SI1135391T1 - Novel triazolo(4,5-d)pyrimidine compounds - Google Patents

Novel triazolo(4,5-d)pyrimidine compounds

Info

Publication number
SI1135391T1
SI1135391T1 SI9930550T SI9930550T SI1135391T1 SI 1135391 T1 SI1135391 T1 SI 1135391T1 SI 9930550 T SI9930550 T SI 9930550T SI 9930550 T SI9930550 T SI 9930550T SI 1135391 T1 SI1135391 T1 SI 1135391T1
Authority
SI
Slovenia
Prior art keywords
pyrimidine compounds
novel triazolo
triazolo
novel
pyrimidine
Prior art date
Application number
SI9930550T
Other languages
English (en)
Slovenian (sl)
Inventor
Simon Astra Charnwood Guile
David Astra Charnwood Hardern
Anthony Astra Charnwood Ingall
Brian Astra Charnwood SPRINGTHORPE
Paul Astra Charnwood WILLIS
Original Assignee
Astrazeneca Ab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26663448&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SI1135391(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from SE9804211A external-priority patent/SE9804211D0/xx
Priority claimed from SE9901271A external-priority patent/SE9901271D0/xx
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of SI1135391T1 publication Critical patent/SI1135391T1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • 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
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/33Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C211/39Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton
    • C07C211/40Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton containing only non-condensed rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Diabetes (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Vascular Medicine (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
SI9930550T 1998-12-04 1999-12-02 Novel triazolo(4,5-d)pyrimidine compounds SI1135391T1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE9804211A SE9804211D0 (sv) 1998-12-04 1998-12-04 Novel compounds
SE9901271A SE9901271D0 (sv) 1999-04-09 1999-04-09 Novel compounds
EP99963796A EP1135391B1 (fr) 1998-12-04 1999-12-02 Nouveaux composes de triazolo(4,5-d)pyrimidine
PCT/SE1999/002256 WO2000034283A1 (fr) 1998-12-04 1999-12-02 Nouveaux composes de triazolo(4,5-d)pyrimidine

Publications (1)

Publication Number Publication Date
SI1135391T1 true SI1135391T1 (en) 2004-08-31

Family

ID=26663448

Family Applications (3)

Application Number Title Priority Date Filing Date
SI9931026T SI1386921T1 (sl) 1998-12-04 1999-12-02 Intermediati za pripravo antitrombotičnih 4H-ciklopenta-1,3-dioksolnih derivatov
SI9930550T SI1135391T1 (en) 1998-12-04 1999-12-02 Novel triazolo(4,5-d)pyrimidine compounds
SI9931059T SI1386917T1 (sl) 1998-12-04 1999-12-02 Intermediati za pripravo nekaterih triazolopirimidinov kot P2T antagonistov

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SI9931026T SI1386921T1 (sl) 1998-12-04 1999-12-02 Intermediati za pripravo antitrombotičnih 4H-ciklopenta-1,3-dioksolnih derivatov

Family Applications After (1)

Application Number Title Priority Date Filing Date
SI9931059T SI1386917T1 (sl) 1998-12-04 1999-12-02 Intermediati za pripravo nekaterih triazolopirimidinov kot P2T antagonistov

Country Status (36)

Country Link
US (12) US6525060B1 (fr)
EP (5) EP1386909A1 (fr)
JP (4) JP4202607B2 (fr)
KR (4) KR100776484B1 (fr)
CN (1) CN1128801C (fr)
AR (3) AR023920A1 (fr)
AT (3) ATE261970T1 (fr)
AU (1) AU766618B2 (fr)
BR (1) BRPI9915883B8 (fr)
CA (1) CA2351709C (fr)
CY (3) CY1110501T1 (fr)
CZ (3) CZ295234B6 (fr)
DE (4) DE69915675D1 (fr)
DK (3) DK1386921T3 (fr)
EG (1) EG24814A (fr)
ES (3) ES2216623T3 (fr)
FR (1) FR11C0016I2 (fr)
HK (3) HK1039933B (fr)
HU (2) HU228589B1 (fr)
ID (1) ID29927A (fr)
IL (6) IL143232A0 (fr)
LT (1) LTPA2011004I1 (fr)
LU (1) LU91819I2 (fr)
MY (1) MY121867A (fr)
NO (3) NO319806B1 (fr)
NZ (1) NZ511778A (fr)
PL (1) PL201283B1 (fr)
PT (2) PT1135391E (fr)
RU (3) RU2317990C2 (fr)
SA (1) SA99200848B1 (fr)
SI (3) SI1386921T1 (fr)
SK (1) SK286007B6 (fr)
TR (1) TR200101567T2 (fr)
TW (1) TWI229674B (fr)
WO (1) WO2000034283A1 (fr)
ZA (1) ZA200104094B (fr)

