MA33105B1 - Esters (1-phényl-2-pyridin-4-yl) éthyliques d'acide benzoïque en tant qu'inhibiteurs de la phosphodiestérase - Google Patents

Esters (1-phényl-2-pyridin-4-yl) éthyliques d'acide benzoïque en tant qu'inhibiteurs de la phosphodiestérase

Info

Publication number
MA33105B1
MA33105B1 MA34150A MA34150A MA33105B1 MA 33105 B1 MA33105 B1 MA 33105B1 MA 34150 A MA34150 A MA 34150A MA 34150 A MA34150 A MA 34150A MA 33105 B1 MA33105 B1 MA 33105B1
Authority
MA
Morocco
Prior art keywords
phenyl
inhibitors
phosphodiesterase
pyridin
benzoic acid
Prior art date
Application number
MA34150A
Other languages
Arabic (ar)
English (en)
Inventor
Gabriele Amari
Elisabetta Armani
Maurizio Delcanale
Original Assignee
Chiesi Farma Spa
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=40674203&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA33105(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Chiesi Farma Spa filed Critical Chiesi Farma Spa
Publication of MA33105B1 publication Critical patent/MA33105B1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00—Inhalators
    • A61M15/0065—Inhalators with dosage or measuring devices
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4704—2-Quinolinones, e.g. carbostyril
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10—Preparation of respiratory gases or vapours
    • A61M16/14—Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/61—Halogen atoms or nitro radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Anesthesiology (AREA)
  • Biophysics (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Otolaryngology (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE DES INHIBITEURS DE L'ENZYME PHOSPHODIESTÉRASE 4 (PDE4). PLUS PARTICULIÈREMENT, L'INVENTION CONCERNE DES COMPOSÉS QUI SONT DÉRIVÉS D'ALCOOLS 1-PHÉNYL-2-PYRIDINYL ALKYLIQUES, DES PROCÉDÉS DE PRÉPARATION DESDITS COMPOSÉS, DES COMPOSITIONS LES COMPRENANT, LEURS COMBINAISONS ET LEURS UTILISATIONS THÉRAPEUTIQUES. DANS LA FORMULE (I), N REPRÉSENTE O OU 1; R1 ET R2 PEUVENT ÊTRE IDENTIQUES OU DIFFÉRENTS, ET SONT SÉLECTIONNÉS DANS LE GROUPE CONSTITUÉ PAR: - ALKYLE C1-C6 LINÉAIRE OU RAMIFIÉ; - OR3 OÙ R3 REPRÉSENTE ALKYLE C1-C6 ÉVENTUELLEMENT SUBSTITUÉ PAR UN OU PLUSIEURS GROUPES CYCLOALKYLES C3-C7; ET - HNSO2R4 OÙ R4 REPRÉSENTE ALKYLE C1-C4 ÉVENTUELLEMENT SUBSTITUÉ PAR UN OU PLUSIEURS ATOMES D'HALOGÈNE OU PAR UN GROUPE C1-C4, R1 ET/OU R2 REPRÉSENTANT HNSO2R4. LES AUTRES VARIABLES SONT TELLES QUE DÉFINIES DANS LES REVENDICATIONS.
MA34150A 2009-02-06 2010-02-04 Esters (1-phényl-2-pyridin-4-yl) éthyliques d'acide benzoïque en tant qu'inhibiteurs de la phosphodiestérase MA33105B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09001660A EP2216327A1 (fr) 2009-02-06 2009-02-06 Benzoate de (1-Phenyl-2-Pyridin-4-yl)ethyle en tant qu'inhibiteurs de phosphodiestérase
PCT/EP2010/000676 WO2010089107A1 (fr) 2009-02-06 2010-02-04 Esters (1-phényl-2-pyridin-4-yl) éthyliques d'acide benzoïque en tant qu'inhibiteurs de la phosphodiestérase

Publications (1)

