AR064026A1 - Derivados de azacicloalcanos como inhibidores de estearoil-coenzima a delta-9 desaturasa - Google Patents
Derivados de azacicloalcanos como inhibidores de estearoil-coenzima a delta-9 desaturasaInfo
- Publication number
- AR064026A1 AR064026A1 ARP070105302A ARP070105302A AR064026A1 AR 064026 A1 AR064026 A1 AR 064026A1 AR P070105302 A ARP070105302 A AR P070105302A AR P070105302 A ARP070105302 A AR P070105302A AR 064026 A1 AR064026 A1 AR 064026A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- group
- heteroaryl
- independently
- Prior art date
Links
Classifications
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- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
-
- 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
-
- 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
- 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
-
- 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
- C07D417/14—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 three or more hetero rings
Abstract
Son de utilidad para la prevencion y tratamiento de afecciones relacionadas con la síntesis y metabolismo anormales de lípidos, incluidas enfermedades cardiovasculares, tales como aterosclerosis; obesidad; diabetes; enfermedad neurologica; síndrome metabolico; resistencia a insulina; y esteatosis hepática. Reivindicacion 1: Un compuesto de la formula estructural 1: o una sal farmacéuticamente aceptable de la misma; en la que: q es 0 o 1; r es 0 o 1; Z es O, S, o NR4; X-Y es N-C(O), N-CRaRb, CR14-O, CR14-S(O)0-2, o CR13-CRaRb; Ra y Rb son cada uno independientemente hidrogeno o alquilo C1-3, en los que el alquilo está opcionalmente sustituido con de uno a tres sustituyentes que se seleccionan independientemente a partir de fluor e hidroxi; W es heteroarilo que se selecciona del grupo constituido por el grupo de formulas (2); R1 es heteroarilo que se selecciona del grupo constituido por el grupo de formulas (3) en el que RC es -(CH2)mCO2H, -(CH2)mCO2alquilo C1-3, -(CH2)m-Z- (CH2)pCO2H, o -(CH2)m-Z-(CH2)pCO2alquilo C1-3; en el que cualquier átomo de carbono de los grupos metileno (CH2) de (CH2)m o (CH2)p está opcionalmente sustituido con un hidroxi, un amino o uno u dos átomos de fluor; y en el que dicho anillo heteroarilo R1 está opcionalmente sustituido con un sustituyente que se selecciona independientemente a partir del grupo constituido por ciano, halogeno, alquilo C1-4, alcoxi C1-4, alquiltio C1-4, alquilsulfonilo C1-4, y trifluorometilo; cada R2 se selecciona independientemente a partir del grupo constituido por: hidrogeno, halogeno, hidroxi, ciano, amino, nitro, alquilo C1-4, opcionalmente sustituido con de uno a cinco átomos de fluor, alcoxi C1-4, opcionalmente sustituido con de uno a cinco átomos de fluor, alquiltio C1-4, opcionalmente sustituido con de uno a cinco átomos de fluor, alquil C1-4 sulfonilo, carboxi, alquiloxi C1-4 carbonilo, y alquil C1-4 carbonilo; Ar es fenilo, naftilo, o heteroarilo opcionalmente sustituido con de uno a cinco sustituyentes R3; cada R3 se selecciona Independientemente a partir del grupo constituido por: alquilo C1-6, alquenilo C2-6, (CH2)n-fenilo, (CH2)n-naftilo, (CH2)n-heteroarilo, (CH2)n-heterociclilo, (CH2)n-cicloalquilo 