FR11C0016I2 - NEW TRIAZOLO(4,5-D)PYRIMIDINE COMPOUNDS - Google Patents

NEW TRIAZOLO(4,5-D)PYRIMIDINE COMPOUNDS

Info

Publication number
FR11C0016I2
FR11C0016I2 FR11C0016C FR11C0016C FR11C0016I2 FR 11C0016 I2 FR11C0016 I2 FR 11C0016I2 FR 11C0016 C FR11C0016 C FR 11C0016C FR 11C0016 C FR11C0016 C FR 11C0016C FR 11C0016 I2 FR11C0016 I2 FR 11C0016I2
Authority
FR
France
Prior art keywords
pyrimidine compounds
new triazolo
triazolo
new
pyrimidine
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
FR11C0016C
Other languages
French (fr)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
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=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR11C0016(I2) "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/en
Priority claimed from SE9901271A external-priority patent/SE9901271D0/en
Application filed by AstraZeneca AB filed Critical AstraZeneca AB
Publication of FR11C0016I1 publication Critical patent/FR11C0016I1/fr
Application granted granted Critical
Publication of FR11C0016I2 publication Critical patent/FR11C0016I2/en
Active legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/33—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C211/39—Compounds 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
    • C07C211/40—Compounds 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic 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
    • C07D239/28—Heterocyclic 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
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48—Two nitrogen atoms
FR11C0016C 1998-12-04 2011-05-23 NEW TRIAZOLO(4,5-D)PYRIMIDINE COMPOUNDS Active FR11C0016I2 (en)

Applications Claiming Priority (3)

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

Publications (2)

Publication Number Publication Date
FR11C0016I1 FR11C0016I1 (en) 2011-07-08
FR11C0016I2 true FR11C0016I2 (en) 2012-03-16

Family

ID=26663448

Family Applications (1)

Application Number Title Priority Date Filing Date
FR11C0016C Active FR11C0016I2 (en) 1998-12-04 2011-05-23 NEW TRIAZOLO(4,5-D)PYRIMIDINE COMPOUNDS

Country Status (36)

Country Link
US (12) US6525060B1 (en)
EP (5) EP1386921B1 (en)
JP (4) JP4202607B2 (en)
KR (4) KR100822602B1 (en)
CN (1) CN1128801C (en)
AR (3) AR023920A1 (en)
AT (3) ATE261970T1 (en)
AU (1) AU766618B2 (en)
BR (1) BRPI9915883B8 (en)
CA (1) CA2351709C (en)
CY (3) CY1110501T1 (en)
CZ (3) CZ295234B6 (en)
DE (4) DE69940171D1 (en)
DK (3) DK1386921T3 (en)
EG (1) EG24814A (en)
ES (3) ES2318081T3 (en)
FR (1) FR11C0016I2 (en)
HK (3) HK1039933B (en)
HU (2) HU228589B1 (en)
ID (1) ID29927A (en)
IL (6) IL143232A0 (en)
LT (1) LTC1135391I2 (en)
LU (1) LU91819I2 (en)
MY (1) MY121867A (en)
NO (2) NO319806B1 (en)
NZ (1) NZ511778A (en)
PL (1) PL201283B1 (en)
PT (2) PT1386921E (en)
RU (3) RU2317990C2 (en)
SA (1) SA99200848B1 (en)
SI (3) SI1386921T1 (en)
SK (1) SK286007B6 (en)
TR (1) TR200101567T2 (en)
TW (1) TWI229674B (en)
WO (1) WO2000034283A1 (en)
ZA (1) ZA200104094B (en)

