PE20091826A1 - Derivados de la 2-trifluorometilnicotinamida como agentes para aumentar el hdl-colesterol - Google Patents
Derivados de la 2-trifluorometilnicotinamida como agentes para aumentar el hdl-colesterolInfo
- Publication number
- PE20091826A1 PE20091826A1 PE2009000468A PE2009000468A PE20091826A1 PE 20091826 A1 PE20091826 A1 PE 20091826A1 PE 2009000468 A PE2009000468 A PE 2009000468A PE 2009000468 A PE2009000468 A PE 2009000468A PE 20091826 A1 PE20091826 A1 PE 20091826A1
- Authority
- PE
- Peru
- Prior art keywords
- hydroxy
- cholesterol
- agents
- nicotinamide
- trifluoro
- Prior art date
Links
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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
- 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
- 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
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 2-TRIFLUOROMETILNICOTINAMIDA DE FORMULA (I), DONDE R1 ES HIDROXIALQUILO INFERIOR, CICLOALQUILO SUSTITUIDO O NO POR HIDROXI, HIDROXIALQUILO INFERIOR, ENTRE OTROS; R2, R4 Y R8 SON CADA UNO H; R3 ES ALCOXIALQUILO INFERIOR, HALOALQUILO INFERIOR, HETEROALQUILO INFERIOR, ENTRE OTROS; R5, R6 Y R7 SON CADA UNO H, ALQUILO INFERIOR, HALOALCOXI INFERIOR, ENTRE OTROS. SON COMPUESTOS SELECCIONADOS: 5-(4-CLORO-FENIL)-N-(2-CICLOPROPIL-2-HIDROXI-PROPIL)-6-(2,2,2-TRIFLUORO-ETOXI)-2-TRIFLUOROMETIL-NICOTINAMIDA; N-(2-CICLOPROPIL-2-HIDROXI-PROPIL)-5-(3,4-DICLOROFENIL)-6-(2,2,2-TRIFLUORO-ETOXI)-2-TRIFLUOROMETIL-NICOTINAMIDA; 5-(3-CLORO-FENIL)-N-(CICLOPROPIL-2-HIDROXI-PROPIL)-6-(2,2,2-TRIFLUORO-ETOXI)-2-TRIFLUOROMETIL-NICOTINAMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON AGENTES PARA AUMENTAR EL HDL-COLESTEROL SIENDO UTILES EN EL TRATAMIENTO DE HIPERCOLESTEROLEMIA, HIPERTRIGLICERIDEMIA, INFARTO DE MIOCARDIO, ENTRE OTROS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08153792 | 2008-03-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091826A1 true PE20091826A1 (es) | 2009-11-25 |
Family
ID=40601113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2009000468A PE20091826A1 (es) | 2008-03-31 | 2009-03-30 | Derivados de la 2-trifluorometilnicotinamida como agentes para aumentar el hdl-colesterol |
Country Status (14)
Country | Link |
---|---|
US (1) | US7897621B2 (es) |
EP (1) | EP2262770B1 (es) |
JP (1) | JP5442711B2 (es) |
KR (1) | KR101249668B1 (es) |
CN (1) | CN101981009B (es) |
AR (1) | AR071096A1 (es) |
AU (1) | AU2009231375A1 (es) |
CA (1) | CA2717537A1 (es) |
ES (1) | ES2391371T3 (es) |
IL (1) | IL208021A0 (es) |
MX (1) | MX2010010000A (es) |
PE (1) | PE20091826A1 (es) |
TW (1) | TW200944504A (es) |
WO (1) | WO2009121740A1 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011035324A1 (en) * | 2009-09-21 | 2011-03-24 | Vanderbilt University | O-benzyl nicotinamide analogs as mglur5 positive allosteric modulators |
WO2012031817A1 (en) * | 2010-09-09 | 2012-03-15 | F. Hoffmann-La Roche Ag | Determination of abca1 protein levels in cells |
US8410107B2 (en) | 2010-10-15 | 2013-04-02 | Hoffmann-La Roche Inc. | N-pyridin-3-yl or N-pyrazin-2-yl carboxamides |
US8669254B2 (en) | 2010-12-15 | 2014-03-11 | Hoffman-La Roche Inc. | Pyridine, pyridazine, pyrimidine or pyrazine carboxamides as HDL-cholesterol raising agents |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE0400208D0 (sv) | 2004-02-02 | 2004-02-02 | Astrazeneca Ab | Chemical compounds |
MX2007012213A (es) | 2005-04-06 | 2007-12-10 | Hoffmann La Roche | Derivados de piridin-3-carboxamida como agonistas inversos de canabinoides. |
US7629346B2 (en) | 2006-06-19 | 2009-12-08 | Hoffmann-La Roche Inc. | Pyrazinecarboxamide derivatives as CB1 antagonists |
US7781593B2 (en) * | 2006-09-14 | 2010-08-24 | Hoffmann-La Roche Inc. | 5-phenyl-nicotinamide derivatives |
KR101107896B1 (ko) * | 2006-10-04 | 2012-01-25 | 에프. 호프만-라 로슈 아게 | 고 밀도 지단백질(hdl)-콜레스테롤 상승제로서 3-피리딘카복스아마이드 및 2-피라진카복스아마이드 유도체 |
DE602007006531D1 (de) * | 2006-10-04 | 2010-06-24 | Hoffmann La Roche | Pyrazin-2-carboxamid-derivate als cb2-rezeptormodulatoren |
-
2009
- 2009-03-16 US US12/404,364 patent/US7897621B2/en not_active Expired - Fee Related