3-7, halogeno, nitro, (CH2)nOR4, (CH2)nN(R4)2, (CH2)nC:::N, (CH2)nCO2R4, (CH2)NR4SO2R4, (CH2)nSO2N(R4)2, (CH2)nS(O)0-2R4, (CH2)nNR4C(O)N(R4)2, (CH2)nC(O)N(R4)2, (CH2)nNR4C(O)R4, (CH2)nNR4CO2R4, (CH2)nC(O)R4, O(CH2)nC(O)N(R4)2, (CH2)s-Z-(CH2)t-fenilo, (CH2)s-Z-(CH2)t- naftilo, (CH2)s-Z-(CH2)t-heteroarilo, (CH2)s-Z-(CH2)t-heterociclilo, (CH2)s-Z-(CH2)t-cicIoalquilo C3-7, (CH2)s-Z-(CH2)t-OR4, (CH2)s-Z-(CH2)t-N(R4)2, (CH2)s-Z-(CH2)t-NR4SO2R4, (CH2)s-Z-(CH2)t-C:::N, (CH2)s-Z-(CH2)t-CO2R4, (CH2)s-Z-(CH2)t-SO2N(R4)2, (CH2)s-Z-(CH2)t-S(O)0-2R4, (CH2)s-Z-(CH2)t-NR4C(O)N(R4)2, (CH2)s-Z-(CH2)t-C(O)N(R4)2, (CH2)s-Z-(CH2)t-NR4C(O)R4, (CH2)s-Z-(CH2)t-NR4CO2R4, (CH2)s-Z-(CH2)t-C(O)R4, CF3, CH2CF3, OCF3, y OCH2CF3; en el que fenilo, naftilo, heteroarilo, cicloalquilo, y heterociclilo están opcionalmente sustituidos con de uno a tres sustituyentes que se seleccionan independientemente a partir de halogeno, hidroxi, alquilo C1-4, trifluorometilo, y alcoxi C1-4, opcionalmente sustituido con de uno a cinco átomos de fluor y en el que cualquier átomo de carbono de un metileno (CH2) de R3 está opcionalmente sustituido con de uno a dos grupos que se seleccionan independientemente a partir de fluor, hidroxi, y alquilo C1-4; o dos sustituyentes cuando están en ci mismo grupo metileno (CH2) se toman conjuntamente con el átomo de carbono al que están unidos formando un grupo ciclopropilo; cada R4 se selecciona independientemente a partir del grupo constituido por hidrogeno, alquilo C1-6, (CH2)n-fenilo, (CH2)n- heteroarilo, (CH2)n-naftilo, y (CH2)ncicloalquilo C3-7, en el que alquilo, fenilo, heteroarilo, y cicloalquilo están opcionalmente sustituidos con de uno a tres grupos que se seleccionan independientemente a partir de halogeno, alquilo C1-4 y alcoxi C1-4, o dos grupos R4 junto con el átomo al que están unidos forman un sistema anular cíclico monociclico o bicíclico de 4 a 8 miembros que opcionalmente contiene un heteroátomo adicional que se selecciona a partir de O, S, NH, y Nalquilo C1-4; R5, R6, R7, R8, R9, R10, R11, y R12 son cada uno independientemente hidrogeno, fluor, o alquilo C1-3, en los que el alquilo está opcionalmente sustituido con de uno a tres sustituyentes que se seleccionan independientemente a partir de fluor e hidroxi; R13 es hidrogeno, alquilo C1-3, fluor, o hidroxi; cada R14 es hidrogeno o alquilo C1-3; cada m es independientemente un numero entero de 0 a 4; cada p es independientemente un numero entero de 1 a 3; cada n es independientemente un numero entero de 0 a 2; cada s es independientemente un numero entero de 1 a 3; y cada t es independientemente un numero entero de 1 a 3.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87221606P | 2006-12-01 | 2006-12-01 | |
US89890007P | 2007-02-01 | 2007-02-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR064026A1 true AR064026A1 (es) | 2009-03-04 |
Family
ID=39467388
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070105302A AR064026A1 (es) | 2006-12-01 | 2007-11-29 | Derivados de azacicloalcanos como inhibidores de estearoil-coenzima a delta-9 desaturasa |
Country Status (24)
Country | Link |
---|---|
US (1) | US8063224B2 (es) |
EP (1) | EP2099793B1 (es) |
JP (1) | JP5050061B2 (es) |
KR (1) | KR20090086623A (es) |
AR (1) | AR064026A1 (es) |
AT (1) | ATE543816T1 (es) |
AU (1) | AU2007327276B2 (es) |
BR (1) | BRPI0719702A2 (es) |
CA (1) | CA2670703C (es) |