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 (en) 1999-09-15 1999-09-15 Astra Pharma Prod Novel compounds
SE9904129D0 (en) 1999-11-15 1999-11-15 Astra Pharma Prod Novel compounds
SE9904377D0 (en) * 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
GB0013488D0 (en) 2000-06-02 2000-07-26 Astrazeneca Ab Chemical compound
TWI290549B (en) * 2000-06-02 2007-12-01 Astrazeneca Ab Process for the preparation of cyclopropyl carboxylic acid ester and derivatives
US6897201B2 (en) 2000-08-21 2005-05-24 Inspire Pharmaceuticals, Inc. Compositions and methods for the treatment of glaucoma or ocular hypertension
US7132408B2 (en) 2000-08-21 2006-11-07 Inspire Pharmaceuticals, Inc. Composition and method for inhibiting platelet aggregation
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
SE0101932D0 (en) * 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
EP1650192A4 (en) 2003-07-24 2007-03-21 Astellas Pharma Inc Quinolone derivative or salt thereof
SE0401001D0 (en) 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
SE0400873D0 (en) * 2004-03-31 2004-03-31 Astrazeneca Ab Chemical process
WO2007020935A1 (en) * 2005-08-17 2007-02-22 Ono Pharmaceutical Co., Ltd. Therapeutic agent for pain comprising p2y12 receptor and/or p2y14 receptor blocker
TWI391378B (en) 2006-03-16 2013-04-01 Astellas Pharma Inc Quinolone derivative or pharmaceutically acceptable salt thereof
GB0615620D0 (en) 2006-08-05 2006-09-13 Astrazeneca Ab A process for the preparation of optically active intermediates
TWI482772B (en) * 2006-08-21 2015-05-01 Astrazeneca Ab Compositions, suitable for oral administration, comprising a triazolo(4,5-d)pyrimidin derivate
WO2008024044A1 (en) * 2006-08-21 2008-02-28 Astrazeneca Ab Compositions, suitable for oral administration, comprising a triazolo [4, 5] pyrimidin derivate
US7566722B2 (en) * 2006-10-31 2009-07-28 Janssen Pharmaceutica, N.V. Triazolopyrimidine derivatives as ADP P2Y12 receptor antagonists
TWI496776B (en) * 2007-11-15 2015-08-21 Astrazeneca Ab A process for preparing a diastereomerically pure dibenzoyl-l-tartrate salt of (3ar, 4s, 6r, 6as)-6-amino-2, 2-dimethyltetrahydro-3ah-cyclopenta(d)(1, 3)-dioxol-4-ol
UA100864C2 (en) 2007-12-03 2013-02-11 Астразенека Аб Method for the for the treatment or prevention of abdominal aortic aneurysms
TWI389913B (en) * 2008-09-08 2013-03-21 Lg Life Sciences Ltd Fused heterocyclic compound
ES2558843T3 (en) 2008-09-09 2016-02-09 Astrazeneca Ab Procedure for preparing [1S- [1-alpha, 2-alpha, 3-beta (1S *, 2R *), 5-beta]] - 3- [7- [2- (3,4-difluorophenyl) -cyclopropylamino] -5- (propylthio) -3H-1,2,3-triazolo [4,5-d] pyrimidin-3-yl] -5- (2-hydroxyethoxy) cyclopentane-1,2-diol and its intermediates
EP2361242B1 (en) 2008-10-17 2018-08-01 Oryzon Genomics, S.A. Oxidase inhibitors and their use
WO2010084160A1 (en) 2009-01-21 2010-07-29 Oryzon Genomics S.A. Phenylcyclopropylamine derivatives and their medical use
EP2459564B1 (en) 2009-07-27 2016-09-07 Auspex Pharmaceuticals, Inc. Cyclopropyl modulators of p2y12 receptor
EP2305376A1 (en) 2009-09-23 2011-04-06 Lonza Ltd. Process and catalyst for the catalytic hydrogenation of aromatic and heteroaromatic nitro compounds
MX338041B (en) 2009-09-25 2016-03-30 Oryzon Genomics Sa Lysine specific demethylase-1 inhibitors and their use.
EP2486002B1 (en) 2009-10-09 2019-03-27 Oryzon Genomics, S.A. Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
CA2781182A1 (en) 2009-12-03 2011-06-09 Astrazeneca Ab Co - crystals of a triazolo [4,5 - d] pyrimidine platelet aggregation inhibitor
EA026094B1 (en) 2009-12-23 2017-03-31 Рациофарм Гмбх Solid dosage form of ticagrelor
CA2788072A1 (en) 2010-02-16 2011-08-25 Actavis Group Ptc Ehf Improved processes for preparing ticagrelor intermediate, 4,6-dichloro-5-nitro-2-(propylthio)pyrimidine
