AR070014A1 - Derivados de piridina, su preparacion y uso - Google Patents
Derivados de piridina, su preparacion y usoInfo
- Publication number
- AR070014A1 AR070014A1 ARP080103463A ARP080103463A AR070014A1 AR 070014 A1 AR070014 A1 AR 070014A1 AR P080103463 A ARP080103463 A AR P080103463A AR P080103463 A ARP080103463 A AR P080103463A AR 070014 A1 AR070014 A1 AR 070014A1
- Authority
- AR
- Argentina
- Prior art keywords
- aryl
- alkyl
- heterocyclyl
- alkenyl
- alkoxy
- Prior art date
Links
Classifications
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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
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Virology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Molecular Biology (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
También se revelan procesos para la preparacion de estos derivados, y su uso en la elaboracion de composiciones farmacéuticas para el tratamiento del cáncer y de la inflamacion. Reivindicacion 1: Un compuesto de la formula (1) en donde, A y B se seleccionan independientemente de carbono y nitrogeno; siempre y cuando por lo menos uno de entre A y B sea nitrogeno; R1 se selecciona de hidrogeno, alquilo, alquenilo, alquinilo, acilo, hidroxi, alcoxi, arilo, y ariloxi, o está ausente; R2 se selecciona de hidrogeno, alquilo, alquenilo, alquinilo, acilo, hidroxi, alcoxi, arilo, y ariloxi; R3 se selecciona de hidrogeno, alquilo, alquenilo, alquinilo, acilo, hidroxi, alcoxi, arilo, ariloxi, y -O-R6; o R2 y R3 juntos con el átomo N al cual se encuentran anexos forman un heterociclo de 5 miembros que tiene por lo menos un heteroátomo adicional seleccionado de O, N y S; en donde el heterociclo podrá estar no sustituido o sustituido; o R2 y R3 junto con el átomo N al cual se encuentran anexos forman un heterociclo de 6 o 7 miembros, teniendo opcionalmente uno o más heteroátomos adicionales seleccionados de O, N y S; en donde el heterociclo podrá estar no sustituido o sustituido; R4 y R5 se seleccionan independientemente de hidrogeno, alquilo, haloalquilo, aralquilo, alquenilo, alquinilo, arilo, heterociclilo, cicloalquilo, -O-R6, y -C(O)-T-Q; R6 se selecciona de alquenilo y alquinilo; en donde el alquenilo y el alquinilo podrán estar no sustituidos o sustituidos; T se selecciona de -(CR7R8)n- y -C(R7R8)C(O)-, donde n es un entero de 0 a 5; R7 y R8 se seleccionan independientemente de hidrogeno, alquilo, haloalquilo, cicloalquilo, alquenilo, halogeno, hidroxi, alcoxi, ciano, nitro, arilo, y heterociclilo; y Q se selecciona de hidrogeno, hidroxi, halogeno, ciano, nitro, alquilo, haloalquilo, alcoxi, cicloalquilo, heterociclilo, y arilo; en donde R1, R2, R3, R4, R5, T, R7, R8 y Q son: alquilo y cicloalquilo no sustituido o sustituido con por lo menos un grupo seleccionado de halogeno, hidroxi, carboxi, acetoxi, amino, cicloalquilo, alcoxi, ariloxi, alcoxicarbonilo, aminocarbonilo, aminoarilo, arilo, aralquilo, y heterociclilo; arilo no sustituido o sustituido con por lo menos un grupo seleccionado de halogeno, nitro, alquilo, haloalquilo, alcoxi, amino, heteroarilalquilo, heterociclilo, arilo, y aralquilo; y heterociclilo no sustituido o sustituido con por lo menos un grupo seleccionado de halogeno, hidroxi, alcoxi, oxo, alquilo, haloalquilo, alquenilo, alquinilo, heterociclilo, ariloxi, cicloalquilo, cicloalquilalquilo, acilo, aciloxi, amino, aminoalquilo, hidroxialquilo, heterociclilalquilo, heteroarilalquilo, aralquilo, alquilaminoalquilo, formilo, alquilcarbonilo, arilcarbonilo, arilo, alquilamino, alquilheteroarilamino, alcoxicarbonilo, ariloxicarbonilo, -COOH, -C(O)-O-R6, y -O-R6; con la salvedad de que: cuando R1 se selecciona de hidrogeno, alquilo, alquenilo, alquinilo, acilo, hidroxi, alcoxi, arilo, y ariloxi, entonces por lo menos uno de entre R4 y R5 es -C(O)-T-Q; con la otra salvedad de que: cuando Q se