CL (1) | CL2007003440A1 (es) |
CO (1) | CO6190521A2 (es) |
CR (1) | CR10858A (es) |
EA (1) | EA200970524A1 (es) |
EC (1) | ECSP099375A (es) |
GT (1) | GT200900144A (es) |
IL (1) | IL198824A0 (es) |
MA (1) | MA31017B1 (es) |
MX (1) | MX2009005713A (es) |
NO (1) | NO20092469L (es) |
PE (1) | PE20081199A1 (es) |
SV (1) | SV2009003275A (es) |
TN (1) | TN2009000212A1 (es) |
TW (1) | TW200826936A (es) |
WO (1) | WO2008064474A1 (es) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2001062954A2 (en) * | 2000-02-24 | 2001-08-30 | Xenon Genetics, Inc. | Stearoyl-coa desaturase to identify triglyceride reducing therapeutic agents |
WO2007134457A1 (en) * | 2006-05-22 | 2007-11-29 | Merck Frosst Canada Ltd. | Cyclic amine derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AU2007260527A1 (en) * | 2006-06-12 | 2007-12-21 | Merck Frosst Canada Ltd. | Azetidine derivatives as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
EP2032570A4 (en) | 2006-06-13 | 2010-10-27 | Merck Frosst Canada Ltd | AZACYCLOPENTATE DERIVATIVES AS INHIBITORS OF STEAROYL-COENZYME-A-DELTA-9-DESATURASE |
WO2008017161A1 (en) * | 2006-08-09 | 2008-02-14 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AR064965A1 (es) | 2007-01-26 | 2009-05-06 | Merck Frosst Canada Inc | Derivados de azacicloalcanos como inhibidores de estearoil - coenzima a delta -9 desaturasa |
WO2008128335A1 (en) * | 2007-04-20 | 2008-10-30 | Merck Frosst Canada Ltd. | Novel heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AU2008253512A1 (en) * | 2007-05-23 | 2008-11-27 | Merck Frosst Canada Ltd. | Bicyclic heteroaromatic compounds as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
WO2008157844A1 (en) | 2007-06-21 | 2008-12-24 | Forest Laboratories Holdings Limited | Novel piperazine derivatives as inhibitors of stearoyl-coa desaturase |
UA98799C2 (ru) * | 2007-07-19 | 2012-06-25 | Такеда Фармасьютикал Компани Лимитед | Твердый препарат, включающий алоглиптин и гидрохлорид метформина |
WO2009012573A1 (en) * | 2007-07-20 | 2009-01-29 | Merck Frosst Canada Ltd. | Bicyclic heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AU2009290089A1 (en) * | 2008-09-08 | 2010-03-11 | Merck Frosst Canada Ltd. | Heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
US9168248B2 (en) | 2009-02-17 | 2015-10-27 | Merck Canada Inc. | Spiro compounds useful as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
JP2012518603A (ja) * | 2009-02-23 | 2012-08-16 | メルク カナダ インコーポレイテッド | ステアロイル−コエンザイムaデルタ−9デサチュラーゼの阻害剤としての複素環誘導体 |
WO2010108268A1 (en) * | 2009-03-23 | 2010-09-30 | Merck Frosst Canada Ltd. | Heterocyclic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
WO2011011872A1 (en) | 2009-07-28 | 2011-02-03 | Merck Frosst Canada Ltd. | Novel spiro compounds useful as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
KR20130100903A (ko) | 2010-04-28 | 2013-09-12 | 바이엘 크롭사이언스 아게 | 살진균제로서의 케토헤테로아릴피페리딘 및 케토헤테로아릴피페라진 유도체 |
CA2825684C (en) * | 2011-01-28 | 2021-11-23 | 4Sc Discovery Gmbh | Il17 and ifn-gamma inhibition for the treatment of autoimmune inflammation |
CA2850836A1 (en) | 2011-10-15 | 2013-04-18 | Genentech, Inc. | Methods of using scd1 antagonists |
WO2013062882A1 (en) * | 2011-10-26 | 2013-05-02 | Merck Canada Inc. | Scd inhibitors for the treatment of hcv |
WO2013134546A1 (en) | 2012-03-07 | 2013-09-12 | Mayo Foundation For Medical Education And Research | Methods and materials for treating cancer |
CN104768549A (zh) | 2012-05-22 | 2015-07-08 | 耶路撒冷希伯来大学的益生研究开发有限公司 | 未分化细胞的选择性抑制剂 |
WO2018081167A1 (en) * | 2016-10-24 | 2018-05-03 | Yumanity Therapeutics | Compounds and uses thereof |
US10973810B2 (en) * | 2017-01-06 | 2021-04-13 | Yumanity Therapeutics, Inc. | Methods for the treatment of neurological disorders |
WO2019084157A1 (en) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | COMPOUNDS AND USES THEREOF |
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DE1595923A1 (de) * | 1965-02-20 | 1969-11-27 | Merck Ag E | 1-Aralkyl-4-(thiazolyl-2)-piperazine und Verfahren zu ihrer Herstellung |
DK0876366T3 (da) | 1996-01-15 | 2001-11-05 | Janssen Pharmaceutica Nv | Angiogenese-inhiberende pyridazinaminer |
US20050119251A1 (en) * | 2001-12-21 | 2005-06-02 | Jian-Min Fu | Nicotinamide derivatives and their use as therapeutic agents |
ATE555789T1 (de) | 2003-07-30 | 2012-05-15 | Xenon Pharmaceuticals Inc | Pyridazinderivate und deren verwendung als therapeutische mittel |
US7754711B2 (en) | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
US7345043B2 (en) * | 2004-04-01 | 2008-03-18 | Miikana Therapeutics | Inhibitors of histone deacetylase |
TW200624427A (en) | 2004-09-20 | 2006-07-16 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
MX2007003329A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y biciclicos y su uso como inhibidores de estearoil-coa-desaturasa (scd). |
WO2006034279A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
EP2316458A1 (en) | 2004-09-20 | 2011-05-04 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
US7951805B2 (en) | 2004-09-20 | 2011-05-31 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase |
US7767677B2 (en) * | 2004-09-20 | 2010-08-03 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
AR051026A1 (es) * | 2004-09-20 | 2006-12-13 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa |
JP4958785B2 (ja) | 2004-09-20 | 2012-06-20 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | 複素環誘導体およびステアロイル−CoAデサチュラーゼインヒビターとしてのそれらの使用 |
GT200600046A (es) | 2005-02-09 | 2006-09-25 | Terapia de combinacion | |
WO2006125181A2 (en) | 2005-05-19 | 2006-11-23 | Xenon Pharmaceuticals Inc. | Piperidine derivatives and their use as stearoyl-coa desaturase modulators |
US20090099200A1 (en) * | 2005-06-09 | 2009-04-16 | Chun Sing Li | Azacyclohexane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
JP2009501733A (ja) | 2005-07-20 | 2009-01-22 | メルク フロスト カナダ リミテツド | ステアロイルコエンザイムaデルタ−9デサチュラーゼの阻害剤としてのヘテロ芳香族化合物 |
EP1934205A4 (en) | 2005-10-05 | 2010-06-02 | Merck Frosst Canada Ltd | SUBSTITUTED QUINOLINES AS INHIBITORS OF LEUCOTRIENE BIOSYNTHESIS |
JP2009515839A (ja) | 2005-11-15 | 2009-04-16 | メルク フロスト カナダ リミテツド | ステアロイル−CoAデルタ−9デサチュラーゼ阻害剤としてのアザシクロヘキサン誘導体 |
US7799787B2 (en) | 2005-12-20 | 2010-09-21 | Merck Frosst Canada Ltd. | Heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
WO2007134457A1 (en) | 2006-05-22 | 2007-11-29 | Merck Frosst Canada Ltd. | Cyclic amine derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AU2007260527A1 (en) | 2006-06-12 | 2007-12-21 | Merck Frosst Canada Ltd. | Azetidine derivatives as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
EP2032570A4 (en) | 2006-06-13 | 2010-10-27 | Merck Frosst Canada Ltd | AZACYCLOPENTATE DERIVATIVES AS INHIBITORS OF STEAROYL-COENZYME-A-DELTA-9-DESATURASE |
WO2008017161A1 (en) | 2006-08-09 | 2008-02-14 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
AU2007312866A1 (en) | 2006-10-20 | 2008-04-24 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
AR064965A1 (es) * | 2007-01-26 | 2009-05-06 | Merck Frosst Canada Inc | Derivados de azacicloalcanos como inhibidores de estearoil - coenzima a delta -9 desaturasa |
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2007
- 2007-11-26 TW TW096144835A patent/TW200826936A/zh unknown
- 2007-11-28 WO PCT/CA2007/002139 patent/WO2008064474A1/en active Application Filing
- 2007-11-28 AU AU2007327276A patent/AU2007327276B2/en not_active Ceased
- 2007-11-28 AT AT07845603T patent/ATE543816T1/de active
- 2007-11-28 CA CA2670703A patent/CA2670703C/en not_active Expired - Fee Related
- 2007-11-28 BR BRPI0719702-0A patent/BRPI0719702A2/pt not_active IP Right Cessation
- 2007-11-28 KR KR1020097013826A patent/KR20090086623A/ko not_active Application Discontinuation
- 2007-11-28 EA EA200970524A patent/EA200970524A1/ru unknown
- 2007-11-28 EP EP07845603A patent/EP2099793B1/en active Active
- 2007-11-28 JP JP2009538560A patent/JP5050061B2/ja not_active Expired - Fee Related
- 2007-11-28 MX MX2009005713A patent/MX2009005713A/es unknown
- 2007-11-29 CL CL200703440A patent/CL2007003440A1/es unknown
- 2007-11-29 AR ARP070105302A patent/AR064026A1/es not_active Application Discontinuation
- 2007-11-30 PE PE2007001699A patent/PE20081199A1/es not_active Application Discontinuation
- 2007-11-30 US US11/998,501 patent/US8063224B2/en active Active
-
2009
- 2009-05-19 IL IL198824A patent/IL198824A0/en unknown
- 2009-05-27 GT GT200900144A patent/GT200900144A/es unknown
- 2009-05-27 SV SV2009003275A patent/SV2009003275A/es unknown
- 2009-05-28 CO CO09054946A patent/CO6190521A2/es not_active Application Discontinuation
- 2009-05-29 TN TNP2009000212A patent/TN2009000212A1/fr unknown
- 2009-06-01 EC EC2009009375A patent/ECSP099375A/es unknown
- 2009-06-10 CR CR10858A patent/CR10858A/es unknown
- 2009-06-22 MA MA32023A patent/MA31017B1/fr unknown
- 2009-06-30 NO NO20092469A patent/NO20092469L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP5050061B2 (ja) | 2012-10-17 |
PE20081199A1 (es) | 2008-10-19 |
CA2670703C (en) | 2012-05-15 |
CL2007003440A1 (es) | 2008-04-04 |
MA31017B1 (fr) | 2009-12-01 |
ECSP099375A (es) | 2009-07-31 |
EP2099793A1 (en) | 2009-09-16 |
CA2670703A1 (en) | 2008-06-05 |
MX2009005713A (es) | 2009-06-08 |
CR10858A (es) | 2009-06-25 |
BRPI0719702A2 (pt) | 2013-12-17 |
US8063224B2 (en) | 2011-11-22 |
TN2009000212A1 (en) | 2010-10-18 |
KR20090086623A (ko) | 2009-08-13 |
JP2010510993A (ja) | 2010-04-08 |
US20080132542A1 (en) | 2008-06-05 |
EA200970524A1 (ru) | 2009-12-30 |
SV2009003275A (es) | 2009-11-18 |
AU2007327276B2 (en) | 2011-06-09 |
NO20092469L (no) | 2009-08-27 |
IL198824A0 (en) | 2010-02-17 |
TW200826936A (en) | 2008-07-01 |
ATE543816T1 (de) | 2012-02-15 |
AU2007327276A1 (en) | 2008-06-05 |
EP2099793B1 (en) | 2012-02-01 |
EP2099793A4 (en) | 2010-12-29 |
GT200900144A (es) | 2011-06-23 |
WO2008064474A1 (en) | 2008-06-05 |
CO6190521A2 (es) | 2010-08-19 |
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