NO312960B1 - PDE IV-inhiberende 2-cyanoiminoimidazol-derivater - Google Patents

PDE IV-inhiberende 2-cyanoiminoimidazol-derivater Download PDF

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Publication number
NO312960B1
NO312960B1 NO19991560A NO991560A NO312960B1 NO 312960 B1 NO312960 B1 NO 312960B1 NO 19991560 A NO19991560 A NO 19991560A NO 991560 A NO991560 A NO 991560A NO 312960 B1 NO312960 B1 NO 312960B1
Authority
NO
Norway
Prior art keywords
formula
compounds
acid
hydrogen
dihydro
Prior art date
Application number
NO19991560A
Other languages
English (en)
Norwegian (no)
Other versions
NO991560L (no
NO991560D0 (no
Inventor
Eddy Jean Edgard Freyne
Francisco Javi Fernandez-Gadea
Jose Ignacio Andres-Gil
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of NO991560D0 publication Critical patent/NO991560D0/no
Publication of NO991560L publication Critical patent/NO991560L/no
Publication of NO312960B1 publication Critical patent/NO312960B1/no

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • C07D233/48Nitrogen atoms not forming part of a nitro radical with acyclic hydrocarbon or substituted acyclic hydrocarbon radicals, attached to said nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/88Nitrogen atoms, e.g. allantoin

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
NO19991560A 1996-10-02 1999-03-30 PDE IV-inhiberende 2-cyanoiminoimidazol-derivater NO312960B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP96202749 1996-10-02
PCT/EP1997/005322 WO1998014432A1 (en) 1996-10-02 1997-09-24 Pde iv inhibiting 2-cyanoiminoimidazole derivatives

Publications (3)

Publication Number Publication Date
NO991560D0 NO991560D0 (no) 1999-03-30
NO991560L NO991560L (no) 1999-06-02
NO312960B1 true NO312960B1 (no) 2002-07-22

Family

ID=8224456

Family Applications (1)

Application Number Title Priority Date Filing Date
NO19991560A NO312960B1 (no) 1996-10-02 1999-03-30 PDE IV-inhiberende 2-cyanoiminoimidazol-derivater

Country Status (30)

Country Link
US (1) US6051718A (de)
EP (1) EP0934280B1 (de)
JP (1) JP3068208B2 (de)
KR (1) KR100520002B1 (de)
CN (1) CN1106387C (de)
AR (1) AR008875A1 (de)
AT (1) ATE236884T1 (de)
AU (1) AU719561B2 (de)
BG (1) BG64278B1 (de)
BR (1) BR9712256B1 (de)
CA (1) CA2267322C (de)
CY (1) CY2380B1 (de)
CZ (1) CZ297474B6 (de)
DE (1) DE69720757T2 (de)
DK (1) DK0934280T3 (de)
EE (1) EE03825B1 (de)
ES (1) ES2196308T3 (de)
HU (1) HU225158B1 (de)
IL (2) IL129298A0 (de)
MY (1) MY116980A (de)
NO (1) NO312960B1 (de)
NZ (1) NZ334971A (de)
PL (1) PL194673B1 (de)
PT (1) PT934280E (de)
RU (1) RU2180902C2 (de)
SI (1) SI0934280T1 (de)
SK (1) SK285878B6 (de)
TR (1) TR199900732T2 (de)
UA (1) UA62939C2 (de)
WO (1) WO1998014432A1 (de)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100596664B1 (ko) * 1998-04-01 2006-07-06 얀센 파마슈티카 엔.브이. Pde iv 억제용 피리딘 유도체
US6953774B2 (en) 2000-08-11 2005-10-11 Applied Research Systems Ars Holding N.V. Methods of inducing ovulation
WO2002085855A1 (fr) * 2001-04-19 2002-10-31 Eisai Co., Ltd. Derives de 2-iminopyrrolidine
JP4510383B2 (ja) 2001-05-23 2010-07-21 田辺三菱製薬株式会社 軟骨疾患修復治療用組成物
CN100358514C (zh) * 2001-07-11 2008-01-02 日研化学株式会社 过敏性眼疾病治疗剂
TWI221838B (en) 2001-08-09 2004-10-11 Tanabe Seiyaku Co Pyrazinoisoquinoline compound or naphthalene compound
UA80418C2 (en) 2001-12-14 2007-09-25 Applied Research Systems Methods of inducing ovulation using phosphodiesterase inhibitor as non-polypeptide camp level modulator.and method of collecting oocytes for in vitro fertilization
EP2444393A1 (de) 2003-02-19 2012-04-25 Eisai R&D Management Co., Ltd. Verfahren zur Herstellung von zyklischen Benzamidinderivaten
EP2258359A3 (de) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenese durch Modulation des Muscarinrezeptors mit Sabcomelin
WO2007025177A2 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2377530A3 (de) 2005-10-21 2012-06-20 Braincells, Inc. Modulation von Neurogenese durch PDE-Hemmung
EP1942879A1 (de) 2005-10-31 2008-07-16 Braincells, Inc. Gaba-rezeptor-vermittelte modulation von neurogenese
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
EP2021000A2 (de) 2006-05-09 2009-02-11 Braincells, Inc. Neurogenese mittels angiotensin-modulation
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
US9957247B2 (en) * 2012-06-07 2018-05-01 Georgia State University Research Foundation, Inc. SecA inhibitors and methods of making and using thereof
GB2533925A (en) * 2014-12-31 2016-07-13 Univ Bath Antimicrobial compounds, compositions and methods
CN109438434B (zh) * 2018-11-19 2021-05-04 华南农业大学 一种含噁唑环的2-氰基亚氨基噻唑烷类化合物及其制备方法和应用

