EE04781B1 - 2-fenüülasendatud imidasotriasinoonid kui fosfodiesteraasi inhibiitorid ja nende valmistamismeetod - Google Patents

2-fenüülasendatud imidasotriasinoonid kui fosfodiesteraasi inhibiitorid ja nende valmistamismeetod

Info

Publication number
EE04781B1
EE04781B1 EEP200000291A EEP200000291A EE04781B1 EE 04781 B1 EE04781 B1 EE 04781B1 EE P200000291 A EEP200000291 A EE P200000291A EE P200000291 A EEP200000291 A EE P200000291A EE 04781 B1 EE04781 B1 EE 04781B1
Authority
EE
Estonia
Prior art keywords
phenyl
preparation
phosphodiesterase inhibitors
substituted imidazotriazinones
imidazotriazinones
Prior art date
Application number
EEP200000291A
Other languages
English (en)
Estonian (et)
Inventor
Niew�Hner Ulrich
Es-Sayed Mazen
Haning Helmut
Schenke Thomas
Schlemmer Karl-Heinz
Keldenich J�Rg
Bischoff Erwin
Perzborn Elisabeth
Dembowsky Klaus
Serno Peter
Nowakowski Marc
Original Assignee
Bayer Aktiengesellschaft
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27217917&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EE04781(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from DE19750085A external-priority patent/DE19750085A1/de
Priority claimed from DE1998112462 external-priority patent/DE19812462A1/de
Priority claimed from DE1998140289 external-priority patent/DE19840289A1/de
Application filed by Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Publication of EE200000291A publication Critical patent/EE200000291A/xx
Publication of EE04781B1 publication Critical patent/EE04781B1/xx

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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • 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
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • 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
    • 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
    • A61P9/06Antiarrhythmics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Endocrinology (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Vascular Medicine (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
EEP200000291A 1997-11-12 1998-10-31 2-fenüülasendatud imidasotriasinoonid kui fosfodiesteraasi inhibiitorid ja nende valmistamismeetod EE04781B1 (et)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19750085A DE19750085A1 (de) 1997-11-12 1997-11-12 2-Phenyl-substituierte Imidazotriazinone
DE1998112462 DE19812462A1 (de) 1998-03-23 1998-03-23 2-[2-Ethoxy-5(4-ethyl-piperazin-1-sulfonyl) -phenyl]-5-methyl-7-prophyl-3H-imidazo[5,1-f][1,2,4]triazin-4-on Dihydrochlorid
DE1998140289 DE19840289A1 (de) 1998-09-04 1998-09-04 2-Phenyl-substituierte Imidazotriazinone
PCT/EP1998/006910 WO1999024433A1 (fr) 1997-11-12 1998-10-31 Imidazotriazinones a substitution 2-phenyle utilisees comme inhibiteurs des phosphodiesterases

Publications (2)

Publication Number Publication Date
EE200000291A EE200000291A (et) 2001-06-15
EE04781B1 true EE04781B1 (et) 2007-02-15

Family

ID=27217917

Family Applications (1)

Application Number Title Priority Date Filing Date
EEP200000291A EE04781B1 (et) 1997-11-12 1998-10-31 2-fenüülasendatud imidasotriasinoonid kui fosfodiesteraasi inhibiitorid ja nende valmistamismeetod

Country Status (44)

Country Link
US (9) US6362178B1 (fr)
EP (3) EP1049695B1 (fr)
JP (2) JP3356428B2 (fr)
KR (2) KR100548120B1 (fr)
CN (2) CN1123573C (fr)
AR (2) AR013759A1 (fr)
AT (1) ATE213246T1 (fr)
AU (1) AU738675B2 (fr)
BG (1) BG65257B1 (fr)
BR (2) BR9812785A (fr)
CA (2) CA2309332C (fr)
CH (1) CH693954A5 (fr)
CO (1) CO4980861A1 (fr)
CU (1) CU23063A3 (fr)
CY (1) CY1112949T1 (fr)
CZ (1) CZ301911B6 (fr)
DE (3) DE19881732D2 (fr)
DK (3) DK1049695T3 (fr)
EE (1) EE04781B1 (fr)
ES (3) ES2386420T3 (fr)
FI (1) FI113772B (fr)
GB (1) GB2346877B (fr)
HK (2) HK1031730A1 (fr)
HN (1) HN1998000175A (fr)
HR (2) HRP20000292B1 (fr)
HU (3) HU228196B1 (fr)
ID (1) ID25871A (fr)
IL (3) IL135462A0 (fr)
IN (1) IN188419B (fr)
LU (1) LU90561B1 (fr)
MY (1) MY138535A (fr)
NO (2) NO314940B1 (fr)
NZ (1) NZ504436A (fr)
PE (1) PE131799A1 (fr)
PL (2) PL194801B1 (fr)
PT (2) PT1174431E (fr)
SE (1) SE522809C2 (fr)
SI (2) SI1049695T1 (fr)
SK (1) SK287161B6 (fr)
TR (1) TR200001338T2 (fr)
TW (2) TWI229081B (fr)
UA (1) UA46166C2 (fr)
UY (2) UY25246A1 (fr)
WO (1) WO1999024433A1 (fr)

Families Citing this family (165)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040014761A1 (en) * 1997-10-28 2004-01-22 Place Virgil A. Treatment of female sexual dysfunction with phosphodiesterase inhibitors
US6403597B1 (en) * 1997-10-28 2002-06-11 Vivus, Inc. Administration of phosphodiesterase inhibitors for the treatment of premature ejaculation
EP1049695B1 (fr) * 1997-11-12 2002-02-13 Bayer Ag Imidazotriazinones a substitution 2-phenyle utilisees comme inhibiteurs des phosphodiesterases
DE19827640A1 (de) 1998-06-20 1999-12-23 Bayer Ag 7-Alkyl- und Cycloalkyl-substituierte Imidazotriazinone
US7235625B2 (en) 1999-06-29 2007-06-26 Palatin Technologies, Inc. Multiple agent therapy for sexual dysfunction
DE19944161A1 (de) * 1999-09-15 2001-03-22 Bayer Ag Neue Kombination zur Behandlung von sexueller Dysfunktion
CA2323008C (fr) * 1999-10-11 2005-07-12 Pfizer Inc. Composes pharmaceutiques actifs
US20050070499A1 (en) * 1999-11-08 2005-03-31 Pfizer Inc. Compounds for the treatment of female sexual dysfunction
IL139455A0 (en) * 1999-11-08 2001-11-25 Pfizer Compounds for the treatment of female sexual dysfunction
JP2003519151A (ja) 1999-12-24 2003-06-17 バイエル アクチェンゲゼルシャフト トリアゾロトリアジノンおよびそれらの使用
EP1252165A1 (fr) 1999-12-24 2002-10-30 Bayer Aktiengesellschaft Isoxazolopyrimidinones et leur utilisation
US6803365B2 (en) * 1999-12-24 2004-10-12 Bayer Aktlengesellschaft Imidazo[1,3,5]triazinones and the use thereof
DE10010067A1 (de) 2000-03-02 2001-09-06 Bayer Ag Neue Imidazotriazinone und ihre Verwendung
EP1278522B1 (fr) 2000-04-19 2006-10-25 Lilly Icos LLC Utilisation d'inhibiteurs de phosphodiesterase specifique de gmp cyclique pour le traitement de la maladie de parkinson
US6821978B2 (en) * 2000-09-19 2004-11-23 Schering Corporation Xanthine phosphodiesterase V inhibitors
AU2001290146A1 (en) * 2000-09-29 2002-04-08 Glaxo Group Limited Compounds useful in the treatment of inflammatory diseases
US6548508B2 (en) 2000-10-20 2003-04-15 Pfizer, Inc. Use of PDE V inhibitors for improved fecundity in mammals
US20020091129A1 (en) * 2000-11-20 2002-07-11 Mitradev Boolell Treatment of premature ejaculation
DE10063108A1 (de) * 2000-12-18 2002-06-20 Bayer Ag Verfahren zur Herstellung von Sulfonamid-substituierten Imidazotriazinonen
DE10063106A1 (de) * 2000-12-18 2002-06-20 Bayer Ag Verfahren zur Herstellung von 2-(2-Ethoxyphenyl)-substituierten Imidazotriazinonen
DE10064105A1 (de) 2000-12-21 2002-06-27 Bayer Ag Neue Substituierte Imidazotriazinone
CA2436576A1 (fr) * 2001-02-02 2002-08-08 Pfizer Inc. Traitement du diabete sucre
DE10107639A1 (de) * 2001-02-15 2002-08-22 Bayer Ag 2-Alkoxyphenyl-substituierte Imidazotriazinone
DE10108752A1 (de) * 2001-02-23 2002-09-05 Bayer Ag Neue Substituierte Imidazotriazinone
GB0107751D0 (en) * 2001-03-28 2001-05-16 Pfizer Ltd Pharmaceutically active compounds
DE10118306A1 (de) 2001-04-12 2002-10-17 Bayer Ag Imidazotriazinonhaltige Zusammensetzungen zur nasalen Applikation
ATE348618T1 (de) * 2001-05-09 2007-01-15 Bayer Healthcare Ag Neue verwendung von 2-(2-ethoxy-5-(4-methyl- piperazin-1-sulfonyl)-phenyl)-5-methyl-7-propyl 3h-imidazo(5,1-f)(1,2,4)triazin-4-on
US20070122353A1 (en) 2001-05-24 2007-05-31 Hale Ron L Drug condensation aerosols and kits
US20030051728A1 (en) 2001-06-05 2003-03-20 Lloyd Peter M. Method and device for delivering a physiologically active compound
US7087605B2 (en) 2001-06-01 2006-08-08 Bayer Aktiengesellschaft 5-Ethyl-imidazotriazinones
GB0113344D0 (en) * 2001-06-01 2001-07-25 Bayer Ag Novel heterocycles 3
DE10130167A1 (de) 2001-06-22 2003-01-02 Bayer Ag Imidazotriazine
DE10135815A1 (de) * 2001-07-23 2003-02-06 Bayer Ag Verwendung von 2-Alkoxyphenyl-substituierten Imidazotriazinonen
JP4450365B2 (ja) 2001-08-28 2010-04-14 シェーリング コーポレイション 多環式グアニンホスホジエステラーゼv阻害剤
JP2005509038A (ja) 2001-11-09 2005-04-07 シェーリング コーポレイション 多環式グアニン誘導体ホスホジエステラーゼv阻害剤
GB0129274D0 (en) * 2001-12-06 2002-01-23 Pfizer Ltd Novel kit
CA2439784C (fr) * 2001-12-13 2010-11-02 Daiichi Suntory Pharma Co., Ltd. Derives de pyrazolopyrimidinone possedant une activite inhibitrice de pde7
GB0130219D0 (en) * 2001-12-18 2002-02-06 Pfizer Ltd Compounds for the treatment of sexual dysfunction
GB0209988D0 (en) * 2002-05-01 2002-06-12 Bayer Ag Novel Heterocycles
DE10220570A1 (de) 2002-05-08 2003-11-20 Bayer Ag Carbamat-substituierte Pyrazolopyridine
US7091207B2 (en) 2002-05-22 2006-08-15 Virginia Commonwealth University Method of treating myocardial infarction with PDE-5 inhibitors
RU2004133973A (ru) * 2002-05-23 2005-09-10 Пфайзер Инк. (US) Новая комбинация
SI1509525T1 (sl) 2002-05-31 2006-12-31 Schering Corp Postopek priprave inhibitorjev ksantinske fosfodiesteraze V in njihovih prekurzorjev
GB0214784D0 (en) * 2002-06-26 2002-08-07 Pfizer Ltd Novel combination
DE10229778A1 (de) * 2002-07-03 2004-01-29 Bayer Ag Neue Verwendung von Imidazotriazinonen
DE10230605A1 (de) 2002-07-08 2004-01-29 Bayer Ag Substituierte Imidazotriazine
DE10232113A1 (de) * 2002-07-16 2004-01-29 Bayer Ag Vardenafil Hydrochlorid Trihydrat enthaltende Arzneimittel
GB0219961D0 (en) 2002-08-28 2002-10-02 Pfizer Ltd Oxytocin inhibitors
US7323462B2 (en) 2002-12-10 2008-01-29 Pfizer Inc. Morpholine dopamine agonists
RU2331438C2 (ru) 2002-12-13 2008-08-20 Уорнер-Ламберт Компани Ллс Альфа-2-дельта лиганд для лечения симптомов нижних мочевыводящих путей
JP2006522127A (ja) * 2003-04-01 2006-09-28 スミスクライン ビーチャム コーポレーション イミダゾトリアジン化合物
OA13050A (en) 2003-04-29 2006-11-10 Pfizer Ltd 5,7-diaminopyrazolo [4,3-D] pyrimidines useful in the treatment of hypertension.
US20040220186A1 (en) * 2003-04-30 2004-11-04 Pfizer Inc. PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease
CA2526475A1 (fr) 2003-05-21 2004-12-02 Alexza Pharmaceuticals, Inc. Unite de chauffage autonome a allumage optique ou electrique, et unite d'administration de medicament utilisant cette unite de chauffage
MXPA05012302A (es) 2003-05-22 2006-01-30 Altana Pharma Ag Composicion que comprende un inhibidor de pde4 y un inhibidor de pde5.
CN100374441C (zh) 2003-06-06 2008-03-12 天津倍方科技发展有限公司 二氢吡咯[2,3-d]嘧啶-4-酮衍生物,其制备方法及其制药用途
JP2006219374A (ja) 2003-06-13 2006-08-24 Daiichi Asubio Pharma Co Ltd Pde7阻害作用を有するイミダゾトリアジノン誘導体
US20050079548A1 (en) * 2003-07-07 2005-04-14 Plexxikon, Inc. Ligand development using PDE4B crystal structures
US7291640B2 (en) * 2003-09-22 2007-11-06 Pfizer Inc. Substituted triazole derivatives as oxytocin antagonists
JP2007512345A (ja) * 2003-11-21 2007-05-17 シェーリング コーポレイション ホスホジエステラーゼv阻害剤処方物
US7572799B2 (en) * 2003-11-24 2009-08-11 Pfizer Inc Pyrazolo[4,3-d]pyrimidines as Phosphodiesterase Inhibitors
GB0327323D0 (en) * 2003-11-24 2003-12-31 Pfizer Ltd Novel pharmaceuticals
EP1708718A1 (fr) 2004-01-22 2006-10-11 Pfizer Limited Derives de triazole inhibant l'activite antagoniste de vasopressine
US7569572B2 (en) * 2004-04-07 2009-08-04 Pfizer Inc Pyrazolo[4,3-D]pyrimidines
DE102004023069A1 (de) 2004-05-11 2005-12-08 Bayer Healthcare Ag Neue Darreichungsformen des PDE 5-Inhibitors Vardenafil
JP2008501617A (ja) * 2004-06-11 2008-01-24 アスビオファーマ株式会社 Pde7阻害作用を有するイミダゾトリアジノン誘導体
DE102005001989A1 (de) * 2005-01-15 2006-07-20 Bayer Healthcare Ag Intravenöse Formulierungen von PDE-Inhibitoren
MX2007010144A (es) * 2005-02-18 2008-02-15 Surface Logix Inc Compuestos mejorados farmacocineticamente.
EP1848437A4 (fr) * 2005-02-18 2012-04-25 Surface Logix Inc Procedes de fabrication de composes a amelioration pharmacocinetique comportant des residus ou groupes fonctionnels et compositions pharmaceutiques comportant lesdits composes
DE102005009240A1 (de) * 2005-03-01 2006-09-07 Bayer Healthcare Ag Arzneiformen mit verbesserten pharmakokinetischen Eigenschaften
DE102005009241A1 (de) 2005-03-01 2006-09-07 Bayer Healthcare Ag Arzneiformen mit kontrollierter Bioverfügbarkeit
DE102005016345A1 (de) * 2005-04-09 2006-10-12 Bayer Healthcare Ag Neue Verwendung von 2-Phenyl-substituierten Imidazotriazinon-Derivaten
CN102614176A (zh) 2005-04-19 2012-08-01 奈科明有限责任公司 用于治疗肺动脉高血压的罗氟司特
PL1881985T3 (pl) 2005-05-12 2011-05-31 Pfizer Bezwodne krystaliczne postacie N-[1-(2-etoksyetylo)-5-(N-etylo-N-metyloamino)-7-(4-metylopirydyn-2-yloamino)-1H-pirazolo[4,3-d]pirymidyno-3-karbonylo]metano-sulfonoamidu
US20060264624A1 (en) * 2005-05-20 2006-11-23 Alexander Heim-Riether Methods for synthesizing imidazotriazinones
US20070010525A1 (en) * 2005-06-27 2007-01-11 Meyer Jackson Method and compositions for modulating neuropeptide hormone secretion
CA2618103A1 (fr) * 2005-08-10 2007-02-15 Pfizer Limited Derives de triazole substitues en tant qu'antagonistes d'oxytocine
EP2258359A3 (fr) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline
EP1928437A2 (fr) 2005-08-26 2008-06-11 Braincells, Inc. Neurogenese par modulation du recepteur muscarinique
KR20080056250A (ko) 2005-09-29 2008-06-20 바이엘 헬스케어 아게 비뇨기 장애의 치료를 위한 pde 억제제 및 이들의 조합
WO2007047282A1 (fr) * 2005-10-12 2007-04-26 Lilly Icos Llc Traitement d'une hypertrophie benigne de la prostate et de symptomes dans les voies urinaires inferieures
EP1940389A2 (fr) 2005-10-21 2008-07-09 Braincells, Inc. Modulation de la neurogenese par inhibition de la pde
EP2314289A1 (fr) 2005-10-31 2011-04-27 Braincells, Inc. Modulation de la neurogenese dont la médiation est assurée par récepteur gaba
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
CN101415670A (zh) * 2006-02-17 2009-04-22 惠氏公司 制备磺酰胺取代醇和其中间体的方法
AR059517A1 (es) * 2006-02-17 2008-04-09 Wyeth Corp N- sulfonilacion selectiva de alcoholes sustituidos con 2- aminotrifluoralquilo
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
US7977478B2 (en) * 2006-03-13 2011-07-12 Dr. Reddy's Laboratories Limited Polymorphic forms of vardenafil
SG170737A1 (en) * 2006-03-17 2011-05-30 Univ Johns Hopkins N-hydroxylsulfonamide derivatives as new physiologically useful nitroxyl donors
WO2007124045A2 (fr) * 2006-04-20 2007-11-01 Ampla Pharmaceuticals, Inc. Potentialisation d'activité de récepteur mc4
EP2377531A2 (fr) 2006-05-09 2011-10-19 Braincells, Inc. Neurogénèse par modulation de l'angiotensine
EP2026813A2 (fr) 2006-05-09 2009-02-25 Braincells, Inc. Neurogenèse induite par le récepteur 5ht
WO2008000418A2 (fr) 2006-06-27 2008-01-03 Sandoz Ag Nouveau procédé de préparation de sel
US20090298878A1 (en) * 2006-07-14 2009-12-03 Akira Matsumura Oxime compounds and the use thereof
AU2007287024A1 (en) * 2006-08-24 2008-02-28 Surface Logix, Inc. Pharmacokinetically improved compounds
AR062501A1 (es) 2006-08-29 2008-11-12 Actelion Pharmaceuticals Ltd Composiciones terapeuticas
WO2008030651A1 (fr) 2006-09-08 2008-03-13 Braincells, Inc. Combinaisons contenant un dérivé de 4-acylaminopyridine
DE102006043443A1 (de) * 2006-09-15 2008-03-27 Bayer Healthcare Ag Neue aza-bicyclische Verbindungen und ihre Verwendung
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
US8314119B2 (en) 2006-11-06 2012-11-20 Abbvie Inc. Azaadamantane derivatives and methods of use
WO2008073928A1 (fr) 2006-12-12 2008-06-19 Gilead Colorado, Inc. Composition de traitement de l'hypertension pulmonaire
KR20130122023A (ko) 2007-02-12 2013-11-06 디엠아이 바이오사이언시스 인코포레이티드 트라마돌의 부작용을 감소시키는 방법
WO2008100886A1 (fr) * 2007-02-12 2008-08-21 Auspex Pharmaceuticals, Inc. Modulateurs de la pde5 hautement sélectifs et à longue durée d'action
KR20090121315A (ko) 2007-02-12 2009-11-25 디엠아이 바이오사이언시스 인코포레이티드 조루 및 발기부전을 동시에 치료하는 방법
US20080216828A1 (en) 2007-03-09 2008-09-11 Alexza Pharmaceuticals, Inc. Heating unit for use in a drug delivery device
DE102007027067A1 (de) 2007-06-12 2008-12-18 Ratiopharm Gmbh Verfahren zur Herstellung eines Arzneimittels enthaltend Vardenafil Hydrochlorid Trihydrat
JP2010532319A (ja) * 2007-06-13 2010-10-07 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト 聴覚障害の処置用のpde阻害剤
WO2009030095A1 (fr) * 2007-09-06 2009-03-12 Topharman Shanghai Co., Ltd. Procédé de préparation de vardénafil et de ses intermédiaires
WO2009082845A1 (fr) 2007-12-28 2009-07-09 Topharman Shanghai Co., Ltd. N-{1-[3-(2-éthoxy-5-(4-éthylpipérazinyl)benzènesulfonyl)-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl]éthyl}butyramide, son procédé de préparation et son utilisation
WO2009091777A1 (fr) * 2008-01-15 2009-07-23 Forest Laboratories Holdings Limited Le nébivolol dans le traitement du dysfonctionnement sexuel
DE102008063992A1 (de) 2008-12-19 2010-09-02 Lerner, Zinoviy, Dipl.-Ing. Neue aliphatisch substituierte Pyrazolopyridine und ihre Verwendung
EP2379076B1 (fr) 2008-12-23 2014-11-12 The Trustees of Columbia University in the City of New York Inhibiteurs de la phosphodiestérase et utilisations de ces derniers
WO2010099217A1 (fr) 2009-02-25 2010-09-02 Braincells, Inc. Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine
GB0903493D0 (en) 2009-02-27 2009-04-08 Vantia Ltd New compounds
DE102009020888A1 (de) 2009-05-12 2010-11-18 Ratiopharm Gmbh Schmelztablette, enthaltend ein Vardenafil-Salz
WO2011016016A1 (fr) 2009-08-07 2011-02-10 Ranbaxy Laboratories Limited Procédés de préparation de vardénafil
UY33041A (es) 2009-11-27 2011-06-30 Bayer Schering Pharma Aktienegesellschaft Procedimiento para la preparaciòn de {4,6-diamino-2-[1-(2-fluorobencil)-1h-pirazolo[3,4-b]piridin-3-il]pirimidin-5-il}carbamato de metilo y su purificaciòn para el uso como principio activo farmacèutico
RS59908B1 (sr) 2009-11-27 2020-03-31 Adverio Pharma Gmbh Postupak za proizvodnju metil-{4,6-diamino-2-[1-(2-fluorobenzil)-1h-pirazolo[3,4-b]piridin-3-il]pirimidin-5-il}metilkarbamata
JP5806231B2 (ja) 2009-12-21 2015-11-10 アセフ エス.アー. 勃起障害の治療における血管拡張剤としてのクベビン、ジベンジルブチルロラクトリンリグナン、その半合成誘導体および合成誘導体、ならびに他のリグナンおよびネオリグナン
PL390079A1 (pl) * 2009-12-30 2011-07-04 Zakłady Farmaceutyczne POLPHARMA Spółka Akcyjna Sposób otrzymywania wardenafilu i jego izolacji jako soli z kwasem cytrynowym oraz krystaliczna postać tej soli
JP2013523809A (ja) 2010-04-05 2013-06-17 エスケー ケミカルズ カンパニー リミテッド Pde5抑制剤を含む皮膚しわ改善用組成物
DE102010021637A1 (de) 2010-05-26 2011-12-01 Bayer Schering Pharma Aktiengesellschaft Substituierte 5-Fluor-1H-Pyrazolopyridine und ihre Verwendung
CN102382129B (zh) * 2010-08-19 2014-02-26 山东轩竹医药科技有限公司 螺环取代的磷酸二酯酶抑制剂
CN102372730B (zh) * 2010-08-19 2014-03-26 山东轩竹医药科技有限公司 桥环取代的磷酸二酯酶抑制剂
EP2619208B1 (fr) 2010-09-20 2016-11-09 Ironwood Pharmaceuticals, Inc. Composés imidazotriazinones
AU2011305462B2 (en) 2010-09-23 2015-11-26 Abbvie Bahamas Ltd. Monohydrate of an azaadamantane derivative
