UY28915A1 - Derivados de tetraazabenzo (e)azuleno y sus análogos - Google Patents
Derivados de tetraazabenzo (e)azuleno y sus análogosInfo
- Publication number
- UY28915A1 UY28915A1 UY28915A UY28915A UY28915A1 UY 28915 A1 UY28915 A1 UY 28915A1 UY 28915 A UY28915 A UY 28915A UY 28915 A UY28915 A UY 28915A UY 28915 A1 UY28915 A1 UY 28915A1
- Authority
- UY
- Uruguay
- Prior art keywords
- azuleno
- tetraazabenzo
- analogs
- derivatives
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Esta invención se refiere a agonistas CCK-A de fórmula en que R1-R4, A,B,X,D,E y G son como se definen en la memoria descriptiva, así como, entre otras cosas, las composiciones farmacéuticas que contienen los compuestos y los métodos para usar los compuestos y composiciones. Los compuestos son útiles para tratar la obesidad.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57403304P | 2004-05-25 | 2004-05-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY28915A1 true UY28915A1 (es) | 2005-12-30 |
Family
ID=34967684
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY28915A UY28915A1 (es) | 2004-05-25 | 2005-05-23 | Derivados de tetraazabenzo (e)azuleno y sus análogos |
Country Status (26)
Country | Link |
---|---|
US (2) | US7265104B2 (es) |
EP (1) | EP1753766A1 (es) |
JP (1) | JP4069159B2 (es) |
CN (1) | CN1950374A (es) |
AP (1) | AP2006003768A0 (es) |
AR (1) | AR049187A1 (es) |
AU (1) | AU2005247693A1 (es) |
BR (1) | BRPI0510273A (es) |
CA (1) | CA2568056A1 (es) |
CR (1) | CR8753A (es) |
EA (1) | EA010888B1 (es) |
EC (1) | ECSP067025A (es) |
GE (1) | GEP20094723B (es) |
GT (1) | GT200500119A (es) |
IL (1) | IL178220A0 (es) |
MA (1) | MA28605B1 (es) |
NL (1) | NL1029105C2 (es) |
NO (1) | NO20064288L (es) |
PA (1) | PA8634101A1 (es) |
PE (1) | PE20060363A1 (es) |
SV (1) | SV2006002127A (es) |
TN (1) | TNSN06386A1 (es) |
TW (1) | TWI297688B (es) |
UA (1) | UA84208C2 (es) |
UY (1) | UY28915A1 (es) |
WO (1) | WO2005116034A1 (es) |
Families Citing this family (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060177438A1 (en) * | 2005-02-08 | 2006-08-10 | New England Medical Center | Methods of altering absorption of hydrophobic compounds |
EP1937297A2 (en) * | 2005-09-08 | 2008-07-02 | Gastrotech Pharma A/S | Use of a glp-1 molecule for treatment of biliary dyskinesia and/or biliary pain/discomfort |
JP2010500300A (ja) | 2006-08-08 | 2010-01-07 | サノフィ−アベンティス | アリールアミノアリール−アルキル−置換イミダゾリジン−2,4−ジオン、それらの製造法、それらの化合物を含有する薬剤、およびそれらの使用 |
AU2007320906A1 (en) | 2006-11-13 | 2008-05-22 | Pfizer Products Inc. | Diaryl, dipyridinyl and aryl-pyridinyl derivatives and uses thereof |
JP5313161B2 (ja) * | 2006-12-11 | 2013-10-09 | メルク・シャープ・アンド・ドーム・コーポレーション | ボンベシンレセプターサブタイプ−3調節因子としての置換ジアゼピンスルホンアミド |
AU2008219723A1 (en) * | 2007-02-28 | 2008-09-04 | Merck Sharp & Dohme Corp. | Substituted benzodiazepinones, benzoxazepinones and benzothiazepinones as sodium channel blockers |
ES2748136T3 (es) | 2007-10-15 | 2020-03-13 | United Animal Health Inc | Método para aumentar el rendimiento de las crías |
