EA200400716A1 - 3- (IMIDAZOLYL) -2-ALCOXYPROPIONIC ACIDS AS TAFIA INHIBITORS (THROMBIN-ACTIVATED FIBRINOLYSIS INHIBITOR) - Google Patents

3- (IMIDAZOLYL) -2-ALCOXYPROPIONIC ACIDS AS TAFIA INHIBITORS (THROMBIN-ACTIVATED FIBRINOLYSIS INHIBITOR)

Info

Publication number
EA200400716A1
EA200400716A1 EA200400716A EA200400716A EA200400716A1 EA 200400716 A1 EA200400716 A1 EA 200400716A1 EA 200400716 A EA200400716 A EA 200400716A EA 200400716 A EA200400716 A EA 200400716A EA 200400716 A1 EA200400716 A1 EA 200400716A1
Authority
EA
Eurasian Patent Office
Prior art keywords
alcoxypropionic
thrombin
imidazolyl
acids
fibrinolysis inhibitor
Prior art date
Application number
EA200400716A
Other languages
Russian (ru)
Inventor
Шарлотт Мойра Норфор Аллертон
Дейвид Джон Булл
Марк Эдвард Баннэйдж
Роберт Джон Магайр
Джон Стил
Original Assignee
Пфайзер Инк.
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
Priority claimed from GB0201389A external-priority patent/GB0201389D0/en
Priority claimed from GB0202027A external-priority patent/GB0202027D0/en
Application filed by Пфайзер Инк. filed Critical Пфайзер Инк.
Publication of EA200400716A1 publication Critical patent/EA200400716A1/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
    • C07D233/54Heterocyclic 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/04Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P41/00Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution
    • 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
    • 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
    • A61P9/10Drugs 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
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D403/12Heterocyclic 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 chain containing hetero atoms as chain links

Abstract

Соединения формулы (I), где n равно 0-3, Rпредставляет собой возможно замещенный Cалкил, Cалкенил или Cалкинил, гетероцикл, ароматический гетероцикл, арил или водород, а R, R, R, R, R, R, Rи R, каждый независимо, выбран из водорода и возможно замещенного Cалкила или Rи Rпредставляют собой алкиленовую цепь, являются новыми. Они полезны при лечении тромботических состояний и других патологий, связанных с отложением фибрина.Международная заявка была опубликована вместе с отчетом о международном поиске.The compounds of formula (I), where n is 0-3, R 1 is a possibly substituted C 1-6 alkyl, C 1-6 alkenyl or C 1-6 alkynyl, a heterocycle, an aromatic heterocycle, aryl or hydrogen, and R, R, R, R, R, R, R and R each independently is selected from hydrogen and optionally substituted C 1-6 alkyl or R 8 and R 12 represent an alkylene chain are new. They are useful in the treatment of thrombotic conditions and other pathologies associated with fibrin deposition. The international application was published along with an international search report.

EA200400716A 2002-01-22 2003-01-10 3- (IMIDAZOLYL) -2-ALCOXYPROPIONIC ACIDS AS TAFIA INHIBITORS (THROMBIN-ACTIVATED FIBRINOLYSIS INHIBITOR) EA200400716A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0201389A GB0201389D0 (en) 2002-01-22 2002-01-22 3-(imidazolyl)-2-alkoxypropanoic acids
GB0202027A GB0202027D0 (en) 2002-01-29 2002-01-29 3-(imidazolyl)-2-alkoxypropanoic acids
PCT/IB2003/000060 WO2003061652A1 (en) 2002-01-22 2003-01-10 3-(imidazolyl)-2-alkoxypropanoic acids as tafia inhibitors

Publications (1)

Publication Number Publication Date
EA200400716A1 true EA200400716A1 (en) 2004-12-30

Family

ID=27614792

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200400716A EA200400716A1 (en) 2002-01-22 2003-01-10 3- (IMIDAZOLYL) -2-ALCOXYPROPIONIC ACIDS AS TAFIA INHIBITORS (THROMBIN-ACTIVATED FIBRINOLYSIS INHIBITOR)

Country Status (24)

Country Link
EP (1) EP1467731A1 (en)
JP (1) JP2005520811A (en)
KR (1) KR20040077775A (en)
CN (1) CN1620291A (en)
AP (1) AP2004003084A0 (en)
AR (1) AR038197A1 (en)
BR (1) BR0307016A (en)
CA (1) CA2472238A1 (en)
EA (1) EA200400716A1 (en)
EC (1) ECSP045200A (en)
HR (1) HRP20040659A2 (en)
IL (1) IL162677A0 (en)
IS (1) IS7310A (en)
MA (1) MA27167A1 (en)
MX (1) MXPA04006573A (en)
NO (1) NO20043457L (en)
OA (1) OA12756A (en)
PA (1) PA8563501A1 (en)
PE (1) PE20030929A1 (en)
PL (1) PL371487A1 (en)
TN (1) TNSN04121A1 (en)
TW (1) TW200302094A (en)
UY (1) UY27615A1 (en)
WO (1) WO2003061652A1 (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005051384A1 (en) * 2003-11-25 2005-06-09 Pfizer Limited Stabilised pharmaceutical compositions
WO2006113247A1 (en) * 2005-04-18 2006-10-26 Bayer Schering Pharma Aktiengesellschaft Use of tafi inhibitors for enhanced myocardial reperfusion and facilitated pci
US20110213143A1 (en) 2008-10-29 2011-09-01 Taisho Pharmaceutical Co., Ltd. Compound having tafia inhibitory activity
US8987242B2 (en) 2008-12-05 2015-03-24 Merck Sharp & Dohme Corp. Morpholinone compounds as factor IXA inhibitors
TW201033184A (en) 2008-12-05 2010-09-16 Mochida Pharm Co Ltd Morpholinone compounds as factor IXa inhibitors
EP2548871B1 (en) 2010-03-18 2017-07-19 Daiichi Sankyo Company, Limited Cycloalkyl-substituted imidazole derivative
WO2011115065A1 (en) * 2010-03-18 2011-09-22 第一三共株式会社 Cyclopropanecarboxylic acid derivative
JP6461113B2 (en) 2013-06-10 2019-01-30 サノフイSanofi Macrocyclic urea derivatives as inhibitors of TAFIa, their preparation and use as pharmaceuticals
WO2017170460A1 (en) 2016-03-29 2017-10-05 第一三共株式会社 Inflammatory intestinal disease therapeutic agent
EP3682881A4 (en) 2017-09-14 2021-08-11 Daiichi Sankyo Company, Limited Compound having cyclic structure

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9901572D0 (en) * 1999-05-03 1999-05-03 Astra Ab New compounds
PL361054A1 (en) * 2000-08-17 2004-09-20 Pfizer Inc. Substituted imidazoles as tafia inhibitors

Also Published As

Publication number Publication date
NO20043457L (en) 2004-08-19
PL371487A1 (en) 2005-06-13
UY27615A1 (en) 2003-08-29
TW200302094A (en) 2003-08-01
KR20040077775A (en) 2004-09-06
JP2005520811A (en) 2005-07-14
AR038197A1 (en) 2005-01-05
PA8563501A1 (en) 2004-08-31
CA2472238A1 (en) 2003-07-31
ECSP045200A (en) 2004-08-27
PE20030929A1 (en) 2003-11-05
BR0307016A (en) 2004-11-03
MA27167A1 (en) 2005-01-03
AP2004003084A0 (en) 2004-09-30
TNSN04121A1 (en) 2006-06-01
IL162677A0 (en) 2005-11-20
OA12756A (en) 2006-07-03
WO2003061652A8 (en) 2004-09-10
EP1467731A1 (en) 2004-10-20
HRP20040659A2 (en) 2004-10-31
MXPA04006573A (en) 2004-10-04
WO2003061652A1 (en) 2003-07-31
CN1620291A (en) 2005-05-25
IS7310A (en) 2004-06-14

Similar Documents

Publication Publication Date Title
EA200600358A1 (en) PHENYL OR PYRIDYLAMIDE COMPOUNDS AS ANTAGONISTS PROSTAGLANDINE E2
EA200600509A1 (en) COMPOUNDS OF PYRIMIDOTHIOPHENE
EA200701779A1 (en) DERIVATIVES (1,5-DIPHENYL-1N-PYRAZOL-3-IL) OXADIAZOLE, THEIR RECEIVING AND THEIR USE IN THERAPY
EA200200253A1 (en) INHIBITORS OF CELLULAR ADHESION
DE60332856D1 (en) GLYCINNITRIL BASED DIPEPTIDYLPEPTIDASE IV INHIBITORS
ATE427300T1 (en) HETEROCYCLIC SUBSTITUTED AMIDES AS CALPAIN INHIBITORS
DK0705254T3 (en) Phenyl heterocyclic compounds as cyclooxygenase-2 inhibitors
PT1052254E (en) Nitrogenous heterocyclic derivatives and medicine thereof
EA200801534A1 (en) 3`-ALCOXYPIPROCYCLOPENTILIZED TETRAMIC AND TETRONIC ACIDS
BRPI0508464A (en) sulfonylpyrrols
DK0892780T3 (en) m-Amidinophenyl analogues as factor Xa inhibitors
EA200400716A1 (en) 3- (IMIDAZOLYL) -2-ALCOXYPROPIONIC ACIDS AS TAFIA INHIBITORS (THROMBIN-ACTIVATED FIBRINOLYSIS INHIBITOR)
ATE442139T1 (en) 3-OXO-1,3-DIHYDRO-INDAZOLE-2-CARBONIC ACID AMIDE DERIVATIVES AS PHOSPHOLIPASE INHIBITORS
EA200201071A1 (en) CYCLOPENTYL SUBSTITUTED GLUTARAMIDE DERIVATIVES AS INHIBITORS NEUTRAL ENDOPEPTIDASE INHIBITORS
BR0313969A (en) Oxytocin Inhibitors
DE602004015158D1 (en) OXAZOLIDINONE-CHINOLON HYBRID ANTIBIOTICS
ATE363276T1 (en) TRIPEPTIDYLPEPTIDASE INHIBITORS
ATE235462T1 (en) METALLOPROTEINASE INHIBITORS
MXPA04005940A (en) 3-(imidazolyl)-2-aminopropanoic acids for use as tafi-a inhibitors for the treatment of thrombotic diseases.
EA200200596A1 (en) OX (ADI) AZOLYL HYDROXAMIC ACIDS, USEFUL AS PROGOLAGEN-C-PROTEINASE AS USE AS INHIBITORS
NO970340L (en) Organic compounds
DK1899331T3 (en) Homomorpholinoxazolidones as antibacterial agents
EA199901006A1 (en) FUNGICIDE MIXTURE
BR0317719A (en) Phosphoramide Derivatives
EA200101103A1 (en) NEW 15 MEMBERS 8- AND 9a LACTAMS