PE20060357A1 - Compuestos y composiciones como moduladores de receptor activado de proliferador de peroxisoma (ppar) - Google Patents
Compuestos y composiciones como moduladores de receptor activado de proliferador de peroxisoma (ppar)Info
- Publication number
- PE20060357A1 PE20060357A1 PE2005000536A PE2005000536A PE20060357A1 PE 20060357 A1 PE20060357 A1 PE 20060357A1 PE 2005000536 A PE2005000536 A PE 2005000536A PE 2005000536 A PE2005000536 A PE 2005000536A PE 20060357 A1 PE20060357 A1 PE 20060357A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- compounds
- ppar
- modulators
- isoxazol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
- C07D261/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- 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
Abstract
REFERIDA A UN COMPUESTO DERIVADO DE ISOXAZOL DE FORMULA I, DONDE R1 ES ALQUILO C1-C6, CICLOALQUILO C3-C12, ARILO C6-C10, ENTRE OTROS; X ES UN ENLACE O ALQUILENO C1-C4; R2 ES -XOXOR5, -XOR5, -C(O)OR5, ENTRE OTROS; R3 ES CICLOALQUILO C3-C8, ARILO C6-C10, ENTRE OTROS; R5 ES H, ALQUILO C1-C6. SON COMPUESTOS PREFERIDOS: ACIDO (5-{4-[2-(2,4-DICLORO-FENOXI)-ETIL-CARBAMOIL]-5-FENIL-ISOXAZOL-3-IL}-FENIL)-ACETICO, ACIDO (3-CLORO-4-{4-[2-(2,4-DICLORO-FENOXI)-ETILCARBAMOIL]-5-FENIL-ISOXAZOL-3-IL}FENIL)-ACETICO, ACIDO (3-CLORO-4-{4-[2-(2,4-DICLORO-FENOXI)-ETILCARBAMOIL]-5-p-TOLIL-ISOXAZOL-3-IL}-FENIL)-ACETICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A COMPOSICIONES FARMACEUTICAS. DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR ACTIVADO DE PROLIFERADOR DE PEROXISOMA (PPAR), PARTICULARMENTE LA ACTIVIDAD DE PPARd Y SON UTILES PARA EL TRATAMIENTO DE DISLIPIDEMIA, ATEROSCLEROSIS, FALLA CARDIACA, ENFERMEDADES VASCULARES, ENTRE OTRAS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US57100304P | 2004-05-14 | 2004-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20060357A1 true PE20060357A1 (es) | 2006-05-09 |
Family
ID=35428368
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2005000536A PE20060357A1 (es) | 2004-05-14 | 2005-05-13 | Compuestos y composiciones como moduladores de receptor activado de proliferador de peroxisoma (ppar) |
Country Status (14)
Country | Link |
---|---|
US (1) | US7820705B2 (es) |
EP (1) | EP1745027A4 (es) |
JP (1) | JP2007537286A (es) |
KR (1) | KR20070034993A (es) |
CN (1) | CN1984894A (es) |
AR (1) | AR048789A1 (es) |
AU (2) | AU2005245411B2 (es) |
BR (1) | BRPI0511099A (es) |
CA (1) | CA2564429A1 (es) |
MX (1) | MXPA06013196A (es) |
PE (1) | PE20060357A1 (es) |
RU (1) | RU2408589C2 (es) |
TW (1) | TW200602330A (es) |
WO (1) | WO2005113519A1 (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1707202A1 (de) * | 2005-03-31 | 2006-10-04 | Speedel Experimenta AG | Organische Verbindungen |
WO2007011524A1 (en) * | 2005-07-14 | 2007-01-25 | Franco Folli | Daily dosage regimen for treating diabetes, obsity, metabolic syndrome and polycystic ovary syndrome |
WO2007050485A2 (en) * | 2005-10-25 | 2007-05-03 | Merck & Co., Inc. | Combination of a dipeptidyl peptidase-4 inhibitor and an anti-hypertensive agent for the treatment of diabetes and hypertension |
DE102006014165A1 (de) * | 2006-03-24 | 2007-09-27 | Schebo Biotech Ag | Neue Isooxazol-Derivate und deren Verwendungen |
AR060901A1 (es) * | 2006-05-12 | 2008-07-23 | Jerini Ag | Compuestos heterociclicos para la inhibicion de integrinas y uso de estos |
WO2008035359A2 (en) * | 2006-06-12 | 2008-03-27 | Cadila Healthcare Limited | Oximinophenoxyalkanoic acid and phenylalkanoic acid derivatives |
US20080020014A1 (en) * | 2006-07-19 | 2008-01-24 | Paul Consigny | Implantable devices containing nuclear receptor ligands for the treatment of vascular and related disorders |
US7943619B2 (en) * | 2007-12-04 | 2011-05-17 | Hoffmann-La Roche Inc. | Isoxazolo-pyridazine derivatives |
AU2008333326B2 (en) | 2007-12-04 | 2013-05-30 | F. Hoffmann-La Roche Ag | Isoxazolo-pyridine derivatives |
AU2008333320B2 (en) * | 2007-12-04 | 2012-12-20 | F. Hoffmann-La Roche Ag | Isoxazolo-pyrazine derivatives |
ES2714453T3 (es) * | 2008-06-09 | 2019-05-28 | Univ Muenchen Ludwig Maximilians | Fármacos para inhibir la agregación de proteínas implicadas en enfermedades relacionadas con enfermedades neurodegenerativas y/o agregación de proteínas |
EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
US8785435B2 (en) | 2011-10-20 | 2014-07-22 | Hoffmann-La Roche Inc. | Solid forms |
US8604062B2 (en) | 2011-10-20 | 2013-12-10 | Hoffman-La Roche Inc. | Process for the preparation of isoxazolyl-methoxy nicotinic acids |
US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
CN105030771B (zh) * | 2015-04-10 | 2017-11-17 | 广州市爱菩新医药科技有限公司 | 连吡啶异恶唑类化合物作为法尼醇x受体激动剂的应用 |
CN105622536B (zh) * | 2015-12-30 | 2018-06-29 | 商丘师范学院 | 一种三氟甲基化烯基异噁唑化合物及其制备方法和应用 |
CN105622537A (zh) * | 2016-03-01 | 2016-06-01 | 青岛大学 | 一种3,4,5-三取代异恶唑类化合物的合成方法 |
JP6678779B2 (ja) | 2016-06-13 | 2020-04-08 | ギリアード サイエンシーズ, インコーポレイテッド | Fxr(nr1h4)調節化合物 |
CA2968836A1 (en) | 2016-06-13 | 2017-12-13 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
AU2018243719B2 (en) | 2017-03-28 | 2021-01-21 | Gilead Sciences, Inc. | Therapeutic combinations for treating liver diseases |
AU2020209564B2 (en) | 2019-01-15 | 2022-12-01 | Gilead Sciences, Inc. | FXR (NR1H4) modulating compounds |
CA3233305A1 (en) | 2019-02-19 | 2020-08-27 | Gilead Sciences, Inc. | Solid forms of fxr agonists |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2088996A (en) * | 1935-11-22 | 1937-08-03 | Hoffmann La Roche | Double compounds of secondary amides of 3.5-dimethyl-isoxazole-4-carboxylic acid and process for the manufacture of same |
DE1670249B2 (de) * | 1966-07-25 | 1974-07-18 | Bristol-Myers Co., East Syracuse, N.Y. (V.St.A.) | Verfahren zur Herstellung von 4-Isothiazolcarbonsäuren |
GB1203040A (en) | 1967-02-15 | 1970-08-26 | Geigy Ag J R | 5-nitro-2-furyl-isoxazoles and compositions thereof |
US3466296A (en) | 1967-05-16 | 1969-09-09 | American Home Prod | Process for the preparation of alkyl 3,5-disubstituted-isoxazole-4-carboxylates |
DE3247454A1 (de) | 1982-12-22 | 1984-06-28 | Laboratorios Bago S.A., Buenos Aires | Substituierte 3-phenyl-5-methyl-isoxazol-4-carboxy-anilide, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
IT1228288B (it) | 1989-01-09 | 1991-06-07 | Zambon Spa | Composti ad attivita' antiserotoninica |
