MA33071B1 - Compose a noyau condenses et son utilisation - Google Patents

Compose a noyau condenses et son utilisation

Info

Publication number
MA33071B1
MA33071B1 MA34132A MA34132A MA33071B1 MA 33071 B1 MA33071 B1 MA 33071B1 MA 34132 A MA34132 A MA 34132A MA 34132 A MA34132 A MA 34132A MA 33071 B1 MA33071 B1 MA 33071B1
Authority
MA
Morocco
Prior art keywords
nucleus
intensive
composite
diseases
angiotensin
Prior art date
Application number
MA34132A
Other languages
Arabic (ar)
English (en)
Inventor
Tsuyoshi Maekawa
Hideyuki Igawa
Original Assignee
Takeda Pharmaceutical
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 Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of MA33071B1 publication Critical patent/MA33071B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Emergency Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Endocrinology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

L'invention porte sur un nouveau composé représenté par la formule suivante, dans laquelle chaque symbole est tel que défini dans la description, ou sur un sel de ce composé, qui a une activité antagoniste des récepteurs de l'angiotensine II et une activité agoniste du récepteur ³ activé par les proliférateurs des peroxysomes, et qui est utile en tant qu'agent pour la prophylaxie ou le traitement de maladies circulatoires, telles que l'hypertension et similaire, et/ou de maladies métaboliques, telles que le diabète et similaire, et similaires.
MA34132A 2009-01-30 2010-01-29 Compose a noyau condenses et son utilisation MA33071B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009020720 2009-01-30
PCT/JP2010/051651 WO2010087515A1 (fr) 2009-01-30 2010-01-29 Composé à noyaux condensés et son utilisation

Publications (1)

Publication Number Publication Date
MA33071B1 true MA33071B1 (fr) 2012-02-01

Family

ID=42026435

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34132A MA33071B1 (fr) 2009-01-30 2010-01-29 Compose a noyau condenses et son utilisation

Country Status (36)

Country Link
US (4) US8283353B2 (fr)
EP (1) EP2384327B1 (fr)
JP (2) JP4892649B1 (fr)
KR (1) KR20110113758A (fr)
CN (2) CN102369205B (fr)
AR (1) AR075344A1 (fr)
AU (1) AU2010208863A1 (fr)
CA (1) CA2750710C (fr)
CL (1) CL2011001848A1 (fr)
CO (1) CO6362011A2 (fr)
CR (1) CR20110463A (fr)
CY (1) CY1114530T1 (fr)
DK (1) DK2384327T3 (fr)
DO (1) DOP2011000249A (fr)
EA (1) EA019823B1 (fr)
EC (1) ECSP11011294A (fr)
ES (1) ES2433225T3 (fr)
GE (1) GEP20135961B (fr)
HR (1) HRP20131017T1 (fr)
IL (1) IL214283A0 (fr)
MA (1) MA33071B1 (fr)
ME (1) ME01621B (fr)
MX (1) MX2011008058A (fr)
MY (1) MY152946A (fr)
NZ (1) NZ594606A (fr)
PE (1) PE20120593A1 (fr)
PL (1) PL2384327T3 (fr)
PT (1) PT2384327E (fr)
RS (1) RS53012B (fr)
SG (1) SG173135A1 (fr)
SI (1) SI2384327T1 (fr)
TN (1) TN2011000368A1 (fr)
TW (2) TW201444848A (fr)
UY (1) UY32409A (fr)
WO (1) WO2010087515A1 (fr)
ZA (1) ZA201105867B (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA33071B1 (fr) 2009-01-30 2012-02-01 Takeda Pharmaceutical Compose a noyau condenses et son utilisation
HUE024504T2 (en) 2010-12-23 2016-01-28 Sanofi Sa Pyrimidine derivatives, a process for their preparation and their use in medicine
CZ304252B6 (cs) * 2011-04-11 2014-01-29 Zentiva, K. S. Způsob výroby 2-ethoxy-1-((2´-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)bifenyl-4-yl)methyl)-1H-benzo[d]imidazol-7-karboxylátů a jejich převedení na azilsartan
EP3472168B1 (fr) 2016-06-20 2024-01-10 Novartis AG Formes cristallines d'un composé de triazolopyrimidine
CA3077050A1 (fr) 2017-09-26 2019-04-04 Ecolab Usa Inc. Compositions antimicrobiennes et virocides acides/anioniques et leurs utilisations
DK3804716T3 (da) 2018-05-31 2025-03-03 Hua Medicine Shanghai Ltd Farmaceutisk kombination, sammensætning og kombinationspræparat omfattende glucokinase-aktivator og sglt-2-inhibitor og fremgangsmåder til fremstilling og anvendelser deraf
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
US11472791B2 (en) 2019-03-05 2022-10-18 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as CDK2 inhibitors
WO2020205560A1 (fr) 2019-03-29 2020-10-08 Incyte Corporation Composés sulfonylamides utilisés comme inhibiteurs de la cdk2
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
MX2022001940A (es) 2019-08-14 2022-05-10 Incyte Corp Compuestos de imidazolil pirimidinilamina como inhibidores de cdk2.
CN119930610A (zh) 2019-10-11 2025-05-06 因赛特公司 作为cdk2抑制剂的双环胺
CN112745319B (zh) * 2019-10-30 2022-06-17 中国科学院上海药物研究所 一类取代三环结构的化合物、其制备方法及用途
CN114901072B (zh) 2019-12-16 2024-12-17 埃科莱布美国股份有限公司 阴离子表面活性剂对杀病毒功效的影响
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2672892B1 (fr) * 1991-02-20 1994-01-14 Synthelabo Derives de 4-pyrimidinones, leur preparation et leur application en therapeutique.
US5472967A (en) 1991-02-20 1995-12-05 Synthelabo 4-pyrimidinone derivatives their preparation and their application in therapy
TW251288B (fr) * 1991-06-27 1995-07-11 Takeda Dharm Industry Co Ltd
IL102183A (en) 1991-06-27 1999-11-30 Takeda Chemical Industries Ltd Biphenyl substituted heterocyclic compounds their production and pharmaceutical compositions comprising them
IT1250749B (it) 1991-08-02 1995-04-21 Luso Farmaco Inst Composti eterociclici ad attivita' a ii antagonista
US5389632A (en) 1992-02-24 1995-02-14 Laboratoires Upsa Pyrazolopyrimidine derivatives which are angiotensin II receptor antagonists
FR2687677B1 (fr) * 1992-02-24 1996-10-11 Union Pharma Scient Appl Nouveaux derives de polyazaindenes antagonistes des recepteurs a l'angiotensine ii ; leurs procedes de preparation, compositions pharmaceutiques les contenant.
US5387747A (en) 1992-02-24 1995-02-07 Laboratoires Upsa Triazolopyrimidine derivatives which are angiotensin II receptor antagonists, their methods of preparation and pharmaceutical compositions in which they are present
IT1263804B (it) 1993-01-22 1996-09-03 Luso Farmaco Inst Derivati pirimidinonici fusi con eterocicli azotati ad attivita' a ii antagonista
GB9406573D0 (en) 1994-03-31 1994-05-25 Merck Sharp & Dohme Medicaments
WO1996040256A1 (fr) 1995-06-07 1996-12-19 G.D. Searle & Co. Procede de traitement de la cardiofibrose avec une combinaison de spironolactone et d'un antagoniste de l'angiotensive ii
IL122246A (en) 1995-06-07 2004-06-01 Searle & Co Combination of spironolactone and angiotensin II antagonist for the treatment of heart failure
KR100618466B1 (ko) 1995-06-07 2006-12-13 지.디. 썰 엘엘씨 울혈성심마비의치료를위한에폭시-스테로이드계알도스테론길항제및앤지오탠신ii길항제복합요법
WO1996040255A2 (fr) 1995-06-07 1996-12-19 G.D. Searle & Co. Procede de traitement de la fibrose cardiaque par une combinaison therapeutique d'un antagoniste de l'angiotensine ii et d'un antagoniste de l'aldosterone epoxy-steroide
FR2812876B1 (fr) 2000-08-08 2002-09-27 Galderma Res & Dev Nouveaux composes bi-aromatiques activateurs des recepteurs de type ppar-gamma et leur utilisation dans des compositions cosmetiques ou pharmaceutiques
SE0101579D0 (sv) 2001-05-04 2001-05-04 Astrazeneca Ab New compounds
US7232828B2 (en) 2002-08-10 2007-06-19 Bethesda Pharmaceuticals, Inc. PPAR Ligands that do not cause fluid retention, edema or congestive heart failure
TW200418835A (en) 2003-01-24 2004-10-01 Tanabe Seiyaku Co A pyrazolopyrimidine compound and a process for preparing the same
US20050065184A1 (en) 2003-08-29 2005-03-24 Aaipharma Inc. Method of reducing the risk of oxidative stress
JP2007520559A (ja) * 2004-02-03 2007-07-26 アボット・ラボラトリーズ 治療薬としてのアミノベンゾオキサゾール類
MEP8409A (en) 2004-06-02 2011-12-20 Fused heterocyclic compound
RU2384346C2 (ru) 2004-06-23 2010-03-20 Зольвай Фармасьютиклз Гмбх Фармацевтические композиции, содержащие nep-ингибиторы, ингибиторы эндогенной эндотелинпродуцирующей системы и антагонисты at1-рецептора
US20050288272A1 (en) 2004-06-23 2005-12-29 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising NEP-inhibitors, inhibitors of the endogenous endothelin producing system and AT1 receptor antagonists
AU2006273622A1 (en) 2005-07-27 2007-02-01 Mor Research Applications Ltd. Inhibition of the renin-angiotensin system for the treatment of renal, vascular and cartilage pathology
WO2007053406A1 (fr) 2005-10-28 2007-05-10 Novartis Ag Combinaison de composes organiques hypotenseurs et hypocholesterolemiant
WO2007051007A2 (fr) 2005-10-28 2007-05-03 Novartis Ag Combinaison de composes organiques
US20080064871A1 (en) 2006-05-26 2008-03-13 Japan Tobacco Inc. Production Method of Nitrogen-Containing Fused Ring Compounds
US20080132474A1 (en) 2006-11-09 2008-06-05 Gene Logic Inc. Breast cancer screening and treatment methods
US20090012052A1 (en) 2006-11-09 2009-01-08 Ore Pharmaceuticals Inc. Method for treating er+ breast cancer
MX2009005449A (es) * 2006-11-24 2009-06-02 Takeda Pharmaceutical Compuesto heteromonociclico y uso del mismo.
JPWO2008143262A1 (ja) 2007-05-21 2010-08-12 武田薬品工業株式会社 複素環化合物およびその用途
CN101888776B (zh) 2007-09-20 2015-03-11 罗切斯特大学 治疗或预防炎性病症的方法和组合物
KR101673621B1 (ko) 2008-03-24 2016-11-07 노파르티스 아게 아릴술폰아미드-계 매트릭스 메탈로프로테아제 억제제
EP2279009A4 (fr) 2008-05-05 2011-09-21 Univ Rochester Procédés et compositions pour le traitement ou la prévention d'une remodélisation cardiaque pathologique et d'une insuffisance cardiaque
MA33071B1 (fr) * 2009-01-30 2012-02-01 Takeda Pharmaceutical Compose a noyau condenses et son utilisation

Also Published As

Publication number Publication date
TW201444848A (zh) 2014-12-01
JP2011251970A (ja) 2011-12-15
ECSP11011294A (es) 2011-09-30
AR075344A1 (es) 2011-03-23
IL214283A0 (en) 2011-09-27
PL2384327T3 (pl) 2013-12-31
CN102369205A (zh) 2012-03-07
CN102369205B (zh) 2014-10-29
PE20120593A1 (es) 2012-05-21
CA2750710A1 (fr) 2010-08-05
US8592431B2 (en) 2013-11-26
JP2012513952A (ja) 2012-06-21
CR20110463A (es) 2011-12-01
MY152946A (en) 2014-12-15
JP4892649B1 (ja) 2012-03-07
ME01621B (me) 2014-09-20
GEP20135961B (en) 2013-11-11
KR20110113758A (ko) 2011-10-18
TN2011000368A1 (en) 2013-03-27
SI2384327T1 (sl) 2013-12-31
US9115136B2 (en) 2015-08-25
SG173135A1 (en) 2011-08-29
TWI468410B (zh) 2015-01-11
NZ594606A (en) 2013-06-28
UY32409A (es) 2010-08-31
US20110288087A1 (en) 2011-11-24
MX2011008058A (es) 2011-09-01
EA201101138A1 (ru) 2012-04-30
US20100197683A1 (en) 2010-08-05
CL2011001848A1 (es) 2012-02-03
CY1114530T1 (el) 2017-01-25
ES2433225T3 (es) 2013-12-10
US8283353B2 (en) 2012-10-09
PT2384327E (pt) 2013-11-07
CN103788097B (zh) 2016-03-30
US20110294832A1 (en) 2011-12-01
JP5676379B2 (ja) 2015-02-25
ZA201105867B (en) 2012-10-31
WO2010087515A1 (fr) 2010-08-05
HRP20131017T1 (hr) 2013-12-06
DK2384327T3 (da) 2013-10-28
TW201031669A (en) 2010-09-01
EA019823B1 (ru) 2014-06-30
US20140046056A1 (en) 2014-02-13
US8921379B2 (en) 2014-12-30
CN103788097A (zh) 2014-05-14
EP2384327A1 (fr) 2011-11-09
AU2010208863A1 (en) 2011-09-08
HK1162505A1 (en) 2012-08-31
DOP2011000249A (es) 2011-09-15
CA2750710C (fr) 2018-09-04
CO6362011A2 (es) 2012-01-20
EP2384327B1 (fr) 2013-07-31
RS53012B (sr) 2014-04-30

Similar Documents

Publication Publication Date Title
MA33071B1 (fr) Compose a noyau condenses et son utilisation
MA31084B1 (fr) Derives de piperidine agonistes de gpcr
MA30528B1 (fr) Antagoniste du recepteur il-8.
MA32614B1 (fr) Compositions therapeutiques contenant du macitentan
MA31189B1 (fr) Composés à cycles fusionnés utiles en tant qu'agonistes partiels de ppar-gamma
MA46286B1 (fr) Dérivé de pyrazolopyridine ayant un effet agoniste du récepteur glp-1
EA200701705A1 (ru) Антагонисты рецепторы глюкагона, получение и терапевтическое применение
MA37866B1 (fr) Dérivés de type aza-indazole ou diaza-indazole pour le traitement de la douleur
MA33840B1 (fr) Nouveau composé de spiropipéridine
MA32903B1 (fr) Inhibiteurs de proteine-kinases
MX2011011156A (es) COMPUESTOS DIAMIDA QUE TIENE ACTIVIDAD COMO ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS Y COMO AGONISTAS DE LOS RECEPTORES ANDRENERGICOS ß2.
EP2324029A4 (fr) Inhibiteurs hétérocyliques des récepteurs de l'histamine destinés au traitement d'une maladie
BRPI0714315B8 (pt) arilamidas substituídas com tetrazol, seu uso e composição farmacêutica que as compreende
MA33178B1 (fr) Pipéridines substituées comme antagonistes de ccr3
TN2014000243A1 (fr) Benzopyrannes nouveaux, compositions les contenant et leurs utilisations
ATE464304T1 (de) Carboxamid-spirolactam-cgrp-rezeptor-antagonist n
MA34545B1 (fr) Co-cristaux et sels d'inhibiteurs de ccr3
EA201070535A1 (ru) Новые агонисты глюкокортикоидных рецепторов
MA30556B1 (fr) COMPOSES A BASE DE DIALKYLPHENYLE AYANT UNE ACTIVITE AGONISTE DU RECEPTEUR ADRENERGIQUE ß2 ET ANTAGONISTE DU RECEPTEUR MUSCARINIQUE.
CY1110922T1 (el) Ανταγωνιστες υποδοχεα γλυκαγονης, παρασκευη και θεραπευτικες χρησεις
DK1735278T3 (da) Histamin H3-receptormidler, fremstilling og terapeutiske anvendelser
TNSN08337A1 (fr) Piperidinoylpyrrolidines agonistes du recepteur de melanocortine de type 4
DK2081572T3 (da) Benzimidazol-cannabinoid-agonister med en substitueret heterocyklisk gruppe
MA33836B1 (fr) Compositions pharmaceutiques contenant des ligands des récepteurs sigma
ATE552246T1 (de) Substituierte aryloxy-n- bicyclomethylacetamidverbindungen als vr1- antagonisten