PL2637664T3 (pl) 2010-10-15 2017-09-29 Gilead Sciences, Inc. Kompozycje i metody leczenia nadciśnienia płucnego
TWI462739B (zh) 2010-11-02 2014-12-01 Univ Kaohsiung Medical Sildenafil-同族物四級銨哌嗪鹽類之製備及醫療用途
CN102134242B (zh) * 2011-01-21 2013-08-28 浙江大德药业集团有限公司 一种用于治疗阳痿的快速长效的化合物
MX370433B (es) 2011-10-10 2019-12-13 H Lundbeck As Derivados de 7h-imidazo [1-5-a] pirazin-8-ona como inhibidores de la fosfodiasterasa 9(pde9); y el uso de los mismos en el tratamiento de trastornos neurodegenerativos.
AT512084A1 (de) * 2011-10-20 2013-05-15 Univ Wien Tech Diazabicyclo- und diazaspiro-alkanderivate als phosphodiesterase-5 inhibitoren
US9402877B2 (en) 2011-11-04 2016-08-02 Xion Pharmaceuticals Corporation Methods and compositions for oral administration of melanocortin receptor agonist compounds
CZ303877B6 (cs) * 2011-11-24 2013-06-05 Zentiva, K.S. Zpusob prípravy a izolace solí vardenafilu s kyselinami
EP2804603A1 (fr) 2012-01-10 2014-11-26 President and Fellows of Harvard College Composés promoteurs de réplication des cellules bêta et leurs procédés d'utilisation
WO2013109738A1 (fr) 2012-01-17 2013-07-25 The Trustees Of Columbia University In The City Of New York Nouveaux inhibiteurs de la phosphodiestérase et utilisations de ceux-ci
AP2014007820A0 (en) 2012-01-26 2014-07-31 Lundbeck & Co As H PDE9 inhibitors with imidazo triazinone backbone
CN104168895B (zh) 2012-02-28 2020-02-21 首尔制药株式会社 包含西地那非作为活性成分的掩蔽苦味的高含量快速溶解膜
EP2828262A4 (fr) 2012-03-19 2015-09-23 Forum Pharmaceuticals Inc Composés d'imidazotriazinone
CN103374002B (zh) * 2012-04-19 2015-07-15 山东轩竹医药科技有限公司 磷酸二酯酶-5抑制剂
CZ307091B6 (cs) 2012-09-14 2018-01-10 Zentiva, K.S. Stabilní farmaceutický přípravek obsahující Vardenafil hydrochlorid
CN109498628A (zh) 2012-12-04 2019-03-22 株式会社阿丽浱欧 包含5型磷酸二酯酶抑制剂的神经细胞的细胞凋亡抑制用组合物的用途
KR101953735B1 (ko) 2012-12-14 2019-03-04 한미약품 주식회사 포스포다이에스터라제-5 억제제를 포함하는 츄정
BR112015019571A2 (pt) 2013-02-21 2017-07-18 Adverio Pharma Gmbh formas de {4,6-diamino-2-[1-(2-fluorobenzil)-1h-pirazolo[3,4-b]piridino-3-il]pirimidino-5-il}metilcarbamato de metila
CN104109164B (zh) * 2013-04-18 2016-05-25 广州朗圣药业有限公司 一种适合工业化的高纯度盐酸伐地那非三水合物的制备方法
ES2776353T3 (es) 2013-07-17 2020-07-30 Univ Columbia Inhibidores de la fosfodiesterasa novedosos y usos de los mismos
WO2015089105A1 (fr) 2013-12-09 2015-06-18 Respira Therapeutics, Inc. Formulations en poudre d'inhibiteur pde5 et procédés y associés
PL223869B1 (pl) * 2013-12-16 2016-11-30 Starogardzkie Zakłady Farm Polpharma Spółka Akcyjna Sposób otrzymywania wardenafilu i jego soli
KR101645652B1 (ko) 2014-11-03 2016-08-08 (주)퓨젠바이오농업회사법인 세리포리아 락세라타에 의해 생산되는 세포외다당체를 유효성분으로 함유하는 성기능개선용 조성물
DK3303339T3 (da) 2015-07-07 2021-04-12 H Lundbeck As Pde9-inhibitorer med imidazotriazinonskelet og imidazopyrazinonskelet til behandling af perifere sygdomme
CN108290896B (zh) 2015-11-16 2021-09-28 托帕杜制药公司 2-苯基-3,4-二氢吡咯并[2,1-f][1,2,4]三嗪酮衍生物及其用途
WO2017168174A1 (fr) 2016-04-02 2017-10-05 N4 Pharma Uk Limited Nouvelles formes pharmaceutiques du sildénafil
EP3554507A1 (fr) 2016-12-14 2019-10-23 Respira Therapeutics, Inc. Procédés et compositions de traitement de l'hypertension pulmonaire et d'autres troubles des poumons
KR20200010228A (ko) 2017-05-22 2020-01-30 토파두르 파마 아게 가용성 구아닐레이트 사이클라제 활성제 및 포스포디에스테라제 억제제의 신규한 이중 작용 방식 및 이의 용도
CN107445964A (zh) * 2017-07-29 2017-12-08 合肥创新医药技术有限公司 一种盐酸伐地那非杂质的合成方法
JP2021506986A (ja) 2017-12-20 2021-02-22 クラリア・ファルマ・ホールディング・アクチボラグ バルデナフィルを含むフィルム配合物、その調製法、およびその使用
CA3103695A1 (fr) 2018-06-14 2019-12-19 Astrazeneca Uk Limited Methodes de traitement d'une dysfonction erectile avec une composition pharmaceutique d'inhibiteur de phosphodiesterase 5 specifique de cgmp
CN112997258A (zh) 2018-06-14 2021-06-18 阿斯利康(英国)有限公司 用cGMP特异性磷酸二酯酶5抑制剂药物组合物治疗勃起功能障碍的方法
EP3887376A1 (fr) * 2018-11-28 2021-10-06 Topadur Pharma AG Nouveaux activateurs de la guanylate cyclase solubles à double mode d'action, inhibiteurs de phosphodiestérase et leurs utilisations
CN113518771A (zh) 2019-03-13 2021-10-19 大塚制药株式会社 向含有仲胺的化合物的胺部分导入氘代低级烷基的方法
WO2021245192A1 (fr) 2020-06-04 2021-12-09 Topadur Pharma Ag Nouveaux activateurs de la guanylate cyclase soluble à double mode d'action et inhibiteurs de phosphodiestérase et leurs utilisations
JP2023552632A (ja) * 2020-12-11 2023-12-18 イルドン ファーマシューティカル カンパニー リミテッド アンドロゲン受容体及びホスホジエステラーゼ二重阻害剤としての新規化合物
CN114085225A (zh) * 2021-06-04 2022-02-25 广东西捷药业有限公司 一种伐地那非类似物及其合成方法和应用
IL310526A (en) 2021-09-29 2024-03-01 Topadur Pharma Ag Topical compounds of 2-phenyl-4,3-dihydropyrrolo[2,F-L][4,2,1]triazinone derivatives and their uses
WO2023166013A1 (fr) 2022-03-02 2023-09-07 Topadur Pharma Ag Compositions topiques et leurs utilisations
KR20230129639A (ko) 2022-03-02 2023-09-11 연세대학교 산학협력단 이중작용 pde5 억제제/질산유기에스터의 국소 혈류 증진을 위한 경피 투약 형태

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US26565A (en) * 1859-12-27 Improved register for railroad-cars
DE812845C (de) 1944-12-07 1951-09-06 Georges Lissac Brille
US2705715A (en) 1952-10-29 1955-04-05 American Cyanamid Co Purine compounds and methods of preparing the same
CH367510A (de) 1957-11-27 1963-02-28 Ciba Geigy Verfahren zur Herstellung neuer Sulfonamide
GB1042471A (en) 1963-01-16 1966-09-14 Ilford Ltd Penta-azaindenes, their production and use in photographic emulsions
GB1051734A (fr) 1963-01-16
US3169129A (en) 1963-05-10 1965-02-09 American Cyanamid Co 2-ortho-hydroxy-phenyl-4-(3h)-quinazolinones
USRE26565E (en) 1966-03-02 1969-04-29 Table iii
GB1338235A (en) 1970-12-15 1973-11-21 May & Baker Ltd Azapurinones
GB1493685A (en) 1970-12-15 1977-11-30 May & Baker Ltd 8-azapurinones
BE791025A (fr) * 1971-11-19 1973-05-07 Allen & Hanburys Ltd Composes heterocycliques
GB1457873A (en) * 1973-01-04 1976-12-08 Allen & Hanburys Ltd Imidazotriazines
US4052390A (en) 1973-06-12 1977-10-04 May & Baker Limited Azapurinones
US4060615A (en) 1976-02-18 1977-11-29 Mead Johnson & Company 2-Piperazinyl-6,7-dimethoxyquinazolines
GB1561345A (en) 1976-10-22 1980-02-20 May & Baker Ltd 8 - azapuring - 6 - ones
US4159330A (en) 1976-11-02 1979-06-26 Carlo Erba S.P.A. 2-Disubstituted phenyl-3,4-dihydro-4-oxo-quinazoline derivatives and process for their preparation
DK109578A (da) 1977-03-25 1978-09-26 Allen & Hanburys Ltd Fremgangsmaade til fremstilling af heterocycliske forbindelser
GB1584461A (en) 1977-03-25 1981-02-11 Allen & Hanburys Ltd Imidazotriazines imidazotriazinones and pharmaceutical compositions containing them
US4308384A (en) 1978-09-18 1981-12-29 Glaxo Group Limited Production of triazinones
US4287673A (en) * 1980-01-11 1981-09-08 Sunbeam Corporation Hair dryer diffuser
EP0054132B1 (fr) 1980-12-12 1984-10-10 Dr. Karl Thomae GmbH Pyrimidones, leur préparation et médicaments les contenant
US4431440A (en) 1981-02-20 1984-02-14 American Cyanamid Company Method to alter or control the development and/or the life cycle of various plant species
JPS60246396A (ja) 1984-05-22 1985-12-06 Sankyo Co Ltd 酵素阻害物質ジヒドロデスオキシグリゼオ−ル酸及びその塩類
US4666908A (en) 1985-04-05 1987-05-19 Warner-Lambert Company 5-Substituted pyrazolo[4,3-d]pyrimidine-7-ones and methods of use
CA1303037C (fr) 1987-02-02 1992-06-09 Smith Kline & French Laboratories Limited Derives de purinone utilises comme bronchodilatateurs,vasodilatateurs et agents anti-allergiques
US5254571A (en) 1988-04-21 1993-10-19 Smith Kline & French Laboratories Ltd. Chemical compounds
GB8814352D0 (en) 1988-06-16 1988-07-20 Smith Kline French Lab Chemical compounds
ES2058527T3 (es) 1988-06-16 1994-11-01 Smith Kline French Lab Derivados de pirimidina condensados procedimiento y compuestos intermedios para su preparacion y composiciones farmaceuticas que los contienen.
US5075310A (en) 1988-07-01 1991-12-24 Smith Kline & French Laboratories, Ltd. Pyrimidone derivatives as bronchodilators
US4923874A (en) 1988-07-21 1990-05-08 G. D. Searle & Co. Use of 8-azapurin-6-one derivatives for control of hypertension
GB8817651D0 (en) 1988-07-25 1988-09-01 Smith Kline French Lab Chemical compounds
GB8827988D0 (en) 1988-11-30 1989-01-05 Smith Kline French Lab Chemical compounds
