IT1218420B - Agenti terapeutici comprendenti 3-1 (immidazolilalchil) indoli (e loro sali di addizione) - Google Patents

Agenti terapeutici comprendenti 3-1 (immidazolilalchil) indoli (e loro sali di addizione)

Info

Publication number
IT1218420B
IT1218420B IT20399/80A IT2039980A IT1218420B IT 1218420 B IT1218420 B IT 1218420B IT 20399/80 A IT20399/80 A IT 20399/80A IT 2039980 A IT2039980 A IT 2039980A IT 1218420 B IT1218420 B IT 1218420B
Authority
IT
Italy
Prior art keywords
immidazolylalkyl
indoles
therapeutic agents
addition salts
agents including
Prior art date
Application number
IT20399/80A
Other languages
English (en)
Italian (it)
Other versions
IT8020399A0 (it
Inventor
Peter Edward Cross
Roger Peter Dickinson
Original Assignee
Pfizer
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 filed Critical Pfizer
Publication of IT8020399A0 publication Critical patent/IT8020399A0/it
Application granted granted Critical
Publication of IT1218420B publication Critical patent/IT1218420B/it

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
IT20399/80A 1979-03-07 1980-03-06 Agenti terapeutici comprendenti 3-1 (immidazolilalchil) indoli (e loro sali di addizione) IT1218420B (it)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB7908123 1979-03-07

Publications (2)

Publication Number Publication Date
IT8020399A0 IT8020399A0 (it) 1980-03-06
IT1218420B true IT1218420B (it) 1990-04-19

Family

ID=10503707

Family Applications (1)

Application Number Title Priority Date Filing Date
IT20399/80A IT1218420B (it) 1979-03-07 1980-03-06 Agenti terapeutici comprendenti 3-1 (immidazolilalchil) indoli (e loro sali di addizione)

Country Status (36)

Country Link
US (1) US4273782A (cg-RX-API-DMAC7.html)
JP (1) JPS55133380A (cg-RX-API-DMAC7.html)
KR (1) KR850000760B1 (cg-RX-API-DMAC7.html)
AR (1) AR227015A1 (cg-RX-API-DMAC7.html)
AT (1) AT375366B (cg-RX-API-DMAC7.html)
AU (1) AU516957B2 (cg-RX-API-DMAC7.html)
BE (1) BE882113A (cg-RX-API-DMAC7.html)
CA (1) CA1120479A (cg-RX-API-DMAC7.html)
CH (1) CH649546A5 (cg-RX-API-DMAC7.html)
CS (1) CS253702B2 (cg-RX-API-DMAC7.html)
DD (1) DD149525A5 (cg-RX-API-DMAC7.html)
DE (1) DE3008632A1 (cg-RX-API-DMAC7.html)
DK (1) DK151884C (cg-RX-API-DMAC7.html)
ES (2) ES489220A0 (cg-RX-API-DMAC7.html)
FI (1) FI66860C (cg-RX-API-DMAC7.html)
FR (1) FR2450832A1 (cg-RX-API-DMAC7.html)
GR (1) GR67237B (cg-RX-API-DMAC7.html)
HK (1) HK89884A (cg-RX-API-DMAC7.html)
HU (1) HU184727B (cg-RX-API-DMAC7.html)
IE (1) IE49542B1 (cg-RX-API-DMAC7.html)
IL (1) IL59524A (cg-RX-API-DMAC7.html)
IT (1) IT1218420B (cg-RX-API-DMAC7.html)
KE (1) KE3467A (cg-RX-API-DMAC7.html)
LU (1) LU82224A1 (cg-RX-API-DMAC7.html)
MY (1) MY8500285A (cg-RX-API-DMAC7.html)
NL (1) NL182959C (cg-RX-API-DMAC7.html)
NO (1) NO152217C (cg-RX-API-DMAC7.html)
NZ (1) NZ193052A (cg-RX-API-DMAC7.html)
PH (1) PH15198A (cg-RX-API-DMAC7.html)
PL (1) PL128296B1 (cg-RX-API-DMAC7.html)
PT (1) PT70914A (cg-RX-API-DMAC7.html)
SE (1) SE440778B (cg-RX-API-DMAC7.html)
SG (1) SG67284G (cg-RX-API-DMAC7.html)
SU (1) SU1277894A3 (cg-RX-API-DMAC7.html)
YU (1) YU41911B (cg-RX-API-DMAC7.html)
ZA (1) ZA801328B (cg-RX-API-DMAC7.html)

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DE3786030T2 (de) 1986-03-27 1993-12-02 Merck Frosst Canada Inc Tetrahydrocarbazole Ester.
JPH0832679B2 (ja) * 1986-09-05 1996-03-29 理化学研究所 N―フタルイシド誘導体及びその製造法
GR871809B (en) * 1986-11-28 1988-03-07 Glaxo Group Ltd Process for the preparation of tricyclic ketones
KR920700210A (ko) * 1989-03-31 1992-02-19 기따미 가즈히꼬 신규 이미다졸 유도체, 그의 제법 및 그의 의약용도
US5399574A (en) * 1990-06-07 1995-03-21 Burroughs Wellcome Co. Indolyl tetrahydropyridines for treating migraine
DE4023215A1 (de) * 1990-07-21 1992-01-23 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, sie enthaltende mittel und deren verwendung
KR930702334A (ko) * 1990-09-13 1993-09-08 데이비드 로버트 5 하이드록시트립타민 수용체 길항제로서의 인돌우레아
US5162337A (en) * 1990-10-05 1992-11-10 Merck & Co., Inc. Animal growth promotion
US5120749A (en) * 1991-02-20 1992-06-09 Abbott Laboratories Platelet activating antagonists
US5463074A (en) * 1991-12-18 1995-10-31 Schering Corporation Imidazolyl or imidazoylalkyl substituted with a four or five membered nitrogen containing heterocyclic ring
US5538973A (en) * 1992-03-27 1996-07-23 Kyoto Pharmaceutical Industries, Ltd. Imidazole derivative, pharmaceutical use thereof, and intermediate therefor
EP0597112A4 (en) * 1992-03-27 1994-06-22 Kyoto Pharma Ind Novel imidazole derivative, pharmaceutical use thereof, and intermediate therefor.
JPH0632913U (ja) * 1992-09-18 1994-04-28 三洋電機株式会社 床暖房用パネル
OA11622A (en) * 1998-03-31 2004-09-16 Inst For Pharm Discovery Inc Substituted indolealkanoic acids.
NZ537979A (en) * 2002-09-12 2007-08-31 Hoffmann La Roche N-substituted-1H-indol-5-propionic acid compounds as PPAR agonists useful for the treatment of diabetes
CA2505545C (en) * 2002-11-25 2011-06-07 F. Hoffmann-La Roche Ag Indolyl derivatives
JP2006514640A (ja) * 2002-12-10 2006-05-11 ワイス プラスミノゲンアクティベータインヒビターのインヒビターとしての置換3−アルキル及び3−アリールアルキル1h−イル酢酸誘導体
GB0324763D0 (en) * 2003-10-23 2003-11-26 Oxagen Ltd Use of compounds in therapy
NZ550447A (en) * 2004-05-03 2010-06-25 Hoffmann La Roche Hexafluoro-indolyl derivatives as liver-x-receptor modulators
MX2007004525A (es) * 2004-10-12 2007-09-19 Decode Genetics Inc Sulfonamidas biciclicas peri-sustituidas para enfermedad de arteria oclusiva.
BRPI0615307A2 (pt) * 2005-08-25 2009-08-04 Schering Corp agonistas de adrenorreceptor alfa2c
US7977359B2 (en) * 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
US8399666B2 (en) * 2005-11-04 2013-03-19 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
GB2431927B (en) * 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
RU2008149518A (ru) * 2006-05-16 2010-06-27 Декод Дженетикс, Ехф. (Is) Способ получения 7-(акрилоил) индолов
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TW200920369A (en) * 2007-10-26 2009-05-16 Amira Pharmaceuticals Inc 5-lipoxygenase activating protein (flap) inhibitor
EP2234608A2 (en) 2007-12-11 2010-10-06 Viamet Pharmaceuticals, Inc. Metalloenzyme inhibitors using metal binding moieties in combination with targeting moieties
US7750027B2 (en) * 2008-01-18 2010-07-06 Oxagen Limited Compounds having CRTH2 antagonist activity
DK2250161T3 (da) 2008-01-18 2014-01-27 Atopix Therapeutics Ltd Forbindelser med CRTH2-antagonistaktivitet
EP2240444A1 (en) * 2008-01-22 2010-10-20 Oxagen Limited Compounds having crth2 antagonist activity
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BRPI0912267A2 (pt) * 2008-05-23 2015-10-13 Amira Pharmaceuticals Inc sal farmaceuticamente aceitável, composição farmacêutica, artigo de fabricação, métodos para tratar asma, rinite alérgica, doença, lesões gástricas e dor, métodos para prevenir broncoconstrição e rinite alérgica, uso de um sal farmaceuticamente aceitável, e, processo para a preparação de um sal farmaceuticamente aceitável.
US8546431B2 (en) 2008-10-01 2013-10-01 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
CN103929961A (zh) * 2011-06-20 2014-07-16 美国阿尔茨海默病研究所公司 化合物及其治疗应用
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US11530186B2 (en) * 2018-03-29 2022-12-20 H. Lee Moffitt Cancer Center and Research Center Institute, Inc. Inhibitors for the β-catenin / T-cell factor protein-protein interaction

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US3370063A (en) * 1964-10-05 1968-02-20 Mcneilab Inc Substituted dimethoxy indoles and method of making the same
US3621027A (en) * 1968-03-18 1971-11-16 Endo Lab 1-aminoalkyl-2,6-diaryl 4,5,6,7 tetrahydro-4-oxindales
US3931229A (en) * 1973-08-23 1976-01-06 Warner-Lambert Company 3-Thiomethyl-2[2-(dialkylamino)ethyl]indoles
US4059583A (en) * 1975-11-13 1977-11-22 Mcneil Laboratories, Incorporated Substituted indoles
AU523536B2 (en) * 1977-08-26 1982-08-05 Wellcome Foundation Limited, The Imidazoles and methods of preparing them
US4140858A (en) * 1977-12-19 1979-02-20 Warner-Lambert Company 3-(1H-imidazol-1-ylmethyl)-2-(disubstitutedaminomethyl)indoles and a method for their production
DE2960547D1 (en) * 1978-02-24 1981-11-05 Pfizer Ltd 3-(imidazol-1-ylalkyl)indoles as selective inhibitors of thromboxane synthetase,pharmaceutical compositions thereof, and methods for preparing them

Also Published As

Publication number Publication date
JPS55133380A (en) 1980-10-17
YU61480A (en) 1983-12-31
JPS6141513B2 (cg-RX-API-DMAC7.html) 1986-09-16
US4273782A (en) 1981-06-16
AT375366B (de) 1984-07-25
CH649546A5 (de) 1985-05-31
DE3008632A1 (de) 1980-10-16
NO152217B (no) 1985-05-13
ES496889A0 (es) 1982-08-01
FI800672A7 (fi) 1980-09-08
LU82224A1 (fr) 1980-06-06
HU184727B (en) 1984-10-29
IE800453L (en) 1980-09-07
DE3008632C2 (cg-RX-API-DMAC7.html) 1988-02-25
FI66860B (fi) 1984-08-31
FR2450832B1 (cg-RX-API-DMAC7.html) 1983-04-22
SU1277894A3 (ru) 1986-12-15
PL128296B1 (en) 1984-01-31
ES8104278A1 (es) 1981-04-01
ATA125780A (de) 1983-12-15
AU516957B2 (en) 1981-07-02
HK89884A (en) 1984-11-23
MY8500285A (en) 1985-12-31
CA1120479A (en) 1982-03-23
KE3467A (en) 1984-11-09
AR227015A1 (es) 1982-09-15
PH15198A (en) 1982-09-17
KR830001928A (ko) 1983-05-19
ZA801328B (en) 1981-03-25
CS253702B2 (en) 1987-12-17
DK151884B (da) 1988-01-11
IT8020399A0 (it) 1980-03-06
ES8205789A1 (es) 1982-08-01
SE8001736L (sv) 1980-09-08
KR850000760B1 (ko) 1985-05-25
DK42580A (da) 1980-09-08
PL222470A1 (cg-RX-API-DMAC7.html) 1980-12-01
IE49542B1 (en) 1985-10-30
SE440778B (sv) 1985-08-19
BE882113A (fr) 1980-09-08
AU5623180A (en) 1980-09-11
NO800650L (no) 1980-09-08
IL59524A (en) 1982-11-30
DD149525A5 (de) 1981-07-15
ES489220A0 (es) 1981-04-01
NO152217C (no) 1985-08-21
IL59524A0 (en) 1980-06-30
PT70914A (en) 1980-04-01
FI66860C (fi) 1984-12-10
DK151884C (da) 1988-06-13
SG67284G (en) 1985-03-15
NL8001351A (nl) 1980-09-09
GR67237B (cg-RX-API-DMAC7.html) 1981-06-25
NZ193052A (en) 1984-07-06
NL182959C (nl) 1988-06-16
YU41911B (en) 1988-02-29
FR2450832A1 (fr) 1980-10-03

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