |
-
2003
- 2003-04-14 AU AU2003232204A patent/AU2003232204B8/en not_active Ceased
- 2003-04-14 CN CNB038093839A patent/CN1329386C/zh not_active Expired - Fee Related
- 2003-04-14 AT AT03749855T patent/ATE346056T1/de active
- 2003-04-14 DK DK03749855T patent/DK1501815T3/da active
- 2003-04-14 PL PL03373701A patent/PL373701A1/xx not_active Application Discontinuation
- 2003-04-14 HR HR20040953A patent/HRP20040953A2/hr not_active Application Discontinuation
- 2003-04-14 JP JP2004503454A patent/JP4091600B2/ja not_active Expired - Fee Related
- 2003-04-14 PT PT03749855T patent/PT1501815E/pt unknown
- 2003-04-14 CA CA002482346A patent/CA2482346C/en not_active Expired - Fee Related
- 2003-04-14 ES ES03749855T patent/ES2276097T3/es not_active Expired - Lifetime
- 2003-04-14 EP EP03749855A patent/EP1501815B1/en not_active Expired - Lifetime
- 2003-04-14 KR KR1020047017204A patent/KR100669587B1/ko not_active Expired - Fee Related
- 2003-04-14 NZ NZ535706A patent/NZ535706A/en unknown
- 2003-04-14 DE DE60309856T patent/DE60309856T2/de not_active Expired - Lifetime
- 2003-04-14 WO PCT/EP2003/003844 patent/WO2003095438A1/en not_active Ceased
- 2003-04-14 BR BR0309546-0A patent/BR0309546A/pt not_active IP Right Cessation
- 2003-04-14 UA UA20041109723A patent/UA80427C2/uk unknown
- 2003-04-14 RS YUP-936/04A patent/RS93604A/sr unknown
- 2003-04-14 EA EA200401398A patent/EA011297B1/ru not_active IP Right Cessation
- 2003-04-14 MX MXPA04010605A patent/MXPA04010605A/es active IP Right Grant
- 2003-04-23 TW TWSUBSTITUTA patent/TWI281917B/zh active
- 2003-04-23 US US10/421,109 patent/US7105671B2/en not_active Expired - Fee Related
- 2003-04-24 PE PE2003000409A patent/PE20040451A1/es not_active Application Discontinuation
- 2003-04-24 AR ARP030101426A patent/AR039665A1/es active IP Right Grant
- 2003-04-24 PA PA20038572301A patent/PA8572301A1/es unknown
- 2003-04-24 GT GT200300096A patent/GT200300096A/es unknown
- 2003-04-24 MY MYPI20031564A patent/MY135222A/en unknown
- 2003-04-28 UY UY27787A patent/UY27787A1/es not_active Application Discontinuation
-
2004
- 2004-10-04 ZA ZA200407986A patent/ZA200407986B/xx unknown
- 2004-10-20 TN TNP2004000211A patent/TNSN04211A1/fr unknown
- 2004-10-21 IL IL164780A patent/IL164780A/en not_active IP Right Cessation
- 2004-10-21 NO NO20044534A patent/NO20044534L/no not_active Application Discontinuation
- 2004-10-22 EC EC2004005382A patent/ECSP045382A/es unknown
- 2004-10-26 MA MA27915A patent/MA27113A1/fr unknown
-
2006
- 2006-04-10 US US11/402,167 patent/US7259166B2/en not_active Expired - Fee Related
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR039665A1 (es) | Fenilacetamidas sustituidas y su uso como activadores de glucoquinasa | |
| CO6260076A2 (es) | Derivados de uracilo o timina para el tratamiento de la hepatitis c | |
| BR122017028096B8 (pt) | composto, composição farmacêutica, e, uso do composto | |
| AR073412A1 (es) | Derivados de espiro imidazolona como antagonistas del receptor glucagon y composiciones que los comprende. | |
| BRPI0810929B8 (pt) | uso de um composto de fórmula 1 | |
| CO5721006A2 (es) | Derivados de pirazolo-quinazolina, proceso para su preparacion y su uso como inhibidores de quinasa | |
| CO5580815A2 (es) | Derivados de adamantana, procesos para su preparacion y composiciones farmaceuticas que los contienen | |
| BR0108303A (pt) | Derivados do 1h-imidazopiridina | |
| AR044152A1 (es) | Derivados de alquilarilo, metodo de preparacion y uso para el tratamiento de la obesidad | |
| BRPI0718966B8 (pt) | composto, composição farmacêutica, inibidor plk1 e agente antitumoral | |
| NO20054856D0 (no) | 4-anilo-kinazolinderivater som antiproliferative midler | |
| BR112015019790A2 (pt) | derivado de piridina monocíclica | |
| AR056964A1 (es) | Derivados de aminosulfonilo, composiciones farmaceuticas y sus usos | |
| AR054081A1 (es) | Derivados de pirimidina, procesos de obtencion y composiciones farmaceuticas | |
| AR038536A1 (es) | N-aril-2-oxazolidinona-5- carboxamidas y sus derivados | |
| NO20074763L (no) | (1,5-difenyl-1H-pyrazol-3-yl)oksadiazolderivater, fremgangsmate ved fremstilling derav og anvendelse av samme i terapi | |
| NO20072688L (no) | Aminpyridinderivat med aurora A-selektiv inhiberende virkning | |
| ATE260275T1 (de) | Substituierte thien-3-yl- sulfonylamino(thio)carbonyl-triazolin(thi)one | |
| CO6190626A2 (es) | Compuestos y composiciones como inhibidores de proteasa activadora de canal | |
| AR064521A1 (es) | Activador de glucoquinasa | |
| CO5601027A2 (es) | Derivados de imidazol-4-il-etinil-piridina | |
| MX2010000658A (es) | Derivados de pirimidina 934. | |
| CO5690593A2 (es) | Nuevos derivados de pirimidin 2-amina | |
| PA8573501A1 (es) | Derivados de benzoxazina y su empleo | |
| AR043487A1 (es) | Heterociclos fusionados de pirimidina y usos de los mismos |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |