NZ197828A - Tri-substituted imidazoles and pharmaceuticals - Google Patents

Tri-substituted imidazoles and pharmaceuticals

Info

Publication number
NZ197828A
NZ197828A NZ197828A NZ19782881A NZ197828A NZ 197828 A NZ197828 A NZ 197828A NZ 197828 A NZ197828 A NZ 197828A NZ 19782881 A NZ19782881 A NZ 19782881A NZ 197828 A NZ197828 A NZ 197828A
Authority
NZ
New Zealand
Prior art keywords
phenyl
carbon atoms
substituted
lower alkoxy
formula
Prior art date
Application number
NZ197828A
Other languages
English (en)
Inventor
A Sallmann
Original Assignee
Ciba Geigy Ag
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 Ciba Geigy Ag filed Critical Ciba Geigy Ag
Priority to NZ207254A priority Critical patent/NZ207254A/en
Publication of NZ197828A publication Critical patent/NZ197828A/en

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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
    • C07D213/44Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/53Nitrogen atoms
    • 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
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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
    • C07D213/44Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/46Oxygen atoms
    • C07D213/50Ketonic radicals
    • 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
    • C07D233/20Heterocyclic 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 substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/26Radicals substituted by carbon atoms having three bonds to hetero 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
    • C07D233/64Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Cosmetics (AREA)
NZ197828A 1980-07-25 1981-07-24 Tri-substituted imidazoles and pharmaceuticals NZ197828A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NZ207254A NZ207254A (en) 1980-07-25 1981-07-24 Heterocyclyl-substituted oxazoles and pharmaceuticals

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH571580 1980-07-25

Publications (1)

Publication Number Publication Date
NZ197828A true NZ197828A (en) 1985-11-08

Family

ID=4298165

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ197828A NZ197828A (en) 1980-07-25 1981-07-24 Tri-substituted imidazoles and pharmaceuticals

Country Status (23)

Country Link
US (1) US4447431A (OSRAM)
EP (1) EP0045081B1 (OSRAM)
JP (1) JPS5756466A (OSRAM)
KR (13) KR850000883B1 (OSRAM)
AR (1) AR230269A1 (OSRAM)
AT (1) ATE17349T1 (OSRAM)
AU (2) AU7340481A (OSRAM)
CA (1) CA1175431A (OSRAM)
DD (2) DD201677A5 (OSRAM)
DE (1) DE3173434D1 (OSRAM)
DK (1) DK331881A (OSRAM)
ES (8) ES8301472A1 (OSRAM)
FI (1) FI812326A7 (OSRAM)
GB (1) GB2080805B (OSRAM)
GR (1) GR75287B (OSRAM)
IE (1) IE52071B1 (OSRAM)
IL (1) IL63410A (OSRAM)
NO (1) NO812542L (OSRAM)
NZ (1) NZ197828A (OSRAM)
PL (8) PL237003A1 (OSRAM)
PT (1) PT73424B (OSRAM)
SU (8) SU1235454A3 (OSRAM)
ZA (1) ZA815078B (OSRAM)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1983002613A1 (fr) * 1981-07-20 1983-08-04 Sallmann, Alfred Composes oxazoiques a triple substitution
EP0084756A1 (de) * 1982-01-22 1983-08-03 Ciba-Geigy Ag Trisubstituierte Oxazaverbindungen
FR2633291B1 (fr) * 1988-06-27 1990-09-07 Oreal Derives d'hydroxy-4 isoxazoles, leur procede de preparation et compositions cosmetiques et pharmaceutiques les contenant
US5252322A (en) * 1989-09-22 1993-10-12 The Gillette Company Skin tanning compositions containing imidazoles
NZ239161A (en) * 1990-07-31 1994-01-26 Smithkline Beecham Corp Substituted [1h-imidazol-5-yl] alkanoic acid derivatives; medicaments,
IL104369A0 (en) * 1992-01-13 1993-05-13 Smithkline Beecham Corp Novel compounds and compositions
US5916891A (en) * 1992-01-13 1999-06-29 Smithkline Beecham Corporation Pyrimidinyl imidazoles
US5593992A (en) * 1993-07-16 1997-01-14 Smithkline Beecham Corporation Compounds
US5670527A (en) * 1993-07-16 1997-09-23 Smithkline Beecham Corporation Pyridyl imidazole compounds and compositions
US5593991A (en) * 1993-07-16 1997-01-14 Adams; Jerry L. Imidazole compounds, use and process of making
JPH09505055A (ja) * 1993-11-08 1997-05-20 スミスクライン・ビーチャム・コーポレイション サイトカイン媒介疾患治療用オキサゾール
US5723477A (en) * 1994-11-10 1998-03-03 Sibia Neurosciences, Inc. Modulators of acetylcholine receptors
IL118544A (en) * 1995-06-07 2001-08-08 Smithkline Beecham Corp History of imidazole, the process for their preparation and the pharmaceutical preparations containing them
US5739143A (en) * 1995-06-07 1998-04-14 Smithkline Beecham Corporation Imidazole compounds and compositions
US6369068B1 (en) 1995-06-07 2002-04-09 Smithkline Beecham Corporation Amino substituted pyrimidine containing compounds
ZA9610687B (en) * 1995-12-22 1997-09-29 Smithkline Beecham Corp Novel synthesis.
AP9700912A0 (en) 1996-01-11 1997-01-31 Smithkline Beecham Corp Novel cycloalkyl substituted imidazoles
IL125223A0 (en) * 1996-01-11 1999-03-12 Smithkline Beecham Corp Novel substituted imidazole compounds
US6046208A (en) * 1996-01-11 2000-04-04 Smithkline Beecham Corporation Substituted imidazole compounds
ZA97175B (en) * 1996-01-11 1997-11-04 Smithkline Beecham Corp Novel substituted imidazole compounds.
WO1997035856A1 (en) * 1996-03-25 1997-10-02 Smithkline Beecham Corporation Novel treatment for cns injuries
EP0956018A4 (en) 1996-08-21 2000-01-12 Smithkline Beecham Corp IMIDAZOLE COMPOUNDS, COMPOSITIONS CONTAINING THEM AND THEIR USE
US5929076A (en) * 1997-01-10 1999-07-27 Smithkline Beecham Corporation Cycloalkyl substituted imidazoles
EP1028954B1 (en) * 1997-04-24 2003-07-02 Ortho-McNeil Pharmaceutical, Inc. Substituted imidazoles useful in the treatment of inflammatory diseases
JP2002504909A (ja) 1997-06-13 2002-02-12 スミスクライン・ビーチャム・コーポレイション 新規な置換ピラゾールおよびピラゾリン化合物
US6610695B1 (en) 1997-06-19 2003-08-26 Smithkline Beecham Corporation Aryloxy substituted pyrimidine imidazole compounds
AR016294A1 (es) * 1997-07-02 2001-07-04 Smithkline Beecham Corp Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion
US6562832B1 (en) 1997-07-02 2003-05-13 Smithkline Beecham Corporation Substituted imidazole compounds
US6489325B1 (en) 1998-07-01 2002-12-03 Smithkline Beecham Corporation Substituted imidazole compounds
TW517055B (en) 1997-07-02 2003-01-11 Smithkline Beecham Corp Novel substituted imidazole compounds
US7301021B2 (en) * 1997-07-02 2007-11-27 Smithkline Beecham Corporation Substituted imidazole compounds
CA2295762A1 (en) 1997-07-02 1999-01-14 Ravi Shanker Garigipati Novel cycloalkyl substituted imidazoles
US6362193B1 (en) 1997-10-08 2002-03-26 Smithkline Beecham Corporation Cycloalkenyl substituted compounds
US6335340B1 (en) 1997-12-19 2002-01-01 Smithkline Beecham Corporation compounds of heteroaryl substituted imidazole, their pharmaceutical compositons and uses
CN1302296A (zh) * 1998-05-22 2001-07-04 史密丝克莱恩比彻姆公司 新的2-烷基取代咪唑化合物
US6858617B2 (en) 1998-05-26 2005-02-22 Smithkline Beecham Corporation Substituted imidazole compounds
ATE266399T1 (de) * 1998-08-20 2004-05-15 Smithkline Beecham Corp Neue substituierte triazolverbindungen
JP2002528506A (ja) * 1998-11-04 2002-09-03 スミスクライン・ビーチャム・コーポレイション ピリジン−4−イルまたはピリミジン−4−イル置換ピラジン
WO2000029399A1 (en) * 1998-11-12 2000-05-25 Boehringer Ingelheim (Canada) Ltd. Antiherpes compounds
US6239279B1 (en) 1998-12-16 2001-05-29 Smithkline Beecham Corporation Synthesis for 4-aryl-5-pyrimidine imidazole substituted derivatives
ATE281451T1 (de) 1999-11-22 2004-11-15 Smithkline Beecham Plc Imidazolderivate und deren verwendung als raf kinase inhibitoren
AU1781601A (en) 1999-11-23 2001-06-04 Smithkline Beecham Corporation 3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors
EP1233950B1 (en) 1999-11-23 2005-10-05 Smithkline Beecham Corporation 3,4-DIHYDRO-(1H)QUINAZOLIN-2-ONE COMPOUNDS AS CSBP/P39 kINASE INHIBITORS
US7053098B1 (en) 1999-11-23 2006-05-30 Smithkline Beecham Corporation 3,4-Dihydro-(1H) quinazolin-2-one compounds as CSBP/P38 kinase inhibitors
US6759410B1 (en) * 1999-11-23 2004-07-06 Smithline Beecham Corporation 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors
US7235551B2 (en) * 2000-03-02 2007-06-26 Smithkline Beecham Corporation 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
GB0005357D0 (en) 2000-03-06 2000-04-26 Smithkline Beecham Plc Compounds
JP2003525936A (ja) * 2000-03-06 2003-09-02 スミスクライン ビーチャム パブリック リミテッド カンパニー Rafキナーゼ阻害物質としてのイミダゾール誘導体
CZ20031125A3 (cs) * 2000-10-23 2003-10-15 Smithkline Beecham Corporation Nové sloučeniny
GB0112348D0 (en) * 2001-05-19 2001-07-11 Smithkline Beecham Plc Compounds
US20040192689A1 (en) * 2001-09-05 2004-09-30 Dean David Kenneth Heterocycle-carboxamide derivatives as raf kinase inhibitors
JP4361798B2 (ja) * 2001-12-18 2009-11-11 エフ.ホフマン−ラ ロシュ アーゲー Mdm2インヒビターとしてのシス−イミダゾリン
TW200505446A (en) * 2003-01-17 2005-02-16 Fuj Isawa Pharmaceutical Co Ltd Inhibitor of cox
WO2004099130A2 (en) * 2003-05-08 2004-11-18 Astellas Pharma Inc. 1,2-diarylimidazoles useful as inhibitors of cox
UY29440A1 (es) * 2005-03-25 2006-10-02 Glaxo Group Ltd Nuevos compuestos
WO2006104917A2 (en) * 2005-03-25 2006-10-05 Glaxo Group Limited Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1h)-one derivatives
WO2013049272A2 (en) 2011-09-29 2013-04-04 Theraceutix, Llc Composition and method for treatment of symptoms associated with various skin conditions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3558645A (en) * 1968-07-08 1971-01-26 Sandoz Ag 2-(4-(4',5-diphenyl - 2 - imidazolyl)-phenoxy) lower aliphatic monocarboxylic acids
CH561718A5 (OSRAM) * 1971-05-10 1975-05-15 Ciba Geigy Ag
GB1469532A (en) * 1973-06-28 1977-04-06 Dumex Ltd As Imimdazolyl-alkanoic acid derivatives
US4372964A (en) * 1980-10-30 1983-02-08 E. I. Du Pont De Nemours And Company Antiinflammatory 4,5-diaryl-1H-imidazole-2-methanols

Also Published As

Publication number Publication date
US4447431A (en) 1984-05-08
KR850002756A (ko) 1985-05-15
KR850002754A (ko) 1985-05-15
NO812542L (no) 1982-01-26
ES514579A0 (es) 1983-05-16
KR850000888B1 (ko) 1985-06-26
ES514582A0 (es) 1983-05-16
ES8306122A1 (es) 1983-05-16
ES514580A0 (es) 1983-05-16
IE811680L (en) 1982-01-25
SU1145928A3 (ru) 1985-03-15
PL236997A1 (en) 1983-01-03
GB2080805B (en) 1984-03-07
GB2080805A (en) 1982-02-10
KR850002749A (ko) 1985-05-15
ATE17349T1 (de) 1986-01-15
KR850000890B1 (ko) 1985-06-26
IL63410A0 (en) 1981-10-30
KR850000873B1 (ko) 1985-06-22
KR850000911B1 (ko) 1985-06-27
KR850000884B1 (ko) 1985-06-26
ZA815078B (en) 1982-07-28
PL237005A1 (en) 1983-02-28
KR850000885B1 (ko) 1985-06-26
CA1175431A (en) 1984-10-02
PL237001A1 (en) 1983-02-28
ES8306121A1 (es) 1983-05-16
SU1205763A3 (ru) 1986-01-15
DD202554A5 (de) 1983-09-21
KR850002753A (ko) 1985-05-15
ES8306123A1 (es) 1983-05-16
DK331881A (da) 1982-01-26
ES8306120A1 (es) 1983-05-16
ES514585A0 (es) 1983-07-01
KR850002755A (ko) 1985-05-15
KR850002745A (ko) 1985-05-15
GR75287B (OSRAM) 1984-07-13
ES504257A0 (es) 1982-12-01
IL63410A (en) 1986-04-29
DD201677A5 (de) 1983-08-03
SU1138023A3 (ru) 1985-01-30
PL237002A1 (en) 1983-02-28
KR850000891B1 (ko) 1985-06-26
PT73424B (en) 1983-06-20
EP0045081B1 (de) 1986-01-08
PL135822B1 (en) 1985-12-31
SU1152520A3 (en) 1985-04-23
SU1169534A3 (ru) 1985-07-23
SU1235454A3 (ru) 1986-05-30
KR850002746A (ko) 1985-05-15
SU1227112A3 (ru) 1986-04-23
ES514581A0 (es) 1983-05-16
KR850002747A (ko) 1985-05-15
ES8306124A1 (es) 1983-05-16
JPS5756466A (en) 1982-04-05
AU5655586A (en) 1986-09-11
ES514583A0 (es) 1983-05-16
PL237004A1 (en) 1983-02-28
ES8301472A1 (es) 1982-12-01
IE52071B1 (en) 1987-06-10
KR850000883B1 (ko) 1985-06-26
KR850002748A (ko) 1985-05-15
KR850002744A (ko) 1985-05-15
KR850002752A (ko) 1985-05-15
PL237003A1 (en) 1983-02-28
KR850000889B1 (ko) 1985-06-26
PL232352A1 (OSRAM) 1982-12-20
FI812326L (fi) 1982-01-26
SU1205764A3 (ru) 1986-01-15
EP0045081A3 (en) 1982-04-07
ES8307245A1 (es) 1983-07-01
KR850002750A (ko) 1985-05-15
PL237000A1 (en) 1983-02-28
PT73424A (en) 1981-08-01
FI812326A7 (fi) 1982-01-26
KR850000886B1 (ko) 1985-06-26
KR850001064B1 (ko) 1985-07-25
ES514584A0 (es) 1983-05-16
ES8306119A1 (es) 1983-05-16
AU7340481A (en) 1982-01-28
KR850000887B1 (ko) 1985-06-26
DE3173434D1 (en) 1986-02-20
KR850000892B1 (ko) 1985-06-26
EP0045081A2 (de) 1982-02-03
AR230269A1 (es) 1984-03-01
KR830006230A (ko) 1983-09-20

Similar Documents

Publication Publication Date Title
US4447431A (en) Tri-substituted imidazole derivatives, pharmaceutical preparations containing them, and their use
US5602152A (en) Benzoxepines
NZ238407A (en) 5-hydroxy-2-(substituted methyl)amino pyridine derivatives and pharmaceuticals compositions
JPH0153671B2 (OSRAM)
HUT65693A (en) Process for preparing substituted cyclohexane derivatives and pharmaceutical compositions containing them
EP0022578A1 (en) Pharmaceutical compositions containing 3-Amino-pyrazoline derivatives
WO1983002611A1 (fr) Composes diazoiques a triple substitution
US4622421A (en) Phenylalkanoic acid derivatives and their use
US3524860A (en) (2-imidazolin-2-yl)alkyl-substituted 7-azaindoles
NZ203317A (en) 2,3-diaryl-5-halo-thiophene derivatives;pharmaceutical compositions
JP2004538278A (ja) 緑内障および近視を処置するためのベンゾ[g]キノリン誘導体
US3833594A (en) Amino derivatives of pyrazolopyridine carboxylic acids and esters
US5137904A (en) Thiohydantoin inhibitors of collagen-induced and ADP-induced platelet aggregation
NZ198074A (en) Diaryl-imidazoles,and pharmaceutical compositions
US4447607A (en) Dibenzo diazacines
KR20010041765A (ko) IgE 항체생산 억제제 및 자기면역질환 억제제
JPS63253072A (ja) 置換ヒダントイン化合物
EP0162217A1 (de) 1,2,4-Triazacycloalkadienderivate
EP1133471B1 (en) Hydrazine derivatives
US6174908B1 (en) Potassium channel inhibitors
JPH0753730B2 (ja) イミダゾピラゾール誘導体
US4595689A (en) 4-(8-bromodibenz[b,f]oxepin-10-yl)-1,2,3,6-tetrahydro-1-methylpyridine and 4-(2-bromodibenzo[a,d]cyclophetatriene-11-yl)-1,2,3,6-tetrahydro-1-methylpyridine for dermal inflammation
US12398142B2 (en) Abelson non-tyrosine kinase compounds for the treatment of neurodegenerative diseases
EP0011854A1 (en) 4-(2'-Pyridylamino)-phenylacetic acid derivatives, process for their preparation, pharmaceuticals containing these compounds and their use
US5428058A (en) Phospholipase A2 inhibitors