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0784461B2 (ja) * 1986-12-19 1995-09-13 日本バイエルアグロケム株式会社 殺虫性ニトロイミノ又はシアノイミノ化合物
JPH05310650A (ja) * 1991-08-22 1993-11-22 Nippon Soda Co Ltd 新規なアミン誘導体、その製造方法及び殺虫剤
DE69333688T2 (de) * 1992-07-28 2005-11-03 Aventis Pharma Ltd., West Malling Inhibitoren von c-amp phosphodiesterase
JP3100984B2 (ja) * 1992-12-02 2000-10-23 ファイザー・インク. 選択的pde▲下i▼▲下v▼阻害物質としてのカテコールジエーテル類
GB9304919D0 (en) * 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
ZA945609B (en) * 1993-07-28 1995-05-12 Rhone Poulenc Rorer Ltd [Di(ether or thioether)heteroaryl or fluoro substituted aryl] compounds
JPH09502170A (ja) * 1993-08-19 1997-03-04 スミスクライン・ビーチャム・コーポレイション フェネチルアミン化合物
GB9401460D0 (en) * 1994-01-26 1994-03-23 Rhone Poulenc Rorer Ltd Compositions of matter
JP3056788B2 (ja) * 1994-06-24 2000-06-26 ユーロ−セルティーク,エス.エイ. ホスホジエステラーゼivの阻害化合物および阻害方法
TW332201B (en) * 1995-04-06 1998-05-21 Janssen Pharmaceutica Nv 1,3-Dihydro-1-(phenylalkyl)-2H-imidazol-2-one derivatives
TW375612B (en) * 1995-04-06 1999-12-01 Janssen Pharmaceutica Nv 1,3-dihydro-2H-imidazol-2-one derivatives for the treatment of disease states related to an abnormal enzymatic or catalytic activity of phosphodiesterase type IV, preparation thereof and pharmaceutical composition containing the same
TW424087B (en) * 1995-04-06 2001-03-01 Janssen Pharmaceutica Nv 1,3-dihydro-1-(phenylalkenyl)-2H-imidazol-2-one derivatives

Also Published As

Publication number Publication date
SI0934280T1 (en) 2003-12-31
CA2267322A1 (en) 1998-04-09
AR008875A1 (es) 2000-02-23
HUP9904063A2 (hu) 2000-09-28
KR20000029964A (ko) 2000-05-25
TR199900732T2 (xx) 1999-08-23
AU4779297A (en) 1998-04-24
US6051718A (en) 2000-04-18
SK285878B6 (sk) 2007-10-04
PL194673B1 (pl) 2007-06-29
DE69720757T2 (de) 2004-03-04
JP2000503678A (ja) 2000-03-28
NO991560L (no) 1999-06-02
CZ297474B6 (cs) 2006-12-13
EP0934280A1 (de) 1999-08-11
CN1232456A (zh) 1999-10-20
HUP9904063A3 (en) 2000-11-28
EE03825B1 (et) 2002-08-15
HU225158B1 (en) 2006-07-28
EE9900112A (et) 1999-10-15
KR100520002B1 (ko) 2005-10-13
MY116980A (en) 2004-04-30
ES2196308T3 (es) 2003-12-16
PL332573A1 (en) 1999-09-27
IL129298A (en) 2006-04-10
CZ102899A3 (cs) 1999-07-14
BR9712256A (pt) 1999-08-24
CY2380B1 (en) 2004-06-04
JP3068208B2 (ja) 2000-07-24
ATE236884T1 (de) 2003-04-15
AU719561B2 (en) 2000-05-11
DK0934280T3 (da) 2003-07-21
IL129298A0 (en) 2000-02-17
BG103220A (en) 1999-11-30
EP0934280B1 (de) 2003-04-09
CN1106387C (zh) 2003-04-23
RU2180902C2 (ru) 2002-03-27
BG64278B1 (bg) 2004-08-31
HK1020344A1 (en) 2000-04-14
CA2267322C (en) 2007-11-06
NO991560D0 (no) 1999-03-30
WO1998014432A1 (en) 1998-04-09
PT934280E (pt) 2003-08-29
SK34499A3 (en) 2000-04-10
DE69720757D1 (de) 2003-05-15
BR9712256B1 (pt) 2011-04-19
UA62939C2 (uk) 2004-01-15
NZ334971A (en) 2000-09-29

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