US5574020A (en) * 1989-09-28 1996-11-12 Eli Lilly And Company Tilmicosin formulation
GB8928346D0 (en) 1989-12-15 1990-02-21 Smith Kline French Lab Chemical compounds
JPH05506011A (ja) * 1990-04-11 1993-09-02 ジ・アップジョン・カンパニー 流動床コーティングによるイブプロフェンの味覚マスキング
GB9013750D0 (en) * 1990-06-20 1990-08-08 Pfizer Ltd Therapeutic agents
US5250534A (en) 1990-06-20 1993-10-05 Pfizer Inc. Pyrazolopyrimidinone antianginal agents
GB9114760D0 (en) * 1991-07-09 1991-08-28 Pfizer Ltd Therapeutic agents
US5316906A (en) 1991-08-23 1994-05-31 Molecular Probes, Inc. Enzymatic analysis using substrates that yield fluorescent precipitates
GB9119704D0 (en) * 1991-09-14 1991-10-30 Pfizer Ltd Therapeutic agents
GB9121028D0 (en) * 1991-10-03 1991-11-13 Pfizer Ltd Therapeutic agents
GB9126260D0 (en) * 1991-12-11 1992-02-12 Pfizer Ltd Therapeutic agents
US5294612A (en) 1992-03-30 1994-03-15 Sterling Winthrop Inc. 6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereof
GB9213623D0 (en) * 1992-06-26 1992-08-12 Pfizer Ltd Therapeutic agents
US5734053A (en) 1992-06-26 1998-03-31 Pfizer Inc Purinone antianginal agents
GB9218322D0 (en) 1992-08-28 1992-10-14 Pfizer Ltd Therapeutic agents
GB9311920D0 (en) * 1993-06-09 1993-07-28 Pfizer Ltd Therapeutic agents
GB9312210D0 (en) 1993-06-14 1993-07-28 Smithkline Beecham Plc Chemical compounds
GB9315017D0 (en) 1993-07-20 1993-09-01 Glaxo Lab Sa Chemical compounds
WO1995007267A1 (fr) 1993-09-10 1995-03-16 Eisai Co., Ltd. Compose de quinazoline
US6143746A (en) * 1994-01-21 2000-11-07 Icos Corporation Tetracyclic cyclic GMP-specific phosphodiesterase inhibitors, process of preparation and use
US5374053A (en) * 1994-01-21 1994-12-20 Heidelberger Druckmaschinen Ag Device for changing the transport position of products
US5556847A (en) * 1994-10-27 1996-09-17 Duquesne University Of The Holy Ghost Methods of effecting memory enhancement mediated by steroid sulfatase inhibitors
GB9423911D0 (en) * 1994-11-26 1995-01-11 Pfizer Ltd Therapeutic agents
GB9514464D0 (en) 1995-07-14 1995-09-13 Glaxo Lab Sa Medicaments
GB9612514D0 (en) * 1996-06-14 1996-08-14 Pfizer Ltd Novel process
EP1049695B1 (fr) * 1997-11-12 2002-02-13 Bayer Ag Imidazotriazinones a substitution 2-phenyle utilisees comme inhibiteurs des phosphodiesterases
US6221402B1 (en) * 1997-11-20 2001-04-24 Pfizer Inc. Rapidly releasing and taste-masking pharmaceutical dosage form
DE19827640A1 (de) * 1998-06-20 1999-12-23 Bayer Ag 7-Alkyl- und Cycloalkyl-substituierte Imidazotriazinone
UA67802C2 (uk) * 1998-10-23 2004-07-15 Пфайзер Рісьоч Енд Дівелепмент Компані, Н.В./С.А. Фармацевтична композиція з контрольованим вивільненням інгібітора цгмф фде-5 (варіанти), спосіб її одержання та спосіб лікування еректильної дисфункції
US6075028A (en) * 1999-09-23 2000-06-13 Graham; Richard Method of treating Tourette's syndrome and related CNS disorders
CA2323008C (fr) * 1999-10-11 2005-07-12 Pfizer Inc. Composes pharmaceutiques actifs
US6803365B2 (en) * 1999-12-24 2004-10-12 Bayer Aktlengesellschaft Imidazo[1,3,5]triazinones and the use thereof
ATE348618T1 (de) * 2001-05-09 2007-01-15 Bayer Healthcare Ag Neue verwendung von 2-(2-ethoxy-5-(4-methyl- piperazin-1-sulfonyl)-phenyl)-5-methyl-7-propyl 3h-imidazo(5,1-f)(1,2,4)triazin-4-on
DE10232113A1 (de) * 2002-07-16 2004-01-29 Bayer Ag Vardenafil Hydrochlorid Trihydrat enthaltende Arzneimittel