US9186337B2 (en) 2010-02-24 2015-11-17 Oryzon Genomics S.A. Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae
US9616058B2 (en) 2010-02-24 2017-04-11 Oryzon Genomics, S.A. Potent selective LSD1 inhibitors and dual LSD1/MAO-B inhibitors for antiviral use
KR101794020B1 (en) 2010-04-19 2017-11-06 오리존 지노믹스 에스.에이. Lysine specific demethylase-1 inhibitors and their use
EP2560939A2 (en) 2010-04-20 2013-02-27 Actavis Group Ptc Ehf Novel process for preparing phenylcyclopropylamine derivatives using novel intermediates
RU2013103794A (en) 2010-06-30 2014-08-10 Актавис Груп Птс Ехф NEW METHODS FOR PRODUCING Phenylcyclopropylamine Derivatives AND THEIR APPLICATION FOR PRODUCING TICAGRELOR
US9181198B2 (en) 2010-07-29 2015-11-10 Oryzon Genomics S.A. Arylcyclopropylamine based demethylase inhibitors of LSD1 and their medical use
WO2012013727A1 (en) 2010-07-29 2012-02-02 Oryzon Genomics S.A. Cyclopropylamine derivatives useful as lsd1 inhibitors
WO2012045883A1 (en) 2010-10-08 2012-04-12 Oryzon Genomics S.A. Cyclopropylamine inhibitors of oxidases
WO2012063126A2 (en) 2010-11-09 2012-05-18 Actavis Group Ptc Ehf Improved processes for preparing pure (3ar,4s,6r,6as)-6-amino-2,2-dimethyltetrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol and its key starting material
WO2012072713A2 (en) 2010-11-30 2012-06-07 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
MX2013007115A (en) 2010-12-20 2014-02-10 Actavis Group Ptc Ehf Novel processes for preparing triazolo[4,5-d]pyrimidine derivatives and intermediates thereof.
EP2712315B1 (en) 2011-02-08 2021-11-24 Oryzon Genomics, S.A. Lysine demethylase inhibitors for myeloproliferative disorders
CN102653539B (en) * 2011-03-01 2014-09-17 秦引林 Compound for resisting platelet aggregation and medicament combination thereof
CA2832570A1 (en) 2011-04-06 2012-10-11 Teva Pharmaceutical Industries Ltd. New intermediates and processes for preparing ticagrelor
CN102731510B (en) * 2011-04-07 2015-12-16 博瑞生物医药（苏州）股份有限公司 The derivative of ADZ6140, preparation method and pharmaceutical use thereof
CZ2011229A3 (en) * 2011-04-19 2012-08-15 Zentiva, K.S. Optically active salts of (3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopenta-[d][1,3]dioxol-4-ole and process for their preparation
BR112013028936B1 (en) * 2011-05-13 2021-10-19 Astrazeneca Ab PROCESS FOR THE PREPARATION OF BENZYL [(3AS,4R,6S,6AR)-6-HYDROXY-2,2-DIMETHYLTETRA-HYDRO-3AHCYCLOPENTA[D]DIOXOL]-4-YL]CARBAMATE AND INTERMEDIATE COMPOUNDS IN THE PROCESS
WO2012156537A2 (en) * 2011-05-19 2012-11-22 Oryzon Genomics, S.A. Lysine demethylase inhibitors for thrombosis and cardiovascular diseases
WO2012156531A2 (en) * 2011-05-19 2012-11-22 Oryzon Genomics, S.A. Lysine demethylase inhibitors for inflammatory diseases or conditions
KR20140028011A (en) 2011-06-01 2014-03-07 아스트라제네카 아베 Novel ticagrelor co-crystal
US20140206867A1 (en) 2011-06-15 2014-07-24 Actavis Group Ptc Ehf Process for Preparing Cyclopentylamine Derivatives and Intermediates Thereof
CN102924457A (en) * 2011-08-12 2013-02-13 上海恒瑞医药有限公司 Triazolopyrimidine derivatives, preparation method and uses thereof
EP2570405A1 (en) 2011-09-14 2013-03-20 LEK Pharmaceuticals d.d. Synthesis of Triazolopyrimidine Compounds
HUE031673T2 (en) 2011-09-14 2017-07-28 Lek Pharmaceuticals Synthesis of triazolopyrimidine compounds
CN107266345B (en) 2011-10-20 2021-08-17 奥瑞泽恩基因组学股份有限公司 (hetero) arylcyclopropylamine compounds as LSD1 inhibitors
RS58475B1 (en) 2011-10-20 2019-04-30 Oryzon Genomics Sa (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
WO2013060837A1 (en) 2011-10-27 2013-05-02 Lek Pharmaceuticals D.D. Synthesis of triazolopyrimidine compounds
EP2586773A1 (en) 2011-10-27 2013-05-01 LEK Pharmaceuticals d.d. Synthesis of Triazolopyrimidine Compounds
EP2589587A1 (en) 2011-11-04 2013-05-08 Chemo Ibérica, S.A. Synthesis of nitrogen substituted cyclopropanes
BR112014013085A2 (en) 2011-11-30 2017-06-13 Actavis Group Ptc Ehf ticagrelor crystalline form, process for preparing ticagrelor crystalline form, pharmaceutical composition and process for preparing a pharmaceutical composition
EP2607355A1 (en) * 2011-12-23 2013-06-26 LEK Pharmaceuticals d.d. Synthesis of triazolopyrimidine compounds
EP2794575B1 (en) * 2011-12-23 2018-12-05 LEK Pharmaceuticals d.d. Synthesis of triazolopyrimidine compounds
EP2628721A1 (en) 2012-02-20 2013-08-21 LEK Pharmaceuticals d.d. Synthesis of 2-(3,4-difluorophenyl)cyclopropanecarboxylic acid
EP2644590A1 (en) 2012-03-30 2013-10-02 LEK Pharmaceuticals d.d. Synthesis of 2-(3,4-difluorophenyl)cyclopropanamine derivatives and salts
CN104603098B (en) 2012-03-30 2016-06-29 桑多斯股份公司 The synthesis of 2-(3,4-difluorophenyl) cyclopropyl amine derivatives and salt
WO2013150495A2 (en) 2012-04-05 2013-10-10 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
WO2013163892A1 (en) * 2012-05-02 2013-11-07 Sunshine Lake Pharma Co., Ltd. Novel triazolo pyrimidine compounds and a process of preparation thereof
CN102659815B (en) * 2012-05-04 2013-07-17 开原亨泰制药股份有限公司 Method for preparing selective anticoagulant ticagrelor and intermediates thereof
EP2666771A1 (en) 2012-05-24 2013-11-27 LEK Pharmaceuticals d.d. Synthesis of Aminocyclopentanetriol Derivatives
ITMI20121142A1 (en) * 2012-06-28 2013-12-29 Chemo Iberica Sa CHEMOENZYMATIC PROCESS FOR THE PRODUCTION OF FENYL CYCLOPROPYLAMINE
BR112014032085A2 (en) * 2012-06-29 2017-06-27 Zentiva Ks ticagrelor solvate, processes for the preparation of a solvate and for the preparation of a cocrystal, ticagrelor cocrystal, and, uses of a solvate and a cocrystal
WO2014006091A1 (en) 2012-07-04 2014-01-09 Lek Pharmaceuticals D.D. Ticagrelor adducts with divalent metal salts
CN103626743B (en) * 2012-08-23 2018-06-08 广东东阳光药业有限公司 New intermediate of Ticagrelor and preparation method thereof
CN102875537A (en) * 2012-09-10 2013-01-16 常州制药厂有限公司 Novel preparation method of antithrombosis medicine
CZ2012705A3 (en) 2012-10-16 2014-04-23 Zentiva, K.S. Solid oral pharmaceutical formulation containing ticagrelor
WO2014083139A1 (en) 2012-11-29 2014-06-05 Actavis Group Ptc Ehf Novel amorphous form of ticagrelor
WO2014102830A1 (en) 2012-12-31 2014-07-03 Megafine Pharma (P) Ltd. A process for preparation of ticagrelor and intermediates thereof
CN104045620B (en) * 2013-03-12 2017-05-10 博瑞生物医药（苏州）股份有限公司 Preparation method of intermediate of ticagrelor
CZ307217B6 (en) 2013-03-14 2018-04-04 Zentiva, K.S. An improved manufacturing process and new intermediates for synthesis of ticagrelor
IN2013MU01111A (en) * 2013-03-25 2015-05-01 Glenmark Generics Ltd
ITMI20130487A1 (en) 2013-03-29 2014-09-30 Chemo Res S L SELECTIVE ALCHILATION OF CYCLOPENTILALCULES
CN107573333B (en) 2013-04-10 2019-10-18 江苏恒瑞医药股份有限公司 The preparation method of intermediate of ticagrelor and preparation method thereof and ticagrelor
EP2813216A1 (en) 2013-06-10 2014-12-17 Zentiva, a.s. Stabilized amorphous ticagrelor
WO2014170026A1 (en) 2013-04-18 2014-10-23 Zentiva, K.S. Stabilized amorphous ticagrelor
CN104230818B (en) * 2013-06-06 2018-01-12 郝聪梅 The improvement preparation method of ticagrelor midbody
EP2816043A1 (en) 2013-06-21 2014-12-24 LEK Pharmaceuticals d.d. Spherical ticagrelor particles
WO2014206187A1 (en) 2013-06-24 2014-12-31 苏州明锐医药科技有限公司 Preparation method of ticagrelor and intermediates thereof
CN104250251B (en) * 2013-06-25 2017-05-17 上海京新生物医药有限公司 Preparation method for ticagrelor
WO2015001489A1 (en) 2013-07-01 2015-01-08 Ranbaxy Laboratories Limited Pharmaceutical compositions of ticagrelor
