YU65995A - Inhibitori 5-lipoksigenaze i njihove farmaceutske kompozicije - Google Patents

Inhibitori 5-lipoksigenaze i njihove farmaceutske kompozicije

Info

Publication number
YU65995A
YU65995A YU65995A YU65995A YU65995A YU 65995 A YU65995 A YU 65995A YU 65995 A YU65995 A YU 65995A YU 65995 A YU65995 A YU 65995A YU 65995 A YU65995 A YU 65995A
Authority
YU
Yugoslavia
Prior art keywords
pharmaceutical compositions
phenylene
inhibitors
lipoxygenasis
treating
Prior art date
Application number
YU65995A
Other languages
English (en)
Inventor
W. Rodney Stevens
Takashi Mano
Kazunari Nakao
Yoshiyuki Okumura
Original Assignee
Pfizer Inc.
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 Pfizer Inc. filed Critical Pfizer Inc.
Publication of YU65995A publication Critical patent/YU65995A/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • 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
    • A61P37/08Antiallergic agents
    • 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
    • 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
    • C07D233/56Heterocyclic 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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Opisani su inhibitori 5-lipoksigenaze formule: njihove farmaceutski primenljive soli i kompozicije, pri čemu Ar1 predstavlja 2-alkilimidazolil ili pirolil; X1 je direktna veza ili CH2; Ar2 je 1,4-fenilen; X2 je -A-X- ili -X-A-, gde je A direktna veza ili C1-4-alkilen, a X je oksi, tio, sulfinil ili sulfonil grupa, Ar3 je 1,3-fenilen ili 5-fluoro-1,3-fenilen; Y je CONH2; i R1 i R2 su svako C1-4 alkil. Ova jedinjenja su korisna pri tretiranju ili ublažavanju inflamatornih obolenja, alergija i kardiovaskularnih obolenja kod sisara i kao aktivni sastojak u farmaceutskim kompozicijama za tretiranje takvih stanja.
YU65995A 1994-10-18 1995-10-17 Inhibitori 5-lipoksigenaze i njihove farmaceutske kompozicije YU65995A (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9401747 1994-10-18

Publications (1)

Publication Number Publication Date
YU65995A true YU65995A (sh) 1999-06-15

Family

ID=14098722

Family Applications (1)

Application Number Title Priority Date Filing Date
YU65995A YU65995A (sh) 1994-10-18 1995-10-17 Inhibitori 5-lipoksigenaze i njihove farmaceutske kompozicije

Country Status (31)

Country Link
EP (1) EP0787127B1 (sh)
JP (1) JP3032579B2 (sh)
CN (1) CN1093536C (sh)
AT (1) ATE198474T1 (sh)
AU (1) AU681520B2 (sh)
BG (1) BG61768B1 (sh)
CA (1) CA2202057C (sh)
CO (1) CO4480026A1 (sh)
CZ (1) CZ287350B6 (sh)
DE (1) DE69519804T2 (sh)
DK (1) DK0787127T3 (sh)
ES (1) ES2153033T3 (sh)
FI (1) FI971632A0 (sh)
GR (1) GR3035471T3 (sh)
HU (1) HU221543B (sh)
IL (1) IL115581A (sh)
LV (1) LV11468B (sh)
MY (1) MY114680A (sh)
NO (1) NO314629B1 (sh)
NZ (1) NZ285163A (sh)
PE (1) PE49196A1 (sh)
PL (1) PL180104B1 (sh)
RU (1) RU2136666C1 (sh)
SI (1) SI9500392A (sh)
SK (1) SK281577B6 (sh)
TR (1) TR199501274A2 (sh)
TW (1) TW411339B (sh)
UA (1) UA45312C2 (sh)
WO (1) WO1996011911A1 (sh)
YU (1) YU65995A (sh)
ZA (1) ZA958748B (sh)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6239285B1 (en) 1998-02-06 2001-05-29 Pfizer Inc Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems
US6194585B1 (en) * 1998-12-22 2001-02-27 Pfizer Inc. Process for preparing 5-lipoxygenase inhibitors
SG87145A1 (en) * 1999-08-31 2002-03-19 Pfizer Prod Inc Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems
US6344563B1 (en) * 1999-08-31 2002-02-05 Timothy Norris Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems
US6346624B1 (en) * 1999-08-31 2002-02-12 Pfizer Inc Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems
AU4589701A (en) 2000-03-24 2001-10-08 Cocensys Inc Aryl substituted pyrazoles, triazoles and tetrazoles, and the use thereof
DK1383874T3 (da) * 2001-04-20 2010-05-03 Novozymes As Varianter af lipogygenase og deres anvendelse
GB0302094D0 (en) 2003-01-29 2003-02-26 Pharmagene Lab Ltd EP4 receptor antagonists
GB0324269D0 (en) 2003-10-16 2003-11-19 Pharmagene Lab Ltd EP4 receptor antagonists
GEP20125386B (en) * 2006-11-27 2012-01-25 Pfizer Prod Inc Pyrazole analogs
EP2225229A1 (en) 2007-11-26 2010-09-08 Pfizer Inc. Pyrazole derivatives as 5-lo inhibitors
KR20140138243A (ko) * 2012-02-28 2014-12-03 피라말 엔터프라이지즈 리미티드 G 단백질 연결 수용체 작용물질로서의 페닐알칸산 유도체
BR112020018094A2 (pt) 2018-03-08 2020-12-22 Incyte Corporation Compostos de aminopirazina diol como inibidores de pi3k-¿
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2001730A6 (es) * 1987-01-14 1988-06-01 Ferrer Int Procedimiento de obtencion del acio 2,3-dihidro-5-(b-(1h-imidazol-1-il) etoxi)-1h-inden-1-carboxilico
EP0462830B1 (en) * 1990-06-21 1995-10-18 Zeneca Limited Cyclic ether derivatives
IE913866A1 (en) * 1990-11-28 1992-06-03 Ici Plc Aryl derivatives
EP0505122A1 (en) * 1991-03-21 1992-09-23 Zeneca Limited Alpha, alpha-dialkylbenzyl derivatives
EP0540165A1 (en) * 1991-10-03 1993-05-05 Zeneca Limited Alkanoic acid derivatives
ES2103130T3 (es) * 1993-06-14 1997-08-16 Pfizer Inhibidores imidazoles como la lipoxigenasa.

Also Published As

Publication number Publication date
ATE198474T1 (de) 2001-01-15
MY114680A (en) 2002-12-31
UA45312C2 (uk) 2002-04-15
PL180104B1 (pl) 2000-12-29
BG100070A (bg) 1996-05-31
HUT77363A (hu) 1998-03-30
CO4480026A1 (es) 1997-07-09
TW411339B (en) 2000-11-11
CA2202057C (en) 2001-10-09
RU2136666C1 (ru) 1999-09-10
DK0787127T3 (da) 2001-02-05
SK281577B6 (sk) 2001-05-10
ZA958748B (en) 1997-04-17
SK128795A3 (en) 1996-07-03
IL115581A0 (en) 1996-01-19
LV11468A (lv) 1996-08-20
CZ287350B6 (en) 2000-10-11
EP0787127A1 (en) 1997-08-06
CN1093536C (zh) 2002-10-30
JPH11507322A (ja) 1999-06-29
AU2417495A (en) 1996-05-06
HU221543B (hu) 2002-11-28
CZ117797A3 (cs) 1998-06-17
SI9500392A (en) 1996-08-31
TR199501274A2 (tr) 1996-06-21
NO971773D0 (no) 1997-04-17
IL115581A (en) 1999-10-28
PL319727A1 (en) 1997-08-18
WO1996011911A1 (en) 1996-04-25
ES2153033T3 (es) 2001-02-16
LV11468B (en) 1996-12-20
NO971773L (no) 1997-06-17
NZ285163A (en) 1998-08-26
DE69519804D1 (de) 2001-02-08
NO314629B1 (no) 2003-04-22
CN1169722A (zh) 1998-01-07
AU681520B2 (en) 1997-08-28
DE69519804T2 (de) 2001-04-19
JP3032579B2 (ja) 2000-04-17
GR3035471T3 (en) 2001-05-31
EP0787127B1 (en) 2001-01-03
FI971632A7 (fi) 1997-04-17
BG61768B1 (bg) 1998-05-29
CA2202057A1 (en) 1996-04-25
PE49196A1 (es) 1996-11-21
FI971632A0 (fi) 1997-04-17

Similar Documents

Publication Publication Date Title
YU65995A (sh) Inhibitori 5-lipoksigenaze i njihove farmaceutske kompozicije
NO2006002I2 (no) Posakonazol eventuelt i form av en ester og/eller et farmasøytisk akseptabelt salt derav.
YU18101A (sh) 4-amino supstituisani-2-supstituisani-1,2,3,4- tetrahidrohinolini kao inhibitori cetp
YU69902A (sh) Novi derivati piperazina
EA200100202A1 (ru) 4-карбоксиамино-2-замещенные-1,2,3,4-тетрагидрохинолины в качестве сетр-ингибиторов
EA200100376A1 (ru) Арилсульфонанилидмочевины
MX9102209A (es) Derivados de acido hidroxamico y n-hidroxiurea novedosos y su uso.
ES2194986T3 (es) Compuestos de carbonil-piperazinilo y piperidinilo que inhiben la farnesil-protein-transferasa.
YU60198A (sh) Supstituisani derivati indazola i njihova upotreba kao fosfodiesteraze (pde) tipa iv i inhibitora faktora nekroze tumora (tnf)
EA200200262A1 (ru) Пиперазиновые производные и их применение в качестве противовоспалительных агентов
EA200101036A1 (ru) Противовоспалительные и иммуносупрессорные соединения, ингибирующие клеточную адгезию
PT1023267E (pt) Compostos de piridilo e composicoes farmaceuticas que os contem
NO158017C (no) Analogifremgangsmaate for fremstilling av terapeutisk aktive imidazolderivater.
DE69315699D1 (de) Inhibitoren gegen die aggregation von blutplättchen
YU7191A (sh) Oralno aktivni inhibitori renina
YU6396A (sh) Kombinacija inhibitora hiv proteaze sa drugim jedinjenjima za terapiju hiv infekcija
ES2138211T3 (es) N-hidroxiureas como agentes antiinflamatorios.
DE69629474D1 (de) Antifungale tetrahydrofurane
DE69103773D1 (de) Derivate von hydroxaminsäure die lipoxygenase hemmen.
EA200200292A1 (ru) Производные гигромицина
EA199700302A1 (ru) Биологически активные уреидо-производные, полезные при лечении рассеянного склероза
YU32601A (sh) Derivati higromicina kao antibakterijski agensi
ATE146167T1 (de) Cyclopropyl-n-hydroxyharnstoff als lypoxygenaseinhibitoren
SE9902596D0 (sv) Pharmaceutically active compounds
ATE268768T1 (de) Antithrombosemittel