US20100317642A1 (en) * | 2007-10-15 | 2010-12-16 | Inventis Dds Pvt Limited | Pharmaceutical composition of orlistat |
US8470841B2 (en) | 2008-07-09 | 2013-06-25 | Sanofi | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
MX2011004575A (es) * | 2008-11-13 | 2011-06-01 | Hoffmann La Roche | Espiro-5,6-dihidro-4h-2,3,5,10b-tetraaza-benzo [e] azulenos. |
JP5384659B2 (ja) * | 2008-11-18 | 2014-01-08 | エフ.ホフマン−ラ ロシュ アーゲー | ジヒドロテトラアザベンゾアズレンのアルキルシクロヘキシルエーテル |
MY150837A (en) * | 2008-11-28 | 2014-02-28 | Hoffmann La Roche | Arylcyclohexylethers of dihydrotetraazabenzoazulenes for use as vasopressin via receptor antagonists |
WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
WO2010067233A1 (en) | 2008-12-08 | 2010-06-17 | Pfizer Inc. | 1,2,4 triazolo [4, 3 -a] [1,5] benzodiazepin-5 (6h) -ones as agonists of the cholecystokinin-1 receptor (cck-ir) |
JP2012515760A (ja) | 2009-01-20 | 2012-07-12 | ファイザー・インク | 置換ピラジノンアミド |
WO2010086820A1 (en) | 2009-02-02 | 2010-08-05 | Pfizer Inc. | 4-amino-5-oxo-7, 8-dihydropyrimido [5,4-f] [1,4] oxazepin-6 (5h) -yl) phenyl derivatives, pharmaceutical compositions and uses thereof |
TW201040174A (en) | 2009-02-03 | 2010-11-16 | Pfizer | 4-amino-7,8-dihydropyrido[4,3-d]pyrimidin-5(6H)-one derivatives |
TW201040175A (en) | 2009-02-04 | 2010-11-16 | Pfizer | 4-amino-7,8-dihydropyrido[4,3-d]pyrimidin-5(6H)-one derivatives |
PL2406253T3 (pl) | 2009-03-11 | 2013-10-31 | Pfizer | Pochodne benzofuranylu jako inhibitory glukokinazy |
EP2406230A1 (en) | 2009-03-11 | 2012-01-18 | Pfizer Inc. | Substituted indazole amides and their use as glucokinase activators |
US20120095028A1 (en) | 2009-03-20 | 2012-04-19 | Pfizer Inc. | 3-oxa-7-azabicyclo[3.3.1]nonanes |
PE20120399A1 (es) | 2009-06-05 | 2012-04-24 | Pfizer | Derivados del l-(piperidin-4-il)-pirazol como moduladores de gpr 119 |
CN102482312A (zh) | 2009-08-26 | 2012-05-30 | 赛诺菲 | 新颖的杂芳族氟代糖苷结晶水合物、含有这些化合物的药物和它们的用途 |
EP2480551A1 (en) | 2009-09-23 | 2012-08-01 | Pfizer Inc. | Gpr 119 modulators |
CA2777857C (en) | 2009-11-02 | 2014-12-02 | Pfizer Inc. | Dioxa-bicyclo[3.2.1]octane-2,3,4-triol derivatives |
JP2013510191A (ja) | 2009-11-10 | 2013-03-21 | ファイザー・インク | N−2ピラゾロスピロケトンアセチル−CoAカルボキシラーゼ阻害薬 |
PL2499139T3 (pl) | 2009-11-10 | 2014-04-30 | Pfizer | N1-pirazolospiroketonowe inhibitory karboksylazy acetylo-CoA |
US20120295845A1 (en) | 2009-11-23 | 2012-11-22 | Pfizer Inc | Imidazo-pyrazoles as gpr119 inhibitors |
US20110160143A1 (en) * | 2009-12-28 | 2011-06-30 | Perricone Nicholas V | Topical Acyl Glutathione Psoriasis Compositions |
RS54383B1 (en) | 2010-03-19 | 2016-04-28 | Pfizer Inc. | 2,3-DIHYDRO-1H-INDEN-1-IL-2,7-DIAZASPIRO DERIVATIVES [3.6] NONANES AND THEIR USE AS ANTAGONISTS OR INVERNING AGELISTS OF GRELIN RECEPTORS |
US8420633B2 (en) | 2010-03-31 | 2013-04-16 | Hoffmann-La Roche Inc. | Aryl-cyclohexyl-tetraazabenzo[e]azulenes |