selecciona de cicloalquilo, heterociclilo, y arilo, entonces R2 y R3 junto con el átomo N al cual se encuentran anexos forman un heterociclo de 5 miembros que tiene por lo menos un heteroátomo adicional seleccionado de O, N y S; en donde el heterociclo podrá estar no sustituido o sustituido; o R2 y R3 junto con el átomo N al cual se encuentran anexo forman un heterociclo de 6 o 7 miembros, que tiene opcionalmente uno o más heteroátomos adicionales seleccionados de O, N y S; en donde el heterociclo podrá estar no sustituido o sustituido; y las formas estereoisoméricas y tautoméricas y mezclas de las misma en todos sus índices, sales farmacéuticamente aceptables, solvatos farmacéuticamente aceptables, polimorfos farmacéuticamente aceptables y prodrogas de los mismos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95443707P | 2007-08-07 | 2007-08-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR070014A1 true AR070014A1 (es) | 2010-03-10 |
Family
ID=40083721
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080103463A AR070014A1 (es) | 2007-08-07 | 2008-08-07 | Derivados de piridina, su preparacion y uso |
Country Status (4)
Country | Link |
---|---|
US (1) | US8314103B2 (es) |
AR (1) | AR070014A1 (es) |
TW (1) | TW200908984A (es) |
WO (1) | WO2009019656A1 (es) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
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US7588924B2 (en) | 2006-03-07 | 2009-09-15 | Procter & Gamble Company | Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase |
EP4095127A1 (en) | 2006-06-26 | 2022-11-30 | Akebia Therapeutics Inc. | Prolyl hydroxylase inhibitors and methods of use |
TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
CA2774046C (en) | 2009-11-06 | 2014-01-21 | Aerpio Therapeutics Inc. | Compositions comprising n-benzyl or n-sulfonylaryl-3-hydroxypyridin-2-(1h)-ones and their use for treating colitis |
US9315491B2 (en) | 2009-12-28 | 2016-04-19 | Development Center For Biotechnology | Pyrimidine compounds as mTOR and PI3K inhibitors |
WO2011080568A2 (en) * | 2009-12-28 | 2011-07-07 | Development Center For Biotechnology | Novel pyrimidine compounds as mtor and p13k inhibitors |
WO2011130908A1 (en) * | 2010-04-21 | 2011-10-27 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2012082765A2 (en) * | 2010-12-16 | 2012-06-21 | The United State Of America. As Represented By The Secretary Department Of Health And Human Services | Methods for decreasing body weight and treating diabetes |
CN103270026A (zh) * | 2010-12-21 | 2013-08-28 | 诺瓦提斯公司 | 作为vps34抑制剂的联-杂芳基化合物 |
NO2686520T3 (es) | 2011-06-06 | 2018-03-17 | ||
CN103717214A (zh) | 2011-06-06 | 2014-04-09 | 阿克比治疗有限公司 | 用于稳定低氧诱导因子-2α作为治疗癌症的方法的化合物和组合物 |
WO2013008162A1 (en) | 2011-07-08 | 2013-01-17 | Novartis Ag | Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease |
WO2013066835A2 (en) * | 2011-10-31 | 2013-05-10 | Glaxosmithkline Llc | Compounds and methods |
WO2013080120A1 (en) | 2011-11-28 | 2013-06-06 | Novartis Ag | Novel trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease |
EA029473B1 (ru) | 2011-12-15 | 2018-03-30 | Новартис Аг | Применение ингибиторов pi3k для лечения острой и церебральной малярии |
BR112015031027A2 (pt) | 2013-06-13 | 2017-08-29 | Akebia Therapeutics Inc | Uso de um composto, método in vitro, composição farmacêutica e forma de dosagem única |
AR097631A1 (es) * | 2013-09-16 | 2016-04-06 | Bayer Pharma AG | Trifluorometilpirimidinonas sustituidas con heterociclos y sus usos |
MX2021001169A (es) | 2013-11-15 | 2023-02-10 | Akebia Therapeutics Inc | Formas sólidas de ácido {[5-(3-clorofenil)-3-hidroxipiridin-2-carb onil]amino}acético, composiciones, y usos de las mismas. |
EP3730590A1 (de) * | 2014-03-10 | 2020-10-28 | Merck Patent GmbH | Flüssigkristalline medien mit homöotroper ausrichtung |
JP2017114765A (ja) * | 2014-04-25 | 2017-06-29 | 大正製薬株式会社 | トリアゾリルで置換されたヘテロアリール化合物 |