Also Published As

Publication number Publication date
HU228196B1 (en) 2013-01-28
US7314871B2 (en) 2008-01-01
CN1508137A (zh) 2004-06-30
EP1049695B1 (fr) 2002-02-13
EP1049695A1 (fr) 2000-11-08
SE522809C2 (sv) 2004-03-09
KR100430355B1 (ko) 2004-05-04
HU230154B1 (hu) 2015-09-28
GB2346877B (en) 2001-12-05
SK287161B6 (sk) 2010-02-08
DK200000766A (da) 2000-05-09
EP1174431B1 (fr) 2012-05-30
IL135462A0 (en) 2001-05-20
SI1049695T1 (en) 2002-06-30
DE19881732C1 (de) 2002-01-31
US7122540B2 (en) 2006-10-17
TWI229081B (en) 2005-03-11
CA2395558C (fr) 2007-07-17
DE19881732D2 (de) 2000-08-24
US7704999B2 (en) 2010-04-27
BG65257B1 (bg) 2007-10-31
SE0001745D0 (sv) 2000-05-11
US20130059844A1 (en) 2013-03-07
US6566360B1 (en) 2003-05-20
SK7092000A3 (en) 2001-03-12
IN188419B (fr) 2002-09-21
CN100430396C (zh) 2008-11-05
CY1112949T1 (el) 2016-04-13
ES2386420T3 (es) 2012-08-20
PL194801B1 (pl) 2007-07-31
PL201336B1 (pl) 2009-03-31
EP1174431A2 (fr) 2002-01-23
BR9816155B1 (pt) 2010-07-27
ATE213246T1 (de) 2002-02-15
HN1998000175A (es) 1999-01-08
DK176852B1 (en) 2009-12-14
ID25871A (id) 2000-11-09
EP2295436A1 (fr) 2011-03-16
PL340400A1 (en) 2001-01-29
GB2346877A (en) 2000-08-23
JP2002348290A (ja) 2002-12-04
CZ20001759A3 (cs) 2000-10-11
IL135462A (en) 2006-04-10
HUP0100394A3 (en) 2002-05-28
MY138535A (en) 2009-06-30
SI1174431T1 (sl) 2012-09-28
CA2395558A1 (fr) 1999-05-20
US20040067945A1 (en) 2004-04-08
JP2001522851A (ja) 2001-11-20
NO20002444D0 (no) 2000-05-11
DK1049695T3 (da) 2002-05-13
US20060189615A1 (en) 2006-08-24
AU738675B2 (en) 2001-09-20
UY25671A1 (es) 2000-03-31
US6362178B1 (en) 2002-03-26
CN1123573C (zh) 2003-10-08
IL163475A (en) 2015-11-30
ES2172945T3 (es) 2002-10-01
US7696206B2 (en) 2010-04-13
TR200001338T2 (tr) 2000-08-21
PT1174431E (pt) 2012-07-24
US20050070541A1 (en) 2005-03-31
BG104406A (en) 2001-08-31
AR013759A1 (es) 2001-01-10
UA46166C2 (uk) 2002-05-15
DK1174431T3 (da) 2012-08-20
US20100016323A1 (en) 2010-01-21
CO4980861A1 (es) 2000-11-27
WO1999024433A1 (fr) 1999-05-20
NO20021714L (no) 2000-05-11
CN1278822A (zh) 2001-01-03
HK1031730A1 (en) 2001-06-22
TW513431B (en) 2002-12-11
PT1049695E (pt) 2002-07-31
US6890922B2 (en) 2005-05-10
ES2194567A1 (es) 2003-11-16
HRP20020585A2 (en) 2005-10-31
HK1067124A1 (en) 2005-04-01
NO314940B1 (no) 2003-06-16
KR100548120B1 (ko) 2006-02-02
FI113772B (fi) 2004-06-15
EE200000291A (et) 2001-06-15
US20110009367A1 (en) 2011-01-13
UY25246A1 (es) 2001-08-27
HRP20020585B1 (hr) 2013-02-28
JP4388729B2 (ja) 2009-12-24
AR035972A2 (es) 2004-07-28
FI20001086A (fi) 2000-05-09
HUP0100394A2 (hu) 2001-09-28
CZ301911B6 (cs) 2010-07-28
SE0001745L (sv) 2000-05-11
US20080113972A1 (en) 2008-05-15
EP1174431A3 (fr) 2002-01-30
GB0010974D0 (en) 2000-06-28
CU23063A3 (es) 2005-07-19
BR9812785A (pt) 2000-10-10
JP3356428B2 (ja) 2002-12-16
CH693954A5 (de) 2004-05-14
HRP20000292B1 (en) 2008-09-30
CA2309332C (fr) 2002-12-03
NO20021714D0 (no) 2002-04-11
AU1558799A (en) 1999-05-31
KR20040014591A (ko) 2004-02-14
NZ504436A (en) 2001-08-31
CA2309332A1 (fr) 1999-05-20
DE59803108D1 (de) 2002-03-21
KR20010031944A (ko) 2001-04-16
PE131799A1 (es) 1999-12-30
LU90561B1 (de) 2000-12-01
HRP20000292A2 (en) 2001-04-30
NO20002444L (no) 2000-05-11
ES2194567B1 (es) 2005-03-01
HU227841B1 (en) 2012-05-02

Similar Documents

Publication Publication Date Title
EE04781B1 (et) 2-fenüülasendatud imidasotriasinoonid kui fosfodiesteraasi inhibiitorid ja nende valmistamismeetod
PT916675E (pt) Processo para preparacao de sildenafil
IL136308A0 (en) Antipicornaviral compounds and methods for their use and preparation
AR017655A1 (es) Metodo para preparar eteres de monofluormetilo
ZA988469B (en) Pyrrolidin-2-one compounds and their use as neuraminidase inhibitors
HU9801540D0 (en) Process for manufacturing components made of steel
FI951514A (fi) Uusia mono- ja bisyklisiä DNA-gyraasiinhibiittoreita
BR9800557A (pt) Processo contínuo para preparação de 4-aminopiperidinas
PT912603E (pt) Processo para preparar certos aza ciclo-hexapeptidos
FI964310A (fi) Imidatsolijohdannainen ja menetelmä sen valmistamiseksi
AU1354199A (en) Process for the preparation of urea
NO996432L (no) Fremgangsmåte for fremstilling av 4-substituert-1H-indol-3- glykosamider
PT998470E (pt) Processo de preparacao de derivados aminados de alquiloxifuranona compostos provenientes desse processo e utilizacao desses compostos
NO995388D0 (no) Fremgangsmåte for fremstilling av formylfosfonsyre
BR9804794A (pt) Processo para prepara-Æo de 1-alquil-4-(2-cloro-3-alcÄxi-4-alquil-sulfonil-benzoil) -5-hidrÄxi-pirazol e compostos relacioonados
ZA987741B (en) Process for the preparation of oxazaphosphorine-2-amines
IL120322A0 (en) Process for the preparation of thifluzamide
HUP0001757A3 (en) Improved process for the preparation of halo-4-phenoxyquinolines
IL135553A0 (en) Process for the preparation of azacycloalkyalkanoyl pseudotetrapeptides
NO20003077D0 (no) FremgangsmÕte for fremstilling av klorbenzooksazolen
FI971964A (fi) Menetelmä 1-halo-3-trialkyylisilasnyylibentseenijohdannaisten valmistamiseksi
EE200100333A (et) Meetod 2-halo-3-nitro-4-aminopüridiini valmistamiseks ja selleks vajalike vaheühendite saamine
ZA988190B (en) Process for the preparation of 1-phenylpyrazoline-3-carboxylic acid derivatives
NO994557D0 (no) Fremgangsmaate for fremstilling av arylaminotriazolopyridiner
IL131765A0 (en) Process for the purification of substituted p-nitrodiphenylethers

Legal Events

Date Code Title Description
GB1A Change in the ownership or in the address of the owner
KB4A Valid patent at the end of a year

Effective date: 20071231

KB4A Valid patent at the end of a year

Effective date: 20081231

GB1A Change in the ownership or in the address of the owner
KB4A Valid patent at the end of a year

Effective date: 20101231