WO2011123678A2 (en) | 2010-03-31 | 2011-10-06 | Arqule, Inc. | Substituted benzo-pyrido-triazolo-diazepine compounds |
US8461151B2 (en) | 2010-04-13 | 2013-06-11 | Hoffmann-La Roche Inc. | Aryl-/heteroaryl-cyclohexenyl-tetraazabenzo[e]azulenes |
US8492376B2 (en) | 2010-04-21 | 2013-07-23 | Hoffmann-La Roche Inc. | Heteroaryl-cyclohexyl-tetraazabenzo[e]azulenes |
US8481528B2 (en) | 2010-04-26 | 2013-07-09 | Hoffmann-La Roche Inc. | Heterobiaryl-cyclohexyl-tetraazabenzo[e]azulenes |
US8513238B2 (en) | 2010-05-10 | 2013-08-20 | Hoffmann-La Roche Inc. | Heteroaryl-cyclohexyl-tetraazabenzo[E]azulenes |
WO2011158149A1 (en) | 2010-06-18 | 2011-12-22 | Pfizer Inc. | 2-(3,5-disubstitutedphenyl)pyrimidin-4(3h)-one derivatives |
EP2621493B1 (en) | 2010-09-30 | 2016-08-17 | Pfizer Inc | N1-PYRAZOLOSPIROKETONE ACETYL-CoA CARBOXYLASE INHIBITORS |
MX2013004733A (es) | 2010-10-29 | 2013-07-02 | Pfizer | Inhibidores de n1/n2-lactama acetil-coa carboxilasa. |
AU2011346670B2 (en) | 2010-12-23 | 2015-05-07 | Pfizer Inc. | Glucagon receptor modulators |
CN104744370A (zh) | 2011-02-08 | 2015-07-01 | 辉瑞大药厂 | 胰高血糖素受体调节剂 |
AU2012221704B2 (en) | 2011-02-23 | 2013-12-05 | Coeruleus Ltd. | Flumazenil complexes, compositions comprising same and uses thereof |
US8895547B2 (en) | 2011-03-08 | 2014-11-25 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
WO2012120054A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120055A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2683702B1 (de) | 2011-03-08 | 2014-12-24 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
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 |
WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2683698B1 (de) | 2011-03-08 | 2017-10-04 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
SG194142A1 (en) | 2011-04-22 | 2013-11-29 | Pfizer | Pyrazolospiroketone derivatives for use as acetyl - coa carboxylase inhibitors |
CA2841757A1 (en) | 2011-07-15 | 2013-01-24 | Etzer Darout | Gpr 119 modulators |
CN103732578B (zh) | 2011-07-22 | 2015-08-12 | 辉瑞大药厂 | 喹啉基胰高血糖素受体调节剂 |
JP6043355B2 (ja) | 2011-08-31 | 2016-12-14 | ファイザー・インク | ヘキサヒドロピラノ[3,4−d][1,3]チアジン−2−アミン化合物 |
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 |
JP2015515472A (ja) | 2012-04-06 | 2015-05-28 | ファイザー・インク | ジアシルグリセロールアシルトランスフェラーゼ2阻害薬 |
US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
CA2872154C (en) | 2012-05-04 | 2016-08-23 | Pfizer Inc. | Heterocyclic substituted hexahydropyrano [3,4-d] [1,3] thiazin-2-amine compounds as inhibitors of app, bace1 and bace2 |
BR112014032913A2 (pt) | 2012-06-29 | 2017-06-27 | Pfizer | novas 4-(amino-substituídas)-7h-pirrolo[2,3-d]pirimidinas como inibidores de lrrk2 |
US9260455B2 (en) | 2012-09-20 | 2016-02-16 | Pfizer Inc. | Alkyl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
JP2016502978A (ja) | 2012-12-11 | 2016-02-01 | ファイザー・インク | BACE1の阻害剤としてのヘキサヒドロピラノ[3,4−d][1,3]チアジン−2−アミン化合物 |
CA2893333C (en) | 2012-12-19 | 2017-10-24 | Pfizer Inc. | Carbocyclic-and heterocyclic-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
