UA73181C2 - CRYSTALLINE AND AMORPHOUS FORMS OF TRIAZOL(4,5-d)PIRIMIDIN, METHOD FOR OBTAINING THEREOF, PHARMACEUTICAL COMPOSITON AND METHOD OF THERAPY OR PROPHILAXIS OF ARTERIAL THROMBOTIC COMPLICATIONS - Google Patents
CRYSTALLINE AND AMORPHOUS FORMS OF TRIAZOL(4,5-d)PIRIMIDIN, METHOD FOR OBTAINING THEREOF, PHARMACEUTICAL COMPOSITON AND METHOD OF THERAPY OR PROPHILAXIS OF ARTERIAL THROMBOTIC COMPLICATIONS Download PDFInfo
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- UA73181C2 UA73181C2 UA20021210808A UA20021210808A UA73181C2 UA 73181 C2 UA73181 C2 UA 73181C2 UA 20021210808 A UA20021210808 A UA 20021210808A UA 20021210808 A UA20021210808 A UA 20021210808A UA 73181 C2 UA73181 C2 UA 73181C2
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- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
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- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0013407.2A GB0013407D0 (en) | 2000-06-02 | 2000-06-02 | Forms of a chemical compound |
PCT/SE2001/001239 WO2001092262A1 (en) | 2000-06-02 | 2001-05-31 | New crystalline and amorphous form of a triazolo(4,5-d)pyrimidine compound |
Publications (1)
Publication Number | Publication Date |
---|---|
UA73181C2 true UA73181C2 (en) | 2005-06-15 |
Family
ID=9892841
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA20021210808A UA73181C2 (en) | 2000-06-02 | 2001-05-31 | CRYSTALLINE AND AMORPHOUS FORMS OF TRIAZOL(4,5-d)PIRIMIDIN, METHOD FOR OBTAINING THEREOF, PHARMACEUTICAL COMPOSITON AND METHOD OF THERAPY OR PROPHILAXIS OF ARTERIAL THROMBOTIC COMPLICATIONS |
Country Status (36)
Country | Link |
---|---|
US (3) | US20030181469A1 (de) |
EP (3) | EP2292622A1 (de) |
JP (3) | JP5036947B2 (de) |
KR (1) | KR100781864B1 (de) |
CN (2) | CN1817883B (de) |
AR (2) | AR032335A1 (de) |
AT (2) | ATE555115T1 (de) |
AU (4) | AU6287401A (de) |
BG (3) | BG65837B1 (de) |
BR (1) | BR0111328A (de) |
CA (1) | CA2408596C (de) |
CY (1) | CY1113047T1 (de) |
CZ (2) | CZ307468B6 (de) |
DE (1) | DE60117972T2 (de) |
DK (2) | DK1493745T3 (de) |
EE (1) | EE05222B1 (de) |
ES (2) | ES2384708T3 (de) |
GB (1) | GB0013407D0 (de) |
HK (2) | HK1052347B (de) |
HU (2) | HU229374B1 (de) |
IL (4) | IL152777A0 (de) |
IS (2) | IS2609B (de) |
MX (1) | MXPA02011795A (de) |
MY (2) | MY140674A (de) |
NO (3) | NO323780B1 (de) |
NZ (1) | NZ522638A (de) |
PH (1) | PH12011000127A1 (de) |
PL (2) | PL359172A1 (de) |
PT (2) | PT1493745E (de) |
RU (3) | RU2325391C2 (de) |
SG (1) | SG135965A1 (de) |
SI (2) | SI1289992T1 (de) |
SK (1) | SK287817B6 (de) |
UA (1) | UA73181C2 (de) |
WO (1) | WO2001092262A1 (de) |
ZA (1) | ZA200209324B (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114634489A (zh) * | 2022-04-19 | 2022-06-17 | 奎马特里克斯有限公司 | 结晶形式 |
Families Citing this family (65)
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 |
GB0013488D0 (en) * | 2000-06-02 | 2000-07-26 | Astrazeneca Ab | Chemical compound |
GB0013407D0 (en) | 2000-06-02 | 2000-07-26 | Astrazeneca Ab | Forms of a chemical compound |
JP4298212B2 (ja) * | 2002-03-29 | 2009-07-15 | 大日本印刷株式会社 | 塩酸エピナスチン高融点型結晶の製造法 |
WO2008024044A1 (en) * | 2006-08-21 | 2008-02-28 | Astrazeneca Ab | Compositions, suitable for oral administration, comprising a triazolo [4, 5] pyrimidin derivate |