WO2016113205A1 (de) | 2015-01-13 | 2016-07-21 | Bayer Pharma Aktiengesellschaft | Substituierte pentafluorethylpyrimidinone und ihre verwendung |
JP6693425B2 (ja) * | 2015-01-14 | 2020-05-13 | Jnc株式会社 | 重合性基を有する化合物、液晶組成物および液晶表示素子 |
BR112017015852A2 (pt) | 2015-01-23 | 2018-03-27 | Akebia Therapeutics Inc | forma de cristal, sal hemicálcico, sal hemicálcico di-hidratado, sal monossódico hidratado, sal bissódico monoidratado, sal monossódico anidro e método para preparar o composto 1 |
IL292262B2 (en) | 2015-04-01 | 2024-02-01 | Akebia Therapeutics Inc | Formulation of an oral administration form of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid |
CN107849457B (zh) * | 2015-07-23 | 2021-11-30 | 捷恩智株式会社 | 液晶组合物及液晶显示元件 |
US10492494B2 (en) | 2015-11-13 | 2019-12-03 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
US20180354920A1 (en) | 2015-11-13 | 2018-12-13 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
AR106679A1 (es) | 2015-11-13 | 2018-02-07 | Basf Se | Oxadiazoles sustituidos para combatir hongos fitopatógenos |
JP2018537457A (ja) | 2015-11-19 | 2018-12-20 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 植物病原菌を駆除するための置換オキサジアゾール |
US10986839B2 (en) | 2016-04-11 | 2021-04-27 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
CN116903526A (zh) * | 2017-08-23 | 2023-10-20 | 思普瑞特生物科学公司 | 吡啶基吡啶酮化合物 |
US11434249B1 (en) | 2018-01-02 | 2022-09-06 | Seal Rock Therapeutics, Inc. | ASK1 inhibitor compounds and uses thereof |
MX2020011845A (es) | 2018-05-09 | 2021-01-15 | Akebia Therapeutics Inc | Proceso para preparar acido 2-[[5-(3-clorofenil)-3-hidroxipiridina -2-carbonil]amino]acetico. |
CN109678852B (zh) * | 2018-12-20 | 2022-04-19 | 南京中医药大学 | 6-氧代六氢嘧啶衍生物、其制备方法及制药应用 |
US11524939B2 (en) | 2019-11-13 | 2022-12-13 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid |
UY39854A (es) | 2021-07-15 | 2022-11-30 | Kumiai Chemical Industry Co | Derivado de formamida y agente de control hortícola y agrícola para el control de enfermedades de la |
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MX9300433A (es) | 1992-01-28 | 1994-07-29 | Kirin Brewery | Compuestos de piridincarboximidamina y composiciones farmaceuticas que los contienen. |
HUP0400179A3 (en) * | 2001-06-12 | 2004-10-28 | Neurogen Corp Branford | 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines, their use and pharmaceutical compositions containing them |
EP1270551A1 (en) | 2001-06-26 | 2003-01-02 | Aventis Pharma Deutschland GmbH | Urea derivatives with antiproteolytic activity |
WO2004048365A1 (en) | 2002-11-21 | 2004-06-10 | Chiron Corporation | 2,4,6-trisubstituted pyrimidines as phosphotidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer |
US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
US20050119243A1 (en) | 2003-11-07 | 2005-06-02 | Harris Wayne B. | HIF-1 inhibitors and methods of use thereof |
UY29300A1 (es) | 2004-12-22 | 2006-07-31 | Astrazeneca Ab | Compuestos quimicos |
WO2006094292A2 (en) | 2005-03-02 | 2006-09-08 | Fibrogen, Inc. | Thienopyridine compounds, and methods of use thereof |
GB0520657D0 (en) | 2005-10-11 | 2005-11-16 | Ludwig Inst Cancer Res | Pharmaceutical compounds |
AU2008213808B2 (en) * | 2007-02-06 | 2011-11-10 | Novartis Ag | PI 3-kinase inhibitors and methods of their use |
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2008
- 2008-08-05 TW TW097129745A patent/TW200908984A/zh unknown
- 2008-08-06 WO PCT/IB2008/053151 patent/WO2009019656A1/en active Application Filing
- 2008-08-06 US US12/672,485 patent/US8314103B2/en not_active Expired - Fee Related
- 2008-08-07 AR ARP080103463A patent/AR070014A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
TW200908984A (en) | 2009-03-01 |
WO2009019656A1 (en) | 2009-02-12 |
US8314103B2 (en) | 2012-11-20 |
US20110077252A1 (en) | 2011-03-31 |
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