CA2897678A1 (en) | 2013-02-13 | 2014-08-21 | Pfizer Inc. | Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
US9233981B1 (en) | 2013-02-15 | 2016-01-12 | Pfizer Inc. | Substituted phenyl hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
EP3055300B1 (en) | 2013-10-09 | 2018-03-07 | Pfizer Inc | Antagonists of prostaglandin ep3 receptor |
CN103664675B (zh) * | 2013-11-27 | 2016-05-18 | 浙江省诸暨合力化学对外贸易有限公司 | 一种2-氯-n-(4-氟苯基)-n-异丙基乙酰胺的制备方法 |
US9695171B2 (en) | 2013-12-17 | 2017-07-04 | Pfizer Inc. | 3,4-disubstituted-1 H-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7H-pyrrolo[2,3-c]pyridazines as LRRK2 inhibitors |
CN106103425A (zh) | 2014-03-17 | 2016-11-09 | 辉瑞公司 | 用于治疗代谢及相关病症的二酰甘油酰基转移酶2抑制剂 |
JP6111002B1 (ja) | 2014-04-10 | 2017-04-05 | ファイザー・インク | 2−アミノ−6−メチル−4,4a,5,6−テトラヒドロピラノ[3,4−d][1,3]チアジン−8a(8H)−イル−1,3−チアゾール−4−イルアミド |
WO2016092413A1 (en) | 2014-12-10 | 2016-06-16 | Pfizer Inc. | Indole and indazole compounds that activate ampk |
JP2017538769A (ja) | 2014-12-22 | 2017-12-28 | ファイザー・インク | プロスタグランジンep3受容体の拮抗薬 |
CN107787322B (zh) | 2015-06-17 | 2023-07-07 | 辉瑞大药厂 | 三环化合物以及它们作为磷酸二酯酶抑制剂的用途 |
EP3350178B1 (en) | 2015-09-14 | 2021-10-20 | Pfizer Inc. | Novel imidazo [4,5-c]quinoline and imidazo [4,5-c][1,5]naphthyridine derivatives as lrrk2 inhibitors |
JP2018531923A (ja) | 2015-09-24 | 2018-11-01 | ファイザー・インク | N−[2−(2−アミノ−6,6−二置換−4,4a,5,6−テトラヒドロピラノ[3,4−d][1,3]チアジン−8a(8H)−イル)−1,3−チアゾール−4−イル]アミド |
WO2017051303A1 (en) | 2015-09-24 | 2017-03-30 | Pfizer Inc. | Tetrahydropyrano[3,4-d][1,3]oxazin derivatives and their use as bace inhibitors |
WO2017051294A1 (en) | 2015-09-24 | 2017-03-30 | Pfizer Inc. | N-[2-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2h-1,2,4-thiadiazin-5-yl)-1,3-thiazol-4-yl] amides useful as bace inhibitors |
RU2696269C1 (ru) | 2015-12-29 | 2019-08-01 | Пфайзер Инк. | Замещенные 3-азабицикло[3.1.0]гексаны в качестве ингибиторов кетогексокиназы |
CN105524069A (zh) * | 2016-02-25 | 2016-04-27 | 江苏理工学院 | 一种新型胆囊收缩毒受体拮抗剂类似物及其合成方法 |
AR109179A1 (es) | 2016-08-19 | 2018-11-07 | Pfizer | Inhibidores de diacilglicerol aciltransferasa 2 |
CN112955147A (zh) | 2018-08-31 | 2021-06-11 | 辉瑞公司 | 用于治疗nash/nafld和相关疾病的组合 |
EP3972596A1 (en) | 2019-05-20 | 2022-03-30 | Pfizer Inc. | Combinations comprising benzodioxol as glp-1r agonists for use in the treatment of nash/nafld and related diseases |
JP2022552655A (ja) | 2019-10-07 | 2022-12-19 | キャリーオペ,インク. | Gpr119アゴニスト |
CN112573494B (zh) * | 2020-12-23 | 2022-06-21 | 西南石油大学 | 一种利用水合物法的氦精制装置 |
WO2023026180A1 (en) | 2021-08-26 | 2023-03-02 | Pfizer Inc. | Amorphous form of (s)-2-(5-((3-ethoxypyridin-2-yl)oxy)pyridin-3-yl)-n-(tetrahydrofuran-3- yl)pyrimidine-5-carboxamide |
WO2023169456A1 (en) | 2022-03-09 | 2023-09-14 | Gasherbrum Bio , Inc. | Heterocyclic glp-1 agonists |
WO2023198140A1 (en) | 2022-04-14 | 2023-10-19 | Gasherbrum Bio, Inc. | Heterocyclic glp-1 agonists |
