CY1113992T1 - Αναλογα κιναζολινης ως αναστολεις υποδοχεων κινασης της τυροσινης - Google Patents
Αναλογα κιναζολινης ως αναστολεις υποδοχεων κινασης της τυροσινηςInfo
- Publication number
- CY1113992T1 CY1113992T1 CY20131100122T CY131100122T CY1113992T1 CY 1113992 T1 CY1113992 T1 CY 1113992T1 CY 20131100122 T CY20131100122 T CY 20131100122T CY 131100122 T CY131100122 T CY 131100122T CY 1113992 T1 CY1113992 T1 CY 1113992T1
- Authority
- CY
- Cyprus
- Prior art keywords
- tyrosine kinase
- inhibitors
- kinazolin
- analogues
- kinase receptors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Η παρούσα εφεύρεση παρέχει ανάλογα κιναζολίνης του Τύπου (I): όπου το Α είναι συνδεδεμένο με τουλάχιστον ένα από τους άνθρακες στις θέσεις 5, 6, 7 ή 8 θέση του δικυκλικού δακτυλίου, και ο δακτύλιος είναι υποκατεστημένος με έως και δύο ανεξάρτητες R 3 ομάδες. Η εφεύρεση περιλαμβάνει επίσης μεθόδους χρήσης των ενώσεων του τύπου (I) ως αναστολέων υποδοχέων τύπου I της κινάσης της τυροσίνης και την θεραπευτική αγωγή των υπερπολλαπλασιαστικών νόσων όπως ο καρκίνος.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/642,440 US7501427B2 (en) | 2003-08-14 | 2003-08-14 | Quinazoline analogs as receptor tyrosine kinase inhibitors |
US55171804P | 2004-03-10 | 2004-03-10 | |
EP04780990A EP1660090B1 (en) | 2003-08-14 | 2004-08-10 | Quinazoline analogs as receptor tyrosine kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1113992T1 true CY1113992T1 (el) | 2016-07-27 |
Family
ID=34198338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20131100122T CY1113992T1 (el) | 2003-08-14 | 2013-02-08 | Αναλογα κιναζολινης ως αναστολεις υποδοχεων κινασης της τυροσινης |
Country Status (24)
Country | Link |
---|---|
US (2) | US7452895B2 (el) |
EP (1) | EP1660090B1 (el) |
JP (1) | JP4828421B2 (el) |
KR (2) | KR100953246B1 (el) |
CN (3) | CN102432552B (el) |
AR (1) | AR045378A1 (el) |
AU (1) | AU2004264937B2 (el) |
BR (1) | BRPI0413565B8 (el) |
CA (1) | CA2535614C (el) |
CL (1) | CL2004002066A1 (el) |
CY (1) | CY1113992T1 (el) |
DK (1) | DK1660090T3 (el) |
ES (1) | ES2399427T3 (el) |
HK (1) | HK1085400A1 (el) |
IL (1) | IL173593A (el) |
IS (1) | IS8288A (el) |
MX (1) | MXPA06001767A (el) |
NO (1) | NO336275B1 (el) |
NZ (1) | NZ545459A (el) |
PL (1) | PL1660090T3 (el) |
PT (1) | PT1660090E (el) |
RU (1) | RU2350605C2 (el) |
TW (1) | TWI353982B (el) |
WO (1) | WO2005016346A1 (el) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7488823B2 (en) * | 2003-11-10 | 2009-02-10 | Array Biopharma, Inc. | Cyanoguanidines and cyanoamidines as ErbB2 and EGFR inhibitors |
US7501427B2 (en) | 2003-08-14 | 2009-03-10 | Array Biopharma, Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
CA2535614C (en) * | 2003-08-14 | 2009-12-22 | Array Biopharma Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
PL1971601T3 (pl) | 2005-11-15 | 2010-03-31 | Array Biopharma Inc | Pochodne N4-fenylo-chinazolino-4-aminy i związki pokrewne jako inhibitory receptorowych kinaz tyrozynowych ErbB typu I do leczenia chorób cechujących się nadmierną proliferacją komórek |
CA2852060A1 (en) | 2011-10-14 | 2013-04-18 | Array Biopharma Inc. | Polymorphs of arry-380, a selective herb2 inhibitor and pharmaceutical compositions containing them |
SI2765990T1 (sl) | 2011-10-14 | 2017-11-30 | Array Biopharma, Inc. | Trdna disperzija |
