NO20023009D0 - Pyrrolidiner som inhiberer CAMP-spesifikk PDE - Google Patents

Pyrrolidiner som inhiberer CAMP-spesifikk PDE

Info

Publication number
NO20023009D0
NO20023009D0 NO20023009A NO20023009A NO20023009D0 NO 20023009 D0 NO20023009 D0 NO 20023009D0 NO 20023009 A NO20023009 A NO 20023009A NO 20023009 A NO20023009 A NO 20023009A NO 20023009 D0 NO20023009 D0 NO 20023009D0
Authority
NO
Norway
Prior art keywords
pyrrolidines
specific pde
inhibit camp
camp
inhibit
Prior art date
Application number
NO20023009A
Other languages
English (en)
Other versions
NO20023009L (no
Inventor
Timothy J Martins
Kerry W Fowler
Joshua Odingo
Laurence E Burgess
Stephen T Schlachter
Original Assignee
Icos Corp
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 Icos Corp filed Critical Icos Corp
Publication of NO20023009D0 publication Critical patent/NO20023009D0/no
Publication of NO20023009L publication Critical patent/NO20023009L/no

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    • 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
    • A61K31/40—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
    • A61K31/40—Heterocyclic 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
    • A61K31/4025—Heterocyclic 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 not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • 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
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Veterinary Medicine (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Life Sciences & Earth Sciences (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
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  • Neurosurgery (AREA)
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  • Pulmonology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Endocrinology (AREA)
  • Cardiology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Dermatology (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Reproductive Health (AREA)
  • Ophthalmology & Optometry (AREA)
  • Oncology (AREA)
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NO20023009A 1999-12-23 2002-06-21 Pyrrolidiner som inhiberer CAMP-spesifikk PDE NO20023009L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US17202399P 1999-12-23 1999-12-23
PCT/US2000/034116 WO2001047879A1 (en) 1999-12-23 2000-12-15 Pyrrolidines which inhibit camp-specific pde

Publications (2)

Publication Number Publication Date
NO20023009D0 true NO20023009D0 (no) 2002-06-21
NO20023009L NO20023009L (no) 2002-08-19

Family

ID=22626053

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20023009A NO20023009L (no) 1999-12-23 2002-06-21 Pyrrolidiner som inhiberer CAMP-spesifikk PDE

Country Status (16)

Country Link
US (1) US6376489B1 (no)
EP (1) EP1244619A1 (no)
JP (1) JP2003519122A (no)
KR (1) KR20020063601A (no)
CN (1) CN1246311C (no)
AU (1) AU778795B2 (no)
BR (1) BR0016687A (no)
CA (1) CA2395173A1 (no)
EA (1) EA007589B1 (no)
HU (1) HUP0300169A3 (no)
IL (1) IL150287A0 (no)
MX (1) MXPA02006206A (no)
NO (1) NO20023009L (no)
PL (1) PL355893A1 (no)
WO (1) WO2001047879A1 (no)
ZA (1) ZA200205015B (no)

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US6680336B2 (en) * 1999-12-15 2004-01-20 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6794192B2 (en) * 2000-06-29 2004-09-21 Pfizer Inc. Target
WO2002022605A1 (en) 2000-09-15 2002-03-21 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6660731B2 (en) 2000-09-15 2003-12-09 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6989385B2 (en) 2000-12-21 2006-01-24 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US20050101000A1 (en) * 2002-12-11 2005-05-12 Isis Pharmaceuticals Inc. Modulation of phosphodiesterase 4B expression
EA200500299A1 (ru) 2002-08-02 2005-08-25 Вертекс Фармасьютикалз Инкорпорейтед Пиразольные композиции, используемые в качестве ингибиторов gsk-3
US7138423B2 (en) * 2004-07-20 2006-11-21 Bristol-Myers Squibb Company Arylpyrrolidine derivatives as NK-1 /SSRI antagonists
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP2275095A3 (en) 2005-08-26 2011-08-17 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
JP2009512711A (ja) 2005-10-21 2009-03-26 ブレインセルス，インコーポレイティド Ｐｄｅ阻害による神経新生の調節
CA2625210A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
AU2007249435A1 (en) 2006-05-09 2007-11-22 Braincells, Inc. 5 HT receptor mediated neurogenesis
WO2007134136A2 (en) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenesis by modulating angiotensin
KR20090064418A (ko) 2006-09-08 2009-06-18 브레인셀즈 인코퍼레이션 4-아실아미노피리딘 유도체 포함 조합물
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
US20150119399A1 (en) 2012-01-10 2015-04-30 President And Fellows Of Harvard College Beta-cell replication promoting compounds and methods of their use
JO3264B1 (ar) * 2013-03-13 2018-09-16 Lilly Co Eli مركبات ازيتيدينيل أوكسي فينيل بيروليدين
DK3150578T3 (da) * 2014-05-29 2021-01-18 Mitsubishi Tanabe Pharma Corp Ny pyrrolidinforbindelse og anvendelse som melanocortin-receptoragonist
ES2967094T3 (es) 2017-09-29 2024-04-26 Mitsubishi Tanabe Pharma Corp Compuesto de pirrolidina ópticamente activo y procedimiento de producción del mismo
WO2020125627A1 (zh) * 2018-12-18 2020-06-25 湖北生物医药产业技术研究院有限公司 苯基吡咯烷类化合物及其用途
CN113563246A (zh) * 2020-04-29 2021-10-29 广东东阳光药业有限公司 取代的氮杂五元环类衍生物及其在药物中的应用

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JPS5821622B2 (ja) 1973-02-28 1983-05-02 ウェルファイド株式会社 ピロリジンメタノ−ル ノ セイゾウホウ
PT100441A (pt) 1991-05-02 1993-09-30 Smithkline Beecham Corp Pirrolidinonas, seu processo de preparacao, composicoes farmaceuticas que as contem e uso
SK279285B6 (sk) * 1991-05-02 1998-09-09 Daiichi Pharmaceutical Co. Použitie n-(2,6-dimetylfenyl)-2-(2-oxo-1-pyrolidin
US5665754A (en) 1993-09-20 1997-09-09 Glaxo Wellcome Inc. Substituted pyrrolidines
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CA2143143A1 (en) 1994-03-08 1995-09-09 Toshihiko Tanaka 3-phenylpyrrolidine derivatives
DE19601938A1 (de) 1996-01-12 1997-07-17 Schering Ag Neue Phosphodiesteraseinhibitoren
US5908858A (en) * 1996-04-05 1999-06-01 Sankyo Company, Limited 1,2-diphenylpyrrole derivatives, their preparation and their therapeutic uses

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PL355893A1 (en) 2004-05-31
BR0016687A (pt) 2003-02-25
JP2003519122A (ja) 2003-06-17
CA2395173A1 (en) 2001-07-05
EA200200591A1 (ru) 2002-12-26
KR20020063601A (ko) 2002-08-03
CN1246311C (zh) 2006-03-22
HUP0300169A3 (en) 2009-03-30
IL150287A0 (en) 2002-12-01
HUP0300169A2 (en) 2003-05-28
WO2001047879A1 (en) 2001-07-05
EA007589B1 (ru) 2006-12-29
NO20023009L (no) 2002-08-19
US6376489B1 (en) 2002-04-23
MXPA02006206A (es) 2004-02-26
CN1434798A (zh) 2003-08-06
AU778795B2 (en) 2004-12-23
ZA200205015B (en) 2004-04-08
EP1244619A1 (en) 2002-10-02
AU2106501A (en) 2001-07-09

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