WO2024118524A1 (en) | 2022-11-28 | 2024-06-06 | Cerevel Therapeutics, Llc | Azaindole compounds and their use as phosphodiesterase inhibitors |
WO2024125602A1 (en) | 2022-12-15 | 2024-06-20 | Gasherbrum Bio, Inc. | Salts and solid forms of a compound having glp-1 agonist activity |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2318673A1 (de) * | 1973-04-13 | 1974-11-07 | Boehringer Sohn Ingelheim | Neue substituierte triazolo-1,5benzodiazepine |
IE41197B1 (en) * | 1973-05-29 | 1979-11-07 | Squibb & Sons Inc | 4h-s-triazolo (4,3-a)(1,5)benzodiazepin-5-ones |
US4080323A (en) * | 1977-03-07 | 1978-03-21 | Hoffmann-La Roche Inc. | Imidazo [1,5-a][1,5] benzodiazepines |
US4118386A (en) | 1977-04-04 | 1978-10-03 | Hoffmann-La Roche Inc. | Synthesis of imidazo[1,5-a]diazepine-3-carboxylates |
CA1146866A (en) | 1979-07-05 | 1983-05-24 | Yamanouchi Pharmaceutical Co. Ltd. | Process for the production of sustained release pharmaceutical composition of solid medical material |
DE3438830A1 (de) | 1984-10-23 | 1986-04-30 | Rentschler Arzneimittel | Nifedipin enthaltende darreichungsform und verfahren zu ihrer herstellung |
AU1537292A (en) | 1991-04-16 | 1992-11-17 | Nippon Shinyaku Co. Ltd. | Method of manufacturing solid dispersion |
US5340591A (en) | 1992-01-24 | 1994-08-23 | Fujisawa Pharmaceutical Co., Ltd. | Method of producing a solid dispersion of the sparingly water-soluble drug, nilvadipine |
JP3265680B2 (ja) | 1992-03-12 | 2002-03-11 | 大正製薬株式会社 | 経口製剤用組成物 |
GB9307833D0 (en) * | 1993-04-15 | 1993-06-02 | Glaxo Inc | Modulators of cholecystokinin and gastrin |
FR2716195B1 (fr) | 1994-02-14 | 1996-06-21 | Sanofi Sa | Dérivés de 3-acylamino-5-phényl-1,4-benzodiazépin-2-one polysubstitués, leur procédé de préparation et les compositions pharmaceutiques les contenant. |
KR970702274A (ko) | 1994-04-14 | 1997-05-13 | 앨런 헤스케쓰 | 콜레시스토키닌 또는 가스트린을 조절하는 5-헤테로시클릭-1, 5-벤조디아제핀(CCK or Gastrin Modulating 5-Heterocyclic-1,5-Benzodiazepines) |
PE27497A1 (es) * | 1994-04-15 | 1997-08-07 | Glaxo Inc | Derivados de 1,5 benzodiazepina |
DE19504832A1 (de) | 1995-02-14 | 1996-08-22 | Basf Ag | Feste Wirkstoff-Zubereitungen |
PT901786E (pt) | 1997-08-11 | 2007-08-07 | Pfizer Prod Inc | Disperções farmacêuticas sólidas com biodisponibilidade melhorada |
WO2000027845A1 (en) | 1998-11-10 | 2000-05-18 | Merck & Co., Inc. | Spiro-indolines as y5 receptor antagonists |
AR022044A1 (es) | 1999-05-06 | 2002-09-04 | Glaxo Group Ltd | Derivados de 1,5-benzodiazepina |
TWI279402B (en) | 1999-08-20 | 2007-04-21 | Banyu Pharma Co Ltd | Spiro compounds having NPY antagonistic activities and agents containing the same |
US6462053B1 (en) | 1999-08-20 | 2002-10-08 | Banyu Pharmaceutical Co., Ltd. | Spiro compounds |
US6566367B2 (en) | 2000-12-12 | 2003-05-20 | Pfizer Inc. | Spiro[isobenzofuran-1,4′-piperidin]-3-ones and 3H-spiroisobenzofuran-1,4′-piperidines |
US6924291B2 (en) | 2001-01-23 | 2005-08-02 | Merck & Co., Inc. | Process for making spiro isobenzofuranone compounds |