RS57140B1 (sr) | 2012-03-23 | 2018-07-31 | Array Biopharma Inc | Amorfna čvrsta disperzija za korišćenje u lečenju raka mozga |
WO2017037292A1 (en) | 2015-09-04 | 2017-03-09 | Aslan Pharmaceuticals Pte Limited | Combination of a dhodh inhibitor and a her inhibitor for use in the treatment of cancer |
US20190134034A1 (en) * | 2016-04-21 | 2019-05-09 | Aslan Pharmaceuticals Pte. Ltd. | Method of Treating Liver Cancer |
GB201611580D0 (en) * | 2016-07-01 | 2016-08-17 | Aslan Pharmaceuticals Pte Ltd | Method |
CN106279135A (zh) * | 2016-08-09 | 2017-01-04 | 浙江医药高等专科学校 | 一种噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂 |
CN106349231A (zh) * | 2016-08-09 | 2017-01-25 | 浙江医药高等专科学校 | 一类含卤代噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂 |
CN106317040A (zh) * | 2016-08-09 | 2017-01-11 | 浙江医药高等专科学校 | 含噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂、制备方法及用途 |
CN106317039A (zh) * | 2016-08-09 | 2017-01-11 | 浙江医药高等专科学校 | 一种含噻吩磺酰胺结构的乙氧苯并喹唑啉类酪氨酸激酶抑制剂、制备方法及用途 |
CN106349230A (zh) * | 2016-08-09 | 2017-01-25 | 浙江医药高等专科学校 | 一种含硝基噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂及用途 |
WO2018038684A1 (en) | 2016-08-26 | 2018-03-01 | Agency For Science, Technology And Research | Macrophage stimulating protein receptor (or ron - recepteur d' origine nantais) antibodies and uses thereof |
WO2018160138A1 (en) | 2017-03-02 | 2018-09-07 | Aslan Pharmaceuticals Pte Ltd | Dhodh inhibitor for treating haematological cancer |
AU2018258663B2 (en) | 2017-04-28 | 2022-08-04 | Seagen Inc. | Treatment of HER2 positive cancers |
WO2018222134A1 (en) | 2017-06-02 | 2018-12-06 | Aslan Pharmaceuticals Pte Ltd | Cancer therapy |
WO2018222135A1 (en) | 2017-06-02 | 2018-12-06 | Aslan Pharmaceuticals Pte Ltd | Cancer therapy |
EP4360713A3 (en) | 2018-09-18 | 2024-05-22 | F. Hoffmann-La Roche AG | Quinazoline derivatives as antitumor agents |
SG11202104073XA (en) * | 2018-10-09 | 2021-05-28 | Aslan Pharmaceuticals Pte Ltd | Malonate salt of varlitinib |
CN111499622B (zh) * | 2019-07-08 | 2023-06-06 | 山东省科学院菏泽分院 | 一种治疗胆管癌的药物的制备方法 |
TW202214641A (zh) | 2020-06-30 | 2022-04-16 | 美商艾瑞生藥股份有限公司 | Her2突變抑制劑 |
AU2023243776A1 (en) * | 2022-03-28 | 2024-09-12 | Jiangsu Hengrui Pharmaceuticals Co., Ltd. | Nitrogen-containing heterocyclic compound, preparation method therefor, and pharmaceutical application thereof |
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AR004010A1 (es) | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
PL194689B1 (pl) | 1996-02-13 | 2007-06-29 | Astrazeneca Uk Ltd | Pochodne chinazoliny, ich kompozycje farmaceutyczne oraz ich zastosowania |
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PL190489B1 (pl) | 1996-04-12 | 2005-12-30 | Warner Lambert Co | Nieodwracalne inhibitory kinaz tyrozyny, kompozycja farmaceutyczna je zawierająca i ich zastosowanie |
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CA2355470C (en) | 1999-01-13 | 2008-09-30 | Warner-Lambert Company | Benzoheterocycles and their use as mek inhibitors |
PL205557B1 (pl) * | 1999-02-10 | 2010-05-31 | Astrazeneca Ab | Pochodne indolu |
WO2001021594A1 (en) | 1999-09-21 | 2001-03-29 | Astrazeneca Ab | Quinazoline compounds and pharmaceutical compositions containing them |
GB9922171D0 (en) * | 1999-09-21 | 1999-11-17 | Zeneca Ltd | Chemical compounds |
