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MA31072B1 - Composes tetrahydrocyclopenta [b] indole comme modulateurs du recepteur des androgenes - Google Patents

Composes tetrahydrocyclopenta [b] indole comme modulateurs du recepteur des androgenes

Info

Publication number
MA31072B1
MA31072B1 MA32013A MA32013A MA31072B1 MA 31072 B1 MA31072 B1 MA 31072B1 MA 32013 A MA32013 A MA 32013A MA 32013 A MA32013 A MA 32013A MA 31072 B1 MA31072 B1 MA 31072B1
Authority
MA
Morocco
Prior art keywords
formula
tetrahydrocyclopenta
modulators
compound
androgen receptor
Prior art date
Application number
MA32013A
Other languages
English (en)
Inventor
Konstantinos Gavardinas
Jonathan Edward Green
Prabhakar Kondaji Jadhav
Donald Paul Matthews
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of MA31072B1 publication Critical patent/MA31072B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56Ring systems containing three or more rings
    • C07D209/58[b]- or [c]-condensed
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10Drugs for genital or sexual disorders; Contraceptives for impotence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56Ring systems containing three or more rings
    • C07D209/58[b]- or [c]-condensed
    • C07D209/70[b]- or [c]-condensed containing carbocyclic rings other than six-membered

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Endocrinology (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Reproductive Health (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Psychiatry (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pulmonology (AREA)
  • Anesthesiology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UN COMPOSÉ DE FORMULE : FORMULE (I) OU UN SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI; DES COMPOSITIONS PHARMACEUTIQUES COMPRENANT LE COMPOSÉ AA DE FORMULE (I) EN ASSOCIATION AVEC UN TRANSPORTEUR APPROPRIÉ, UN DILUANT, OU UN EXCIPIENT; ET DES PROCÉDÉS POUR TRAITER DES TROUBLES PHYSIOLOGIQUES, EN PARTICULIER UNE MASSE OSSEUSE RÉDUITE, UNE OSTÉOPOROSE, UNE OSTÉOPÉNIE, OU UNE MASSE OU FORCE MUSCULAIRE RÉDUITE, COMPRENANT L'ADMINISTRATION D'UN COMPOSÉ DE FORMULE (I), OU D'UN SEL PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI.
MA32013A 2006-11-20 2009-06-17 Composes tetrahydrocyclopenta [b] indole comme modulateurs du recepteur des androgenes MA31072B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US86648406P 2006-11-20 2006-11-20

Publications (1)

Publication Number Publication Date
MA31072B1 true MA31072B1 (fr) 2010-01-04

Family

ID=39415431

Family Applications (1)

Application Number Title Priority Date Filing Date
MA32013A MA31072B1 (fr) 2006-11-20 2009-06-17 Composes tetrahydrocyclopenta [b] indole comme modulateurs du recepteur des androgenes

Country Status (36)

Country Link
US (1) US7968587B2 (fr)
EP (1) EP2094658B1 (fr)
JP (1) JP5399259B2 (fr)
KR (1) KR101121471B1 (fr)
CN (1) CN101541749B (fr)
AR (1) AR063559A1 (fr)
AT (1) ATE538091T1 (fr)
AU (1) AU2007324046B2 (fr)
BR (1) BRPI0719092B8 (fr)
CA (1) CA2670340C (fr)
CL (1) CL2007003182A1 (fr)
CO (1) CO6190513A2 (fr)
CR (1) CR10802A (fr)
CY (1) CY1112284T1 (fr)
DK (1) DK2094658T3 (fr)
EA (1) EA015627B1 (fr)
EC (1) ECSP099350A (fr)
ES (1) ES2376048T3 (fr)
HR (1) HRP20120032T1 (fr)
IL (1) IL198410A (fr)
JO (1) JO2800B1 (fr)
MA (1) MA31072B1 (fr)
MX (1) MX2009005251A (fr)
MY (1) MY154547A (fr)
NO (1) NO342531B1 (fr)
NZ (1) NZ576296A (fr)
PE (1) PE20081161A1 (fr)
PL (1) PL2094658T3 (fr)
PT (1) PT2094658E (fr)
RS (1) RS52191B (fr)
SI (1) SI2094658T1 (fr)
TN (1) TN2009000189A1 (fr)
TW (1) TWI398438B (fr)
UA (1) UA98777C2 (fr)
WO (1) WO2008063867A2 (fr)
ZA (1) ZA200903096B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2716320C (fr) 2008-02-22 2014-01-28 Radius Health, Inc. Modulateurs selectifs du recepteur de l'androgene
US8268872B2 (en) 2008-02-22 2012-09-18 Radius Health, Inc. Selective androgen receptor modulators
BRPI0912394A2 (pt) * 2008-05-16 2016-07-26 Lilly Co Eli moduladores do receptor de androgênio à base de tetra-hidrociclopenta[b]indol
AR078862A1 (es) 2009-11-13 2011-12-07 Lilly Co Eli Ester isopropilico del acido ((s)-7-ciano-4-((2r,3s)-3-hidroxitetrahidrofuran-2-ilmetil)-1,2,3,4-tetrahidro-ciclopenta(b)indol-2-il)carbamico, composiciones farmaceuticas que lo comprenden y su uso en terapia
CA2788907A1 (fr) 2010-02-04 2011-08-11 Radius Health, Inc. Modulateurs selectifs du recepteur des androgenes
EP3106159A1 (fr) 2010-05-12 2016-12-21 Radius Health, Inc. Régimes thérapeutiques
US8642632B2 (en) 2010-07-02 2014-02-04 Radius Health, Inc. Selective androgen receptor modulators
JP5965909B2 (ja) 2010-09-28 2016-08-10 ラジウス ヘルス,インコーポレイテッド 選択的アンドロゲン受容体モジュレーター
EP2707373A1 (fr) 2011-05-10 2014-03-19 Bayer Intellectual Property GmbH (thio)carbonylamidines bicycliques
CN103265479B (zh) * 2013-06-14 2017-12-08 南开大学 一种6‑氯甲基烟酸叔丁酯的合成方法
CA2943611A1 (fr) 2014-03-28 2015-10-01 Duke University Methode de traitement du cancer faisant intervenir des modulateurs selectifs des recepteurs des ƒstrogenes
US9421264B2 (en) 2014-03-28 2016-08-23 Duke University Method of treating cancer using selective estrogen receptor modulators
TWI744723B (zh) 2014-06-20 2021-11-01 美商基利科學股份有限公司 多環型胺甲醯基吡啶酮化合物之合成
JOP20180072A1 (ar) * 2014-09-11 2019-01-30 Lilly Co Eli علاج الأعراض المرتبطة بالعلاج بالحرمان من الأندروجين
CA3027563C (fr) 2016-06-22 2024-07-02 Ellipses Pharma Ltd Methodes ar+ de traitement du cancer du sein
US20180185347A1 (en) 2016-11-16 2018-07-05 Transition Therapeutics (Ireland 2) Limited Tetrahydrocyclopenta[b]indole compounds and phosphodiesterase inhibitors for the treatment of the signs and symptoms of bhp
JP7481115B2 (ja) 2017-01-05 2024-05-10 ラジウス ファーマシューティカルズ,インコーポレイテッド Rad1901-2hclの多形性形態
IL279853B2 (en) 2018-07-04 2025-01-01 Radius Pharmaceuticals Inc Polymorphic forms of RAD 1901-2HCL
CN119390714A (zh) 2019-02-12 2025-02-07 雷迪厄斯制药公司 方法和化合物
AU2021213297A1 (en) * 2020-01-27 2022-08-18 Eirgen Pharma Ltd. Tetrahydrocyclopenta[b]indole compounds for the treatment of renal disease
US11986461B1 (en) * 2023-08-24 2024-05-21 King Faisal University 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1H-imidazol-2-yl)pyridin-2-ol as an antitumor and antimicrobial compound

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4988820A (en) * 1986-02-21 1991-01-29 Bayer Aktiengesellschaft Cycloalkano(1,2-B) indole-sulponamides
GB8924392D0 (en) * 1989-10-30 1989-12-20 Bayer Ag Substituted cycloalkano/b/dihydroindole-and-indolesulphonamides
GB9008108D0 (en) * 1990-04-10 1990-06-06 Bayer Ag Cycloalkano(b)dihydroindoles and-indolesulphonamides substituted by heterocycles
DE4027278A1 (de) * 1990-08-29 1992-03-05 Bayer Ag Heterocyclisch substituierte indolsulfonamide
DE4131346A1 (de) * 1991-09-20 1993-03-25 Bayer Ag Indolsulfonamid substituierte dihydropyridine, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln
AU7558900A (en) * 1999-10-14 2001-04-23 Kaken Pharmaceutical Co., Ltd. Tetrahydroquinoline derivatives
WO2003014082A1 (fr) 2001-08-09 2003-02-20 Eli Lilly And Company Derives de cyclopenta b indole utilises comme inhibiteurs de spla2
DE10164564B4 (de) * 2001-12-14 2007-05-16 Zentaris Gmbh Tetrahydrocarbazolderivate als Liganden für G-Protein gekoppelte Rezeptoren (GPCR)
EP2423190A1 (fr) * 2002-05-16 2012-02-29 Shionogi&Co., Ltd. Composés présentant un antagonisme du récepteur PGD 2
US20060074124A1 (en) * 2003-09-12 2006-04-06 Andrew Napper Methods of treating a disorder
US20050245540A1 (en) * 2003-12-09 2005-11-03 Fujisawa Pharmaceutical Co., Ltd. New methods
US7019022B2 (en) 2003-12-15 2006-03-28 Merck Frosst Canada & Co. Substituted tetrahydrocarbazole and cyclopentanoindole derivatives
BRPI0507657A (pt) * 2004-03-03 2007-07-10 Lilly Co Eli composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, método para tratar um distúrbio, e, uso de um composto ou um sal farmaceuticamente aceitável do mesmo
JP2008520674A (ja) * 2004-11-22 2008-06-19 スミスクライン ビーチャム コーポレーション Hcvインヒビター
JP2008520742A (ja) 2004-11-23 2008-06-19 ピーティーシー セラピューティクス, インコーポレイテッド Vegf産生の阻害に有用なカルバゾール誘導体、カルボリン誘導体およびインドール誘導体
JP2008530229A (ja) 2005-02-17 2008-08-07 ワイス シクロアルキル縮合インドール、ベンゾチオフェン、ベンゾフランおよびインデン誘導体
DK1902026T3 (da) 2005-06-24 2010-04-26 Lilly Co Eli Tetrahydrocarbazol-derivater, der kan anvendes som androgen-receptor-modulatorer (SARM)
WO2007047604A2 (fr) 2005-10-18 2007-04-26 Elixir Pharmaceuticals, Inc. Inhibition de sirt1
WO2008019825A1 (fr) 2006-08-14 2008-02-21 Santhera Pharmaceuticals (Schweiz) Ag Utilisation de dérivés d'indole tricycliques pour le traitement de maladies musculaires
BRPI0912394A2 (pt) 2008-05-16 2016-07-26 Lilly Co Eli moduladores do receptor de androgênio à base de tetra-hidrociclopenta[b]indol

Also Published As

Publication number Publication date
MY154547A (en) 2015-06-30
EP2094658A2 (fr) 2009-09-02
ATE538091T1 (de) 2012-01-15
JP2010510231A (ja) 2010-04-02
CN101541749A (zh) 2009-09-23
WO2008063867A3 (fr) 2008-07-31
NO20092103L (no) 2009-05-28
CL2007003182A1 (es) 2008-06-27
CN101541749B (zh) 2013-03-27
US7968587B2 (en) 2011-06-28
TWI398438B (zh) 2013-06-11
EA015627B1 (ru) 2011-10-31
CO6190513A2 (es) 2010-08-19
SI2094658T1 (sl) 2012-04-30
TW200827347A (en) 2008-07-01
CA2670340C (fr) 2014-05-20
PL2094658T3 (pl) 2012-05-31
TN2009000189A1 (en) 2010-10-18
MX2009005251A (es) 2009-08-19
BRPI0719092A2 (pt) 2013-12-03
WO2008063867A2 (fr) 2008-05-29
CA2670340A1 (fr) 2008-05-29
IL198410A (en) 2013-09-30
CY1112284T1 (el) 2015-12-09
NZ576296A (en) 2011-11-25
ECSP099350A (es) 2009-06-30
AU2007324046B2 (en) 2012-04-05
AR063559A1 (es) 2009-02-04
BRPI0719092B8 (pt) 2021-05-25
DK2094658T3 (da) 2012-02-13
US20100069404A1 (en) 2010-03-18
KR101121471B1 (ko) 2012-02-28
ES2376048T3 (es) 2012-03-08
NO342531B1 (no) 2018-06-11
JP5399259B2 (ja) 2014-01-29
UA98777C2 (en) 2012-06-25
EA200970500A1 (ru) 2009-10-30
ZA200903096B (en) 2010-07-28
BRPI0719092B1 (pt) 2020-08-18
AU2007324046A1 (en) 2008-05-29
EP2094658B1 (fr) 2011-12-21
RS52191B (sr) 2012-10-31
PE20081161A1 (es) 2008-08-15
PT2094658E (pt) 2012-02-22
CR10802A (es) 2009-07-13
KR20090082229A (ko) 2009-07-29
HRP20120032T1 (hr) 2012-02-29
IL198410A0 (en) 2010-02-17
HK1134089A1 (en) 2010-04-16
JO2800B1 (en) 2014-03-15

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