US6605720B1 (en) | 2002-01-28 | 2003-08-12 | Merck & Co., Inc. | Process for making spirolactone compounds |
-
2005
- 2005-05-13 GE GEAP20059708A patent/GEP20094723B/en unknown
- 2005-05-13 BR BRPI0510273-1A patent/BRPI0510273A/pt not_active IP Right Cessation
- 2005-05-13 AU AU2005247693A patent/AU2005247693A1/en not_active Abandoned
- 2005-05-13 CA CA002568056A patent/CA2568056A1/en not_active Abandoned
- 2005-05-13 WO PCT/IB2005/001469 patent/WO2005116034A1/en active Application Filing
- 2005-05-13 EP EP05739440A patent/EP1753766A1/en not_active Withdrawn
- 2005-05-13 JP JP2007514174A patent/JP4069159B2/ja not_active Expired - Fee Related
- 2005-05-13 EA EA200601773A patent/EA010888B1/ru not_active IP Right Cessation
- 2005-05-13 UA UAA200612379A patent/UA84208C2/ru unknown
- 2005-05-13 AP AP2006003768A patent/AP2006003768A0/xx unknown
- 2005-05-13 CN CNA2005800147946A patent/CN1950374A/zh active Pending
- 2005-05-19 US US11/134,790 patent/US7265104B2/en not_active Expired - Fee Related
- 2005-05-20 GT GT200500119A patent/GT200500119A/es unknown
- 2005-05-23 UY UY28915A patent/UY28915A1/es not_active Application Discontinuation
- 2005-05-23 PE PE2005000568A patent/PE20060363A1/es not_active Application Discontinuation
- 2005-05-23 AR ARP050102117A patent/AR049187A1/es not_active Application Discontinuation
- 2005-05-24 TW TW094116913A patent/TWI297688B/zh active
- 2005-05-24 PA PA20058634101A patent/PA8634101A1/es unknown
- 2005-05-24 NL NL1029105A patent/NL1029105C2/nl not_active IP Right Cessation
- 2005-05-25 SV SV2005002127A patent/SV2006002127A/es not_active Application Discontinuation
-
2006
- 2006-09-20 IL IL178220A patent/IL178220A0/en unknown
- 2006-09-21 NO NO20064288A patent/NO20064288L/no not_active Application Discontinuation
- 2006-11-16 CR CR8753A patent/CR8753A/es not_active Application Discontinuation
- 2006-11-24 EC EC2006007025A patent/ECSP067025A/es unknown
- 2006-11-24 MA MA29486A patent/MA28605B1/fr unknown
- 2006-11-24 TN TNP2006000386A patent/TNSN06386A1/fr unknown
-
2007
- 2007-07-20 US US11/780,988 patent/US7358242B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
GEP20094723B (en) | 2009-07-10 |
AP2006003768A0 (en) | 2006-10-31 |
AU2005247693A1 (en) | 2005-12-08 |
US7265104B2 (en) | 2007-09-04 |
TWI297688B (en) | 2008-06-11 |
JP4069159B2 (ja) | 2008-04-02 |
GT200500119A (es) | 2006-01-12 |
US7358242B2 (en) | 2008-04-15 |
NL1029105A1 (nl) | 2005-11-30 |
SV2006002127A (es) | 2006-02-15 |
US20070265193A1 (en) | 2007-11-15 |
PE20060363A1 (es) | 2006-05-08 |
MA28605B1 (fr) | 2007-05-02 |
UA84208C2 (en) | 2008-09-25 |
JP2008500326A (ja) | 2008-01-10 |
CR8753A (es) | 2006-12-13 |
PA8634101A1 (es) | 2006-06-02 |
WO2005116034A1 (en) | 2005-12-08 |
TW200609235A (en) | 2006-03-16 |
NL1029105C2 (nl) | 2006-06-13 |
ECSP067025A (es) | 2006-12-29 |
IL178220A0 (en) | 2006-12-31 |
TNSN06386A1 (fr) | 2008-02-22 |
EA200601773A1 (ru) | 2007-06-29 |
CN1950374A (zh) | 2007-04-18 |
BRPI0510273A (pt) | 2007-10-30 |