WO2001060784A1 (en) | 2000-02-17 | 2001-08-23 | Bristol-Myers Squibb Co. | Aniline-derived ligands for the thyroid receptor |
PT1287001E (pt) | 2000-06-06 | 2004-12-31 | Pfizer Prod Inc | Derivados de tiofeno uteis como agentes anticancerigenos |
MXPA02012870A (es) | 2000-06-22 | 2003-05-14 | Pfizer Prod Inc | Derivados biciclicos sustituidos para el tratamiento del crecimiento celular anormal. |
BR0111947A (pt) * | 2000-06-30 | 2003-05-06 | Glaxo Group Ltd | Composto, composição farmacêutica, método para o tratamento de um distúrbio em um mamìfero, uso de um composto e processo para preparar, um composto |
WO2003015778A1 (en) | 2001-08-17 | 2003-02-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
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KR20050042055A (ko) * | 2001-11-03 | 2005-05-04 | 아스트라제네카 아베 | 항종양제로서의 퀴나졸린 유도체 |
ATE446093T1 (de) * | 2001-12-24 | 2009-11-15 | Astrazeneca Ab | Substituierte chinazolin-derivate als aurora- kinase inhibitoren |
US7488823B2 (en) | 2003-11-10 | 2009-02-10 | Array Biopharma, Inc. | Cyanoguanidines and cyanoamidines as ErbB2 and EGFR inhibitors |
JP2006515871A (ja) | 2003-01-23 | 2006-06-08 | ティー.ケイ. シグナル リミテッド | 上皮増殖因子受容体チロシンキナーゼの不可逆阻害剤ならびにその使用 |
PE20040945A1 (es) | 2003-02-05 | 2004-12-14 | Warner Lambert Co | Preparacion de quinazolinas substituidas |
BRPI0410720A (pt) | 2003-05-27 | 2006-06-20 | Pfizer Prod Inc | quinazolinas e pirido[3,4-d]pirimidinas como inibidores do receptor de tirosina cinase |
US7501427B2 (en) * | 2003-08-14 | 2009-03-10 | Array Biopharma, Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
CA2535614C (en) | 2003-08-14 | 2009-12-22 | Array Biopharma Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
MXPA06001989A (es) | 2003-08-18 | 2006-05-17 | Pfizer Prod Inc | Programa de dosificacion para un nuevo agente anticanceroso. |
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KR100735639B1 (ko) | 2004-12-29 | 2007-07-04 | 한미약품 주식회사 | 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 및 이의제조방법 |
PL1971601T3 (pl) | 2005-11-15 | 2010-03-31 | Array Biopharma Inc | Pochodne N4-fenylo-chinazolino-4-aminy i związki pokrewne jako inhibitory receptorowych kinaz tyrozynowych ErbB typu I do leczenia chorób cechujących się nadmierną proliferacją komórek |
-
2004
- 2004-08-10 CA CA002535614A patent/CA2535614C/en not_active Expired - Lifetime
- 2004-08-10 WO PCT/US2004/026235 patent/WO2005016346A1/en active Application Filing
- 2004-08-10 EP EP04780990A patent/EP1660090B1/en not_active Expired - Lifetime
- 2004-08-10 CN CN201110283526.1A patent/CN102432552B/zh not_active Expired - Lifetime
- 2004-08-10 CN CN201310428856.4A patent/CN103664802B/zh not_active Expired - Lifetime
- 2004-08-10 RU RU2006103493/04A patent/RU2350605C2/ru active
- 2004-08-10 BR BRPI0413565A patent/BRPI0413565B8/pt active IP Right Grant
- 2004-08-10 US US10/914,974 patent/US7452895B2/en active Active
- 2004-08-10 PL PL04780990T patent/PL1660090T3/pl unknown
- 2004-08-10 ES ES04780990T patent/ES2399427T3/es not_active Expired - Lifetime
- 2004-08-10 CN CN201310581100.3A patent/CN103772373B/zh not_active Expired - Lifetime
- 2004-08-10 KR KR1020067003060A patent/KR100953246B1/ko active IP Right Grant
- 2004-08-10 PT PT47809900T patent/PT1660090E/pt unknown
- 2004-08-10 DK DK04780990.0T patent/DK1660090T3/da active