Publication Number Publication Date
MA33105B1 true MA33105B1 (fr) 2012-03-01

Family

ID=40674203

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34150A MA33105B1 (fr) 2009-02-06 2010-02-04 Esters (1-phényl-2-pyridin-4-yl) éthyliques d'acide benzoïque en tant qu'inhibiteurs de la phosphodiestérase

Country Status (34)

Country Link
US (5) US8440834B2 (fr)
EP (2) EP2216327A1 (fr)
JP (2) JP5612610B2 (fr)
KR (1) KR101337728B1 (fr)
CN (1) CN102317262B (fr)
AR (1) AR075243A1 (fr)
AU (1) AU2010211274B2 (fr)
BR (1) BRPI1005695A8 (fr)
CA (1) CA2751494C (fr)
CL (1) CL2011001876A1 (fr)
CO (1) CO6400217A2 (fr)
CY (1) CY1113764T1 (fr)
EA (1) EA019113B1 (fr)
ES (1) ES2395528T3 (fr)
GE (1) GEP20135919B (fr)
HK (1) HK1162508A1 (fr)
HR (1) HRP20121004T1 (fr)
IL (1) IL214446A (fr)
JO (1) JO2761B1 (fr)
MA (1) MA33105B1 (fr)
ME (1) ME02325B (fr)
MX (1) MX2011007857A (fr)
MY (1) MY152048A (fr)
NZ (1) NZ594413A (fr)
PE (1) PE20120055A1 (fr)
PL (1) PL2393782T3 (fr)
PT (1) PT2393782E (fr)
RS (1) RS52605B (fr)
SG (1) SG173208A1 (fr)
SI (1) SI2393782T1 (fr)
TN (1) TN2011000346A1 (fr)
TW (1) TWI459945B (fr)
UA (1) UA102574C2 (fr)
WO (1) WO2010089107A1 (fr)

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EP2022783A1 (fr) * 2007-08-08 2009-02-11 CHIESI FARMACEUTICI S.p.A. Dérivés d'alcools 1-phényl-2-pyridinylalkyliques en tant qu'inhibiteurs de la phosphodiestérase
EP2216327A1 (fr) 2009-02-06 2010-08-11 CHIESI FARMACEUTICI S.p.A. Benzoate de (1-Phenyl-2-Pyridin-4-yl)ethyle en tant qu'inhibiteurs de phosphodiestérase
MA34449B1 (fr) * 2010-08-03 2013-08-01 Chiesi Farma Spa Formulation de poudre seche comprenant un inhibiteur de phosphodiesterase
CN103052378A (zh) 2010-08-03 2013-04-17 奇斯药制品公司 包含磷酸二酯酶抑制剂的药物制剂
CN106946848B (zh) 2011-06-06 2022-01-04 奇斯药制品公司 作为磷酸二酯酶抑制剂的1-苯基-2-吡啶基烷基醇的衍生物
CN103827088B (zh) * 2011-09-26 2017-10-13 奇斯药制品公司 作为磷酸二酯酶抑制剂的1‑苯基‑2‑吡啶基烷基醇的衍生物
WO2013057013A2 (fr) 2011-10-21 2013-04-25 Chiesi Farmaceutici S.P.A. Dérivés d'alcools 1-phényl-2-pyridinylalkyliques utilisés comme inhibiteurs de phosphodiestérase
WO2013087749A1 (fr) * 2011-12-16 2013-06-20 Chiesi Farmaceutici S.P.A. Potentialisation induite par des inhibiteurs de pdea dans le traitement de la leucémie
BR112014029642A2 (pt) * 2012-06-04 2017-06-27 Chiesi Farm Spa composto, combinação de um composto, composição farmacêutica, uso de um composto, dispositivo e kit
KR20150090253A (ko) * 2012-12-05 2015-08-05 키에시 파르마슈티시 엣스. 피. 에이. Pde4-억제제로서 페닐에틸피리딘 유도체
PL2928869T3 (pl) 2012-12-05 2019-08-30 Chiesi Farmaceutici S.P.A. Pochodne alkoholu 1-fenylo-2-pirydynyloalkilowego jako inhibitory fosfodiesterazy
EP2928880B1 (fr) * 2012-12-05 2018-02-14 Chiesi Farmaceutici S.p.A. Dérivés de phenylethylpyridine comme inhibiteurs de pde4 et en tant qu'antagonistes des récepteurs muscariniques
WO2014086855A1 (fr) * 2012-12-05 2014-06-12 Chiesi Farmaceutici S.P.A. Dérivés de phényléthylpyridine en tant qu'inhibiteurs de pde4
US9427376B2 (en) 2013-10-10 2016-08-30 Chiesi Farmaceutici S.P.A. Process for preparing pharmaceutical formulations for inhalation comprising a high-dosage strength active ingredient
EP3293176B1 (fr) 2013-10-22 2020-12-02 Chiesi Farmaceutici S.p.A. Forme crystalline d'un inhibiteur pde4
US9145409B2 (en) 2013-12-05 2015-09-29 Chiesi Farmaceutici S.P.A Benzhydryl derivatives
TW201607944A (zh) 2013-12-05 2016-03-01 吉斯藥品公司 雜芳基衍生物
WO2015185128A1 (fr) * 2014-06-04 2015-12-10 Chiesi Farmaceutici S.P.A. Dérivés de 3,5-dichloro,4-(3,4-(cyclo-)alcoxyphényl)-2-carbonyloxy)éthyl)pyridine utilisés comme inhibiteurs de pde-4
WO2015185130A1 (fr) * 2014-06-04 2015-12-10 Chiesi Farmaceutici S.P.A. Dérivés de 3,5-dichloro,4-(3,4-(cyclo-)alcoxyphényl)--2-carbonyloxy)éthyl)pyridine utilisés comme inhibiteurs de pde-4
US9763924B2 (en) * 2014-06-05 2017-09-19 Chiesi Farmaceutici S.P.A. Aminoester derivatives
US9326976B2 (en) * 2014-06-05 2016-05-03 Chiesi Farmaceutici S.P.A. Carbamate derivatives
WO2017089347A1 (fr) 2015-11-25 2017-06-01 Inserm (Institut National De La Sante Et De La Recherche Medicale) Procédés et compositions pharmaceutiques pour le traitement de mélanomes résistant aux inhibiteurs de braf
US20190275022A1 (en) * 2016-07-20 2019-09-12 Allergan, Inc. Methods, compositions, and compounds for treatment of dermatological and ocular conditions
BR112020012972A2 (pt) * 2017-12-28 2020-11-24 Chiesi Farmaceutici S.P.A. uso de derivados de álcool 1-fenil-2-piridinil alquílico para tratar fibrose cística
US11813360B2 (en) 2018-07-27 2023-11-14 Chiesi Farmaceutici S.P.A. Carrier particles for dry powder formulations for inhalation
CN115466169B (zh) * 2021-06-10 2024-03-26 中国医学科学院药物研究所 取代邻苯二酚醚类化合物及其制备方法和应用
CN118475343A (zh) 2021-12-21 2024-08-09 凯西制药公司 填充在具有改善的耐湿性的吸入器中的干粉制剂
WO2023208982A1 (fr) 2022-04-27 2023-11-02 Chiesi Farmaceutici S.P.A. Forme cristalline d'un inhibiteur de pde4
WO2024027901A1 (fr) 2022-08-02 2024-02-08 Chiesi Farmaceutici S.P.A. Biomarqueur prédictif de réponse clinique à un inhibiteur de pde4
WO2024062005A1 (fr) 2022-09-22 2024-03-28 Chiesi Farmaceutici S.P.A. Inhalateur à capsule pour l'administration d'un inhibiteur de phosphodiestérase-4
WO2024062006A1 (fr) 2022-09-22 2024-03-28 Chiesi Farmaceutici S.P.A. Inhalateur à capsule pour l'administration d'un inhibiteur de phosphodiestérase-4
WO2024062007A1 (fr) 2022-09-22 2024-03-28 Chiesi Farmaceutici S.P.A. Inhalateur à capsule pour l'administration d'un inhibiteur de phosphodiestérase-4