AR049187A1 (es) | 2006-07-05 |
CA2568056A1 (en) | 2005-12-08 |
US20050267100A1 (en) | 2005-12-01 |
NO20064288L (no) | 2006-10-23 |
EA010888B1 (ru) | 2008-12-30 |
EP1753766A1 (en) | 2007-02-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY28915A1 (es) | Derivados de tetraazabenzo (e)azuleno y sus análogos | |
ECSP088221A (es) | Agonistas adrenoreceptores alfa2c | |
CU23464B7 (es) | (1,8)naftidirin-2-onas y compuestos relacionados para el tratamiento de la esquizofrenia | |
GT200600117A (es) | Nuevos compuestos farmaceuticos | |
CL2008002132A1 (es) | Compuestos derivados de sulfonamidas, moduladores de trpm8; composiciones farmaceuticas que comprenden a dichos compuestos; y uso de dichos compuestos en el tratamiento del dolor neuropatico, dolor inflamatorio, ansiedad, depresion, hiperalgesia inflamatoria, entre otras. | |
UY30748A1 (es) | Compuesto0s novedosos | |
UY30498A1 (es) | Nueva clase de compuestos de benzimidazolilo, sus sales, composiciones farmacéuticas conteniéndolos y aplicaciones | |
ECSP088590A (es) | Derivados de aminoácido multicíclicos y sus métodos de uso | |
ECSP109987A (es) | Métodos y compuestos útiles para preparar inhibidores del co-transportador 2 sodio glucosa | |
UY29886A1 (es) | Derivados de pirazol novedosos, composiciones farmaccuticas que los contienen, procedimientos para la preparacinn de los mismos y aplicaciones | |
DOP2006000061A (es) | Derivados de pirimidina para el tratamiento de trastornos hiperproliferativos | |
DOP2009000133A (es) | Derivados de indol como agonistas de los receptores s1p1 | |
ECSP109844A (es) | Espirociclos como inhibidores de la 11-beta hidroxiesteroide deshidrogenasa de tipo 1 | |
UY29360A1 (es) | Nuevos derivados de pirazol, composiciones farmacéuticas que los contienen, procedimientos de preparación y aplicaciones. | |
ECSP088306A (es) | Agentes para prevenir y tratar los trastornos que involucran la modulación de los receptores ryr | |
NO20061845L (no) | Fenyl-piperazinderivater som modulatorer for muskarine reseptorer | |
UY28215A1 (es) | Quinazolinas utiles como moduladores de canales iónicos | |
ECSP088854A (es) | Moduladores bencimidazolicos de vr1 | |
DOP2011000076A (es) | Derivados de heteroaril amidas y su uso como activadores de glucoquinasa | |
ECSP088099A (es) | Nuevos derivados de la 2-azetidinona para el tratamiento de enfermedades hiperlipidémicas | |
SV2010003598A (es) | Derivados de tiazol usados como inhibidores de pi 3-cinasa | |
ECSP055912A (es) | Compuestos de 2-aminocarbonil-quinolina como antagonistas del receptor de difosfato de adenosina en plaquetas | |
AR057222A1 (es) | Agonistas del receptor del neuropeprtido -2 | |
CR10060A (es) | 3-aminociclopentanocarboxamidas como moduladores de receptores de quimioquinas | |
UY29003A1 (es) | Nuevos derivados de hidantoína, procesos para su preparación, composiciones farmacéuticas que los contienen y su uso en terapia |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20160518 |