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 |
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 |
KR101473207B1 (ko) * | 2007-04-13 | 2014-12-16 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | Xa 인자 억제제로서 작용하는 화합물과의 병용 항응고 요법 |
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 |
EP2340252B1 (de) | 2008-09-09 | 2015-11-11 | AstraZeneca AB | Verfahren zur herstellung von [1s-[1-alpha, 2-alpha, 3-beta(1s*,2r*)5-beta]]-3-[7-[2-(3,4- difluorphenyl)cyclopropylamino]-5- (propylthio)-3h-1,2,3-triazolo[4,5-d] pyrimidin-3-yl]-5-(2-hydroxyethoxy) cyclopentan-1,2-diol und zwischenprodukten davon |
CA2768043A1 (en) | 2009-07-27 | 2011-02-10 | Auspex Pharmaceuticals, Inc. | Cyclopropyl modulators of p2y12 receptor |
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 |
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 |
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 |
RU2014126351A (ru) * | 2011-11-30 | 2016-01-27 | Актавис Груп Птс Ехф | Новая кристаллическая форма тикагрелора и способ ее получения |
EP2834247A4 (de) | 2012-04-05 | 2016-03-30 | Reddys Lab Ltd Dr | Herstellung von ticagrelor |
WO2014000719A1 (en) | 2012-06-29 | 2014-01-03 | Zentiva, K.S. | Novel pharmaceutical solid forms of (1s,2s,3r,5s)-3-[7-[(1r,2s)-2-(3,4difluorophenyl)cyclopropylamino]-5-(propylthio)-3h-[1,2,3]triazolo[4,5-d]pyrimidin-3yl]-5-(2-hydroxyethoxy)cyclopentane-l,2-diol |
CA2877541C (en) | 2012-07-04 | 2020-06-30 | Lek Pharmaceuticals D.D. | Ticagrelor adducts with divalent metal salts |
CZ2012705A3 (cs) | 2012-10-16 | 2014-04-23 | Zentiva, K.S. | Pevná orální farmaceutická formulace obsahující ticagrelor |
CN103772393B (zh) * | 2012-10-18 | 2017-08-04 | 博瑞生物医药(苏州)股份有限公司 | 替卡格雷的晶型及其制备方法 |
WO2014083139A1 (en) * | 2012-11-29 | 2014-06-05 | Actavis Group Ptc Ehf | Novel amorphous form of ticagrelor |
CN103848836B (zh) * | 2012-12-07 | 2016-08-03 | 天津市汉康医药生物技术有限公司 | 替卡格雷倍半水合物及其制备方法 |
WO2014118808A2 (en) * | 2013-02-04 | 2014-08-07 | Hetero Research Foundation | Ticagrelor solid dispersion |
CZ307217B6 (cs) | 2013-03-14 | 2018-04-04 | Zentiva, K.S. | Zlepšený způsob výroby a nové intermediáty syntézy ticagreloru |
WO2014155389A2 (en) * | 2013-03-25 | 2014-10-02 | Glenmark Pharmaceuticals Limited; Glenmark Generics Limited | Process for preparation of ticagrelor |
CN104098570A (zh) * | 2013-04-07 | 2014-10-15 | 杭州领业医药科技有限公司 | 替卡格雷晶型及其制备方法和用途 |
CN104098572A (zh) * | 2013-04-08 | 2014-10-15 | 博瑞生物医药技术(苏州)有限公司 | 替卡格雷共晶型 |
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 (de) | 2013-06-10 | 2014-12-17 | Zentiva, a.s. | Stabilisiertes amorphes Ticagrelor |
WO2014170026A1 (en) | 2013-04-18 | 2014-10-23 | Zentiva, K.S. | Stabilized amorphous ticagrelor |
WO2014191321A1 (en) | 2013-05-29 | 2014-12-04 | Ratiopharm Gmbh | Solid pharmaceutical dosage form |
CN106496234B (zh) * | 2013-06-03 | 2019-08-30 | 杭州领业医药科技有限公司 | 结晶形态的三唑[4,5-d]嘧啶化合物及其制备方法和用途 |
EP3004113A2 (de) * | 2013-06-04 | 2016-04-13 | Dr. Reddy's Laboratories Ltd. | Herstellung von ticagrelor |
EP2816043A1 (de) | 2013-06-21 | 2014-12-24 | LEK Pharmaceuticals d.d. | Kugelförmige Ticagrelorteilchen |
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