- 2004-08-10 KR KR1020107000942A patent/KR101028952B1/ko active IP Right Grant
- 2004-08-10 NZ NZ545459A patent/NZ545459A/en unknown
- 2004-08-10 JP JP2006523384A patent/JP4828421B2/ja not_active Expired - Lifetime
- 2004-08-10 MX MXPA06001767A patent/MXPA06001767A/es active IP Right Grant
- 2004-08-10 AU AU2004264937A patent/AU2004264937B2/en active Active
- 2004-08-13 CL CL200402066A patent/CL2004002066A1/es unknown
- 2004-08-13 AR ARP040102929A patent/AR045378A1/es active IP Right Grant
- 2004-08-13 TW TW093124336A patent/TWI353982B/zh active
-
2006
- 2006-02-07 IS IS8288A patent/IS8288A/is unknown
- 2006-02-07 IL IL173593A patent/IL173593A/en active IP Right Grant
- 2006-03-13 NO NO20061171A patent/NO336275B1/no unknown
- 2006-06-05 HK HK06106407.8A patent/HK1085400A1/xx not_active IP Right Cessation
-
2008
- 2008-10-10 US US12/249,421 patent/US8278314B2/en active Active
-
2013
- 2013-02-08 CY CY20131100122T patent/CY1113992T1/el unknown
Also Published As
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---|---|---|
CY1113992T1 (el) | Αναλογα κιναζολινης ως αναστολεις υποδοχεων κινασης της τυροσινης | |
HN2002000067A (es) | Inhibidores de la rho - quinasa. | |
UY27225A1 (es) | Inhibidores de la rho-quinasa | |
CR7643A (es) | Derivados de 1-heterociclialquil -3-sulfonilazaindol o azaindazol como ligandos de 5-hidroxitriptamina-6 | |
CY1116610T1 (el) | Ετεροδιμερη γλουτamiνiκου οξεος | |
CY1118112T1 (el) | Διυποκατεστημενες βενζοθειενυλ-πυρρολοτριαζινες και η χρηση τους ως αναστολεις κινασης υποδοχεα του αυξητικου παραγοντα των ινοβλαστων (fgfr) | |
EA200801001A1 (ru) | Соединения, которые обладают активностью по отношению к рецепторам м, и их применения в медицине | |
CY1108186T1 (el) | Παραγωγα κουιναζολινης ως αναστολεις της κινασης τυροσινης | |
CY1114277T1 (el) | ΕΝΩΣΕΙΣ ΙΜΙΔΑΖΟ[1,2-a]ΠΥΡΙΔΙΝΗΣ ΩΣ ΑΝΑΣΤΟΛΕΙΣ ΥΠΟΔΟΧΕΑ ΚΙΝΑΣΗΣ ΤΥΡΟΣΙΝΗΣ | |
CY1105053T1 (el) | Υποκατεστημενες ομοιαζουσες με ινδολιζινη ενωσεις και μεθοδοι χρησης | |
CY1106405T1 (el) | Παραγωγα κουιναζολινης | |
CY1108378T1 (el) | 4-υποκατεστημενα παραγωγα 1-αμινοκυκλοεξανιου για την χρησιμοποιηση σαν προσδεματα υποδοχεα orl1 ή οπιακου υποδοχεα mu | |
CY1113324T1 (el) | Υποκατεστημενα αμιδικα παραγωγα ως αναστολεις πρωτεϊνικων κινασων | |
EA200501504A1 (ru) | Лиганды каннабиноидных рецепторов и их применение | |
PE20021010A1 (es) | Derivados espirociclicos como inhibidores de fosfodiesterasa-7 | |
CR8530A (es) | Intermediarios de quinolona como inhibidores de receptores de tirosina quinasas y la sintesis de los mismos | |
UY27551A1 (es) | Derivados de benzotiazol | |
ECSP055964A (es) | Heterociclil-3-sulfonilindazoles como ligandos de 5-hidroxitriptamina-6 | |
CY1109662T1 (el) | Ενωσεις πυρρολοτριαζινης ως αναστολεις κινασης | |
CY1105705T1 (el) | Παραγωγα ινδολυλαλκυλαμινης σαν συνδετηρες 5-υδροξυτρυπταμινης-6 | |
UY28516A1 (es) | Derivados de quinazolina | |
DE602005023732D1 (de) | Pyrrolotriazinverbindungen | |
ECSP055693A (es) | Proceso para la síntesis de intermediarios útiles para la síntesis de inhibidores de la tubulina | |
ECSP034811A (es) | Derivados heterocicliloxi-, -tioxi - y - aminobenzazole tales como ligandos 5-hidroxitriptamina-6 | |
ECSP045473A (es) | Derivados de 1-(aminoalquil)-3-sulfonilindol y 1-aminoalquil-3-sulfonilindazol como ligandos de 5-hidroxitriptamina-6 |