DE4219247A1 (de) * | 1992-06-12 | 1993-12-16 | Bayer Ag | Verwendung von 3-arylsubstituierten 5-Alkyl-isoxazol-4-carbonsäurederivaten zur Bekämpfung von Endoparasiten, neue 3-arylsubstituierte 5-Alkyl-isoxazol-4-carbonsäurederivate und Verfahren zu ihrer Herstellung |
CA2247439A1 (en) | 1996-02-27 | 1997-09-04 | Sankyo Company, Limited | Isoxazole derivatives |
US6369070B1 (en) * | 1998-04-08 | 2002-04-09 | Eli Lilly And Company | Methods for inhibiting mrp1 |
ES2255294T3 (es) * | 1998-08-07 | 2006-06-16 | Chiron Corporation | Derivados de isoxazol sustituidos como moduladores del receptor de estrogenos. |
WO2001016116A1 (en) * | 1999-09-01 | 2001-03-08 | Chemrx Advanced Technologies, Inc. | Process for synthesizing isoxazolines and isoxazoles |
WO2001096346A1 (en) * | 2000-06-14 | 2001-12-20 | Eli Lilly And Company | Tricyclic compounds as mrp1-inhibitors |
GB0119911D0 (en) * | 2001-08-15 | 2001-10-10 | Novartis Ag | Organic Compounds |
US6875780B2 (en) | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
WO2004024939A2 (en) | 2002-09-13 | 2004-03-25 | Georgetown University | Ligands for the peroxisome proliferator-activated receptor, and methods of use thereof |
ATE399165T1 (de) * | 2003-09-12 | 2008-07-15 | Rigel Pharmaceuticals Inc | Chinolinverbindungen und deren verwendungen |
-
2005
- 2005-05-12 AU AU2005245411A patent/AU2005245411B2/en not_active Ceased
- 2005-05-12 WO PCT/US2005/016672 patent/WO2005113519A1/en active Application Filing
- 2005-05-12 JP JP2007513366A patent/JP2007537286A/ja active Pending
- 2005-05-12 CA CA002564429A patent/CA2564429A1/en not_active Abandoned
- 2005-05-12 MX MXPA06013196A patent/MXPA06013196A/es not_active Application Discontinuation
- 2005-05-12 EP EP05769154A patent/EP1745027A4/en not_active Withdrawn
- 2005-05-12 RU RU2006144124/04A patent/RU2408589C2/ru not_active IP Right Cessation
- 2005-05-12 US US11/596,596 patent/US7820705B2/en not_active Expired - Fee Related
- 2005-05-12 BR BRPI0511099-8A patent/BRPI0511099A/pt not_active IP Right Cessation
- 2005-05-12 KR KR1020067023769A patent/KR20070034993A/ko not_active Application Discontinuation
- 2005-05-12 CN CNA2005800196529A patent/CN1984894A/zh active Pending
- 2005-05-13 PE PE2005000536A patent/PE20060357A1/es not_active Application Discontinuation
- 2005-05-13 AR ARP050101972A patent/AR048789A1/es unknown
- 2005-05-13 TW TW094115655A patent/TW200602330A/zh unknown
-
2009
- 2009-07-09 AU AU2009202781A patent/AU2009202781A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1745027A1 (en) | 2007-01-24 |
AU2005245411A1 (en) | 2005-12-01 |
US20080114044A1 (en) | 2008-05-15 |
WO2005113519A1 (en) | 2005-12-01 |
EP1745027A4 (en) | 2009-06-03 |
AU2005245411B2 (en) | 2009-04-23 |
CA2564429A1 (en) | 2005-12-01 |
AU2009202781A1 (en) | 2009-07-30 |
US7820705B2 (en) | 2010-10-26 |
JP2007537286A (ja) | 2007-12-20 |
MXPA06013196A (es) | 2007-02-14 |
RU2006144124A (ru) | 2008-06-20 |
BRPI0511099A (pt) | 2007-12-26 |
RU2408589C2 (ru) | 2011-01-10 |
TW200602330A (en) | 2006-01-16 |
KR20070034993A (ko) | 2007-03-29 |
CN1984894A (zh) | 2007-06-20 |
AR048789A1 (es) | 2006-05-24 |
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Legal Events
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FC | Refusal |