CZ2013866A3 (en) 2013-11-08 2015-05-20 Zentiva, K.S. Novel crystalline form of ticagrelor synthesis intermediate and process for preparing thereof
WO2015110952A1 (en) 2014-01-21 2015-07-30 Wockhardt Limited Solid oral pharmaceutical compositions comprising ticagrelor or salt thereof
CN103992323B (en) * 2014-04-18 2017-03-29 南通常佑药业科技有限公司 A kind of preparation method of ticagrelor
WO2015162630A1 (en) 2014-04-25 2015-10-29 Anlon Chemical Research Organization Novel processes for preparing triazolo [4,5-d]- pyrimidines, including ticagrelor, vianew intermediates and new route of synthesis.
DE102014108210A1 (en) 2014-06-11 2015-12-17 Dietrich Gulba rodenticide
US10011605B2 (en) 2014-06-18 2018-07-03 Flamma Spa Process for the preparation of triazolo[4,5-D] pyrimidine cyclopentane compounds
CN105272985B (en) * 2014-06-24 2017-11-21 珠海联邦制药股份有限公司 Triazol [4,5 d] pyrimidine compound and its synthetic method, purposes, composition
WO2016001851A1 (en) * 2014-07-02 2016-01-07 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
US9982061B2 (en) * 2014-10-01 2018-05-29 Medimmune Limited Antibodies to ticagrelor and methods of use
WO2016116942A1 (en) 2015-01-20 2016-07-28 Anlon Chemical Research Organization Novel pharmaceutical compounds comprising ticagrelor with salts of aspirin
CN105985346B (en) * 2015-03-06 2019-10-18 苏州朗科生物技术股份有限公司 A kind of new ticagrelor compounds process for production thereof and its midbody compound
US9789087B2 (en) 2015-08-03 2017-10-17 Thomas Jefferson University PAR4 inhibitor therapy for patients with PAR4 polymorphism
CN105237540B (en) * 2015-09-21 2017-10-03 南京正大天晴制药有限公司 Preparation method, detection method and purposes of a kind of ticagrelor about material
US20190002471A1 (en) 2016-01-05 2019-01-03 Amneal Pharmaceuticals Company Gmbh Crystalline Form Of Ticagrelor
TR201601835A2 (en) 2016-02-12 2017-08-21 Ali Raif Ilac Sanayi Ve Ticaret Anonim Sirketi PRODUCTION METHOD FOR FORMULATIONS CONTAINING TIKAGRELOR
US20170296666A1 (en) 2016-04-18 2017-10-19 Amneal Pharmaceuticals Company Gmbh Stable Pharmaceutical Composition Of Amorphous Ticagrelor
EA201892150A1 (en) 2016-04-21 2019-05-31 Астразенека Аб DECOMING IN THE ORAL CAVITY TABLETS
RU2019108464A (en) * 2016-08-26 2020-09-28 Мицубиси Танабе Фарма Корпорейшн BICYCLIC NITROGEN-CONTAINING HETEROCYCLIC COMPOUND
DK3292867T3 (en) 2016-09-09 2019-07-22 Univ Liege NEW USE OF TRIAZOL (4,5-D) PYRIMIDINE DERIVATIVES FOR USE IN THE PREVENTION AND TREATMENT OF BACTERIAL INFECTION
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 (en) * 2017-11-24 2018-03-20 常州沃腾化工科技有限公司 The process for purification of the rosickyite yl pyrimidines ester of 4,6 dichloro, 5 amino 2
EP3527571A1 (en) * 2018-02-14 2019-08-21 Université de Liège Pyrimidine derivatives for prevention and treatment of bacterial infection
WO2020021110A1 (en) 2018-07-27 2020-01-30 Krka, D.D., Novo Mesto Pharmaceutical composition of ticagrelor
CN109761785A (en) * 2019-02-16 2019-05-17 安徽诺全药业有限公司 The synthetic method of one kind (1R, 2R) -2- (3,4- difluorophenyl) cyclopropane-carboxylic acid
GB201910656D0 (en) 2019-07-25 2019-09-11 Univ Liege New use of triazolo(4,5-d)Pyrimidine deerivatives
EP3919497A1 (en) 2020-06-04 2021-12-08 Zaklady Farmaceutyczne Polpharma S.A. Process for the preparation of ticagrelor
CN112876485A (en) * 2021-01-25 2021-06-01 郭丽伟 Compound for treating uterine smooth muscle high-frequency tonic contraction related diseases
EP4070658A1 (en) 2021-04-06 2022-10-12 BIORoxx GmbH Use of anticoagulant active compounds as rodenticide
WO2023213198A1 (en) * 2022-05-04 2023-11-09 华东师范大学 Use of aromatic fused ring compound as trek-1 activator, and pharmaceutical composition and analgesic containing same

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 (en) 1967-06-08 1970-10-19 C F Boehringer Soehne Gmbh
DE1670265A1 (en) 1967-08-25 1971-01-28 Boehringer Mannheim Gmbh 2-amino-adenosine derivatives and processes for their preparation
CH558137A (en) 1971-05-17 1975-01-31 Ciba Geigy Ag MEANS OF INFLUENCING PLANT GROWTH.
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
CA1339896C (en) 1988-01-20 1998-06-02 Robert Vince Dideoxydidehydrocarbocyclic nucleosides
WO1990006671A2 (en) 1988-12-12 1990-06-28 Palese Peter M Methods and compositions for the prophylaxis and treatment of hepatitis b virus infections
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 (en) 1991-01-23 1992-08-06 Gensia, Inc. Adenosine kinase inhibitors
ES2078654T3 (en) 1991-04-06 1995-12-16 Astra Pharma Prod 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 (en) 1991-09-09 1998-04-30 Sankyo Co Process for the preparation of tetrahydrothione nopyridine derivatives useful as a drug
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
ES2108425T3 (en) 1993-02-10 1997-12-16 Astra Pharma Prod ATP ANALOGS REPLACED WITH N-ALKYL-2.
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
EP0840740B1 (en) 1995-07-11 2002-05-02 AstraZeneca AB New inhibitors of platelet aggregation
EP0864572B1 (en) 1995-09-01 2001-04-25 Hokuriku Seiyaku Co., Ltd. Crystal of hydrate and process for preparation thereof
DE69632830T2 (en) 1995-11-21 2005-08-25 Euroscreen S.A. RECEPTOR AND NUCLEIC ACID MOLECULAR CODING THEREFOR
US5948437A (en) 1996-05-23 1999-09-07 Zeneca Limited Pharmaceutical compositions using thiazepine
WO1998028300A1 (en) * 1996-12-20 1998-07-02 Astra Pharmaceuticals Ltd. Triazolo[4,5-d]pyrimidinyl derivatives and their use as medicaments
JPH10258654A (en) 1997-03-18 1998-09-29 Delta Tsuuring:Kk Reclining seat
AR017014A1 (en) * 1997-07-22 2001-08-22 Astrazeneca Ab TRIAZOL COMPOUNDS [4,5-D] PYRIMIDINE, PHARMACEUTICAL COMPOSITIONS, USE OF THE SAME TO PREPARE MEDICATIONS AND PROCESSES FOR THE PREPARATION OF SUCH COMPOUNDS
SE9702775D0 (en) 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9702772D0 (en) * 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9702773D0 (en) 1997-07-22 1997-07-22 Astra Pharma Prod Novel compounds
SE9704709D0 (en) 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 (en) 1999-06-21 2005-05-11 Yamamoto Chemicals, Inc. Polymethine compounds, method of producing the same, and use thereof
SE9903759D0 (en) 1999-10-18 1999-10-18 Astra Ab Pharmaceutically active compounds
WO2001034604A2 (en) 1999-11-12 2001-05-17 Biogen, Inc. Adenosine receptor antagonists and methods of making and using the same
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
BR0215193A (en) 2001-12-21 2004-11-16 Pfizer Prod Inc Directly compressible azithromycin formulations
TWI482772B (en) 2006-08-21 2015-05-01 Astrazeneca Ab Compositions, suitable for oral administration, comprising a triazolo(4,5-d)pyrimidin derivate
ES2558843T3 (en) 2008-09-09 2016-02-09 Astrazeneca Ab Procedure for preparing [1S- [1-alpha, 2-alpha, 3-beta (1S *, 2R *), 5-beta]] - 3- [7- [2- (3,4-difluorophenyl) -cyclopropylamino] -5- (propylthio) -3H-1,2,3-triazolo [4,5-d] pyrimidin-3-yl] -5- (2-hydroxyethoxy) cyclopentane-1,2-diol and its intermediates
CA2788072A1 (en) 2010-02-16 2011-08-25 Actavis Group Ptc Ehf Improved processes for preparing ticagrelor intermediate, 4,6-dichloro-5-nitro-2-(propylthio)pyrimidine
RU2013103794A (en) 2010-06-30 2014-08-10 Актавис Груп Птс Ехф NEW METHODS FOR PRODUCING Phenylcyclopropylamine Derivatives AND THEIR APPLICATION FOR PRODUCING TICAGRELOR
MX2013007115A (en) 2010-12-20 2014-02-10 Actavis Group Ptc Ehf Novel processes for preparing triazolo[4,5-d]pyrimidine derivatives and intermediates thereof.
CA2832570A1 (en) 2011-04-06 2012-10-11 Teva Pharmaceutical Industries Ltd. New intermediates and processes for preparing ticagrelor
US20140206867A1 (en) 2011-06-15 2014-07-24 Actavis Group Ptc Ehf Process for Preparing Cyclopentylamine Derivatives and Intermediates Thereof
BR112014013085A2 (en) 2011-11-30 2017-06-13 Actavis Group Ptc Ehf ticagrelor crystalline form, process for preparing ticagrelor crystalline form, pharmaceutical composition and process for preparing a pharmaceutical composition
WO2013150495A2 (en) 2012-04-05 2013-10-10 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
WO2014083139A1 (en) 2012-11-29 2014-06-05 Actavis Group Ptc Ehf Novel amorphous form of ticagrelor
WO2014102830A1 (en) 2012-12-31 2014-07-03 Megafine Pharma (P) Ltd. A process for preparation of ticagrelor and intermediates thereof
WO2014118808A2 (en) 2013-02-04 2014-08-07 Hetero Research Foundation Ticagrelor solid dispersion
CN107573333B (en) 2013-04-10 2019-10-18 江苏恒瑞医药股份有限公司 The preparation method of intermediate of ticagrelor and preparation method thereof and ticagrelor
WO2014195861A2 (en) 2013-06-04 2014-12-11 Dr. Reddy’S Laboratories Limited Preparation of ticagrelor
WO2016001851A1 (en) 2014-07-02 2016-01-07 Dr. Reddy's Laboratories Limited Preparation of ticagrelor
RU2707959C2 (en) 2015-01-27 2019-12-03 Астразенека Аб Method of treating or preventing atherothrombotic events in patients with myocardial infarction in past history

Also Published As

Publication number Publication date
KR20060091056A (en) 2006-08-17
KR100764417B1 (en) 2007-10-05
BRPI9915883B1 (en) 2015-08-18
US6525060B1 (en) 2003-02-25
CY1111759T1 (en) 2015-10-07
NO319806B1 (en) 2005-09-19
HUP0105081A3 (en) 2004-11-29
DE122011100004I1 (en) 2011-09-08
SK7492001A3 (en) 2002-01-07
NO2011007I2 (en) 2012-07-09
IL143232A (en) 2008-12-29
IL143232A0 (en) 2002-04-21
DE69915675D1 (en) 2004-04-22
US20130072503A1 (en) 2013-03-21
KR100822602B1 (en) 2008-04-16
CZ300373B6 (en) 2009-05-06
CY2011005I1 (en) 2014-04-09
RU2317990C2 (en) 2008-02-27
RU2012121883A (en) 2013-11-27
JP2011016831A (en) 2011-01-27
NO2011007I1 (en) 2011-06-06
HUS1300048I1 (en) 2017-03-28
DE69915675T4 (en) 2012-08-30
DE69915675T2 (en) 2005-02-17
IL198040A (en) 2015-06-30
CA2351709C (en) 2010-04-06
US20100069408A1 (en) 2010-03-18
BR9915883A (en) 2001-08-21
KR100776484B1 (en) 2007-11-28
PT1135391E (en) 2004-07-30
JP2007084551A (en) 2007-04-05
CN1128801C (en) 2003-11-26
EP1135391A1 (en) 2001-09-26
IL183969A (en) 2011-03-31
RU2007133926A (en) 2009-03-20
ID29927A (en) 2001-10-25
CZ20011962A3 (en) 2001-11-14
PL348724A1 (en) 2002-06-03
AR023920A1 (en) 2002-09-04
CN1334816A (en) 2002-02-06
MY121867A (en) 2006-02-28
CY2011005I2 (en) 2014-04-09
KR20070086540A (en) 2007-08-27
US6974868B2 (en) 2005-12-13
US20120165348A1 (en) 2012-06-28
EG24814A (en) 2010-09-21
HK1039933B (en) 2004-10-08
EP1386917A1 (en) 2004-02-04
HK1061246A1 (en) 2004-09-10
SK286007B6 (en) 2008-01-07
US20080214812A1 (en) 2008-09-04
US20030144305A1 (en) 2003-07-31
US7250419B2 (en) 2007-07-31
NO20012725D0 (en) 2001-06-01
BRPI9915883B8 (en) 2021-05-25
CZ300280B6 (en) 2009-04-08
EP1386921A1 (en) 2004-02-04
PT1386921E (en) 2009-02-23
JP2008266345A (en) 2008-11-06
AU2016500A (en) 2000-06-26
LTPA2011004I1 (en) 2022-04-11
USRE46276E1 (en) 2017-01-17
IL198040A0 (en) 2009-12-24
NZ511778A (en) 2003-10-31
HUP0105081A2 (en) 2002-05-29
FR11C0016I1 (en) 2011-07-08
US20150152111A1 (en) 2015-06-04
AU766618B2 (en) 2003-10-23
IL169013A (en) 2015-10-29
SI1135391T1 (en) 2004-08-31
ATE513816T1 (en) 2011-07-15
RU2593201C2 (en) 2016-08-10
US20070265282A1 (en) 2007-11-15
LTC1135391I2 (en) 2022-04-11
ES2366902T3 (en) 2011-10-26
JP4202607B2 (en) 2008-12-24
ZA200104094B (en) 2002-08-19
ATE418547T1 (en) 2009-01-15
TWI229674B (en) 2005-03-21
EP2322513A3 (en) 2011-08-24
KR20070007971A (en) 2007-01-16
JP5043749B2 (en) 2012-10-10
DK1386917T3 (en) 2011-08-29
WO2000034283A1 (en) 2000-06-15
CA2351709A1 (en) 2000-06-15
SI1386917T1 (en) 2011-09-30
HK1061684A1 (en) 2004-09-30
LU91819I2 (en) 2011-08-01
EP1386917B1 (en) 2011-06-22
EP1135391B1 (en) 2004-03-17
US20060025590A1 (en) 2006-02-02
EP1386909A1 (en) 2004-02-04
DK1386921T3 (en) 2009-03-23
TR200101567T2 (en) 2001-12-21
CZ295234B6 (en) 2005-06-15
US20140296258A1 (en) 2014-10-02
AR058967A2 (en) 2008-03-05
SA99200848B1 (en) 2006-11-04
EP1386921B1 (en) 2008-12-24
PL201283B1 (en) 2009-03-31
JP2002531567A (en) 2002-09-24
HU228589B1 (en) 2013-04-29
DK1135391T3 (en) 2004-06-28
AR072756A2 (en) 2010-09-22
IL183969A0 (en) 2009-02-11
US20130109702A1 (en) 2013-05-02
JP5415383B2 (en) 2014-02-12
KR20010081054A (en) 2001-08-25
SI1386921T1 (en) 2009-04-30
CY1110501T1 (en) 2015-04-29
KR100742924B1 (en) 2007-07-25
HK1039933A1 (en) 2002-05-17
DE69940171D1 (en) 2009-02-05
IL210398A0 (en) 2011-03-31
NO20012725L (en) 2001-07-31
ATE261970T1 (en) 2004-04-15
EP2322513A2 (en) 2011-05-18
ES2216623T3 (en) 2004-10-16
ES2318081T3 (en) 2009-05-01

Similar Documents

Publication Publication Date Title
FR11C0016I2 (en) NEW TRIAZOLO(4,5-D)PYRIMIDINE COMPOUNDS
IS2461B (en) Pyrrolo [2,3-dl] pyrimidine compounds
FR14C0019I2 (en) PYRROLO 2,3d]PYRIMIDINE COMPOUNDS
IS2236B (en) Triazolo (4,5-d) pyrimidine derivatives as anti-thrombotic agents
EE05351B1 (en) Pyrrolo [2,3-d] pyrimidine compounds
NO20021694D0 (en) Pyrazolo [4,3-d] pyrimidine
DE59903421D1 (en) DIHYDRO [1,2,3] triazolo [4,5-D] PYRIMIDINE-7-ON
NO20004089D0 (en) New triazolo (4,5-d) pyrimidine compounds
DE50001191D1 (en) PYRAZOLO [4, 3-D] PYRIMIDINE
SI0996621T1 (en) TRIAZOLO(4,5-d)PYRIMIDINE DERIVATIVES AS ANTI-THROMBOTIC AGENTS