Families Citing this family (124)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI229674B (en) 1998-12-04 2005-03-21 Astra Pharma Prod Novel triazolo[4,5-d]pyrimidine compounds, pharmaceutical composition containing the same, their process for preparation and uses
SE9903290D0 (sv) * 1999-09-15 1999-09-15 Astra Pharma Prod Novel compounds
SE9904129D0 (sv) 1999-11-15 1999-11-15 Astra Pharma Prod Novel compounds
SE9904377D0 (sv) * 1999-12-01 1999-12-01 Astra Pharma Prod Pharmaceutical combinations
GB0013407D0 (en) * 2000-06-02 2000-07-26 Astrazeneca Ab Forms of a chemical compound
TWI290549B (en) * 2000-06-02 2007-12-01 Astrazeneca Ab Process for the preparation of cyclopropyl carboxylic acid ester and derivatives
GB0013488D0 (en) * 2000-06-02 2000-07-26 Astrazeneca Ab Chemical compound
US6897201B2 (en) 2000-08-21 2005-05-24 Inspire Pharmaceuticals, Inc. Compositions and methods for the treatment of glaucoma or ocular hypertension
US7115585B2 (en) 2000-08-21 2006-10-03 Inspire Pharmaceuticals, Inc. Compositions for treating epithelial and retinal tissue diseases
US7452870B2 (en) 2000-08-21 2008-11-18 Inspire Pharmaceuticals, Inc. Drug-eluting stents coated with P2Y12 receptor antagonist compound
US7018985B1 (en) 2000-08-21 2006-03-28 Inspire Pharmaceuticals, Inc. Composition and method for inhibiting platelet aggregation
US7132408B2 (en) 2000-08-21 2006-11-07 Inspire Pharmaceuticals, Inc. Composition and method for inhibiting platelet aggregation
SE0101932D0 (sv) * 2001-05-31 2001-05-31 Astrazeneca Ab Pharmaceutical combinations
US7435724B2 (en) 2002-02-27 2008-10-14 Inspire Pharmaceutical, Inc. Degradation-resistant mononucleoside phosphate compounds
CA2530352A1 (fr) * 2003-07-24 2005-02-03 Astellas Pharma Inc. Derive de quinolone ou sel de ce dernier
SE0400873D0 (sv) * 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
SE0401001D0 (sv) 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
JPWO2007020935A1 (ja) * 2005-08-17 2009-02-26 小野薬品工業株式会社 P2y12受容体および/またはp2y14受容体ブロッカーを含有してなる疼痛治療剤
TWI391378B (zh) 2006-03-16 2013-04-01 Astellas Pharma Inc 喹啉酮衍生物或其製藥學上可被容許之鹽
GB0615620D0 (en) 2006-08-05 2006-09-13 Astrazeneca Ab A process for the preparation of optically active intermediates
TWI482772B (zh) 2006-08-21 2015-05-01 Astrazeneca Ab 適合口服且包含三唑并[4,5-d]嘧啶衍生物之組合物
WO2008024044A1 (fr) * 2006-08-21 2008-02-28 Astrazeneca Ab Compositions pour administration orale comprenant un dérivé de triazolo [4, 5] pyrimidine
JP2010508350A (ja) 2006-10-31 2010-03-18 ヤンセン ファーマシューティカ エヌ.ベー. Adpp2y12レセプターアンタゴニストとしてのトリアゾロピリミジン誘導体
TWI496776B (zh) * 2007-11-15 2015-08-21 Astrazeneca Ab 製備(3aR,4S,6R,6aS)-6-胺基-2,2-二甲基四氫-3aH-環戊并[d][1,3]二氧雜環戊烯-4-醇之純非對映異構性之二苯甲醯-L-酒石酸鹽之方法
UA100864C2 (uk) * 2007-12-03 2013-02-11 Астразенека Аб Спосіб лікування або запобігання аневризмі черевної аорти
TWI389913B (zh) * 2008-09-08 2013-03-21 Lg Life Sciences Ltd 并合雜環化合物
EP2340252B1 (fr) * 2008-09-09 2015-11-11 AstraZeneca AB Procédé pour préparer le [1s-[1-alpha,2-alpha,3-bêta(1s*,2r*)-5-bêta]]-3-[7-[2-(3,4-difluorophényl)-cyclopropylamino]-5-(propylthio)-3h-1,2,3-triazolo[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyéthoxy)cyclopentane-1,2-diol et ses intermédiaires
WO2010043721A1 (fr) 2008-10-17 2010-04-22 Oryzon Genomics, S.A. Inhibiteurs d’oxydases et leur utilisation
WO2010084160A1 (fr) 2009-01-21 2010-07-29 Oryzon Genomics S.A. Dérivés de phénylcyclopropylamine et leur utilisation médicale
CA2768043A1 (fr) * 2009-07-27 2011-02-10 Auspex Pharmaceuticals, Inc. Modulateurs cyclopropyles du recepteur p2y12
EP2305376A1 (fr) 2009-09-23 2011-04-06 Lonza Ltd. Procédé et catalyseur pour l'hydrogénation catalytique de composés de nitro aromatiques et hétéro-aromatiques