- 2009-03-23 WO PCT/EP2009/053343 patent/WO2009121740A1/en active Application Filing
- 2009-03-23 EP EP09727590A patent/EP2262770B1/en not_active Not-in-force
- 2009-03-23 MX MX2010010000A patent/MX2010010000A/es active IP Right Grant
- 2009-03-23 CN CN2009801105525A patent/CN101981009B/zh not_active Expired - Fee Related
- 2009-03-23 AU AU2009231375A patent/AU2009231375A1/en not_active Abandoned
- 2009-03-23 JP JP2011502334A patent/JP5442711B2/ja not_active Expired - Fee Related
- 2009-03-23 ES ES09727590T patent/ES2391371T3/es active Active
- 2009-03-23 CA CA2717537A patent/CA2717537A1/en not_active Abandoned
- 2009-03-23 KR KR1020107021707A patent/KR101249668B1/ko not_active IP Right Cessation
- 2009-03-27 AR ARP090101099A patent/AR071096A1/es unknown
- 2009-03-30 PE PE2009000468A patent/PE20091826A1/es not_active Application Discontinuation
- 2009-03-30 TW TW098110488A patent/TW200944504A/zh unknown
-
2010
- 2010-09-06 IL IL208021A patent/IL208021A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL208021A0 (en) | 2010-12-30 |
ES2391371T3 (es) | 2012-11-23 |
KR101249668B1 (ko) | 2013-04-01 |
CA2717537A1 (en) | 2009-10-08 |
JP2011516444A (ja) | 2011-05-26 |
US7897621B2 (en) | 2011-03-01 |
TW200944504A (en) | 2009-11-01 |
AR071096A1 (es) | 2010-05-26 |
CN101981009B (zh) | 2013-09-11 |
EP2262770B1 (en) | 2012-08-01 |
KR20100117142A (ko) | 2010-11-02 |
MX2010010000A (es) | 2010-09-30 |
CN101981009A (zh) | 2011-02-23 |
AU2009231375A1 (en) | 2009-10-08 |
WO2009121740A1 (en) | 2009-10-08 |
US20090247588A1 (en) | 2009-10-01 |
JP5442711B2 (ja) | 2014-03-12 |
EP2262770A1 (en) | 2010-12-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20131377A1 (es) | Triazina-oxadiazoles | |
PE20160843A1 (es) | Pirrolidinonas herbicidas | |
PE20120693A1 (es) | Compuestos heterociclos como moduladores de la piruvato cinasa m2 (pkm2) | |
PE20060691A1 (es) | Serinamidas sustituidas por benzoilo | |
PE20091842A1 (es) | Pirrolidinonas como activadores de glucoquinasa | |
PE20141974A1 (es) | Compuestos de heterociclilo | |
PE20080927A1 (es) | Derivados de benzoil-amino-heterociclilo como activadores de la glucoquinasa (glk) | |
PE20070407A1 (es) | Compuestos derivados de pirazina como antagonistas del receptor a2b de adenosina | |
PE20180177A1 (es) | Derivados de 1-(het) arilsulfonil-(pirrolidin o piperidin)-2-carboxamida y su uso como antagonistas de trpa1 | |
PE20120691A1 (es) | Derivados de n1-sulfonil-5-fluoropirimidinona | |
PE20141203A1 (es) | Benzilindazoles sustituidos para uso como inhibidores de la quinasa bub1 en el tratamiento de enfermedades hiperproliferativas | |
PE20110397A1 (es) | Compuestos que modulan selectivamente el receptor cb2 | |
PE20121050A1 (es) | Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog | |
PE20090714A1 (es) | Imidazopiridazinas y pirrolo-pirimidinas sustituidas como inhibidores de cinasa de lipido | |
PE20160751A1 (es) | Moduladores de tetrahidropiridopirazinas de gpr6 | |
PE20191142A1 (es) | 2,4 diamino-quinolina sustituida como nuevos agentes anti-cancerigenos | |
PE20121058A1 (es) | Compuestos que modulan el receptor de androgenos | |
PE20141682A1 (es) | Derivados de (4-fenilimidazol-2-il) etilamina utiles como moduladores de canal de sodio | |
AR096446A1 (es) | Compuestos heterocíclicos como plaguicidas | |
PE20090888A1 (es) | Compuestos heterociclicos como agentes moduladores del receptor acoplado a la proteina g gpr119 | |
PE20150621A1 (es) | Derivados de 2,4-diamino-pirimidina n2, n4-disustituidos como inhibidores de jak3 | |
PE20080890A1 (es) | DERIVADOS DE IMIDAZOLONA E IMIDAZOLIDINONA COMO INHIBIDORES DE LA 11b-HSD1 PARA LA DIABETES | |
PE20081665A1 (es) | Antagonistas del receptor de dopamina 2 de rapida disociacion | |
PE20090890A1 (es) | Compuestos derivados de 1-(2,3-dihidrobenzo[1,4]dioxin-2-ilmetil)azaciclos como antagonistas del suptipo adrenoreceptor alfa2c | |
PE20080150A1 (es) | Derivados de piridinona n-aril y n-heteroaril sustituidos como antagonistas del receptor de la hormona concentradora de melanina (mch) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |