PE20120732A1 - Agonistas del receptor de esfingosina-1-fosfato - Google Patents

Agonistas del receptor de esfingosina-1-fosfato

Info

Publication number
PE20120732A1
PE20120732A1 PE2012000174A PE2012000174A PE20120732A1 PE 20120732 A1 PE20120732 A1 PE 20120732A1 PE 2012000174 A PE2012000174 A PE 2012000174A PE 2012000174 A PE2012000174 A PE 2012000174A PE 20120732 A1 PE20120732 A1 PE 20120732A1
Authority
PE
Peru
Prior art keywords
phenyl
alkyl
oxadiazol
sphingosine
crdrd
Prior art date
Application number
PE2012000174A
Other languages
English (en)
Inventor
John L Gilmore
James E Sheppeck
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20120732A1 publication Critical patent/PE20120732A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/14Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

SE REFIERE A COMPUESTOS HETEROCICLICOS DE FORMULA (I) DONDE R1 ES -(CRdRd)aOH, -(CRdRd)aCOOH, ENTRE OTROS, EN DONDE Rd ES H, OH, ALQUILO(C1-C4), ALCOXI(C1-C4), ENTRE OTROS; a ES DE 0 A 3; R2 ES HALO, -OH, ALQUILO(C1-C4), ENTRE OTROS; R3 Y R4 SON CADA UNO H, ALQUILO(C1-C6) O JUNTO AL ATOMO DE C AL QUE ESTAN UNIDOS FORMAN UN ANILLO DE 3 A 6 MIEMBROS; R5 ES H O ALQUILO(C1-C4); R6 ES ALQUILO(C1-C3), HALO, HALOALQUILO(C1-C3), ENTRE OTROS; m Y n SON CADA UNO 1 O 2; x ES DE 0 A 2; t ES DE 0 A 4; W ES O, CH2 O NH; A ES UN COMPUESTO DE FORMULA (i), (ii), (iii) O (iv), EN DONDE Q ES HETEROARILO MONOCICLICO DE 5 MIEMBROS. SON COMPUESTOS PREFERIDOS: ACIDO 1-(2-HIDROXI-2-(4-(5-(5-FENIL-4-PROPILISOXAZOL-3-IL)-1,2,4-OXADIAZOL-3-IL)FENIL)ETIL)ACETIDINA-3-CARBOXILICO; ACIDO (S)-1-((R)-2-HIDROXI-2-(4-(5-(3-FENIL-4-(TRIFLUOROMETIL)ISOXAZOL-5-IL)-1,2,4-OXADIAZOL-3-IL)FENIL)ETIL)PIPERIDINA-3-CARBOXILICO; 2-(3-(HIDROXIMETIL)PIPERIDIN-1-IL)-1-(4-(5-(3-FENIL-4-(TRIFLUOROMETIL)ISOXAZOL-5-IL)-1,2,4-OXADIAZOL-3-IL)FENIL)ETANOL; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON AGONISTAS DEL RECEPTOR DE ESFINGOSINA-1-FOSFATO (S1P1) SIENDO UTILES EN EL TRATAMIENTO DE LUPUS ERITEMATOSO SISTEMICO, ARTRITIS REUMATOIDE, ESCLEROSIS MULTIPLE
PE2012000174A 2009-08-07 2010-08-06 Agonistas del receptor de esfingosina-1-fosfato PE20120732A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23205409P 2009-08-07 2009-08-07

Publications (1)

Publication Number Publication Date
PE20120732A1 true PE20120732A1 (es) 2012-06-20

Family

ID=43029859

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2012000174A PE20120732A1 (es) 2009-08-07 2010-08-06 Agonistas del receptor de esfingosina-1-fosfato

Country Status (19)

Country Link
US (1) US8399451B2 (es)
EP (1) EP2462139B1 (es)
JP (1) JP5602230B2 (es)
KR (1) KR20120108963A (es)
CN (1) CN102548989A (es)
AR (1) AR077819A1 (es)
AU (1) AU2010279354A1 (es)
BR (1) BR112012002824A2 (es)
CA (1) CA2770194A1 (es)
CL (1) CL2012000326A1 (es)
CO (1) CO6430439A2 (es)
EA (1) EA201270266A1 (es)
ES (1) ES2533095T3 (es)
MX (1) MX2012001160A (es)
PE (1) PE20120732A1 (es)
SG (1) SG177691A1 (es)
TW (1) TW201109323A (es)
WO (1) WO2011017578A1 (es)
ZA (1) ZA201200641B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010507619A (ja) * 2006-10-25 2010-03-11 ノイロサーチ アクティーゼルスカブ オキサジアゾール及びチアジアゾール化合物並びにニコチン性アセチルコリン受容体調節物質としてのその使用
CN103119038B (zh) * 2010-04-23 2016-05-04 百时美施贵宝公司 作为1-磷酸鞘氨醇1受体激动剂的4-(5-异噁唑基或5-吡唑基-1,2,4-噁二唑基-3-基)扁桃酰胺
ES2539256T3 (es) 2010-07-20 2015-06-29 Bristol-Myers Squibb Company Compuestos de 3-fenil-1,2,4-oxadiazol sustituidos
WO2012040532A1 (en) 2010-09-24 2012-03-29 Bristol-Myers Squibb Company Substituted oxadiazole compounds and their use as s1p1 agonists
US8629282B2 (en) 2010-11-03 2014-01-14 Bristol-Myers Squibb Company Heterocyclic compounds as S1P1 agonists for the treatment of autoimmune and vascular diseases
UY35338A (es) 2013-02-21 2014-08-29 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware Compuestos bicíclicos moduladores de la actividad de s1p1 y composiciones farmacéuticas que los contienen
UY36274A (es) 2014-08-20 2016-02-29 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware Compuestos bicíclicos sustituidos como agonistas selectivos de la actividad del receptor s1p1 acoplado a la proteína g
TW202023386A (zh) * 2018-09-13 2020-07-01 瑞士商先正達合夥公司 殺有害生物活性唑-醯胺化合物
CN114181276A (zh) * 2021-12-17 2022-03-15 安徽大学 硫酯肽合成方法

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4200750A (en) 1977-01-07 1980-04-29 Westwood Pharmaceuticals Inc. 4-Substituted imidazo [1,2-a]quinoxalines
JPS6480026A (en) 1987-09-21 1989-03-24 Mitsubishi Electric Corp Resist coater
DE4102024A1 (de) * 1991-01-24 1992-07-30 Thomae Gmbh Dr K Biphenylderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
TW432061B (en) 1994-08-09 2001-05-01 Pfizer Res & Dev Lactams
US6069143A (en) * 1994-12-20 2000-05-30 Smithkline Beecham Corporation Fibrinogen receptor antagonists
JP2000516234A (ja) 1996-08-16 2000-12-05 デュポン ファーマシューティカルズ カンパニー アミジノフェニル―ピロリジン類、アミジノフェニル―ピロリン類、およびアミジノフェニル―イソオキサゾリジン類およびそれらの誘導体
EP1575964B1 (en) * 2002-01-18 2009-11-11 Merck & Co., Inc. N-(benzyl)aminoalkyl carboxylate, phosphinates, phosphonates and tetrazoles as edg receptor agonists
WO2003062252A1 (en) * 2002-01-18 2003-07-31 Merck & Co., Inc. Edg receptor agonists
AU2003216054B2 (en) 2002-01-18 2007-01-04 Merck & Co., Inc. Selective S1P1/Edg1 receptor agonists
US7309721B2 (en) * 2002-03-01 2007-12-18 Merck + Co., Inc. Aminoalkylphosphonates and related compounds as Edg receptor agonists
GEP20074148B (en) * 2002-04-23 2007-07-10 Bristol Myers Squibb Co Pyrrolo-triazine aniline compounds useful as kinase inhibitors
JP2005533058A (ja) * 2002-06-17 2005-11-04 メルク エンド カムパニー インコーポレーテッド Edg受容体アゴニストとしての1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)アゼチジン−3−カルボキシラートおよび1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)ピロリジン−3−カルボキシラート
WO2004035538A1 (en) 2002-10-15 2004-04-29 Merck & Co., Inc. Process for making azetidine-3-carboxylic acid
JP4516430B2 (ja) 2002-12-20 2010-08-04 メルク・シャープ・エンド・ドーム・コーポレイション 1−(アミノ)インダン並びに(1,2−ジヒドロ−3−アミノ)−ベンゾフラン、ベンゾチオフェン及びインドール
EP1594508B1 (en) 2003-02-11 2012-08-08 Irm Llc Novel bicyclic compounds and compositions
WO2004103279A2 (en) 2003-05-15 2004-12-02 Merck & Co., Inc. 3-(2-amino-1-azacyclyl)-5-aryl-1,2,4-oxadiazoles as s1p receptor agonists
MXPA05012461A (es) 2003-05-19 2006-02-22 Irm Llc Compuestos y composiciones inmunosupresores.
MY150088A (en) 2003-05-19 2013-11-29 Irm Llc Immunosuppressant compounds and compositions
US7060697B2 (en) 2003-05-19 2006-06-13 Irm Llc Immunosuppressant compounds and compositions
BRPI0410746A (pt) 2003-05-19 2006-06-27 Irm Llc compostos e composições imunossupressoras
US20070043014A1 (en) 2003-10-01 2007-02-22 Merck & Co., Inc. 3,5-Aryl, heteroaryl or cycloalkyl substituted-1,2,4-oxadiazoles as s1p receptor agonists
WO2005058848A1 (en) 2003-12-17 2005-06-30 Merck & Co., Inc. (3,4-disubstituted)propanoic carboxylates as s1p (edg) receptor agonists
TW200538433A (en) 2004-02-24 2005-12-01 Irm Llc Immunosuppressant compounds and compositiions
JP2008517915A (ja) 2004-10-22 2008-05-29 メルク エンド カムパニー インコーポレーテッド S1p受容体アゴニストとしての2−(アリール)アザシクリルメチルカルボキシレート、スルホネート、ホスホネート、ホスフィネート及びヘテロ環
JP2008530135A (ja) 2005-02-14 2008-08-07 ユニバーシティ オブ バージニア パテント ファンデーション アミノ基およびフェニル基で置換されたシクロアルカンならびに5員の複素環を含むスフィンゴシン=1−リン酸アゴニスト
PT1863787E (pt) 2005-03-23 2011-07-29 Actelion Pharmaceuticals Ltd Derivados de benzo(c)tiofenos hidrogenados como imunomoduladores
MX2007011672A (es) 2005-03-23 2007-11-15 Actelion Pharmaceuticals Ltd Nuevos derivados de tiofeno como agonistas del receptor de esfingosina-1-fosfato-1.
CA2605594A1 (en) 2005-04-22 2006-11-02 Daiichi Sankyo Company, Limited Heterocyclic compound
US20080306124A1 (en) 2005-06-08 2008-12-11 Rainer Albert Polycyclic Oxadiazoles or I Soxazoles and Their Use as Sip Receptor Ligands
RU2008101805A (ru) 2005-06-24 2009-07-27 Актелион Фармасьютиклз Лтд (Ch) Новые производные тиофена
BRPI0615133A2 (pt) 2005-08-23 2011-05-03 Irm Llc compostos imunossupressores, composições farmacêuticas contendo os mesmos assim como referido uso
TW200800911A (en) 2005-10-20 2008-01-01 Biolipox Ab Pyrazoles useful in the treatment of inflammation
EP1965807A4 (en) * 2005-11-23 2010-10-27 Epix Delaware Inc S1P RECEPTOR MODULATING COMPOUNDS AND THEIR USE
TWI404706B (zh) 2006-01-11 2013-08-11 Actelion Pharmaceuticals Ltd 新穎噻吩衍生物
GB0601744D0 (en) 2006-01-27 2006-03-08 Novartis Ag Organic compounds
TW200806611A (en) 2006-02-09 2008-02-01 Daiichi Seiyaku Co Novel amidopropionic acid derivatives and medicine containing the same
AU2007227274A1 (en) * 2006-03-21 2007-09-27 Epix Delaware, Inc. S1P receptor modulating compounds
CA2648303C (en) 2006-04-03 2014-07-15 Astellas Pharma Inc. 5-[monocyclic(hetero)arylsubstituted-1,2,4-oxadliazol-3-yl]-(fused heteroaryl substituted) compounds and their use as s1p1 agonists
US20080070866A1 (en) 2006-08-01 2008-03-20 Praecis Pharmaceuticals Incorporated Chemical compounds
JP2009269819A (ja) 2006-08-25 2009-11-19 Asahi Kasei Pharma Kk アミン化合物
CA2662852A1 (en) 2006-09-07 2008-03-13 Allergan, Inc. Heteroaromatic compounds having sphingosine-1-phosphate (s1p) receptor agonist and/or antagonist biological activity
TWI408139B (zh) 2006-09-07 2013-09-11 Actelion Pharmaceuticals Ltd 新穎噻吩衍生物
AU2007292993B2 (en) 2006-09-07 2013-01-24 Idorsia Pharmaceuticals Ltd Pyridin-4-yl derivatives as immunomodulating agents
AU2007292992B2 (en) * 2006-09-08 2013-01-10 Actelion Pharmaceuticals Ltd Pyridin-3-yl derivatives as immunomodulating agents
EP2081888A1 (en) 2006-09-08 2009-07-29 Novartis AG N-biaryl (hetero) arylsulphonamide derivatives useful in the treatment of diseases mediated by lymphocytes interactions
AU2007298593A1 (en) 2006-09-21 2008-03-27 Actelion Pharmaceuticals Ltd Phenyl derivatives and their use as immunomodulators
AU2007302262A1 (en) 2006-09-29 2008-04-03 Novartis Ag Oxadiazole derivatives with anti-inflammatory and immunosuppressive properties
EP2097397A1 (en) 2006-11-21 2009-09-09 University Of Virginia Patent Foundation Tetralin analogs having sphingosine 1-phosphate agonist activity
AU2007334436A1 (en) 2006-12-15 2008-06-26 Abbott Laboratories Novel oxadiazole compounds
GB0625648D0 (en) 2006-12-21 2007-01-31 Glaxo Group Ltd Compounds
JO2701B1 (en) 2006-12-21 2013-03-03 جلاكسو جروب ليميتد Vehicles
MX2009006751A (es) 2006-12-21 2009-06-30 Abbott Lab Compuestos agonistas y antagonistas del receptor de esfingosina-1-fosfato.
WO2008091967A1 (en) 2007-01-26 2008-07-31 Smithkline Beecham Corporation Chemical compounds
MX2009009597A (es) 2007-03-16 2009-09-16 Actelion Pharmaceuticals Ltd Derivados de amino-piridina como agonistas del receptor s1p1/edg1.
MX2009011155A (es) * 2007-04-19 2009-10-30 Glaxo Group Ltd Derivados de indazol oxadiazol sustituidos para su uso como agonistas de esfingosina-1-fosfato (s1p).
US20090069288A1 (en) 2007-07-16 2009-03-12 Breinlinger Eric C Novel therapeutic compounds
US8202865B2 (en) 2007-10-04 2012-06-19 Merck Serono Sa Oxadiazole derivatives
EP2193126B1 (en) 2007-10-04 2015-06-24 Merck Serono S.A. Oxadiazole diaryl compounds
BRPI0818804A2 (pt) 2007-11-01 2015-04-22 Actelion Pharmaceuticals Ltd Composto derivado de pirimidina, composição farmacêutica que o compreende e uso desse composto.
WO2009080663A1 (en) 2007-12-21 2009-07-02 Merck Serono S.A. Triazole oxadiazoles derivatives
HUE025984T2 (hu) 2008-05-14 2016-05-30 Scripps Research Inst Szfingozin foszfát receptor új modulátorai
JP5537433B2 (ja) 2008-10-06 2014-07-02 昭和電工株式会社 触媒およびその製造方法ならびにその用途
US20100160369A1 (en) * 2008-12-04 2010-06-24 Exelixis, Inc. S1P1 Agonists and Methods of Making And Using
PL2354134T3 (pl) 2008-12-05 2016-07-29 Astellas Pharma Inc Pochodne 2h-chromenowe jako stymulatory receptora 1-fosforanu sfingozyny
BRPI0923178A2 (pt) 2008-12-18 2016-02-16 Merck Serono Sa derivados heterocíclicos de oxadiazol fundidos úteis para o tratamento de esclerose múltipla
AR075319A1 (es) 2008-12-23 2011-03-23 Novartis Ag Compuestos de biaril- bencil-amina, procesos para su produccion, su uso como productos farmaceuticos, y composiciones farmaceuticas que los comprenden
EP2202232A1 (en) 2008-12-26 2010-06-30 Laboratorios Almirall, S.A. 1,2,4-oxadiazole derivatives and their therapeutic use
EP2210890A1 (en) 2009-01-19 2010-07-28 Almirall, S.A. Oxadiazole derivatives as S1P1 receptor agonists
CN102361867A (zh) 2009-01-23 2012-02-22 百时美施贵宝公司 在治疗自身免疫疾病和炎性疾病中作为s1p激动剂的取代的噁二唑衍生物
CN102361868A (zh) 2009-01-23 2012-02-22 百时美施贵宝公司 作为1-磷酸-鞘氨醇激动剂的吡唑-1,2,4-噁二唑衍生物
JP2012515788A (ja) 2009-01-23 2012-07-12 ブリストル−マイヤーズ スクイブ カンパニー 自己免疫疾患および炎症性疾患の処置における、s1pアゴニストとしての置換オキサジアゾール誘導体
JP5669363B2 (ja) 2009-03-31 2015-02-12 昭和電工株式会社 樹脂組成物及びこれで処理された紙又は繊維加工品
US8724509B2 (en) 2009-04-03 2014-05-13 Panasonic Corporation Mobile communication method, mobile communication system, and corresponding apparatus