US8859555B2 (en) 2009-09-25 2014-10-14 Oryzon Genomics S.A. Lysine Specific Demethylase-1 inhibitors and their use
US8946296B2 (en) 2009-10-09 2015-02-03 Oryzon Genomics S.A. Substituted heteroaryl- and aryl-cyclopropylamine acetamides and their use
MX2012006375A (es) 2009-12-03 2013-03-21 Astrazeneca Ab Co-cristales de un inhibidor de agregacion de plaquetas de triazolo [4, 5-d] pirimidina.
ES2548845T3 (es) 2009-12-23 2015-10-21 Ratiopharm Gmbh Forma de dosificación farmacéutica sólida de ticagrelor y ácido acetilsalicílico
AU2011216991A1 (en) 2010-02-16 2012-08-30 Actavis Group Ptc Ehf Improved processes for preparing ticagrelor intermediate, 4,6-dichloro-5-nitro-2-(propylthio)pyrimidine
WO2011106106A2 (fr) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Inhibiteurs de lysine déméthylase pour lutter contre les maladies et troubles associés à l'hepadnaviridae
WO2011106574A2 (fr) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Inhibiteurs destinés à une utilisation antivirale
RS55348B1 (sr) 2010-04-19 2017-03-31 Oryzon Gnomics S A Inhibitori lizin specifične demetilaze-1 i njihova upotreba
EP2560939A2 (fr) 2010-04-20 2013-02-27 Actavis Group Ptc Ehf Nouveau procédé de préparation de dérivés de phénylcyclopropylamine par utilisation de nouveaux intermédiaires
CN103003231A (zh) 2010-06-30 2013-03-27 阿特维斯集团公司 制备苯基环丙基胺衍生物的新方法及其用于制备替卡格雷的用途
EP2598482B1 (fr) 2010-07-29 2018-04-04 Oryzon Genomics, S.A. Inhibiteurs de déméthylase lsd1 base d'arylcyclopropylamine et leur utilisation médicale
EP2598480B1 (fr) 2010-07-29 2019-04-24 Oryzon Genomics, S.A. Dérivés de cyclopropylamine utiles en tant qu'inhibiteurs de lsd1
WO2012045883A1 (fr) 2010-10-08 2012-04-12 Oryzon Genomics S.A. Inhibiteurs d'oxydases de cyclopropylamine
WO2012063126A2 (fr) 2010-11-09 2012-05-18 Actavis Group Ptc Ehf Procédés améliorés de préparation de (3ar,4s,6r,6as)-6-amino-2,2-diméthyltétrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol pur et son matériau de départ clé
WO2012072713A2 (fr) 2010-11-30 2012-06-07 Oryzon Genomics, S.A. Inhibiteurs de la déméthylase spécifique de la lysine pour des maladies et troubles liés aux flaviviridés
MX2013007115A (es) 2010-12-20 2014-02-10 Actavis Group Ptc Ehf Procesos novedosos para preparar derivados de triazolo[4, 5 - d] pirimidina e intermediarios de los mismos.
WO2012107498A1 (fr) 2011-02-08 2012-08-16 Oryzon Genomics S.A. Inhibiteurs de lysine diméthylase pour des troubles myéloprolifératifs
CN102653539B (zh) * 2011-03-01 2014-09-17 秦引林 一种抗血小板聚集化合物及其药物组合
BR112013025680A2 (pt) 2011-04-06 2017-01-03 Teva Pharma Novos intermediários e processos para preparar ticagrelor
CN102731510B (zh) * 2011-04-07 2015-12-16 博瑞生物医药(苏州)股份有限公司 替卡格雷的衍生物、制备方法及其药物用途
CZ2011229A3 (cs) * 2011-04-19 2012-08-15 Zentiva, K.S. Opticky aktivní soli (3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyklopenta-[d][1,3]dioxol-4-olu a zpusob jejich prípravy
TWI537256B (zh) * 2011-05-13 2016-06-11 阿斯特捷利康公司 製備[(3aS,4R,6S,6aR)-6-羥基-2,2-二甲基四氫-3aH-環戊并[d][1,3]二氧戊環-4-基]胺甲酸苄基酯之方法及該方法中的中間體
WO2012156531A2 (fr) * 2011-05-19 2012-11-22 Oryzon Genomics, S.A. Inhibiteurs de la lysine déméthylase destinés au traitement de maladies ou états inflammatoires
WO2012156537A2 (fr) * 2011-05-19 2012-11-22 Oryzon Genomics, S.A. Inhibiteurs de la lysine déméthylase destinés au traitement de la thrombose et de maladies cardiovasculaires
CN103764149A (zh) 2011-06-01 2014-04-30 阿斯利康(瑞典)有限公司 新型替卡格雷共晶
EP2721018A1 (fr) 2011-06-15 2014-04-23 Actavis Group Ptc Ehf Procédé amélioré de préparation de dérivés de cyclopentanamine et de leurs intermédiaires
CN102924457A (zh) * 2011-08-12 2013-02-13 上海恒瑞医药有限公司 三唑并嘧啶类衍生物、其制备方法及其用途
EP2570405A1 (fr) 2011-09-14 2013-03-20 LEK Pharmaceuticals d.d. Synthèse de composés de triazolopyrimidines
CA2848621C (fr) 2011-09-14 2019-10-01 Lek Pharmaceuticals D.D. Synthese de composes de triazolopyrimidine
MX356344B (es) 2011-10-20 2018-05-23 Oryzon Genomics Sa Compuestos de (hetero)arilciclopropilamina como inhibidores de lsd1.
IN2014CN03337A (fr) 2011-10-20 2015-07-03 Oryzon Genomics Sa
EP2586773A1 (fr) 2011-10-27 2013-05-01 LEK Pharmaceuticals d.d. Synthèse de composés de type triazolopyrimidine
PL2771326T4 (pl) * 2011-10-27 2018-06-29 Lek Pharmaceuticals D.D. Synteza związków triazolopirymidynowych
EP2589587A1 (fr) 2011-11-04 2013-05-08 Chemo Ibérica, S.A. Synthèse de cyclopropanes à substitution azote
RU2014126351A (ru) 2011-11-30 2016-01-27 Актавис Груп Птс Ехф Новая кристаллическая форма тикагрелора и способ ее получения
EP2794575B1 (fr) * 2011-12-23 2018-12-05 LEK Pharmaceuticals d.d. Synthèse de triazolopyrimidines
EP2607355A1 (fr) * 2011-12-23 2013-06-26 LEK Pharmaceuticals d.d. Synthèse de triazolopyrimidines
EP2628721A1 (fr) 2012-02-20 2013-08-21 LEK Pharmaceuticals d.d. Synthèse de l'acide 2-(3,4-difluorophényl) cyclopropanecarboxylique
CN104603098B (zh) 2012-03-30 2016-06-29 桑多斯股份公司 2-(3,4-二氟苯基)环丙胺衍生物和盐的合成
EP2644590A1 (fr) 2012-03-30 2013-10-02 LEK Pharmaceuticals d.d. Synthèse de dérivés et sels de 2-(3,4-difluorophényl) cyclopropanamine
EP2834247A4 (fr) 2012-04-05 2016-03-30 Reddys Lab Ltd Dr Préparation de ticagrelor
WO2013163892A1 (fr) * 2012-05-02 2013-11-07 Sunshine Lake Pharma Co., Ltd. Nouveaux composés de triazolopyrimidine et leur procédé de préparation
CN102659815B (zh) * 2012-05-04 2013-07-17 开原亨泰制药股份有限公司 一种制备选择性抗凝血药替卡格雷及其中间体的方法
EP2666771A1 (fr) 2012-05-24 2013-11-27 LEK Pharmaceuticals d.d. Synthèse de dérivés aminocyclopentanétriols
ITMI20121142A1 (it) * 2012-06-28 2013-12-29 Chemo Iberica Sa Processo chemoenzimatico per la produzione di fenil ciclopropilammine
WO2014000719A1 (fr) 2012-06-29 2014-01-03 Zentiva, K.S. Nouvelles formes pharmaceutiques solides de (1s,2s,3r,5s)-3-[7-[(1r,2s)-2-(3,4difluorophényl)cyclopropylamino]-5-(propylthio)-3h-[1,2,3]triazolo[4,5-d]pyrimidin-3yl]-5-(2-hydroxyéthoxy)cyclopentane-l,2-diol
CA2877541C (fr) * 2012-07-04 2020-06-30 Lek Pharmaceuticals D.D. Produits d'addition de ticagrelor et de sels metalliques divalents
CN103626743B (zh) * 2012-08-23 2018-06-08 广东东阳光药业有限公司 替卡格雷的新型中间体及其制备方法
CN102875537A (zh) * 2012-09-10 2013-01-16 常州制药厂有限公司 一种新的抗血栓药物的制备方法
CZ2012705A3 (cs) 2012-10-16 2014-04-23 Zentiva, K.S. Pevná orální farmaceutická formulace obsahující ticagrelor
WO2014083139A1 (fr) 2012-11-29 2014-06-05 Actavis Group Ptc Ehf Nouvelle forme amorphe de ticagrelor
WO2014102830A1 (fr) 2012-12-31 2014-07-03 Megafine Pharma (P) Ltd. Procédé de préparation de ticagrelor et de ses intermédiaires
CN104045620B (zh) * 2013-03-12 2017-05-10 博瑞生物医药(苏州)股份有限公司 一种替卡格雷中间体的制备方法
CZ307217B6 (cs) 2013-03-14 2018-04-04 Zentiva, K.S. Zlepšený způsob výroby a nové intermediáty syntézy ticagreloru
WO2014155389A2 (fr) * 2013-03-25 2014-10-02 Glenmark Pharmaceuticals Limited; Glenmark Generics Limited Procédé de préparation de ticagrelor
ITMI20130487A1 (it) 2013-03-29 2014-09-30 Chemo Res S L Alchilazione selettiva di ciclopentilalcoli
CN104098553B (zh) 2013-04-10 2017-11-28 江苏恒瑞医药股份有限公司 替格瑞洛的中间体及其制备方法和替格瑞洛的制备方法
EP2813216A1 (fr) 2013-06-10 2014-12-17 Zentiva, a.s. Ticagrelor amorphe stabilisé
WO2014170026A1 (fr) 2013-04-18 2014-10-23 Zentiva, K.S. Ticagrelor amorphe stabilisé
CN104230818B (zh) * 2013-06-06 2018-01-12 郝聪梅 替卡格雷中间体的改进制备方法
EP2816043A1 (fr) 2013-06-21 2014-12-24 LEK Pharmaceuticals d.d. Particules Ticagrelor sphériques
WO2014206187A1 (fr) 2013-06-24 2014-12-31 苏州明锐医药科技有限公司 Procédé de préparation du ticagrelor et de ses intermédiaires
CN104250251B (zh) * 2013-06-25 2017-05-17 上海京新生物医药有限公司 一种替格瑞洛的制备方法
WO2015001489A1 (fr) 2013-07-01 2015-01-08 Ranbaxy Laboratories Limited Compositions pharmaceutiques de ticagrélor
CZ2013866A3 (cs) 2013-11-08 2015-05-20 Zentiva, K.S. Způsob výroby a nová krystalická forma intermediátu syntézy ticagreloru
WO2015110952A1 (fr) 2014-01-21 2015-07-30 Wockhardt Limited Compositions pharmaceutiques orales solides comprenant du ticagrelor ou un sel de ce dernier
CN103992323B (zh) * 2014-04-18 2017-03-29 南通常佑药业科技有限公司 一种替格瑞洛的制备方法
WO2015162630A1 (fr) 2014-04-25 2015-10-29 Anlon Chemical Research Organization Nouveaux procédés de préparation de triazolo[4,5-d]-pyrimidines, dont le ticagrelor, via de nouveaux intermédiaires et une nouvelle voie de synthèse
DE102014108210A1 (de) 2014-06-11 2015-12-17 Dietrich Gulba Rodentizid
WO2015193165A1 (fr) 2014-06-18 2015-12-23 Flamma Spa Procédé pour la préparation de composés de triazolo[4,5-d]pyrimidine cyclopentane
CN105272985B (zh) * 2014-06-24 2017-11-21 珠海联邦制药股份有限公司 三唑并[4,5‑d]嘧啶化合物及其合成方法、用途、组合物
WO2016001851A1 (fr) * 2014-07-02 2016-01-07 Dr. Reddy's Laboratories Limited Préparation de ticagrélor
AU2015326869B2 (en) 2014-10-01 2021-04-29 Medimmune Limited Antibodies to ticagrelor and methods of use
WO2016116942A1 (fr) 2015-01-20 2016-07-28 Anlon Chemical Research Organization Nouveaux composés pharmaceutiques comprenant du ticagrélor avec des sels d'aspirine
CN105985346B (zh) * 2015-03-06 2019-10-18 苏州朗科生物技术股份有限公司 一种新的替格瑞洛化合物制备方法及其中间体化合物
US9789087B2 (en) 2015-08-03 2017-10-17 Thomas Jefferson University PAR4 inhibitor therapy for patients with PAR4 polymorphism
CN105237540B (zh) * 2015-09-21 2017-10-03 南京正大天晴制药有限公司 一种替格瑞洛有关物质的制备方法、检测方法及用途
US20190002471A1 (en) 2016-01-05 2019-01-03 Amneal Pharmaceuticals Company Gmbh Crystalline Form Of Ticagrelor
TR201601835A2 (tr) 2016-02-12 2017-08-21 Ali Raif Ilac Sanayi Ve Ticaret Anonim Sirketi Ti̇kagrelor i̇çeren formülasyonlar i̇çi̇n üreti̇m yöntemi̇
US20170296666A1 (en) 2016-04-18 2017-10-19 Amneal Pharmaceuticals Company Gmbh Stable Pharmaceutical Composition Of Amorphous Ticagrelor
IL262312B (en) 2016-04-21 2022-08-01 Astrazeneca Ab Tablets containing ticagrelor that disintegrate upon oral administration and a process for their preparation
RU2019108464A (ru) * 2016-08-26 2020-09-28 Мицубиси Танабе Фарма Корпорейшн Бициклическое азотсодержащее гетероциклическое соединение
DK3292867T3 (da) 2016-09-09 2019-07-22 Univ Liege Ny brug af triazol(4,5-d)pyrimidinderivater til brug i forebyggelsen og behandlingen af bakteriel infektion
US10905691B2 (en) 2016-09-09 2021-02-02 Université de Liège Use of triazolo(4,5-d)pyrimidine derivatives for prevention and treatment of bacterial infection
CN107814772A (zh) * 2017-11-24 2018-03-20 常州沃腾化工科技有限公司 4,6‑二氯‑5‑氨基‑2‑丙硫基嘧啶酯的精制方法
EP3527571A1 (fr) * 2018-02-14 2019-08-21 Université de Liège Dérivés de pyrimidine pour la prévention et le traitement d'infections bactériennes
EP3829547A1 (fr) 2018-07-27 2021-06-09 KRKA, d.d., Novo mesto Composition pharmaceutique de ticagrélor
CN109761785A (zh) * 2019-02-16 2019-05-17 安徽诺全药业有限公司 一种(1r,2r)-2-(3,4-二氟苯基)环丙烷羧酸的合成方法
GB201910656D0 (en) * 2019-07-25 2019-09-11 Univ Liege New use of triazolo(4,5-d)Pyrimidine deerivatives
EP3919497A1 (fr) 2020-06-04 2021-12-08 Zaklady Farmaceutyczne Polpharma S.A. Procédé de préparation de ticagrelor
CN112876485A (zh) * 2021-01-25 2021-06-01 郭丽伟 一种用于治疗子宫平滑肌高频率强直性收缩相关疾病的化合物
EP4070658A1 (fr) 2021-04-06 2022-10-12 BIORoxx GmbH Utilisation de composés anticoagulants comme rodenticides
CN117003756A (zh) * 2022-05-04 2023-11-07 华东师范大学 芳香稠环化合物作为trek-1激活剂的用途、包含其的药物组合物、镇痛剂

Family Cites Families (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3106578A (en) 1960-09-16 1963-10-08 Smith Kline French Lab Nu-phenethyl-2-phenylcyclopropylamine derivatives
SE329623B (fr) 1967-06-08 1970-10-19 C F Boehringer Soehne Gmbh
DE1670265A1 (de) 1967-08-25 1971-01-28 Boehringer Mannheim Gmbh 2-Amino-Adenosinderivate und Verfahren zu deren Herstellung
CH558137A (de) * 1971-05-17 1975-01-31 Ciba Geigy Ag Mittel zur beeinflussung des pflanzenwachstums.
US4016204A (en) 1975-10-31 1977-04-05 Nelson Research & Development Company Method of synthesis of trans-2-phenylcyclopropylamine
US4543255A (en) 1984-05-10 1985-09-24 Southern Research Institute Carbocyclic analogs of purine 2'-deoxyribofuranosides
US4742064A (en) 1985-09-10 1988-05-03 Regents Of The University Of Minnesota Antiviral carbocyclic analogs of xylofuranosylpurines
IT1229531B (it) 1988-01-20 1991-09-04 Univ Minnesota Composti nucleosidi dideossidideidrocarbociclici e formulazione farmaceutica che li contiene
CA2005192A1 (fr) 1988-12-12 1990-06-12 Peter M. Palese Methodes et composes pour la prophylaxie et le traitement des infections par le virus de l'hepatie b
US5110933A (en) 1989-11-13 1992-05-05 Board Of Regents Of Oklahoma State University Salts of 3-azabicyclo[3.3.1]nonanes as antiarrhythmic agents, and precursors thereof
US5652366A (en) 1990-09-25 1997-07-29 Rhone-Poulenc Rorer Pharmaceuticals Inc. DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof
WO1992012718A1 (fr) 1991-01-23 1992-08-06 Gensia, Inc. Inhibiteurs de l'adenosine-kinase
PL297372A1 (en) 1991-04-06 1993-09-06 Fisons Plc Atp analogs
EP0521463A3 (en) 1991-07-04 1993-04-14 Hoechst Aktiengesellschaft Substituted cyclic cycloalkyltriols, process, intermediates for their preparation and their use as antiviral and antiparasitic agents
FI101150B (fi) 1991-09-09 1998-04-30 Sankyo Co Menetelmä lääkeaineina käyttökelpoisten tetrahydrotienopyridiinin johd annaisten valmistamiseksi
US5817660A (en) 1991-12-06 1998-10-06 Hoechst Marion Roussel, Inc. Trans cyclopentanyl purine analogs useful as immunosuppressants
US5338725A (en) 1992-06-30 1994-08-16 The Research Foundation Of The State University Of New York Anti-aggregatory agents for platelets
IL108523A0 (en) 1993-02-03 1994-05-30 Gensia Inc Pharmaceutical compositions containing adenosine kinase inhibitors for preventing or treating conditions involving inflammatory responses and pain
AU679721B2 (en) 1993-02-10 1997-07-10 Astrazeneca Ab N-alkyl-2-substituted ATP analogues
US5688774A (en) 1993-07-13 1997-11-18 The United States Of America As Represented By The Department Of Health And Human Services A3 adenosine receptor agonists
US5620676A (en) 1994-03-08 1997-04-15 The United States Of America As Represented By The Department Of Health And Human Services Biologically active ATP analogs
US5831099A (en) 1995-03-10 1998-11-03 The United States Of America As Represented By The Secretary Of The Army Compounds of 1,5-disubstituted-3,7 diaza bicyclo 3.3.0! octanes and products containing the same
US5712258A (en) 1995-03-23 1998-01-27 The Trustees Of The University Of Pennsylvania Inotropic ADP and ATP analogues and their pharmaceutical compositions
US6143749A (en) 1995-06-07 2000-11-07 Abbott Laboratories Heterocyclic substituted cyclopentane compounds
US5747496A (en) 1995-07-11 1998-05-05 Astra Pharmaceuticals Limited Inhibitors of platelet aggregation
AU6754296A (en) 1995-09-01 1997-03-27 Hokuriku Seiyaku Co. Ltd Crystal of hydrate and process for preparation thereof
CA2235627C (fr) 1995-11-21 2010-08-10 Euroscreen S.A. Recepteur et molecule d'acide nucleique codant ledit recepteur
US5948437A (en) 1996-05-23 1999-09-07 Zeneca Limited Pharmaceutical compositions using thiazepine
EP0946561B1 (fr) * 1996-12-20 2002-02-13 AstraZeneca AB Derives de triazolo(4,5-d)pyrimidinyle et leur utilisation comme medicaments
JPH10258654A (ja) 1997-03-18 1998-09-29 Delta Tsuuring:Kk リクライニングシート
TW530058B (en) * 1997-07-22 2003-05-01 Astra Pharma Prod Triazolo [4,5-d]pyrimidine compounos and their use and process for preparation
SE9702772D0 (sv) 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9702775D0 (sv) 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9702773D0 (sv) 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9704709D0 (sv) 1997-12-17 1997-12-17 Astra Ab Pharmaceutically active compounds
TWI229674B (en) 1998-12-04 2005-03-21 Astra Pharma Prod Novel triazolo[4,5-d]pyrimidine compounds, pharmaceutical composition containing the same, their process for preparation and uses
EP1063231B1 (fr) 1999-06-21 2005-05-11 Yamamoto Chemicals, Inc. Composés polyméthiniques, procédé pour leur préparation et leur utilisation
SE9903759D0 (sv) 1999-10-18 1999-10-18 Astra Ab Pharmaceutically active compounds
TR200301062T2 (tr) 1999-11-12 2003-09-22 Biogen, Inc. Adenosin reseptörü antagonistleri ve bu antagonistlerin yapım ve kullanım yöntemleri
GB0013407D0 (en) 2000-06-02 2000-07-26 Astrazeneca Ab Forms of a chemical compound
US7040429B2 (en) 2001-10-10 2006-05-09 Invacare Corporation Wheelchair suspension
AU2002348884A1 (en) 2001-12-21 2003-07-09 Pfizer Products Inc. Directly compressible formulations of azithromycin
TWI482772B (zh) 2006-08-21 2015-05-01 Astrazeneca Ab 適合口服且包含三唑并[4,5-d]嘧啶衍生物之組合物
EP2340252B1 (fr) 2008-09-09 2015-11-11 AstraZeneca AB Procédé pour préparer le [1s-[1-alpha,2-alpha,3-bêta(1s*,2r*)-5-bêta]]-3-[7-[2-(3,4-difluorophényl)-cyclopropylamino]-5-(propylthio)-3h-1,2,3-triazolo[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyéthoxy)cyclopentane-1,2-diol et ses intermédiaires
AU2011216991A1 (en) 2010-02-16 2012-08-30 Actavis Group Ptc Ehf Improved processes for preparing ticagrelor intermediate, 4,6-dichloro-5-nitro-2-(propylthio)pyrimidine
CN103003231A (zh) 2010-06-30 2013-03-27 阿特维斯集团公司 制备苯基环丙基胺衍生物的新方法及其用于制备替卡格雷的用途
MX2013007115A (es) 2010-12-20 2014-02-10 Actavis Group Ptc Ehf Procesos novedosos para preparar derivados de triazolo[4, 5 - d] pirimidina e intermediarios de los mismos.
BR112013025680A2 (pt) 2011-04-06 2017-01-03 Teva Pharma Novos intermediários e processos para preparar ticagrelor
EP2721018A1 (fr) 2011-06-15 2014-04-23 Actavis Group Ptc Ehf Procédé amélioré de préparation de dérivés de cyclopentanamine et de leurs intermédiaires
RU2014126351A (ru) 2011-11-30 2016-01-27 Актавис Груп Птс Ехф Новая кристаллическая форма тикагрелора и способ ее получения
EP2834247A4 (fr) 2012-04-05 2016-03-30 Reddys Lab Ltd Dr Préparation de ticagrelor
WO2014083139A1 (fr) 2012-11-29 2014-06-05 Actavis Group Ptc Ehf Nouvelle forme amorphe de ticagrelor
WO2014102830A1 (fr) 2012-12-31 2014-07-03 Megafine Pharma (P) Ltd. Procédé de préparation de ticagrelor et de ses intermédiaires
WO2014118808A2 (fr) 2013-02-04 2014-08-07 Hetero Research Foundation Dispersion solide de ticagrelor
CN104098553B (zh) 2013-04-10 2017-11-28 江苏恒瑞医药股份有限公司 替格瑞洛的中间体及其制备方法和替格瑞洛的制备方法
EP3004113A2 (fr) 2013-06-04 2016-04-13 Dr. Reddy's Laboratories Ltd. Préparation de ticagrélor
WO2016001851A1 (fr) 2014-07-02 2016-01-07 Dr. Reddy's Laboratories Limited Préparation de ticagrélor
JP2018502894A (ja) 2015-01-27 2018-02-01 アストラゼネカ アクチボラグ 心筋梗塞の病歴がある患者においてアテローム血栓性イベントを治療または予防する方法

Also Published As

Publication number Publication date
IL143232A0 (en) 2002-04-21
ZA200104094B (en) 2002-08-19
LTC1135391I2 (lt) 2022-04-11
TWI229674B (en) 2005-03-21
IL143232A (en) 2008-12-29
IL198040A (en) 2015-06-30
DE69915675T2 (de) 2005-02-17
AR072756A2 (es) 2010-09-22
ES2366902T3 (es) 2011-10-26
HK1039933A1 (en) 2002-05-17
MY121867A (en) 2006-02-28
US20130072503A1 (en) 2013-03-21
FR11C0016I2 (fr) 2012-03-16
EP1386921B1 (fr) 2008-12-24
EG24814A (en) 2010-09-21
PT1386921E (pt) 2009-02-23
AR058967A2 (es) 2008-03-05
PT1135391E (pt) 2004-07-30
DE69940171D1 (de) 2009-02-05
DE69915675D1 (de) 2004-04-22
ES2216623T3 (es) 2004-10-16
ES2318081T3 (es) 2009-05-01
US6525060B1 (en) 2003-02-25
IL183969A0 (en) 2009-02-11
IL183969A (en) 2011-03-31
HK1039933B (zh) 2004-10-08
EP1135391A1 (fr) 2001-09-26
AU766618B2 (en) 2003-10-23
RU2593201C2 (ru) 2016-08-10
US20070265282A1 (en) 2007-11-15
HU228589B1 (en) 2013-04-29
US20030144305A1 (en) 2003-07-31
NO20012725L (no) 2001-07-31
WO2000034283A1 (fr) 2000-06-15
NZ511778A (en) 2003-10-31
DK1386917T3 (da) 2011-08-29
KR20010081054A (ko) 2001-08-25
PL201283B1 (pl) 2009-03-31
JP4202607B2 (ja) 2008-12-24
CY1110501T1 (el) 2015-04-29
US20120165348A1 (en) 2012-06-28
SK286007B6 (sk) 2008-01-07
CN1334816A (zh) 2002-02-06
EP1386909A1 (fr) 2004-02-04
CZ20011962A3 (cs) 2001-11-14
CA2351709A1 (fr) 2000-06-15
BRPI9915883B1 (pt) 2015-08-18
CN1128801C (zh) 2003-11-26
ATE418547T1 (de) 2009-01-15
AU2016500A (en) 2000-06-26
US20100069408A1 (en) 2010-03-18
JP5415383B2 (ja) 2014-02-12
KR100776484B1 (ko) 2007-11-28
EP1386917A1 (fr) 2004-02-04
HK1061246A1 (en) 2004-09-10
SI1386921T1 (sl) 2009-04-30
NO2022007I1 (no) 2022-03-23
JP2008266345A (ja) 2008-11-06
RU2007133926A (ru) 2009-03-20
US20150152111A1 (en) 2015-06-04
DK1386921T3 (da) 2009-03-23
KR100822602B1 (ko) 2008-04-16
BR9915883A (pt) 2001-08-21
SK7492001A3 (en) 2002-01-07
JP5043749B2 (ja) 2012-10-10
TR200101567T2 (tr) 2001-12-21
PL348724A1 (en) 2002-06-03
CZ300280B6 (cs) 2009-04-08
LU91819I2 (fr) 2011-08-01
KR20070007971A (ko) 2007-01-16
HUP0105081A2 (hu) 2002-05-29
US7250419B2 (en) 2007-07-31
FR11C0016I1 (fr) 2011-07-08
HUS1300048I1 (hu) 2017-03-28
EP2322513A2 (fr) 2011-05-18
IL169013A (en) 2015-10-29
US20140296258A1 (en) 2014-10-02
BRPI9915883B8 (pt) 2021-05-25
KR20070086540A (ko) 2007-08-27
IL210398A0 (en) 2011-03-31
NO319806B1 (no) 2005-09-19
NO2011007I1 (no) 2011-06-06
NO2011007I2 (no) 2012-07-09
EP1386921A1 (fr) 2004-02-04
DE69915675T4 (de) 2012-08-30
EP2322513A3 (fr) 2011-08-24
IL198040A0 (en) 2009-12-24
EP1135391B1 (fr) 2004-03-17
ATE261970T1 (de) 2004-04-15
RU2317990C2 (ru) 2008-02-27
DK1135391T3 (da) 2004-06-28
HK1061684A1 (en) 2004-09-30
HUP0105081A3 (en) 2004-11-29
US20130109702A1 (en) 2013-05-02
CA2351709C (fr) 2010-04-06
KR20060091056A (ko) 2006-08-17
CY2011005I1 (el) 2014-04-09
EP1386917B1 (fr) 2011-06-22
JP2002531567A (ja) 2002-09-24
SA99200848B1 (ar) 2006-11-04
NO20012725D0 (no) 2001-06-01
USRE46276E1 (en) 2017-01-17
DE122011100004I1 (de) 2011-09-08
SI1386917T1 (sl) 2011-09-30
LTPA2011004I1 (lt) 2022-04-11
CZ295234B6 (cs) 2005-06-15
RU2012121883A (ru) 2013-11-27
CY2011005I2 (el) 2014-04-09
CY1111759T1 (el) 2015-10-07
US20060025590A1 (en) 2006-02-02
KR100764417B1 (ko) 2007-10-05
AR023920A1 (es) 2002-09-04
US6974868B2 (en) 2005-12-13
KR100742924B1 (ko) 2007-07-25
JP2007084551A (ja) 2007-04-05
CZ300373B6 (cs) 2009-05-06
JP2011016831A (ja) 2011-01-27
ATE513816T1 (de) 2011-07-15
US20080214812A1 (en) 2008-09-04
ID29927A (id) 2001-10-25

Similar Documents

Publication Publication Date Title
HK1039933A1 (en) Novel triazolo(4,5-d)pyrimidine compounds
EG23758A (en) Pyrrolo (2,3-d) pyrimidine compounds
HK1026421A1 (en) Triazolo(4,5-d) pyrimidine derivatives as anti-thrombotic agents
AP9901584A0 (en) Pyrrolo[2,3-d] pyrimidine compounds
HK1051195A1 (en) Pyrrolo(2,3-d)pyrimidine compounds.
IL137812A0 (en) Novel triazolo (4,5-d) pyrimidine compounds
PL355637A1 (en) Pyrazolo[1,5-d][1,2,4]triazines for enhancing cognition
SI1222195T1 (en) Novel thiazolo(4,5-d)pyrimidine compounds
SI1087970T1 (en) PYRROLO 2,3-d)PYRIMIDINE COMPOUNDS
SI0996621T1 (en) TRIAZOLO(4,5-d)PYRIMIDINE DERIVATIVES AS ANTI-THROMBOTIC AGENTS
ZA994004B (en) Pyrrolo[2,3-d]pyrimidine compounds.