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WO2008006509A1 (fr) * 2006-07-14 2008-01-17 Chiesi Farmaceutici S.P.A. Derivés d'alcools de 1-phényl-2-pyridynyl alkylène en tant qu'inhibiteurs de phosphodiestérase
EP2022783A1 (fr) 2007-08-08 2009-02-11 CHIESI FARMACEUTICI S.p.A. Dérivés d'alcools 1-phényl-2-pyridinylalkyliques en tant qu'inhibiteurs de la phosphodiestérase
EP2070913A1 (fr) 2007-12-14 2009-06-17 CHIESI FARMACEUTICI S.p.A. Dérivés d'ester en tant qu'inhibiteurs de la phosphodiestérase
EP2110375A1 (fr) 2008-04-14 2009-10-21 CHIESI FARMACEUTICI S.p.A. Inhibiteurs de la phosphodiestérase de type 4 appartenant à la classe tertiaire d'amine
EP2216327A1 (fr) 2009-02-06 2010-08-11 CHIESI FARMACEUTICI S.p.A. Benzoate de (1-Phenyl-2-Pyridin-4-yl)ethyle en tant qu'inhibiteurs de phosphodiestérase
CN103052378A (zh) 2010-08-03 2013-04-17 奇斯药制品公司 包含磷酸二酯酶抑制剂的药物制剂
MA34449B1 (fr) 2010-08-03 2013-08-01 Chiesi Farma Spa Formulation de poudre seche comprenant un inhibiteur de phosphodiesterase
CN106946848B (zh) 2011-06-06 2022-01-04 奇斯药制品公司 作为磷酸二酯酶抑制剂的1-苯基-2-吡啶基烷基醇的衍生物
CN103827088B (zh) 2011-09-26 2017-10-13 奇斯药制品公司 作为磷酸二酯酶抑制剂的1‑苯基‑2‑吡啶基烷基醇的衍生物
WO2013057013A2 (fr) 2011-10-21 2013-04-25 Chiesi Farmaceutici S.P.A. Dérivés d'alcools 1-phényl-2-pyridinylalkyliques utilisés comme inhibiteurs de phosphodiestérase
BR112014029642A2 (pt) 2012-06-04 2017-06-27 Chiesi Farm Spa composto, combinação de um composto, composição farmacêutica, uso de um composto, dispositivo e kit
PL2928869T3 (pl) 2012-12-05 2019-08-30 Chiesi Farmaceutici S.P.A. Pochodne alkoholu 1-fenylo-2-pirydynyloalkilowego jako inhibitory fosfodiesterazy

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ES2395528T3 (es) 2013-02-13
HK1162508A1 (en) 2012-08-31
US8859778B2 (en) 2014-10-14
CN102317262B (zh) 2014-08-06
AR075243A1 (es) 2011-03-16
AU2010211274B2 (en) 2016-03-17
CN102317262A (zh) 2012-01-11
TN2011000346A1 (en) 2013-03-27
EP2393782B1 (fr) 2012-09-12
MX2011007857A (es) 2011-08-15
BRPI1005695A2 (pt) 2017-06-06
SI2393782T1 (sl) 2013-01-31
US20140378423A1 (en) 2014-12-25
US20130012487A1 (en) 2013-01-10
UA102574C2 (ru) 2013-07-25
IL214446A (en) 2014-12-31
EP2393782A1 (fr) 2011-12-14
US20100204256A1 (en) 2010-08-12
CL2011001876A1 (es) 2011-10-28
US8648204B2 (en) 2014-02-11
PL2393782T3 (pl) 2013-02-28
US20140179647A1 (en) 2014-06-26
ME02325B (me) 2016-06-20
EP2216327A1 (fr) 2010-08-11
HRP20121004T1 (hr) 2012-12-31
JO2761B1 (en) 2014-03-15
PT2393782E (pt) 2012-12-26
IL214446A0 (en) 2011-09-27
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US20130289010A1 (en) 2013-10-31
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US9056176B2 (en) 2015-06-16
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US8440834B2 (en) 2013-05-14
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