Also Published As

Publication number Publication date
CN102548989A (zh) 2012-07-04
JP2013501729A (ja) 2013-01-17
ES2533095T3 (es) 2015-04-07
EP2462139A1 (en) 2012-06-13
TW201109323A (en) 2011-03-16
KR20120108963A (ko) 2012-10-05
WO2011017578A1 (en) 2011-02-10
MX2012001160A (es) 2012-02-13
US8399451B2 (en) 2013-03-19
EP2462139B1 (en) 2015-01-14
AU2010279354A1 (en) 2012-02-09
SG177691A1 (en) 2012-02-28
CO6430439A2 (es) 2012-04-30
EA201270266A1 (ru) 2012-07-30
AR077819A1 (es) 2011-09-28
JP5602230B2 (ja) 2014-10-08
US20110190255A1 (en) 2011-08-04
CL2012000326A1 (es) 2012-10-19
ZA201200641B (en) 2013-06-26
CA2770194A1 (en) 2011-02-10
BR112012002824A2 (pt) 2019-09-24

Similar Documents

Publication Publication Date Title
PE20120732A1 (es) Agonistas del receptor de esfingosina-1-fosfato
PE20081398A1 (es) Derivados de oxadiazol como agonistas del receptor sensible a 1-fosfato de esfingosina (s1p1)
WO2009051956A3 (en) Pyrazole-substituted isoxazoline insecticides
PE20140207A1 (es) Composiciones y metodos para modular el fxr
RU2009139920A (ru) Изоксазолиновые соединения и их применение в борьбе с вредителями
PE20061038A1 (es) Derivados del 1,5-difenil-1h-pirazol-3-il) oxadiazol como agentes antagonistas cb1 y su preparacion
PE20090992A1 (es) Derivados de fenil-amino-pirimidina como agentes inhibidores de cinasa
EA201101089A1 (ru) Производные оксадиазола в качестве агонистов рецептора s1p1
EA201170096A1 (ru) Замещенные производные пиримидона
CO6220851A2 (es) Compuestos de ciclohexandiona sustituidos en la posicion 5
PE20081199A1 (es) Derivados de azacicloalcanos como inhibidores de estearoil-coenzima a delta-9 desaturasa
JP2010504286A5 (es)
PE20120656A1 (es) 2-acetamido-5-aril-1, 2, 4-triazolonas sustituidas y su uso
TW200732329A (en) Aryl-isoxazolo-4-yl-oxadiazole derivatives
PE20080360A1 (es) Derivados 4-bencilftalazinona 2-sustituidos como antagonistas de histaminas h1 y h3
PE20120690A1 (es) Derivados de 5-fluoropirimidinona
RU2008112691A (ru) Азотсодержащее гетероциклическое соединение и его фармацевтическое применение
PE20140868A1 (es) Antagonistas trpm8 y su uso en tratamientos
PE20090477A1 (es) Derivados de oxazol como inhibidores de los canales de sodio
PE20120657A1 (es) Compuesto para el tratamiento de trastornos metabolicos
PE20070460A1 (es) Derivados de carboxamida como antagonista del receptor muscarinico
PE20120362A1 (es) Derivados de tiadiazoles y oxadiazoles, su preparacion y su aplicacion en terapia
MX338631B (es) 5-(fenil/piridinil-etinil)-2-piridina/ 2-pirimidina-carboxamidas como moduladores del receptor de glutamato metabotropico del subtipo 5 (mglur5).
IN2012DN00770A (es)
PE20120934A1 (es) Piperidinas sustituidas

Legal Events

Date Code Title Description
FD Application declared void or lapsed